G. Oldroyd, J. D. Murray, P. S. Poole, and J. A. Downie, The Rules of Engagement in the Legume-Rhizobial Symbiosis, 2011.

, Annual Review of Genetics, vol.45, pp.472-489

C. Wang, X. Zhang, Y. Fan, Y. Gao, Q. Zhu et al., XA23 Is an executor r protein 702 and confers broad-spectrum disease resistance in rice, Molecular Plant, vol.8, pp.290-302, 2015.

C. S. Wortmann, R. A. Kirkby, C. A. Eledu, and D. J. Allen, Atlas of common bean, 1998.

, Africa. Centro Internacional de Agricultura Tropical (CIAT), vol.297, p.133

K. Yang, Z. Tian, C. Chen, L. Luo, B. Zhao et al., Genome sequencing of adzuki bean 706 (Vigna angularis) provides insight into high starch and low fat accumulation and domestication, Proceedings of the 707 National Academy of Sciences of the United States of America, vol.112, pp.13213-13221, 2015.

N. D. Young, F. Debellé, G. Oldroyd, R. Geurts, S. B. Cannon et al.,

H. , The Medicago genome provides insight into the evolution of rhizobial symbioses, Nature, vol.480, pp.520-524, 2011.

J. M. Young, D. C. Park, H. M. Shearman, and E. Fargier, A multilocus sequence analysis of the genus Xanthomonas, 2008.

, Systematic and Applied Microbiology, vol.31, pp.366-377

K. Yu, S. J. Park, and V. Poysa, Marker-assisted selection of common beans for resistance to common bacterial blight: 713 Efficacy and economics, Plant Breeding, vol.119, pp.411-415, 2000.

H. H. Zahran, Rhizobium-legume symbiosis and nitrogen fixation under severe conditions and in an arid climate, 1999.

, Microbiology and molecular biology reviews : MMBR, vol.63, pp.968-89

X. Zeng, D. Tian, K. Gu, Z. Zhou, X. Yang et al., Genetic engineering of the Xa10 promoter for 717 broad-spectrum and durable resistance to Xanthomonas oryzae pv. oryzae, Plant Biotechnology Journal, vol.13, pp.993-1001, 2015.

, E-mail addresses of all authors, p.11

, Mylène Ruh: mylene.ruh@agrocampus-ouest.fr

, Justine Foucher: justine.foucher@inra.fr

, Anne Préveaux: anne.preveaux@inra.fr

, Sébastien Carrère: sebastien.carrere@toulouse.inra.fr

, Martial Briand: martial.briand@inra.fr

S. Becker,

J. Boch,

M. Jacques,

W. G. Nicolas and . Chen,

Y. Jiang, L. Guo, X. Ma, X. Zhao, B. Jiao et al., The WRKY transcription factors PtrWRKY18 and PtrWRKY35 593 promote Melampsora resistance in Populus, Tree Physiology, vol.37, pp.665-675, 2017.
DOI : 10.1093/treephys/tpx008

URL : https://academic.oup.com/treephys/article-pdf/37/5/665/19484767/tpx008.pdf

A. Juillerat, C. Bertonati, G. Dubois, V. Guyot, S. Thomas et al., BurrH: a new modular DNA binding protein for genome engineering, Scientific reports, vol.595, p.3831, 2014.
DOI : 10.1038/srep03831

URL : https://hal.archives-ouvertes.fr/hal-01606222

S. Kay, J. Boch, and U. Bonas, Characterization of AvrBs3-like effectors from a Brassicaceae pathogen reveals virulence 597 and avirulence activities and a protein with a novel repeat architecture. Molecular plant-microbe interactions, MPMI, vol.18, pp.598-838, 2005.

S. Kay, S. Hahn, E. Marois, G. Hause, and U. Bonas, A bacterial effector acts as a plant transcription factor and induces 600 a cell size regulator, Science, vol.318, pp.648-651, 2007.
DOI : 10.1126/science.1144956

S. Kay, S. Hahn, E. Marois, R. Wieduwild, and U. Bonas, Detailed analysis of the DNA recognition motifs of the 602 Xanthomonas type III effectors AvrBs3 and AvrBs3Deltarep16, Plant Journal, vol.59, pp.859-871, 2009.

J. Krüger, C. M. Thomas, C. Golstein, M. S. Dixon, M. Smoker et al., , p.604, 2002.

, Protease Required for Cf-2-Dependent Disease Resistance and Suppression of Autonecrosis, Science, vol.296, pp.744-747

O. De-lange, T. Schreiber, N. Schandry, J. Radeck, K. H. Braun et al., , 2013.

, Breaking the DNA-binding code of Ralstonia solanacearum TAL effectors provides new possibilities to generate plant 607 resistance genes against bacterial wilt disease, New Phytologist, vol.199, pp.773-786

O. De-lange, . De, C. Wolf, J. Dietze, J. Elsaesser et al., Programmable DNA-binding proteins from, p.609, 2014.

, Burkholderia provide a fresh perspective on the TALE-like repeat domain, Nucleic Acids Research, vol.42, pp.7436-7449

O. De-lange, C. Wolf, P. Thiel, J. Krüger, C. Kleusch et al., DNA-binding proteins from marine 611 bacteria expand the known sequence diversity of TALE-like repeats, Nucleic Acids Research, vol.43, pp.10065-10080, 2015.

Y. Leng, Y. Yang, D. Ren, L. Huang, L. Dai et al., A rice PECTATE LYASE-LIKE 613 gene is required for plant growth and leaf senescence, Plant Physiology, vol.174, pp.1151-1166, 2017.

L. Li, A. Atef, A. Piatek, Z. Ali, M. Piatek et al., , 2013.

, Characterization and DNA-binding specificities of Ralstonia TAL-like effectors, Molecular Plant, vol.6, pp.1318-1330

C. Li, J. Wei, Y. Lin, and H. Chen, Gene silencing using the recessive rice bacterial blight resistance gene xa13 as a new 617 paradigm in plant breeding, Plant Cell Reports, vol.31, pp.851-862, 2012.

M. I. Love, W. Huber, and S. Anders, Moderated estimation of fold change and dispersion for RNA-seq data with, 2014.

. Deseq2, Genome Biology, vol.15, pp.1-21

A. Mak, P. Bradley, A. J. Bogdanove, and B. L. Stoddard, TAL effectors: Function, structure, engineering and 621 applications, Current Opinion in Structural Biology, vol.23, pp.93-99, 2013.

A. N. Mak, P. Bradley, R. A. Cernadas, A. J. Bogdanove, and B. L. Stoddard, The Crystal Structre of TAL Effector PthXo1 623 Bound to Its DNA Target, Science, vol.335, pp.716-719, 2012.

A. C. Mallory and H. Vaucheret, Functions of microRNAs and related small RNAs in plants, Nature Genetics, vol.38, p.31, 2006.

M. C. Marín-rodríguez, J. Orchard, and G. B. Seymour, Pectate lyases, cell wall degradation and fruit softening, Journal 627 of Experimental Botany, vol.53, pp.2115-2119, 2002.

N. Mhedbi-hajri, A. Darrasse, S. Pigné, K. Durand, S. Fouteau et al., , 2011.

, Sensing and adhesion are adaptive functions in the plant pathogenic xanthomonads, BMC evolutionary biology, vol.11, p.67

J. C. Misas-villamil, R. Van-der-hoorn, and G. Doehlemann, Papain-like cysteine proteases as hubs in plant 631 immunity, New Phytologist, vol.212, pp.902-907, 2016.

M. J. Moscou and A. J. Bogdanove, A simple cipher governs DNA recognition by TAL effectors, Science, vol.326, p.1501, 2009.

T. Nakagawa, T. Kurose, T. Hino, K. Tanaka, M. Kawamukai et al., Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for 638 plant transformation, Journal of Bioscience and Bioengineering, vol.637, pp.34-41, 2007.

L. Peng, Y. Fukao, M. Fujiwara, T. Takami, and T. Shikanai, Efficient Operation of NAD(P)H Dehydrogenase Requires 640, 2009.

, Supercomplex Formation with Photosystem I via Minor LHCI in Arabidopsis, The Plant Cell, vol.21, pp.3623-3640

Z. Peng, Y. Hu, J. Xie, N. Potnis, A. Akhunova et al., Long read and single molecule DNA 642 sequencing simplifies genome assembly and TAL effector gene analysis of Xanthomonas translucens, BMC Genomics, vol.17, pp.643-664, 2016.

A. L. Pérez-quintero, R. Lm, A. Dereeper, C. López, R. Koebnik et al., An Improved 645 Method for TAL Effectors DNA-Binding Sites Prediction Reveals Functional Convergence in TAL Repertoires of 646 Xanthomonas oryzae Strains, PLoS ONE, vol.8, p.68464, 2013.

J. Rademaker, F. J. Louws, M. H. Schultz, U. Rossbach, L. Vauterin et al., A comprehensive 648 species to strain taxonomic framework for Xanthomonas, Phytopathology, vol.95, pp.1098-1111, 2005.

P. Römer, S. Hahn, T. Jordan, T. Strauss, U. Bonas et al., Plant pathogen recognition mediated by promoter 650 activation of the pepper Bs3 resistance gene, Science, vol.318, pp.645-648, 2007.

C. Rousseau, E. Belin, E. Bove, D. Rousseau, F. Fabre et al., High throughput quantitative phenotyping of plant resistance using chlorophyll fluorescence image analysis, vol.652, 2013.
URL : https://hal.archives-ouvertes.fr/inserm-00837088

, Plant methods, vol.9, p.17

C. Rousseau, G. Hunault, S. Gaillard, J. Bourbeillon, G. Montiel et al., Phenoplant: a web resource for the exploration of large chlorophyll fluorescence image datasets, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01218602

M. Ruh, M. Briand, S. Bonneau, M. Jacques, and N. Chen, Xanthomonas adaptation to common bean is associated 658 with horizontal transfers of genes encoding TAL effectors, BMC Genomics, vol.18, p.670, 2017.

R. P. Ryan, F. Vorhölter, N. Potnis, J. B. Jones, V. Sluys et al., Pathogenomics of 660 Xanthomonas: understanding bacterium-plant interactions, Nature Reviews Microbiology, vol.9, pp.344-355, 2011.

E. Sallet, J. Gouzy, and T. Schiex, EuGene-PP: A next-generation automated annotation pipeline for prokaryotic 662 genomes, Bioinformatics, vol.30, pp.2659-2661, 2014.

S. Schornack, M. J. Moscou, E. R. Ward, and D. M. Horvath, Engineering Plant Disease Resistance Based on TAL Effectors, 2013.

, Annual Review of Phytopathology, vol.51, pp.383-406

S. Schornack, K. Peter, U. Bonas, and T. Lahaye, Expression levels of avrBs3-like genes affect recognition specificity 666 in tomato Bs4-but not in pepper Bs3-mediated perception, Molecular plant-microbe interactions : MPMI, vol.18, pp.1215-1225, 2005.

A. R. Schwartz, R. Morbitzer, T. Lahaye, and B. J. Staskawicz, TALE-induced bHLH transcription factors that activate a 668 pectate lyase contribute to water soaking in bacterial spot of tomato, Proceedings of the National Academy of Sciences of 669 the United States of America, vol.114, pp.897-903, 2017.

A. R. Schwartz, N. Potnis, S. Timilsina, M. Wilson, J. Patané et al., , p.671

N. Almeida, Phylogenomics of Xanthomonas field strains infecting pepper and tomato reveals diversity in 672 effector repertoires and identifies determinants of host specificity, Frontiers in Microbiology, vol.6, pp.1-17, 2015.

S. Stella, R. Molina, C. Bertonatti, A. Juillerrat, and G. Montoya, Expression, purification, crystallization and 674 preliminary X-ray diffraction analysis of the novel modular DNA-binding protein BurrH in its apo form and in complex 675 with its target DNA, Acta Crystallographica Section F Structural Biology Communications, vol.70, pp.87-91, 2014.

J. Streubel, C. Blücher, A. Landgraf, and J. Boch, TAL effector RVD specificities and efficiencies, Nature Biotechnology, vol.677, pp.593-595, 2012.
DOI : 10.1038/nbt.2304

J. Streubel, C. Pesce, M. Hutin, R. Koebnik, J. Boch et al., Five phylogenetically close rice SWEET genes confer 679 TAL effector-mediated susceptibility to Xanthomonas oryzae pv. oryzae, New Phytologist, vol.200, pp.808-819, 2013.
DOI : 10.1111/nph.12411

URL : https://nph.onlinelibrary.wiley.com/doi/pdf/10.1111/nph.12411

A. Sugio, B. Yang, T. Zhu, and F. F. White, Two type III effector genes of Xanthomonas oryzae pv. oryzae control the 681 induction of the host genes OsTFIIAgamma1 and OsTFX1 during bacterial blight of rice, Proceedings of the National 682 Academy of Sciences of the United States of America, vol.104, pp.10720-10725, 2007.

L. Vauterin, B. Hoste, K. Kersters, and J. Swings, Reclassification of Xanthomonas, International Journal of Systematic, vol.684, pp.472-489, 1995.

L. Wang, F. C. Rinaldi, P. Singh, E. L. Doyle, Z. E. Dubrow et al., TAL 686 effectors drive transcription bidirectionally in plants, Molecular Plant, vol.10, pp.285-296, 2017.
DOI : 10.1016/j.molp.2016.12.002

URL : http://www.cell.com/article/S167420521630301X/pdf

C. Wang, X. Zhang, Y. Fan, Y. Gao, Q. Zhu et al., XA23 Is an executor r protein 688 and confers broad-spectrum disease resistance in rice, Molecular Plant, vol.8, pp.290-302, 2015.
DOI : 10.1093/mp/ssu132

K. E. Wilkins, N. J. Booher, L. Wang, and A. J. Bogdanove, TAL effectors and activation of predicted host targets 690 distinguish Asian from African strains of the rice pathogen Xanthomonas oryzae pv. oryzicola while strict conservation 691 suggests universal importance of five TAL effectors, Frontiers in Plant Science, vol.6, pp.1-15, 2015.

Y. Wu, D. Zhang, J. Y. Chu, P. Boyle, Y. Wang et al., The Arabidopsis NPR1 Protein Is 693 a Receptor for the Plant Defense Hormone Salicylic Acid, Cell Reports, vol.1, pp.639-647, 2012.

Y. Xia, H. Suzuki, J. Borevitz, J. Blount, Z. Guo et al., An Extracellular Aspartic Protease 695 Functions in Arabidopsis Disease Resistance Signaling, EMBO Journal, vol.23, pp.980-988, 2004.
DOI : 10.1038/sj.emboj.7600086

URL : http://emboj.embopress.org/content/23/4/980.full.pdf

X. Xin, K. Nomura, K. Aung, A. C. Velásquez, J. Yao et al., Bacteria establish an 697 aqueous living space in plants crucial for virulence, Nature, vol.539, pp.524-529, 2016.
DOI : 10.1038/nature20166

URL : http://europepmc.org/articles/pmc5135018?pdf=render

B. El-yacoubi, A. M. Brunings, Q. Yuan, S. Shankar, and D. W. Gabriel, In planta horizontal transfer of a major 699 pathogenicity effector gene, Applied and Environmental Microbiology, vol.73, pp.1612-1621, 2007.

Y. Yang and D. W. Gabriel, Intragenic recombination of a single plant pathogen gene provides a mechanism for the 701 evolution of new host specificities . These include : Intragenic Recombination of a Single Plant Pathogen Gene Provides 702 a Mechanism for the Evolution of New Host Specifi, Journal of Bacteriology, vol.177, pp.4963-4968, 1995.

B. Yang, A. Sugio, and F. F. White, Os8N3 is a host disease-susceptibility gene for bacterial blight of rice, Proceedings of 704 the National Academy of Sciences of the United States of America, vol.103, pp.10503-10511, 2006.

B. Yang and F. F. White, Diverse members of the AvrBs3/PthA family of type III effectors are major virulence 706 determinants in bacterial blight disease of rice, Molecular plant-microbe interactions : MPMI, vol.17, pp.1192-200, 2004.

J. Yang, Y. Zhang, P. Yuan, Y. Zhou, C. Cai et al., Complete decoding of TAL effectors 708 for DNA recognition, Cell research, vol.24, pp.628-659, 2014.
DOI : 10.1038/cr.2014.19

URL : https://www.nature.com/articles/cr201419.pdf

Y. Yu, J. Streubel, S. Balzergue, A. Champion, J. Boch et al., Colonization of 710 rice leaf blades by an african strain of Xanthomonas oryzae pv. oryzae depends on a new TAL effector that induces the 711 rice nodulin-3 Os11N3 gene, Molecular Plant-Microbe Interactions, vol.24, pp.1102-1115, 2011.

X. Zeng, D. Tian, K. Gu, Z. Zhou, X. Yang et al., Genetic engineering of the Xa10 promoter for 713 broad-spectrum and durable resistance to Xanthomonas oryzae pv. oryzae, Plant Biotechnology Journal, vol.13, pp.993-1001, 2015.

J. Zhang, Z. Yin, and F. White, TAL effectors and the executor R genes, Frontiers in Plant Science, vol.6, p.641, 2015.
DOI : 10.3389/fpls.2015.00641

URL : https://www.frontiersin.org/articles/10.3389/fpls.2015.00641/pdf

J. Zhou, Z. Peng, J. Long, D. Sosso, B. Liu et al., Gene targeting 716 by the TAL effector PthXo2 reveals cryptic resistance gene for bacterial blight of rice, Plant Journal, vol.82, pp.632-643, 2015.

, PVJaloEEP55800861g0145481 Phvul.007G139200.1 Protein of unknown function (DUF1635) 2

, PVJaloEEP55800679g0128221 Phvul.007G099700.1 No functional annotations 3 PVJaloEEP55800033g0016481 Phvul.007G280100.1 NAD(P)H dehydrogenase 18, vol.117, p.119

, PVJaloEEP55800226g0067831 Phvul.001G041700.1 BTB/POZ domain-containing protein npy1

, PVJaloEEP55800203g0063461 Phvul.001G001500.1 Multi-copper oxidase type I family protein-related 6

, PVJaloEEP55800673g0127691 Phvul.003G148400.1 Allergen V5/TPX-1-related family protein-related 7

, PVJaloEEP55801425g0185111 Phvul.008G144100.1 Beta expansin 6-related 8

, No functional annotations 9 PVJaloEEP55803280g0250741 Phvul.001G125800.1 Two-component response regulator ARR8-related 41 10 PVJaloEEP55801242g0173941 Phvul.007G046100.1 Cysteine and glycine-rich protein, CSRP), p.11

, PVJaloEEP55800057g0024751 Phvul.006G197500.1 Cysteine-rich secretory protein-relate 12

, PVJaloEEP55803218g0249351 Phvul.009G012200.1 Wuschel-related homeobox, vol.13, p.13

, PVJaloEEP55800889g0148081 Phvul.007G071100.1 PAR1 protein 14 PVJaloEEP55801772g0201171 Phvul.003G207400.1 Pectate lyase, pp.22-37

, PVJaloEEP55800459g0104461 Phvul.002G210700.2 Taurine-transporting ATPase 16 PVJaloEEP55800001g0000831 NA NA 17 PVJaloEEP55800401g0096411 Phvul.008G270900.1 Glycosyl hydrolase family 9 protein 18 PVJaloEEP55803316g0251431 Phvul.002G086150.1 Origin recognition complex subunit 6 (ORC6), p.19

, Fruit bromelain 20 PVJaloEEP55800545g0114001 Phvul.009G133600.1 Basic blue protein 21 PVJaloEEP55800018g0010221 Phvul.007G236800.1 Pectate lyase 1-related 221 22 PVJaloEEP55800525g0111851 Phvul

, Glucomannan 4-beta-mannosyltransferase 2 24 PVJaloEEP55803897g0263521 Phvul.001G186700.1 Pre-mRNA cleavage complex 2 protein Pcf11, p.378

, PVJaloEEP55808389g0306631 Phvul.003G143400.2 Peroxidase 16-related 26

, PVJaloEEP55800293g0079661 Phvul.001G225000.1 Nicotianamine synthase 27 PVJaloEEP55820685g0326051 Phvul.008G235300.1 Gibberellin-regulated protein 12-related 28

, PVJaloEEP55800670g0127291 Phvul.005G031700.1 Large subunit ribosomal protein L27 (RP-L27, MRPL27, rpmA), p.30

, PVJaloEEP55802585g0232231 Phvul.003G247700.1 Multi-copper oxidase 31 PVJaloEEP55800091g0037291 Phvul.007G261600.1 No functional annotations, vol.678, p.32

, Glyceraldehyde-3-phosphate dehydrogenase (NADP(+)) (phosphorylating) / Triosephosphate dehydrogenase (NADP+), p.33

, PVJaloEEP55800441g0102071 Phvul.004G059200.1 Pectate lyase 11-related 169 37 PVJaloEEP55801056g0160901 Phvul.005G007700.1 Homogalacturonan degradation 47 PVJaloEEP55801823g0203611 Phvul.004G038700.1 Polygalacturonase QRT3 48 PVJaloEEP55800033g0016451 Phvul.007G279900.1 Acylaminoacyl-peptidase, p.49

, PVJaloEEP55802168g0217871 Phvul

. Expansin-a6,

, PVJaloEEP55800409g0097681 Phvul.010G014300.1 Acetyl-CoA:benzylalcohol acetyltranferase-like protein-related 51

, PVJaloEEP55809283g0310391 Phvul.002G101700.1 L-ascorbate oxidase pectinesterase-like protein pollen-specific protein-like 52

, PVJaloEEP55802633g0233651 Phvul.009G255500.2 No functional annotations 53 PVJaloEEP55806708g0296451 Phvul.008G213400.1 O-glycosyl hydrolases family 17 protein 54 PVJaloEEP55801491g0188491 Phvul.011G085200.1 Xyloglucan: xyloglucosyl transferase 55 PVJaloEEP55800273g0076391 Phvul.008G259500.1 F10K1.18 protein 56 PVJaloEEP55804465g0272661 Phvul.005G135600.1 Protein disulfide-isomerase A3

, Arabinogalactan protein 31 59 PVJaloEEP55800077g0032151 Phvul.002G296900.1 No functional annotations 60 PVJaloEEP55801236g0173451 Phvul.007G204900.1 Isopenicillin-N epimerase 61 PVJaloEEP55800738g0133991 Phvul.002G123300.1 ROP guanine nucleotide exchange factor 14 62 PVJaloEEP55811045g0315771 Phvul.006G013781.1 Acylaminoacyl-peptidase / N-acylpeptide hydrolase 63, PVJaloEEP55800218g0066371 Phvul.009G151900.1 Polyketide cyclase / dehydrase and lipid transport 58 PVJaloEEP55804035g0265871 Phvul.002G229200.1, p.977

, PVJaloEEP55800153g0053091 Phvul.009G059700.1 Mannan endo-1,4-beta-mannosidase (MAN), p.65

, Solute carrier family 25 (mitochondrial oxoglutarate transporter, p.66

, 18 protein 67 PVJaloEEP55800310g0082201 Phvul.011G211600.1 No functional annotations 68 PVJaloEEP55801050g0160441 Phvul.009G144100.1 Aspartyl protease-like protein 69 PVJaloEEP55801236g0173461 Phvul

, No functional annotations 72 PVJaloEEP55801681g0197391 Phvul.001G230700.1 Starch binding scaffold protein-related 73

, PVJaloEEP55800788g0138791 Phvul.007G069800.2 ARM repeat superfamily protein-related 74

, No functional annotations 75 PVJaloEEP55801582g0192871 Phvul.004G011800.1 Pectin lyase-like superfamily protein 76 PVJaloEEP55800409g0097691 Phvul

, Germin-like protein subfamily 3 member 2 78 PVJaloEEP55806990g0298521 Phvul

, PVJaloEEP55806196g0292561 Phvul.004G051600.1 5-methyltetrahydropteroyltriglutamate--homocysteine S-methyltransferase / Tetrahydropteroylglutamate-homocysteine transmethylase 833 82 PVJaloEEP55803576g0256711 Phvul.003G096100.2 ARM repeat superfamily protein-related 83

, Ribosome-releasing factor 2, mitochondrial 84 PVJaloEEP55800273g0076381 Phvul.008G259500.1 F10K1.18 protein 85 PVJaloEEP55800018g0010131 Phvul.007G238300.1 Serinc-domain containing serine and sphingolipid biosynthesis protein 86

, Glyceraldehyde-3-phosphate dehydrogenase (NADP(+)) (phosphorylating) / Triosephosphate dehydrogenase (NADP+), p.87

, PVJaloEEP55802410g0226251 Phvul.007G117700.1 Phosphoinositide 5-phosphatase / Type II inositol-1,4,5-trisphosphate 5-phosphatase 88

, PVJaloEEP55802144g0216701 Phvul.003G199200.1 U-box domain-containing protein 18-related 90

, PVJaloEEP55800086g0035661 Phvul.002G009900.1 Glycosyltransferase 6-related 91

, No functional annotations 92 PVJaloEEP55800744g0134631 Phvul.006G038300.1 Domain of unknown function, vol.4477, p.93

, PVJaloEEP55803083g0246321 Phvul.004G054600.1 Chloride channel protein CLC-A-related 94

, PVJaloEEP55802061g0213511 Phvul.005G024100.1 F17A17.37 protein 95 PVJaloEEP55817413g0324381 Phvul.006G101200.2 Calmodulin-like protein 11-related 96

, PVJaloEEP55801663g0196731 Phvul.005G096300.1 Cold-regulated protein 15B

, PVJaloEEP55800009g0005791 Phvul.006G197200.1 Cysteine-rich secretory protein-related 98

, Transmembrane protein adipocyte-associated 1 1.146 100 PVJaloEEP55800902g0149361 Phvul.009G128000.1 Protein of unknown function, vol.688, p.101

, PVJaloEEP55807175g0299661 Phvul.011G167300.1 Chitinase 102 PVJaloEEP55801155g0168081 Phvul.001G030400.1 No functional annotations 103 PVJaloEEP55800377g0093111 Phvul.002G006000.1 Glycine cleavage system H protein 3, mitochondrial 104 PVJaloEEP55805111g0281611 Phvul.008G219100.1 Amino acid transporter 105 PVJaloEEP55800848g0144211 Phvul.010G028300.1 Interleukin-1 receptor-associated kinase 1 (IRAK1), p.61

, PVJaloEEP55800017g0009571 Phvul.003G187700.1 Cell division protein kinase 107 PVJaloEEP55800093g0037951 Phvul.004G032800.1 Lamin-like protein 108 PVJaloEEP55800433g0100861 Phvul.008G041200.1 Gibberellin-regulated protein 4 109 PVJaloEEP55801386g0183161 Phvul.004G170100.2 Polyketide cyclase / dehydrase and lipid transport (Polyketide_cyc2), p.110

, PVJaloEEP55800378g0093251 NA NA 111 PVJaloEEP55802280g0221721 Phvul.002G084100.1 Homeodomain-like superfamily protein 112 PVJaloEEP55801339g0179861 Phvul, p.113

, PVJaloEEP55800845g0143861 Phvul.010G114700.1 Aspartyl protease-related 114

, PVJaloEEP55800148g0051741 Phvul.001G188900.1 Purple acid phosphatase 21-related 116

, Di-glucose binding protein with Leucine-Rich Repeat domain 117 PVJaloEEP55817868g0324541 Phvul.007G276500.1 No functional annotations 118 PVJaloEEP55800431g0100711 Phvul.007G066500.1 Dehydration-responsive element-binding protein

, Leucine Rich Repeat (LRR_1) // Leucine rich repeat N-terminal domain, vol.2, p.124

, PVJaloEEP55802878g0240401 Phvul.006G041100.1 Purple acid phosphatase 18 125 PVJaloEEP55802997g0243921 Phvul.001G190100.1 Ribonucleoside-diphosphate reductase subunit M2 (RRM2), p.126

, PVJaloEEP55801357g0181231 Phvul.010G022000.1 NINJA-family protein AFP1-related 127

, No functional annotations 129 PVJaloEEP55802858g0239901 Phvul.005G045500.1 Aspartyl protease family protein 130 PVJaloEEP55801236g0173471 NA NA 131 PVJaloEEP55800333g0085641 Phvul.001G071600.1 G2/mitotic-specific cyclin, p.132

, PVJaloEEP55800543g0113821 Phvul.003G266500.1 Aspartyl protease family protein 135 PVJaloEEP55800594g0119371 Phvul.009G142800.1 Expansin-A8

, PVJaloEEP55800826g0142271 Phvul.009G028900.1 Allergen-like protein BRSN20-related 137

, PVJaloEEP55801448g0186351 Phvul.005G175700.1 Domain of unknown function (DUF4666) 560, p.663

, Adenosine kinase 1.312 140 PVJaloEEP55801300g0177501 Phvul.003G217800.1 Monocopper oxidase-like protein SKU5 141 PVJaloEEP55801510g0189631 Phvul.008G290300.1 UDP-glycosyltransferase 71C4 142 PVJaloEEP55802433g0227191 NA NA 143 PVJaloEEP55800880g0147291 Phvul.008G251400.1 Sodium/hydrogen exchanger family, p.144

, PVJaloEEP55804744g0276761 Phvul.003G151400.1 No functional annotations 145 PVJaloEEP55803093g0246581 Phvul.008G120700.1 Expansin-A6

, PVJaloEEP55800023g0012211 Phvul.001G171600.1 Ankyrin repeat-containing protein 147

, Inositol 3-alpha-galactosyltransferase / UDP-alpha-D-galactose:myo-inositol 3-alpha-D-galactosyltransferase 148

, Ethylene-responsive transcription factor ERF018 149 PVJaloEEP55802462g0228081 Phvul.004G077100.1 Dynein light chain type 1-like protein 150 PVJaloEEP55802640g0233881 Phvul.007G123002.1 No functional annotations 151 PVJaloEEP55801443g0186161 Phvul.008G119600.1 Nitrogen metabolic regulation protein

, PVJaloEEP55800238g0069881 Phvul.007G014100.1 Ring zinc finger protein

M. Aamir, V. K. Singh, M. Meena, R. S. Upadhyay, V. K. Gupta et al., Structural and Functional Insights into WRKY3 and WRKY4, 2017.

, Transcription Factors to Unravel the WRKY-DNA (W-Box) Complex Interaction in Tomato (Solanum lycopersicum L.). A Computational Approach, Frontiers in Plant Science, vol.8, pp.1-24

M. H. Abd-alla, S. R. Bashandy, and S. Schnell, Occurrence of xanthomonas axonopodis pv. phaseoli, the causal agent of common bacterial blight disease, on seeds of common bean (Phaseolus vulgaris L.) in upper Egypt, Folia Microbiologica, vol.55, pp.47-52, 2010.

V. Y. Abe and C. E. Benedetti, Additive roles of PthAs in bacterial growth and pathogenicity associated with nucleotide polymorphisms in effector-binding elements of citrus canker susceptibility genes, Molecular Plant Pathology, vol.17, pp.1223-1236, 2016.

N. Ah-you, L. Gagnevin, P. Grimont, S. Brisse, X. Nesme et al., Polyphasic characterization of xanthomonads pathogenic to members of the Anacardiaceae and their relatedness to species of Xanthomonas, International Journal of Systematic and Evolutionary Microbiology, vol.59, pp.306-318, 2009.
URL : https://hal.archives-ouvertes.fr/halsde-00526055

A. Akhavan, M. Bahar, H. Askarian, M. R. Lak, A. Nazemi et al., Bean common bacterial blight: pathogen epiphytic life and effect of irrigation practices, SpringerPlus, vol.2, p.41, 2013.

A. Al-saadi, J. D. Reddy, Y. P. Duan, A. M. Brunings, Q. Yuan et al., All five host-range variants of Xanthomonas citri carry one pthA homolog with 17.5 repeats that determines pathogenicity on citrus, but none determine host-range variation, Molecular plant-microbe interactions : MPMI, vol.20, pp.934-943, 2007.

S. M. Alavi, S. Sanjari, F. Durand, C. Brin, C. Manceau et al., Assessment of the genetic diversity of Xanthomonas axonopodis pv. phaseoli and Xanthomonas fuscans subsp. fuscans as a basis to identify putative pathogenicity genes and a type III secretion system of the SPI-1 family by multiple suppression subtractive h, Applied and Environmental Microbiology, vol.74, pp.3295-3301, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00729841

P. Albuquerque, C. Caridade, A. Marcal, J. Cruz, L. Cruz et al., Identification of Xanthomonas fragariae, Xanthomonas axonopodis pv. phaseoli, and Xanthomonas fuscans subsp. fuscans with novel markers and using a dot blot platform coupled with automatic data, Analysis. Applied and Environmental Microbiology, vol.77, pp.5619-5628, 2011.

R. P. Alexander and I. B. Zhulin, Evolutionary genomics reveals conserved structural determinants of signaling and adaptation in microbial chemoreceptors, Proceedings of the National Academy of Sciences of the United States of America, vol.104, pp.2885-2890, 2007.

G. Alexandre, Coupling metabolism and chemotaxis-dependent behaviours by energy taxis receptors, Microbiology, vol.156, p.2283, 2010.

J. R. Alfano and A. Collmer, Bacterial Pathogens in Plants : Life up against the Wall, The Plant cell, vol.8, pp.1683-1698, 1996.

J. R. Alfano and A. Collmer, TYPE III SECRETION SYSTEM EFFECTOR PROTEINS : Double Agents in Bacterial Disease and Plant Defense, Annual Review of Phytopathology, vol.42, pp.385-414, 2004.

B. Alladassi, S. T. Nkalubo, C. Mukankusi, E. S. Mwale, P. Gibson et al., Inheritance of resistance to common bacterial blight in four selected common bean (Phaseolus vulgaris L.) genotypes, Journal of Plant Breeding and Crop Science, vol.9, pp.71-78, 2017.

C. J. Alteri and H. Mobley, The versatile type VI secretion system, Microbiology Spectrum, vol.4, 2016.

A. Amano, Bacterial adhesins to host components in periodontitis, Periodontology, vol.52, pp.12-37, 2000.

J. C. Anderson, Y. Wan, Y. Kim, L. Pasa-tolic, T. O. Metz et al., Decreased abundance of type III secretion system-inducing signals in Arabidopsis mkp1 enhances resistance against Pseudomonas syringae, Proceedings of the National Academy of Sciences of the United States of America, vol.111, pp.6846-51, 2014.

S. A. Angioi, D. Rau, G. Attene, L. Nanni, E. Bellucci et al., Beans in Europe: Origin and structure of the European landraces of Phaseolus vulgaris L, Theoretical and Applied Genetics, vol.121, pp.829-843, 2010.

G. Antony, J. Zhou, S. Huang, T. Li, B. Liu et al., Rice xa13 recessive resistance to bacterial blight is defeated by induction of the disease susceptibility gene Os-11N3, The Plant cell, vol.22, pp.3864-76, 2010.

F. Aragão, E. Nogueira, M. Tinoco, and J. C. Faria, Molecular characterization of the first commercial transgenic common bean immune to the Bean golden mosaic virus, Journal of Biotechnology, vol.166, pp.42-50, 2013.

V. Aritua, J. Harrison, M. Sapp, R. Buruchara, J. Smith et al., Genome sequencing reveals a new lineage associated with lablab bean and genetic exchange between Xanthomonas axonopodis pv. phaseoli and Xanthomonas fuscans subsp. fuscans, Frontiers in Microbiology, vol.6, pp.1-18, 2015.

V. Aritua, N. Parkinson, R. Thwaites, J. V. Heeney, D. R. Jones et al., Characterization of the Xanthomonas sp. causing wilt of enset and banana and its proposed reclassification as a strain of X. vasicola, Plant Pathology, vol.57, pp.170-177, 2008.

E. Arnaud-santana, E. Pena-matos, D. P. Coyne, and A. K. Vidaver, Longevity of Xanthomonas campestris pv. phaseoli in naturally infested dry bean (Phaseolus vulgaris) debris, Plant Disease, vol.75, pp.952-953, 1991.

P. Audy, A. Laroche, G. Saindon, H. C. Huang, and R. L. Gilbertson, Detection of the Bean Common Blight Bacteria, Xanthomonas campestris pv. phaseoli and X. c. phaseoli var. fuscans, Using the Polymerase Chain Reaction, Molecular Plant Pathology, vol.84, pp.1185-92, 1994.

Y. Bai, T. E. Michaels, and K. P. Pauls, Identification of RAPD markers linked to common bacterial blight resistance genes in Phaseolus vulgaris L, Genome, vol.40, pp.544-551, 1997.

K. F. Baker and S. H. Smith, Dynamics of Seed Transmission of Plant Pathogens, Annual Review of Phytopathology, vol.4, pp.311-332, 1966.

D. A. Baltrus, M. T. Nishimura, A. Romanchuk, J. H. Chang, M. S. Mukhtar et al., Dynamic evolution of pathogenicity revealed by sequencing and comparative genomics of 19 pseudomonas syringae isolates, PLoS Pathogens, vol.7, 2011.

J. C. Baptista, M. A. Machado, R. A. Homem, P. S. Torres, A. A. Vojnov et al., Mutation in the xpsD gene of Xanthomonas axonopodis pv. citri affects cellulose degradation and virulence, Genetics and Molecular Biology, vol.33, pp.146-153, 2010.

J. D. Barak, T. Vancheva, P. Lefeuvre, J. B. Jones, S. Timilsina et al., Whole-Genome Sequences of Xanthomonas euvesicatoria Strains Clarify Taxonomy and Reveal a Stepwise Erosion of Type 3 Effectors, Frontiers in Plant Science, 2016.

I. Barash and S. Manulis-sasson, Recent evolution of bacterial pathogens: the gall-forming Pantoea agglomerans case, Annual Review of Phytopathology, vol.47, pp.133-152, 2009.

B. W. Bardoel, S. Van-der-ent, M. Pel, J. Tommassen, C. Pieterse et al.,

R. Bart, M. Cohn, A. Kassen, E. J. Mccallum, M. Shybut et al., Highthroughput genomic sequencing of cassava bacterial blight strains identifies conserved effectors to target for durable resistance, Proceedings of the National Academy of Sciences of the United States of America, vol.109, pp.1972-1979, 2012.

C. Bartoli, F. Roux, and J. R. Lamichhane, Molecular mechanisms underlying the emergence of bacterial pathogens: An ecological perspective, Molecular Plant Pathology, vol.17, pp.303-310, 2016.

A. Bäumler and F. C. Fang, Host specificity of bacterial pathogens. Cold Spring Harbor perspectives in medicine, vol.3, p.10041, 2013.

S. Becker and J. Boch, Single-molecule biophysics: TALEs spin along, but not around, Nature Chemical Biology, vol.12, pp.5-7, 2016.

R. Belas, I. B. Zhulin, and Z. Yang, Bacterial signaling and motility: Sure bets, Journal of Bacteriology, vol.190, pp.1849-1856, 2008.

T. Belete and K. Bastas, Common Bacterial Blight (Xanthomonas axonopodis pv. phaseoli) of Beans with Special Focus on Ethiopian Condition, Journal of Plant Pathology & Microbiology, vol.8, 2017.

K. Belhaj, A. Chaparro-garcia, S. Kamoun, N. J. Patron, and V. Nekrasov, Editing plant genomes with CRISPR / Cas9, Current Opinion in Biotechnology, vol.32, pp.76-84, 2015.

Y. Benjamini and Y. Hochberg, Controlling the false discovery rate: a practical and powerful approach to multiple testing, Journal of the Royal Statistical Society B, vol.57, pp.289-300, 1995.

H. C. Berg, The Rotatory Motor of Bacterial Flagella, Annual Review of Biochemistry, vol.72, pp.19-54, 2003.

D. J. Bertioli, S. B. Cannon, L. Froenicke, G. Huang, A. D. Farmer et al., The genome sequences of Arachis duranensis and Arachis ipaensis, the diploid ancestors of cultivated peanut, Nature genetics, vol.48, pp.438-446, 2016.

P. Birch, L. J. Hyman, R. Taylor, A. F. Opio, C. Bragard et al., RAPD PCR-based differentiation of Xanthomonas campestris pv. phaseoli and Xanthomonas campestris pv. phaseoli var. fuscans, European Journal of Plant Pathology, vol.103, pp.809-814, 1997.

E. Bitocchi, D. Rau, E. Bellucci, M. Rodriguez, M. L. Murgia et al., Beans (Phaseolus ssp.) as a Model for Understanding Crop Evolution, Frontiers in Plant Science, vol.8, pp.1-21, 2017.

S. Blanvillain-baufumé, M. Reschke, M. Solé, F. Auguy, H. Doucoure et al., Targeted promoter editing for rice resistance to Xanthomonas oryzae pv. oryzae reveals differential activities for SWEET14-inducing TAL effectors, Plant biotechnology journal, vol.15, pp.306-317, 2017.

S. Blanvillain, D. Meyer, A. Boulanger, M. Lautier, C. Guynet et al., Plant carbohydrate scavenging through TonB-dependent receptors: A feature shared by phytopathogenic and aquatic bacteria, PLoS ONE, vol.2, 2007.

J. Boch and U. Bonas, Xanthomonas AvrBs3 family-type III effectors: discovery and function, Annual Review of Phytopathology, vol.48, pp.419-455, 2010.

J. Boch, U. Bonas, and T. Lahaye, TAL effectors -pathogen strategies and plant resistance engineering, New Phytologist, vol.204, p.823, 2014.

J. Boch, H. Scholze, S. Schornack, A. Landgraf, S. Hahn et al., Breaking the code of DNA binding specificity of TAL-type III effectors, Science, vol.326, pp.1509-1521, 2009.

A. J. Bogdanove, Principles and applications of TAL effectors for plant physiology and metabolism, Current Opinion in Plant Biology, vol.19, pp.99-104, 2014.

A. J. Bogdanove, R. Koebnik, H. Lu, A. Furutani, S. V. Angiuoli et al., Two new complete genome sequences offer insight into host and tissue specificity of plant pathogenic Xanthomonas spp, Journal of Bacteriology, vol.193, pp.5450-5464, 2011.

A. J. Bogdanove, S. Schornack, and T. Lahaye, TAL effectors: Finding plant genes for disease and defense, Current Opinion in Plant Biology, vol.13, pp.394-401, 2010.

.. J. Bogdanove-a and D. F. Voytas, TAL Effectors: Customizable Proteins for DNA Targeting, Science, vol.333, pp.1843-1846, 2011.

A. J. Bogdanove, Z. M. Wei, L. Zhao, and S. V. Beer, Erwinia amylovora secretes harpin via a type III pathway and contains a homolog of yopN of Yersinia spp, Journal of Bacteriology, vol.178, pp.1720-1730, 1996.

T. Boller and S. Y. He, Innate Immunity in Plants : An Arms Race, Science, vol.324, pp.742-746, 2009.

S. Bolot, A. M. Bodnar, S. Cunnac, E. Ortiz, B. Szurek et al., Draft Genome Sequence of the Xanthomonas cassavae Type Strain CFBP 4642, Genome announcements, vol.1, pp.679-692, 2013.

S. Bolot, E. Guy, S. Carrere, V. Barbe, M. Arlat et al., Xanthomonas campestris pv. campestris Strain Xca5, Genome Announcements, vol.1, pp.32-44, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01455989

U. Bonas, J. Conrads-strauch, and I. Balbo, Resistance in tomato to Xanthomonas campestris pv vesicatoria is determined by alleles of the pepper-specific avirulence gene avrBs3, Molecular & general genetics : MGG, vol.238, pp.261-269, 1993.

U. Bonas, R. E. Stall, and B. Staskawicz, Genetic and structural characterization of the avirulence gene avrBs3 from Xanthomonas campestris pv. vesicatoria, Molecular & general genetics : MGG, vol.218, pp.127-136, 1989.

K. Bonfim, J. C. Faria, E. Nogueira, F. Mendes-e-a,-aragão, . Mendes-É-a et al., RNAi-Mediated Resistance to Bean golden mosaic virus in Genetically Engineered Common Bean (Phaseolus vulgaris), Molecular plant-microbe interactions : MPMI, vol.20, pp.717-726, 2007.

M. F. Boni, D. Posada, and M. W. Feldman, An exact nonparametric method for inferring mosaic structure in sequence triplets, Genetics, vol.176, pp.1035-1047, 2007.

N. J. Booher, S. Carpenter, R. P. Sebra, L. Wang, S. L. Salzberg et al., Single molecule real-time sequencing of Xanthomonas oryzae genomes reveals a dynamic structure and complex TAL (transcription activator-like) effector gene relationships, 2015.

, Microbial Genomics, vol.1, pp.1-22

L. Bortesi and R. Fischer, The CRISPR / Cas9 system for plant genome editing and beyond, Biotechnology Advances, vol.33, pp.41-52, 2015.

A. Boulanger and L. D. Noël, Xanthomonas Whole Genome Sequencing: Phylogenetics, Host Specificity and Beyond, Frontiers in Microbiology, vol.7, pp.1-2, 2016.
URL : https://hal.archives-ouvertes.fr/hal-02090750

T. Boureau, M. Kerkoud, F. Chhel, G. Hunault, A. Darrasse et al., A multiplex-PCR assay for identification of the quarantine plant pathogen Xanthomonas axonopodis pv. phaseoli, Journal of Microbiological Methods, vol.92, pp.42-50, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01199317

J. F. Bradbury, Guide to plant pathogenic bacteria, 1986.

M. Briand, R. Gaborieau, M. Jacques, M. Barret, T. Boureau et al., SkIf : a tool for rapid identification of genes or regulators of interest, 2016.

W. H. Burkholder, The bacterial diseases of the bean, Memoirs. Cornell University Agricultural Experiment Station, vol.127, pp.1-88, 1930.

D. Büttner and U. Bonas, Getting across-bacterial type III effector proteins on their way to the plant cell, The Embo Journal, vol.21, p.5313, 2002.

D. Büttner and U. Bonas, Regulation and secretion of Xanthomonas virulence factors, FEMS Microbiology Reviews, vol.34, pp.107-133, 2010.

D. Büttner and S. Y. He, Type III protein secretion in plant pathogenic bacteria, Plant physiology, vol.150, pp.1656-1664, 2009.

P. Lo-cantore, V. Shanmugaiah, and N. S. Iacobellis, Antibacterial activity of essential oil components and their potential use in seed disinfection, Journal of agricultural and food chemistry, vol.57, pp.9454-61, 2009.

H. Cao, R. L. Baldini, and L. G. Rahme, COMMON MECHANISMS FOR PATHOGENS OF PLANTS AND ANIMALS. Annual Review of Phytopathology, vol.39, pp.259-84, 2011.

T. B. Cao and M. H. Saier, The general protein secretory pathway: Phylogenetic analyses leading to evolutionary conclusions, 2003.

, Biochimica et Biophysica Acta -Biomembranes, vol.1609, pp.115-125

D. Carroll, Genome engineering with targetable nucleases, Annual Review of Biochemistry, vol.83, pp.409-439, 2014.

J. Carvalho, J. De-oliveira-santos, C. Conte, S. Pacheco, E. Nogueira et al., Comparative analysis of nutritional compositions of transgenic RNAi-mediated virus-resistant bean (event EMB-PV051-1) with its non-transgenic counterpart, Transgenic Research, vol.24, pp.813-819, 2015.

L. F. Castiblanco, J. Gil, A. Rojas, D. Osorio, S. Gutiérrez et al., TALE1 from Xanthomonas axonopodis pv. Manihotis acts as a transcriptional activator in plant cells and is important for pathogenicity in cassava plants, Molecular Plant Pathology, vol.14, pp.84-95, 2013.

C. Guerrero, N. A. , I. Mc, D. G. Mendoza-cozatl, and O. Valdes-lopez, Common bean: a legume model on the rise for unraveling responses and adaptations to iron, zinc and phosphate deficiencies, Frontiers in Plant Science, vol.7, pp.1-7, 2016.

H. Celia, N. Noinaj, S. D. Zakharov, E. Bordignon, I. Botos et al., Structural insight into the role of the Ton complex in energy transduction, Nature, vol.538, pp.60-65, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01788473

T. Cermak, E. L. Doyle, M. Christian, L. Wang, Y. Zhang et al., Efficient design and assembly of custom TALEN and other TAL effector-based constructs for DNA targeting, Nucleic Acids Research, vol.39, pp.1-11, 2011.

R. A. Cernadas, E. L. Doyle, D. O. Niño-liu, K. E. Wilkins, T. Bancroft et al., CodeAssisted Discovery of TAL Effector Targets in Bacterial Leaf Streak of Rice Reveals Contrast with Bacterial Blight and a Novel Susceptibility Gene, PLoS Pathogens, vol.10, p.1003972, 2014.

S. Cesbron, M. Briand, S. Essakhi, S. Gironde, T. Boureau et al., Comparative Genomics of Pathogenic and Nonpathogenic Strains of Xanthomonas arboricola Unveil Molecular and Evolutionary Events Linked to Pathoadaptation, Frontiers in Plant Science, vol.6, p.1126, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01455982

S. Chacón, . Mi, B. Pickersgill, D. G. Debouck, and J. S. Arias, Phylogeographic analysis of the chloroplast DNA variation in wild common bean (Phaseolus vulgaris L.) in the Americas, Plant Systematics and Evolution, vol.266, pp.175-195, 2007.

S. Chacón, . Mi, B. Pickersgill, and D. G. Debouck, Domestication patterns in common bean (Phaseolus vulgaris L.) and the origin of the Mesoamerican and Andean cultivated races, Theoretical and Applied Genetics, vol.110, pp.432-444, 2005.

J. Chan and P. H. Goodwin, Differentiation of Xanthomonas campestris pv. phaseoli from Xanthomonas campestris pv. phaseoli var. fuscans by PFGE and RFLP, European Journal of Plant Pathology, vol.105, pp.867-878, 1999.

M. Charpentier and G. Oldroyd, How close are we to nitrogen-fixing cereals?, Current Opinion in Plant Biology, vol.13, pp.556-564, 2010.

L. Q. Chen, SWEET sugar transporters for phloem transport and pathogen nutrition, New Phytologist, vol.201, pp.1150-1155, 2014.

C. Chin, D. H. Alexander, P. Marks, A. A. Klammer, J. Drake et al., , 2013.

. Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data, Nature Methods, vol.10, pp.563-569

D. Chinchilla, Z. Bauer, M. Regenass, T. Boller, and G. Felix, The Arabidopsis Receptor Kinase FLS2 Binds flg22 and Determines the Specificity of Flagellin Perception, The Plant Cell, vol.18, pp.465-476, 2006.

S. T. Chisholm, G. Coaker, B. Day, and B. J. Staskawicz, Host-Microbe Interactions : Shaping the Evolution of the Plant Immune Response, Cell, vol.124, pp.803-814, 2006.

H. Cho, J. G. Kang, J. Lee, J. Lee, S. K. Jeon et al., Direct regulation of E-cadherin by targeted histone methylation of TALE-SET fusion protein in cancer cells, Oncotarget, vol.6, pp.23837-23881, 2015.

H. J. Cho, Y. J. Park, T. H. Noh, Y. T. Kim, J. G. Kim et al., Molecular analysis of the hrp gene cluster in Xanthomonas oryzae pathovar oryzae KACC10859, Microbial Pathogenesis, vol.44, pp.473-483, 2008.

M. Christenhusz and J. W. Byng, The number of known plants species in the world and its annual increase, Phytotaxa, vol.261, p.201, 2016.

M. Christian, T. Cermak, E. L. Doyle, C. Schmidt, F. Zhang et al., Targeting DNA double-strand breaks with TAL effector nucleases, Genetics, vol.186, pp.756-761, 2010.

M. L. Christian, Z. L. Demorest, C. G. Starker, M. J. Osborn, M. D. Nyquist et al.,

G. Targeting and . Effectors, A Comparison of Activities of TALENs Constructed with NN and NK Repeat Variable Di-Residues

, PLoS ONE, vol.7

Z. Chu, B. Fu, H. Yang, C. Xu, Z. Li et al., Targeting xa13, a recessive gene for bacterial blight resistance in rice, Theoretical and Applied Genetics, vol.112, pp.455-461, 2006.

Z. Chu, M. Yuan, J. Yao, X. Ge, B. Yuan et al., Promoter mutations of an essential gene for pollen development result in disease resistance in rice, Genes and Development, vol.20, pp.1250-1255, 2006.

N. P. Cianciotto, Type II secretion: A protein secretion system for all seasons, Trends in Microbiology, vol.13, pp.581-588, 2005.

K. A. Cichy, T. G. Porch, J. S. Beaver, P. Cregan, D. Fourie et al., A Phaseolus vulgaris diversity panel for andean bean improvement, Crop Science, vol.55, pp.2149-2160, 2015.

M. Cohn, R. S. Bart, M. Shybut, D. Dahlbeck, M. Gomez et al., , 2014.

, Xanthomonas axonopodis virulence is promoted by a transcription activator-like effector-mediated induction of a SWEET sugar transporter in cassava, Molecular plant-microbe interactions : MPMI, vol.27, pp.1186-1198

L. Cong, R. Zhou, Y. Kuo, M. Cunniff, and F. Zhang, Comprehensive Interrogation of Natural TALE DNA Binding Modules and Transcriptional Repressor Domains, Nature Communications, vol.3, 2012.

E. C. Constantin, I. Cleenwerck, M. Maes, S. Baeyen, C. Van-malderghem et al., Genetic characterization of strains named as Xanthomonas axonopodis pv. dieffenbachiae leads to a taxonomic revision of the X. axonopodis species complex, Plant Pathology, vol.65, pp.792-806, 2016.

R. R. Corey and M. P. Starr, Colony types of Xanthomonas phaseoli, Journal of Bacteriology, vol.74, pp.137-140, 1957.

G. Cornelis, The type III secretion injectisome, Nature reviews Microbiology, vol.4, pp.811-825, 2006.

J. W. Costerton, K. Cheng, G. G. Geesey, T. I. Ladd, J. C. Nickel et al., BACTERIAL BIOFILMS IN NATlJRE AND DISEASE. Annual Review of Microbiology, vol.41, pp.435-464, 1987.

J. W. Costerton, Z. Lewandowski, D. E. Caldwell, D. R. Korber, and H. M. Lappin-scott, Microbial Biofilms. Annual Review of Microbiology, vol.49, pp.711-745, 1995.

T. A. Coutinho, L. Van-der-westhuizen, J. Roux, S. A. Mcfarlane, and S. N. Venter, Significant host jump of Xanthomonas vasicola from sugarcane to a Eucalyptus grandis clone in South Africa, Plant Pathology, vol.64, pp.576-581, 2015.

K. L. Cox, F. Meng, K. E. Wilkins, F. Li, P. Wang et al., TAL effector driven induction of a SWEET gene confers susceptibility to bacterial blight of cotton, Nature Communications, vol.8, pp.1-14, 2017.

Q. Cronk, I. Ojeda, and R. T. Pennington, Legume comparative genomics: Progress in phylogenetics and phylogenomics, Current Opinion in Plant Biology, vol.9, pp.99-103, 2006.

G. Crooks, G. Hon, J. Chandonia, and S. Brenner, WebLogo: a sequence logo generator, Genome Research, vol.14, pp.1188-1190, 2004.

S. Cunnac, S. Bolot, F. Serna, N. Ortiz, E. Szurek et al., High quality draft genome sequences of two Xanthomonas citri pv. malvacearum strains, Genome announcements, vol.1, pp.674-687, 2013.

S. Cunnac, M. Lindeberg, and A. Collmer, Pseudomonas syringae type III secretion system effectors: repertoires in search of functions, Current Opinion in Microbiology, vol.12, pp.53-60, 2009.

J. L. Dangl, D. M. Horvath, and B. J. Staskawicz, Pivoting the Plant Immune System from Dissection to Deployment, Science, vol.341, p.746, 2013.

T. Danhorn and C. Fuqua, Biofilm Formation by Plant-Associated Bacteria, Annual Review of Microbiology, vol.61, pp.401-422, 2007.
DOI : 10.1146/annurev.micro.61.080706.093316

E. Darmon and D. Leach, Bacterial genome instability. Microbiology and molecular biology reviews : MMBR, vol.78, pp.1-39, 2014.

A. Darrasse, S. Bolot, L. Serres-giardi, E. Charbit, T. Boureau et al., , 2013.

. High-quality, Draft Genome Sequences of Xanthomonas axonopodis pv. glycines Strains CFBP 2526 and CFBP 7119, Genome announcements, vol.1, pp.1036-1049

A. Darrasse, C. Bureau, R. Samson, C. E. Morris, and M. A. Jacques, Contamination of bean seeds by Xanthomonas axonopodis pv. phaseoli associated with low bacterial densities in the phyllosphere under field and greenhouse conditions, European Journal of Plant Pathology, vol.119, pp.203-215, 2007.

A. Darrasse, S. Carrère, V. Barbe, T. Boureau, M. L. Arrieta-ortiz et al., , 2013.

, Genome sequence of Xanthomonas fuscans subsp. fuscans strain 4834-R reveals that flagellar motility is not a general feature of xanthomonads, BMC Genomics, vol.14, p.761

A. Darrasse, A. Darsonval, T. Boureau, M. N. Brisset, D. K. Jacques et al., Transmission of plant-pathogenic bacteria by nonhost seeds without induction of an associated defense reaction at emergence, Applied and Environmental Microbiology, vol.76, p.6787, 2010.

A. Darsonval, A. Darrasse, K. Durand, C. Bureau, S. Cesbron et al., Adhesion and fitness in the bean phyllosphere and transmission to seed of Xanthomonas fuscans subsp. fuscans. Molecular plant-microbe interactions, MPMI, vol.22, pp.747-757, 2009.

A. Darsonval, A. Darrasse, D. Meyer, M. Demarty, K. Durand et al., The Type III Secretion System of Xanthomonas fuscans subsp . fuscans Is Involved in the Phyllosphere Colonization Process and in Transmission to Seeds of Susceptible Beans ?, Applied and environmental microbiology, vol.74, pp.2669-2678, 2008.

A. Degrave, S. Siamer, T. Boureau, and M. A. Barny, The AvrE superfamily: Ancestral type III effectors involved in suppression of pathogen-associated molecular pattern-triggered immunity, Molecular Plant Pathology, vol.16, pp.899-905, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01397129

D. Deng, C. Yan, X. Pan, M. Mahfouz, J. Wang et al., Structural Basis for Sequence-Specific Recognition of DNA by TAL Effectors, Science, vol.335, pp.720-723, 2012.

L. Deslandes and S. Rivas, Catch me if you can: Bacterial effectors and plant targets, Trends in Plant Science, vol.17, pp.644-655, 2012.
DOI : 10.1016/j.tplants.2012.06.011

. Doorn-j-van, P. M. Boonekamp, and B. Oudega, Parital Characterization of Fimbriae of Xanthomonas campestris pv. campestris, Molecular plant-microbe interactions, vol.7, pp.334-378, 1994.

J. Doughari, An Overview of Plant Immunity, Journal of Plant Pathology & Microbiology, vol.6, pp.1-11, 2015.

D. W. Dowson, On the systematic position and generic names of the Gram negative bacterial plant pathogens, Parasitenkunde und Infektionskrankheiten, vol.2, pp.177-193, 1939.

E. L. Doyle, N. J. Booher, D. S. Standage, D. F. Voytas, V. P. Brendel et al., TAL Effector-Nucleotide Targeter (TALE-NT) 2.0: Tools for TAL effector design and target prediction, Nucleic Acids Research, vol.40, pp.117-122, 2012.
DOI : 10.1093/nar/gks608

URL : https://academic.oup.com/nar/article-pdf/40/W1/W117/18785296/gks608.pdf

E. L. Doyle, A. W. Hummel, Z. L. Demorest, C. G. Starker, D. F. Voytas et al., TAL effector specificity for base 0 of the DNA target is altered in a complex, effector-and assay-dependent manner by substitutions for the tryptophan in cryptic repeat -1, PLoS ONE, vol.8, p.82120, 2013.

E. L. Doyle, B. L. Stoddard, D. F. Voytas, and A. J. Bogdanove, TAL effectors: Highly adaptable phytobacterial virulence factors and readily engineered DNA-targeting proteins, Trends in Cell Biology, vol.23, pp.390-398, 2013.
DOI : 10.1016/j.tcb.2013.04.003

URL : http://europepmc.org/articles/pmc3729746?pdf=render

R. W. Duncan, S. P. Singh, and R. L. Gilbertson, Interaction of common bacterial blight bacteria with disease resistance quantitative trait Loci in common bean, Phytopathology, vol.101, pp.425-435, 2011.

D. W. Dye, J. F. Bradbury, M. Goto, A. C. Hayward, R. A. Lelliott et al., International standards for naming pathovars of phytopathogenic bacteria and a list of pathovar names and pathotype strains, Review of Plant Pathology, vol.59, pp.153-159, 1980.

. Efsa-plh-panel, Scientific Opinion on the pest categorisation of Xanthomonas axonopodis pv. phaseoli and Xanthomonas fuscans subsp, fuscans. EFSA Journal, vol.12, p.3856, 2014.

. Efsa-plh-panel, Scientific Opinion on the pest categorisation of Spodoptera littoralis, EFSA Journal, vol.13, p.3987, 2015.

J. Eid, A. Fehr, J. Gray, K. Luong, J. Lyle et al., Single Polymerase Molecules. Science, vol.323, pp.133-138, 2009.

. Eppo/cabi, Xanthomonas axonopodis pv. phaseoli. EPPO quarantine pest, 1986.

A. Erkes, M. Reschke, J. Boch, and J. Grau, Evolution of transcription activator-like effectors in Xanthomonas oryzae, Genome Biology and Evolution, vol.2, pp.1-15, 2017.

A. Escalon, S. Javegny, C. Vernière, L. D. Noël, K. Vital et al., Variations in type III effector repertoires, pathological phenotypes and host range of Xanthomonas citri pv. citri pathotypes, Molecular Plant Pathology, vol.14, pp.483-496, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01199321

T. Eulgem, P. J. Rushton, S. Robatzek, and I. E. Somssich, The WRKY superfamily of plant transcription factors, Trends in Plant Science, vol.5, pp.199-206, 2000.

G. Felix, J. D. Duran, S. Volko, and T. Boller, Plants have a sensitive perception system for the most conserved domain of bacterial flagellin, Plant Journal, vol.18, pp.265-276, 1999.

R. M. Ferreira, A. De-oliveira, L. M. Moreira, J. J. Belasque, E. Gourbeyre et al.,

, A TALE of Transposition: Tn3-like transposons play a major role in the spread of pathogenicity determinants of xanthomonas citri and other xanthomonads, mBio, vol.6, pp.1-12

D. Feyter, R. Yang, Y. Gabriel, and D. W. , Gene-for-genes interactions between cotton R genes and Xanthomonas campestris pv. malvacearum avr genes, Molecular plant-microbe interactions : MPMI, vol.6, pp.225-237, 1993.

A. Figueiredo, F. Monteiro, and M. Sebastiana, Subtilisin-like proteases in plant-pathogen recognition and immune priming: a perspective, Frontiers in Plant Science, vol.5, pp.1-4, 2014.

C. Fininsa, Effect of intercropping bean with maize on bean common bacterial blight and rust diseases, International Journal of Pest Management, vol.42, pp.51-54, 1996.

C. Fininsa, Relationship between common bacterial blight severity and bean yield loss in pure stand and bean-maize intercropping systems, International Journal of Pest Management, vol.49, pp.177-185, 2003.

C. Fininsa and T. Tefera, Effect of primary inoculum sources of bean common bacterial blight on early epidemics, seed yield and quality aspects, International Journal of Pest Managment, vol.47, pp.221-225, 2001.

M. Fischer-le-saux, S. Bonneau, S. Essakhi, C. Manceau, and M. A. Jacques, Aggressive emerging pathovars of Xanthomonas arboricola represent widespread epidemic clones distinct from poorly pathogenic strains, as revealed by multilocus sequence typing, Applied and Environmental Microbiology, vol.81, pp.4651-4668, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01905527

H. H. Flor, Current Status of the Gene-For-Gene Concept, Annual Review of Phytopathology, vol.9, pp.275-296, 1971.

C. H. Foyer, H. Lam, H. T. Nguyen, K. Siddique, R. K. Varshney et al.,

, Neglecting legumes has compromised human health and sustainable food production, Nature Plants, vol.2, p.16112

R. Fronzes, P. J. Christie, and G. Waksmas, The structural biology of type IV secretion systems, Nature Review Microbiology, vol.7, p.703, 2009.

E. Y. Furuya and F. D. Lowy, Antimicrobial-resistant bacteria in the community setting, Nature reviews. Microbiology, vol.4, pp.36-45, 2006.

L. Gagnevin, S. Bolot, J. L. Gordon, O. Pruvost, C. Vernière et al., Draft Genome Sequence of Xanthomonas axonopodis pv. allii Strain CFBP 6369, Genome announcements, vol.2, pp.727-741, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01209994

M. M. Gakuubi, J. M. Wagacha, S. F. Dossaji, and W. Wanzala, Chemical Composition and Antibacterial Activity of Essential Oils of Tagetes minuta (Asteraceae) against Selected Plant Pathogenic Bacteria, International Journal of Microbiology, 2016.

J. E. Galán and A. Collmer, Type III Secretion Machines: Bacterial Devices for Protein Delivery into Host Cells, Science, vol.284, pp.1322-1329, 1999.

B. S. Gaut, The complex domestication history of the common bean, Nature genetics, vol.46, pp.663-667, 2014.

R. Geißler, H. Scholze, S. Hahn, J. Streubel, U. Bonas et al., Transcriptional activators of human genes with programmable DNA-specificity, PLoS ONE, vol.6, p.19509, 2011.

M. Gena, R. Shah, K. S. Jadon, and B. L. Mali, Host range of Xanthomonas axonopodis pv. vignicola, the incitant of bacterial blight in cowpea, Indian Phytopatology, vol.62, pp.539-540, 2009.

R. G. Gerlach and M. Hensel, Protein secretion systems and adhesins: The molecular armory of Gram-negative pathogens, International Journal of Medical Microbiology, vol.297, pp.401-415, 2007.

R. L. Gilbertson and D. P. Maxwell, Common bacterial blight of bean. Plant diseases of international importance. Volume II. Diseases of vegetables and oil seed crops, pp.18-39, 1992.

A. M. Gochez, G. V. Minsavage, N. Potnis, B. I. Canteros, R. E. Stall et al., A functional XopAG homologue in Xanthomonas fuscans pv. aurantifolii strain C limits host range, Plant Pathology, vol.64, pp.1207-1214, 2015.

P. H. Goodwin and C. R. Sopher, Water stress in leaves of Phaseolus vulgaris infected with Xanthomonas campestris pv. phaseoli, Journal of Phytopathology, vol.140, pp.219-226, 1994.

J. L. Gordon, P. Lefeuvre, A. Escalon, V. Barbe, S. Cruveiller et al., Comparative genomics of 43 strains of Xanthomonas citri pv. citri reveals the evolutionary events giving rise to pathotypes with different host ranges, BMC Genomics, vol.16, 2015.

P. H. Graham and P. Ranalli, Common bean (Phaseolus vulgaris L.), Field Crops Research, vol.53, pp.131-146, 1997.

J. Grant, A. S. Arantes, P. Stothard, T. Carver, K. Rutherford et al.,

, Comparing thousands of circular genomes using the CGView Comparison Tool, BMC genomics, vol.13, p.202

S. R. Grant, E. J. Fisher, J. H. Chang, B. M. Mole, and J. L. Dangl, Subterfuge and manipulation: type III effector proteins of phytopathogenic bacteria, Annual Review of Microbiology, vol.60, pp.425-449, 2006.

J. Grau, M. Reschke, A. Erkes, J. Streubel, R. D. Morgan et al., AnnoTALE: bioinformatics tools for identification, annotation, and nomenclature of TALEs from Xanthomonas genomic sequences, Scientific Reports, vol.6, p.21077, 2016.

J. Grau, A. Wolf, M. Reschke, U. Bonas, S. Posch et al., Computational Predictions Provide Insights into the Biology of TAL Effector Target Sites, PLoS Computational Biology, vol.9, 2013.

A. K. Grennan, Plant response to bacterial pathogens. Overlap between innate and gene-for-gene defense response, Plant physiology, vol.142, pp.809-820, 2006.

V. Grimault, V. Olivier, M. Rolland, A. Darrasse, and M. A. Jacques, Seed health testing methods. 7-021: Detection of Xanthomonas axonopodis pv. phaseoli on Phaseolus vulgaris. ISTA International rules for seed testing, International Seed Testing Association, pp.1-20, 2014.

S. H. Guan, C. Gris, S. Cruveiller, C. Pouzet, L. Tasse et al., Experimental evolution of nodule intracellular infection in legume symbionts, The ISME Journal, vol.7, pp.1367-1377, 2013.

K. Gu, J. S. Sangha, Y. Li, and Z. C. Yin, High-resolution genetic mapping of bacterial blight resistance gene Xa10, Theoretical and Applied Genetics, vol.116, pp.155-163, 2008.

K. Gu, D. Tian, C. Qiu, and Z. Yin, Transcription activator-like type III effector AvrXa27 depends on OsTFIIA?5 for the activation of Xa27 transcription in rice that triggers disease resistance to Xanthomonas oryzae pv. oryzae, Molecular Plant Pathology, vol.10, pp.829-835, 2009.

K. Gu, B. Yang, D. Tian, L. Wu, D. Wang et al., R gene expression induced by a type-III effector triggers disease resistance in rice, Nature, vol.435, pp.1122-1125, 2005.

W. Guo, Y. Cui, Y. Li, C. Y. Zhou, L. Yuan et al., Identification of seven Xanthomonas oryzae pv. oryzicola genes potentially involved in pathogenesis in rice, Microbiology, vol.158, pp.505-518, 2012.

A. Hajri, C. Brin, G. Hunault, F. Lardeux, C. Lemaire et al., A «repertoire for repertoire» hypothesis: Repertoires of type three effectors are candidate determinants of host specificity in Xanthomonas, PLoS ONE, vol.4, p.6632, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00729932

A. Hajri, C. Brin, S. Zhao, P. David, J. Feng et al., Multilocus sequence analysis and type III effector repertoire mining provide new insights into the evolutionary history and virulence of Xanthomonas oryzae, Molecular Plant Pathology, vol.13, pp.288-302, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01199331

A. Hajri, D. Meyer, F. Delort, J. Guillaumès, C. Brin et al., Identification of a genetic lineage within Xanthomonas arboricola pv. juglandis as the causal agent of vertical oozing canker of Persian (English) walnut in France, Plant Pathology, vol.59, pp.1014-1022, 2010.

A. Hajri, J. F. Pothier, M. Fischer-le-saux, S. Bonneau, S. Poussier et al., Type Three Effector Gene Distribution and Sequence Analysis Provide New Insights into the Pathogenicity of Plant-Pathogenic Xanthomonas arboricola, Applied and environmental microbiology, vol.78, pp.371-384, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01199341

K. E. Hammond-kosack and K. Kanyuka, Resistance genes (R genes) in plants, Encyclopedia of Life Sciences, pp.1-21, 2007.

J. K. Hane, Y. Ming, L. G. Kamphuis, M. N. Nelson, G. Garg et al., A comprehensive draft genome sequence for lupin (Lupinus angustifolius), an emerging health food: insights into plant-microbe interactions and legume evolution, Plant Biotechnology Journal, vol.15, pp.318-330, 2017.

H. Hashimi, A. Zíková, A. K. Panigrahi, K. D. Stuart, and J. Luke?, TbRGG1 , an essential protein involved in kinetoplastid RNA metabolism that is associated with a novel multiprotein complex, RNA, vol.14, pp.970-980, 2008.

P. Hauck, R. Thilmony, and S. Y. He, A Pseudomonas syringae type III effector suppresses cell wall-based extracellular defense in susceptible Arabidopsis plants, Proceedings of the National Academy of Sciences of the United States of America, vol.100, pp.8577-82, 2003.

J. Hausner, N. Hartmann, M. Jordan, and D. Büttner, The predicted lytic transglycosylase HpaH from Xanthomonas campestris pv. vesicatoria associates with the type III secretion system and promotes effector protein translocation, Infection and Immunity, vol.85, pp.788-804, 2017.

I. Hayat, A. Ahmad, T. Masud, A. Ahmed, and S. Bashir, Nutritional and health perspectives of beans (Phaseolus vulgaris L.): an overview, Critical reviews in food science and nutrition, vol.54, pp.580-92, 2014.

A. C. Hayward, The hosts of Xanthomonas, pp.1-119, 1993.

G. L. Hazelbauer, Bacterial Chemotaxis : The Early Years of Molecular Studies, Annual Review of Microbiology, vol.66, pp.285-303, 2012.

G. L. Hazelbauer, J. J. Falke, and J. S. Parkinson, Bacterial chemoreceptors: high-performance signaling in networked arrays, Trends in Biochemical Sciences, vol.33, pp.9-19, 2008.

S. Y. He, K. Nomura, and T. S. Whittam, Type III protein secretion mechanism in mammalian and plant pathogens, Biochimica et Biophysica Acta (BBA), vol.1694, pp.181-206, 2004.

P. He, L. Shan, N. C. Lin, G. B. Martin, B. Kemmerling et al., Specific Bacterial Suppressors of MAMP Signaling Upstream of MAPKKK in Arabidopsis Innate Immunity, Cell, vol.125, pp.563-575, 2006.

S. He, B. K. Simpson, H. Sun, M. O. Ngadi, Y. Ma et al., Phaseolus vulgaris Lectins: A Systematic Review of Characteristics and Health Implications, Critical reviews in food science and nutrition, 2015.

A. Helmstädter, Beans and diabetes: Phaseolus vulgaris preparations as antihyperglycemic agents, Journal of medicinal food, vol.13, pp.251-255, 2010.

L. Hersemann, D. Wibberg, J. Blom, A. Goesmann, F. Widmer et al., Comparative genomics of host adaptive traits in Xanthomonas translucens pv. graminis, BMC genomics, vol.18, p.35, 2017.

H. Heuer, Y. N. Yin, Q. Y. Xue, K. Smalla, and J. H. Guo, Repeat domain diversity of avrBs3-like genes in Ralstonia solanacearum strains and association with host preferences in the field, Applied and Environmental Microbiology, vol.73, pp.4379-4384, 2007.

R. J. Hillocks, C. S. Madata, R. Chirwa, E. M. Minja, and S. Msolla, Phaseolus bean improvement in Tanzania, Euphytica, vol.150, pp.215-231, 2006.

S. S. Hirano and C. D. Upper, Bacteria in the leaf ecosystem with emphasis on Pseudomonas syringae-a pathogen, ice nucleus, and epiphyte, Microbiology and molecular biology reviews : MMBR, vol.64, pp.624-53, 2000.

K. Hnatuszko-konka, T. Kowalczyk, A. Gerszberg, A. Wiktorek-smagur, and A. K. Kononowicz, Phaseolus vulgaris -Recalcitrant potential, Biotechnology Advances, vol.32, pp.1205-1215, 2014.

C. M. Hopkins, F. F. White, S. H. Choi, A. Guo, and J. E. Leach, Identification of a family of avirulence genes from xanthomonas oryzae pv. oryzae, Molecular plant-microbe interactions : MPMI, vol.5, pp.451-459, 1992.

T. Hruz, O. Laule, G. Szabo, F. Wessendorp, S. Bleuler et al., Genevestigator V3 : A Reference Expression Database for the Meta-Analysis of Transcriptomes, Advances in Bioinformatics, pp.1-5, 2008.

P. D. Hsu, E. S. Lander, and F. Zhang, Development and Applications of CRISPR-Cas9 for Genome Engineering, Cell, vol.157, pp.1262-1278, 2014.

C. Huang, P. Pu, H. Huang, H. Sung, H. Liaw et al., Ecological genomics in Xanthomonas: the nature of genetic adaptation with homologous recombination and host shifts, BMC genomics, vol.16, p.1369, 2015.

Y. Hu, J. Zhang, H. Jia, D. Sosso, T. Li et al., Lateral organ boundaries 1 is a disease susceptibility gene for citrus bacterial canker disease, Proceedings of the National Academy of Sciences of the United States of America, vol.111, pp.521-530, 2014.

J. C. Huguet-tapia, Z. Peng, B. Yang, Z. Yin, S. Liu et al., Complete Genome Sequence of the African Strain AXO1947 of Xanthomonas oryzae pv, oryzae. Genome announcements, vol.4, pp.10-11, 2016.

M. Hulko, F. Berndt, M. Gruber, J. U. Linder, V. Truffault et al., The HAMP Domain Structure Implies Helix Rotation in Transmembrane Signaling, Cell, vol.126, pp.929-940, 2006.

A. W. Hummel, E. L. Doyle, and A. J. Bogdanove, Addition of transcription activator-like effector binding sites to a pathogen strainspecific rice bacterial blight resistance gene makes it effective against additional strains and against bacterial leaf streak, New Phytologist, vol.195, pp.883-893, 2012.

A. W. Hummel, K. E. Wilkins, L. Wang, R. A. Cernadas, and A. J. Bogdanove, A transcription activator-like effector from Xanthomonas oryzae pv. oryzicola elicits dose-dependent resistance in rice, Molecular plant pathology, vol.18, pp.55-56, 2016.

M. Hutin, Criblage de la diversité d'Oryza spp. pour l'identification de nouvelles sources de résistances dépendantes des effecteurs TAL à X. oryzae pv. oryzae, 2015.

M. Hutin, S. Césari, V. Chalvon, C. Michel, T. T. Tran et al., Ectopic activation of the rice NLR heteropair RGA4/RGA5 confers resistance to bacterial blight and bacterial leaf streak diseases, Plant Journal, vol.88, pp.43-55, 2016.

M. Hutin, A. L. Pérez-quintero, C. Lopez, and B. Szurek, MorTAL Kombat: the story of defense against TAL effectors through loss-ofsusceptibility, Frontiers in plant science, vol.6, p.535, 2015.

K. Ifuku, T. Endo, T. Shikanai, and E. Aro, Structure of the chloroplast NADH dehydrogenase-like complex: Nomenclature for nuclear-encoded subunits, Plant and Cell Physiology, vol.52, pp.1560-1568, 2011.

A. Indiana, Rôles du chimiotactisme et de la mobilité flagellaire dans la fitness des Xanthomonas, 2014.

A. Indiana, M. Briand, M. Arlat, L. Gagnevin, R. Koebnik et al., Draft genome sequence of the flagellated Xanthomonas fuscans subsp. fuscans strain CFBP 4884, Genome announcements, vol.2, pp.966-980, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01134880

N. Ishihama and H. Yoshioka, Post-translational regulation of WRKY transcription factors in plant immunity, Current Opinion in Plant Biology, vol.15, pp.431-437, 2012.

F. Islam, J. Renjifo, R. J. Redden, K. E. Basford, and S. Beebe, Association Between Seed Coat Polyphenolics (Tannins) and Disease Resistance in Common Bean, Plant Foods for Human Nutrition, vol.58, pp.285-297, 2003.

J. I?tvánek, M. Jaro?, A. K?enek, and J. ?epková, Genome assembly and annotation for red clover (Trifolium pratense; Fabaceae), 2014.

, American journal of botany, vol.101, pp.327-364

A. S. Iyer and S. R. Mccouch, The rice bacterial blight resistance gene xa5 encodes a novel form of disease resistance. Molecular plantmicrobe interactions, MPMI, vol.17, pp.1348-1354, 2004.

T. Izoré, J. V. Dessen, and A. , Biogenesis, regulation, and targeting of the type III secretion system, Structure, vol.19, pp.603-612, 2011.

J. M. Jacobs, C. Pesce, P. Lefeuvre, and R. Koebnik, Comparative genomics of a cannabis pathogen reveals insight into the evolution of pathogenicity in Xanthomonas, Frontiers in Plant Science, vol.6, p.431, 2015.

M. Jacques, M. Arlat, A. Boulanger, T. Boureau, S. Carrère et al.,

, Using Ecology, Physiology, and Genomics to Understand Host Specificity in Xanthomonas : French Network on Xanthomonads (FNX), Annual Review of Phytopathology, vol.54, pp.163-187

M. A. Jacques, S. Bolot, E. Charbit, A. Darrasse, M. Briand et al., HighQuality Draft Genome Sequence of Xanthomonas alfalfae subsp. alfalfae Strain CFBP 3836, Genome Announcements, vol.1, pp.1035-1048, 2013.

M. Jacques, J. K. Darrasse, A. Samson, and R. , Xanthomonas axonopodis pv. phaseoli ar. fuscans Is Aggregated in Stable Biofilm Population Sizes in the Phyllosphere of Field-Grown Beans, Applied and Environmental Microbiology, vol.71, pp.2008-2015, 2005.
URL : https://hal.archives-ouvertes.fr/hal-01134886

N. Jalan, V. Aritua, D. Kumar, F. Yu, J. B. Jones et al., Comparative genomic analysis of Xanthomonas axonopodis pv. citrumelo F1, which causes citrus bacterial spot disease, and related strains provides insights into virulence and host specificity, Journal of Bacteriology, vol.193, pp.6342-6357, 2011.

N. Jalan, D. Kumar, F. Yu, J. B. Jones, J. H. Graham et al., Complete Genome Sequence of Xanthomonas citri subsp. citri Strain Aw12879, a Restricted-Host-Range Citrus Canker-Causing Bacterium, Genome Announcements, vol.1, pp.235-248, 2013.

G. Jha, R. Rajeshwari, and R. V. Sonti, Functional interplay between two Xanthomonas oryzae pv,. oryzae secretion systems in modulating virulence on rice, Molecular plant-microbe interactions : MPMI, vol.20, pp.31-40, 2007.

Y. Jiang, L. Guo, X. Ma, X. Zhao, B. Jiao et al., The WRKY transcription factors PtrWRKY18 and PtrWRKY35 promote Melampsora resistance in Populus, Tree Physiology, vol.37, pp.665-675, 2017.

T. L. Johnson, J. Abendroth, W. Hol, M. Sandkvist, O. De-lange et al., Breaking the DNAbinding code of Ralstonia solanacearum TAL effectors provides new possibilities to generate plant resistance genes against bacterial wilt disease, FEMS Microbiology Letters, vol.199, pp.773-786, 2006.

O. De-lange, . De, C. Wolf, J. Dietze, J. Elsaesser et al., Programmable DNA-binding proteins from Burkholderia provide a fresh perspective on the TALE-like repeat domain, Nucleic Acids Research, vol.42, pp.7436-7449, 2014.

O. De-lange, C. Wolf, P. Thiel, J. Krüger, C. Kleusch et al., DNA-binding proteins from marine bacteria expand the known sequence diversity of TALE-like repeats, Nucleic Acids Research, vol.43, pp.10065-10080, 2015.

D. Lapin and G. Van-den-ackerveken, Susceptibility to plant disease: More than a failure of host immunity, Trends in Plant Science, vol.18, pp.546-554, 2013.

N. Van-larebeke, G. Engler, M. Holsters, S. Van-den-elascker, I. Zaenen et al., Large plasmid in Agrobacterium tumefaciens essential for crown gall-inducing ability, Nature, vol.252, pp.169-170, 1974.

L. R. Lareo and V. F. González, Acceptability and nutritional quality of common beans (Phaseolus vulgaris L.): A bibliography. Cali Colombia: Centro International de Agricultura Tropical, pp.1-279, 1988.

C. Lau, H. Zhu, J. Tay, Z. Li, F. C. Tay et al., Genetic rearrangements of variable di-residue (RVD)-containing repeat arrays in a baculoviral TALEN system, Molecular therapy. Methods & clinical development, vol.1, p.14050, 2014.

J. Lavigne, E. Botella, and D. O'callaghan, Les systèmes de sécrétions de type IV et leurs effecteurs, Pathologie Biologie, vol.54, p.296, 2006.

M. Lavin, P. S. Herendeen, and M. F. Wojciechowski, Evolutionary rates analysis of leguminosae implicates a rapid diversification of lineages during the tertiary, Systematic Biology, vol.54, pp.575-594, 2005.

G. R. Lazo, R. Roffey, and D. W. Gabriel, Pathovars of Xanthomonas campestris are distinguishable by restriction fragment-length polymorphism, International Journal of Systematic Bacteriology, vol.37, pp.214-221, 1987.

B. M. Lee, Y. J. Park, D. S. Park, H. W. Kang, J. G. Kim et al., The genome sequence of Xanthomonas oryzae pathovar oryzae KACC10331, the bacterial blight pathogen of rice, Nucleic Acids Research, vol.33, pp.577-586, 2005.

Y. Leng, Y. Yang, D. Ren, L. Huang, L. Dai et al., A rice PECTATE LYASE-LIKE gene is required for plant growth and leaf senescence, Plant Physiology, vol.174, pp.1151-1166, 2017.

H. L. Levin and J. V. Moran, Dynamic interactions between transposable elements and their hosts, Nature Reviews Genetics, vol.12, p.615, 2011.

L. Li, A. Atef, A. Piatek, Z. Ali, M. Piatek et al., Characterization and DNAbinding specificities of Ralstonia TAL-like effectors, Molecular Plant, vol.6, pp.1318-1330, 2013.

T. Li, S. Huang, J. Zhou, and B. Yang, Designer TAL effectors induce disease susceptibility and resistance to Xanthomonas oryzae pv. oryzae in rice, Molecular Plant, vol.6, pp.781-789, 2013.

T. Li, B. Liu, M. H. Spalding, D. P. Weeks, and B. Yang, High-efficiency TALEN-based gene editing produces disease-resistant rice, Nature Biotechnology, vol.30, pp.390-392, 2012.

L. Li, C. Stoeckert, and D. S. Roos, OrthoMCL: Identification of Ortholog Groups for Eukaryotic Genomes, Genome Research, vol.13, p.2178, 2003.

J. Li and N. Wang, The gpsX gene encoding a glycosyltransferase is important for polysaccharide production and required for full virulence in Xanthomonas citri subsp. citri, BMC Microbiology, vol.12, 2012.

C. Li, J. Wei, Y. Lin, and H. Chen, Gene silencing using the recessive rice bacterial blight resistance gene xa13 as a new paradigm in plant breeding, Plant Cell Reports, vol.31, pp.851-862, 2012.

R. Li, H. Zhu, J. Ruan, W. Qian, X. Fang et al., De novo assembly of human genomes with massively parallel short read sequencing, Genome Res, vol.20, pp.265-72, 2010.

P. Librado and J. Rozas, DnaSP v5: A software for comprehensive analysis of DNA polymorphism data, Bioinformatics, vol.25, p.1451, 2009.

S. Lin, Y. Zhao, Y. Zhu, M. Gosney, X. Deng et al., An Effective and Inducible System of TAL Effector-Mediated Transcriptional Repression in Arabidopsis, Molecular Plant, vol.9, pp.1546-1549, 2016.

P. B. Lindgren, The role of hrp genes during plant-bacterial interactions, Annual Review of Phytopathology, vol.35, pp.129-152, 1997.

P. B. Lindgren, R. C. Peet, and N. J. Panopoulos, Gene cluster of Pseudomonas syringae pv. 'phaseolicola' controls pathogenicity of bean plants and hypersensitivity of nonhost plants, Journal of Bacteriology, vol.168, pp.512-522, 1986.

S. E. Lindow and M. T. Brandl, Microbiology of the Phyllosphere, Applied and environmental microbiology, vol.69, pp.1875-1883, 2003.

S. Y. Liu, K. Yu, M. Huffner, S. J. Park, M. Banik et al., Construction of a BAC library and a physical map of a major QTL for CBB resistance of common bean (Phaseolus vulgaris L.), Genetica, vol.138, pp.709-716, 2010.

Q. Liu, M. Yuan, Y. Zhou, X. Li, J. Xiao et al., A paralog of the MtN3/saliva family recessively confers race-specific resistance to Xanthomonas oryzae in rice, Plant, Cell and Environment, vol.34, pp.1958-1969, 2011.

S. A. Lloyd, M. Norman, R. Rosqvist, and H. Wolf-watz, Yersinia YopE is targeted for type III secretion by N-terminal, not mRNA, signals, Molecular Microbiology, vol.39, pp.520-531, 2001.

M. I. Love, W. Huber, and S. Anders, Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2, Genome Biology, vol.15, pp.1-21, 2014.

H. Lu, P. Patil, M. A. Van-sluys, F. F. White, R. P. Ryan et al., Acquisition and evolution of plant pathogenesis-associated gene clusters and candidate determinants of tissue-specificity in Xanthomonas, PLoS ONE, vol.3, 2008.

R. Luo, B. Liu, Y. Xie, Z. Li, W. Huang et al., SOAPdenovo2: an empirically improved memoryefficient short-read de novo assembler, vol.1, p.18, 2012.

J. De-lúque and B. Creamer, Major constraints and trends for common bean production and commercialization ; establishing priorities for future research, Agronomía Colombiana, vol.32, pp.423-431, 2014.

W. Ma, F. Dong, J. Stavrinides, and D. S. Guttman, Type III effector diversification via both pathoadaptation and horizontal transfer in response to a coevolutionary arms race, PLoS Genetics, vol.2, pp.2131-2142, 2006.

V. Mageshwaran, S. Walia, and K. Annapurna, Isolation and partial characterization of antibacterial lipopeptide produced by Paenibacillus polymyxa HKA-15 against phytopathogen Xanthomonas campestris pv. phaseoli M-5, World Journal of Microbiology and Biotechnology, vol.28, pp.909-917, 2012.

M. M. Mahfouz, L. Li, M. Piatek, X. Fang, H. Mansour et al., Targeted transcriptional repression using a chimeric TALE-SRDX repressor protein, Plant Molecular Biology, vol.78, pp.311-321, 2012.

A. Mak, P. Bradley, A. J. Bogdanove, and B. L. Stoddard, TAL effectors: Function, structure, engineering and applications, Current Opinion in Structural Biology, vol.23, pp.93-99, 2013.

A. N. Mak, P. Bradley, R. A. Cernadas, A. J. Bogdanove, and B. L. Stoddard, The Crystal Structre of TAL Effector PthXo1 Bound to Its DNA Target, Science, vol.335, pp.716-719, 2012.

A. C. Mallory and H. Vaucheret, Functions of microRNAs and related small RNAs in plants, Nature Genetics, vol.38, pp.31-36, 2006.

M. D. Manson, J. P. Armitage, J. Hoch, and R. M. Macnab, Bacterial Locomotion and Signal Transduction, Journal of bacteriology, vol.180, pp.1009-1022, 1998.

M. C. Marín-rodríguez, J. Orchard, and G. B. Seymour, Pectate lyases, cell wall degradation and fruit softening, Journal of Experimental Botany, vol.53, pp.2115-2119, 2002.

E. Marois, G. Van-den-ackerveken, and U. Bonas, The xanthomonas type III effector protein AvrBs3 modulates plant gene expression and induces cell hypertrophy in the susceptible host, Molecular plant-microbe interactions : MPMI, vol.15, pp.637-646, 2002.

D. P. Martin, B. Murrell, M. Golden, A. Khoosal, and B. Muhire, RDP4: Detection and analysis of recombination patterns in virus genomes, Virus Evolution, vol.1, pp.1-5, 2015.

D. P. Martin, D. Posada, and C. Crandall-k-a,-williamson, A modified bootscan algorithm for automated identification of recombinant sequences and recombination breakpoints, AIDS research and human retroviruses, vol.21, pp.98-102, 2005.

D. Martin and E. Rybicki, RDP: detection of recombination amongst aligned sequences, Bioinformatics, vol.16, p.562, 2000.

L. Mayer, W. P. Da-silva, A. B. Moura, and C. T. Vendruscolo, AFLP analysis of Xanthomonas axonopodis and X. arboricola strains used in xanthan production studies reveal high levels of polymorphism, Brazilian Journal of Microbiology, vol.41, pp.741-748, 2010.

M. Melotto, W. Underwood, J. Koczan, K. Nomura, and S. Y. He, Plant Stomata Function in Innate Immunity against Bacterial Invasion, Cell, vol.126, pp.969-980, 2006.

E. M. Mendenhall, K. E. Williamson, D. Reyon, J. Y. Zou, O. Ram et al., Locus-specific editing of histone modifications at endogenous enhancers using programmable TALE-LSD1 fusions, Nature biotechnology, vol.31, pp.1133-1139, 2013.

A. C. Mercer, T. Gaj, R. P. Fuller, and C. F. Barbas, Chimeric TALE recombinases with programmable DNA sequence specificity, Nucleic Acids Research, vol.40, pp.11163-11172, 2012.

D. Merda, S. Bonneau, J. F. Guimbaud, K. Durand, C. Brin et al., , 2016.

, Recombination-prone bacterial strains form a reservoir from which epidemic clones emerge in agroecosystems, Environmental Microbiology Reports, vol.8, pp.572-581

D. Merda, M. Briand, E. Bosis, C. Rousseau, P. Portier et al., Ancestral acquisitions, gene flow and multiple evolutionary trajectories of the type three secretion system and effectors in Xanthomonas plant pathogens, Molecular Ecology, pp.1-14, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01904571

V. Messina, Nutritional and health benefits of dried beans, The American Journal of Clinical Nutrition, vol.100, pp.437-479, 2014.

C. Meziadi, M. Richard, A. Derquennes, V. Thareau, S. Blanchet et al., Development of molecular markers linked to disease resistance genes in common bean based on whole genome sequence, Plant Science, vol.242, pp.351-357, 2016.

N. Mhedbi, Approches cumulées de phylogénie et d'écologie pour déterminer les bases génétiques de la spécificité d'hôte des bactéries phytopathogènes , cas des Xanthomonas spp, 2010.

N. Mhedbi-hajri, A. Darrasse, S. Pigné, K. Durand, S. Fouteau et al., Sensing and adhesion are adaptive functions in the plant pathogenic xanthomonads, BMC evolutionary biology, vol.11, p.67, 2011.

N. Mhedbi-hajri, A. Hajri, T. Boureau, A. Darrasse, K. Durand et al., Evolutionary History of the Plant Pathogenic Bacterium Xanthomonas axonopodis, PLoS ONE, vol.8, p.58474, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01199308

S. Midha and P. B. Patil, Genomic insights into the evolutionary origin of Xanthomonas axonopodis pv. citri and its ecological relatives, Applied and Environmental Microbiology, vol.80, pp.6266-6279, 2014.

S. Midha, M. Ranjan, V. Sharma, A. K. Pinnaka, and P. B. Patil, Genome sequence of xanthomonas citri pv. mangiferaeindicae strain LMG 941, Journal of Bacteriology, vol.194, p.3031, 2012.

P. N. Miklas, D. P. Coyne, K. F. Grafton, N. Mutlu, J. Reiser et al., A major QTL for common bacterial resistance derives from the common bean great northern landrace cultivar Montana No, Euphytica, vol.131, issue.5, pp.137-146, 2003.

P. N. Miklas, J. D. Kelly, S. E. Beebe, and M. W. Blair, Common bean breeding for resistance against biotic and abiotic stresses: From classical to MAS breeding, Euphytica, vol.147, pp.105-131, 2006.

J. C. Misas-villamil, R. Van-der-hoorn, and G. Doehlemann, Papain-like cysteine proteases as hubs in plant immunity, New Phytologist, vol.212, pp.902-907, 2016.

Y. Miyanari, TAL effector-mediated genome visualization (TGV), Methods, vol.69, pp.198-204, 2014.

Y. Miyanari, C. Ziegler-birling, and M. Torres-padilla, Live visualization of chromatin dynamics with fluorescent TALEs, Nature structural & molecular biology, vol.20, pp.1321-1325, 2013.

A. Mkandawire, R. B. Mabagala, P. Guzmán, P. Gepts, and R. L. Gilbertson, Genetic Diversity and Pathogenic Variation of Common Blight Bacteria (Xanthomonas campestris pv. phaseoli and X. campestris pv. phaseoli var. fuscans) Suggests Pathogen Coevolution with the Common Bean, Phytopathology, vol.94, pp.593-603, 2004.

M. A. Molina, P. Godoy, M. I. Ramos-gonzález, N. Muñoz, J. L. Ramos et al., Role of iron and the TonB system in colonization of corn seeds and roots by Pseudomonas putida KT2440, Environmental Microbiology, vol.7, pp.443-449, 2005.

Y. Mora, R. Díaz, C. Vargas-lagunas, H. Peralta, G. Guerrero et al., Nitrogen-fixing rhizobial strains isolated from common bean seeds: Phylogeny, physiology, and genome analysis, Applied and Environmental Microbiology, vol.80, pp.5644-5654, 2014.

L. M. Moreira, N. F. Almeida, N. Potnis, S. S. Digiampietri-l-a,-adi, J. C. Bortolossi et al., Novel insights into the genomic basis of citrus canker based on the genome sequences of two strains of Xanthomonas fuscans subsp. aurantifolii, BMC Genomics, vol.11, p.238, 2010.

C. E. Morris and J. Monier, THE ECOLOGICAL SIGNIFICANCE OF BIOFILM FORMATION BY PLANT-ASSOCIATED BACTERIA, Annual Review of Phytopathology, vol.41, pp.429-453, 2003.

M. J. Moscou and A. J. Bogdanove, A simple cipher governs DNA recognition by TAL effectors, Science, vol.326, p.1501, 2009.

M. B. Mudgett, New Insights To the Function of Phytopathogenic Bacterial Type Iii Effectors in Plants, Annual Review of Plant Biology, vol.56, pp.509-531, 2005.

M. B. Mudgett, O. Chesnokova, D. Dahlbeck, E. T. Clark, O. Rossier et al., Molecular signals required for type III secretion and translocation of the Xanthomonas campestris AvrBs2 protein to pepper plants, Proceedings of the National Academy of Sciences, vol.97, pp.13324-13329, 2000.

F. Mus, M. B. Crook, K. Garcia, A. G. Costas, B. A. Geddes et al., , 2016.

, Symbiotic Nitrogen Fixation and the Challenges to Its Extension to Nonlegumes, Applied and Environmental Microbiology, vol.82, p.3698

N. Mutlu, A. K. Vidaver, D. P. Coyne, J. R. Steadman, P. A. Lambrecht et al., Differential Pathogenicity of Xanthomonas campestris pv. phaseoli and X. fuscans subsp. fuscans Strains on Bean Genotypes with Common Blight Resistance, Plant Disease, vol.92, pp.546-554, 2008.

T. Nakagawa, T. Kurose, T. Hino, K. Tanaka, M. Kawamukai et al., Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation, Journal of Bioscience and Bioengineering, vol.104, pp.34-41, 2007.

. Nascimento-v-do, O. Arf, M. Tarsitano, N. Garcia, S. Penteado-m-de et al., Economic analysis of rice and common bean production in succession to green manure crops and mecahnical soil decompression in Brazilian Savannah, Revista Ceres, vol.63, pp.315-322, 2016.

L. Navarro, F. Jay, K. Nomura, S. Y. He, and O. Voinnet, Suppression of the microRNA pathway by bacterial effector proteins, Science, vol.321, pp.964-967, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00339296

P. A. Ndakidemi, F. D. Dakora, E. M. Nkonya, D. Ringo, and H. Mansoor, Yield and economic benefits of common bean (Phaseolus vulgaris) and soybean (Glycine max) inoculation in northern Tanzania, Australian Journal of Experimental Agriculture, vol.46, pp.571-577, 2006.

P. D. Newell, C. D. Boyd, H. Sondermann, and G. A. O'toole, A c-di-GMP effector system controls cell adhesion by inside-out signaling and surface protein cleavage, PLoS Biology, vol.9, p.1000587, 2011.

H. Nishimasu, F. A. Ran, P. D. Hsu, S. Konermann, S. I. Shehata et al., Crystal Structure of Cas9 in Complex with Guide RNA and Target DNA, Cell, vol.156, pp.935-949, 2014.

L. Noel, F. Thieme, J. Gabler, D. Buttner, and U. Bonas, XopC and XopJ, two novel type III effector proteins from Xanthomonas campestris pv. vesicatoria, Journal of Bacteriology, vol.185, pp.7092-7102, 2003.

L. Noël, F. Thieme, D. Nennstiel, and U. Bonas, Two Novel Type III-Secreted Proteins of Xanthomonas campestris pv . vesicatoria Are Encoded within the hrp Pathogenicity Island Two Novel Type III-Secreted Proteins of Xanthomonas campestris pv . vesicatoria Are Encoded within the hrp Pathogenicity Island, Journal of Bacteriology, vol.184, pp.1340-1348, 2002.

N. Noinaj, M. Guillier, T. J. Barnard, and S. K. Buchanan, TonB-Dependent Transporters: Regulation, Structure, and Function, Annual Review of Microbiology, vol.64, pp.43-60, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00555668

H. Ochiai, Y. Inoue, M. Takeya, A. Sasaki, and H. Kaku, Genome sequence of Xanthomonas oryzae pv. oryzae suggests contribution of large numbers of effector genes and insertion sequences to its race diversity, Japan Agricultural Research Quarterly, vol.39, pp.275-287, 2005.

. Oepp/cabi, Xanthomonas axonopodis pv . phaseoli. Organismes de Quarantaine Pour l'Europe, 1986.

. Oepp/cabi, Xanthomonas axoponodis pv . citri. Organismes de Quarantaine Pour l'Europe 2ème éditi, 1996.

T. Ojanen-reuhs, N. Kalkkinen, B. Westerlund-wikström, J. Van-doorn, K. Haahtela et al., Characterization of the fimA gene encoding bundle-forming fimbriae of the plant pathogen Xanthomonas campestris pv. vesicatoria, Journal of Bacteriology, vol.179, pp.1280-1290, 1997.

G. Oldroyd, J. D. Murray, P. S. Poole, and J. A. Downie, The Rules of Engagement in the Legume-Rhizobial Symbiosis, Annual Review of Genetics, vol.45, pp.119-144, 2011.

G. De-oliveira-tostes, P. Araujo, J. S. , G. Farias, A. R. et al., Detection and cellular localization of Xanthomonas campestris pv. viticola in seeds of commercial 'Red Globe' grapes, Tropical Plant Pathology, vol.39, pp.134-140, 2014.

T. Van-opijnen, K. L. Bodi, and A. Camilli, Tn-seq: high-throughput parallel sequencing for fitness and genetic interaction studies in microorganisms, Nature Methods, vol.6, pp.767-772, 2009.

T. Van-opijnen and A. Camilli, Transposon insertion sequencing: a new tool for systems-level analysis of microorganisms, Nature Reviews Microbiology, vol.11, pp.435-442, 2013.

A. F. Opio, D. J. Allen, and J. M. Teri, Pathogenic variation in Xanthonomas campestris pv. phaseoli, the causal agent of common bacterial blight in Phaseolus beans, Plant Pathology (United Kingdom), vol.45, pp.1126-1133, 1996.

F. Opio, P. M. Kimani, S. M. Musaana, and R. Buruchara, Research on common blight and halo blight of common beans in east and central Africa, Bean Improvement Cooperative. Annual Report (USA), vol.45, pp.160-161, 2002.

A. Opio, J. Teri, and D. Allen, Studies on Seed Transmission of Xanthomonas campestris pv phaseoli in Common Beans in Uganda, 1993.

, African Crop Science Journal, vol.1, pp.59-67

E. Ormeño-orrillo, L. E. Servín-garcidueñas, M. A. Rogel, V. González, H. Peralta et al.,

, Taxonomy of rhizobia and agrobacteria from the Rhizobiaceae family in light of genomics, Systematic and Applied Microbiology, vol.38, pp.287-291

M. Padidam, S. Sawyer, and C. M. Fauquet, Possible emergence of new geminiviruses by frequent recombination, Virology, vol.265, p.218, 1999.

A. Pandey, S. K. Ray, R. V. Sonti, and R. Rajeshwari, GltB/D mutants of xanthomonas oryzae pv. oryzae are virulence deficient, Current Microbiology, vol.68, pp.105-112, 2014.

E. Paradis, J. Claude, and K. Strimmer, APE: Analyses of phylogenetics and evolution in R language, Bioinformatics, vol.20, pp.289-290, 2004.
URL : https://hal.archives-ouvertes.fr/ird-01887318

N. Parkinson, V. Aritua, J. Heeney, C. Cowie, J. Bew et al., Phylogenetic analysis of Xanthomonas species by comparison of partial gyrase B gene sequences, International Journal of Systematic and Evolutionary Microbiology, vol.57, pp.2881-2887, 2007.

N. Parkinson, C. Cowie, J. Heeney, and D. Stead, Phylogenetic structure of Xanthomonas determined by comparison of gyrB sequences, International Journal of Systematic and Evolutionary Microbiology, vol.59, pp.264-274, 2009.

L. Peng, Y. Fukao, M. Fujiwara, T. Takami, and T. Shikanai, Efficient Operation of NAD(P)H Dehydrogenase Requires Supercomplex Formation with Photosystem I via Minor LHCI in Arabidopsis, The Plant Cell, vol.21, pp.3623-3640, 2009.

Z. Peng, Y. Hu, J. Xie, N. Potnis, A. Akhunova et al., Long read and single molecule DNA sequencing simplifies genome assembly and TAL effector gene analysis of Xanthomonas translucens, BMC Genomics, vol.17, p.21, 2016.

A. Pereira, M. F. Carazzolle, V. Y. Abe, M. De-oliveira, M. N. Domingues et al., Identification of putative TAL effector targets of the citrus canker pathogens shows functional convergence underlying disease development and defense response, BMC Genomics, vol.15, p.157, 2014.

M. L. Pérez-bueno, M. Pineda, E. Díaz-casado, and M. Barón, Spatial and temporal dynamics of primary and secondary metabolism in Phaseolus vulgaris challenged by Pseudomonas syringae, Physiologica Plantarum, vol.153, pp.161-174, 2015.

A. L. Pérez-quintero, Bioinformatic approaches to the study of TAL effector evolution and function, 2017.

A. L. Pérez-quintero, L. Lamy, J. L. Gordon, A. Escalon, S. Cunnac et al., QueTAL: a suite of tools to classify and compare TAL effectors functionally and phylogenetically, Frontiers in Plant Science, vol.6, p.545, 2015.

A. L. Pérez-quintero, R. Lm, A. Dereeper, C. López, R. Koebnik et al., An Improved Method for TAL Effectors DNA-Binding Sites Prediction Reveals Functional Convergence in TAL Repertoires of Xanthomonas oryzae Strains, PLoS ONE, vol.8, p.68464, 2013.

L. M. Perilla-henao and C. L. Casteel, Vector-borne bacterial plant pathogens: Interactions with hemipteran insects and plants, Frontiers in Plant Science, vol.7, p.1163, 2016.

G. Perry, C. Dinatale, W. Xie, A. Navabi, Y. Reinprecht et al., , 2013.

C. Pesce, S. Bolot, E. Berthelot, C. Bragard, S. Cunnac et al., Draft Genome Sequence of Xanthomonas translucens pv. graminis Pathotype Strain CFBP 2053, Genome announcements, vol.3, pp.1174-1189, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01209993

C. Pesce, S. Bolot, S. Cunnac, P. Portier, M. Saux et al., High-Quality Draft Genome Sequence of the Xanthomonas translucens pv. cerealis Pathotype Strain CFBP 2541, Genome announcements, vol.3, p.1574, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01209993

I. Pieretti, M. Royer, V. Barbe, S. Carrere, R. Koebnik et al., The complete genome sequence of Xanthomonas albilineans provides new insights into the reductive genome evolution of the xylemlimited Xanthomonadaceae, BMC Genomics, vol.10, pp.1-15, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00730091

L. Pietrarelli, G. Balestra, and L. Varvaro, Effects of simulated rain on Pseudomonas syringae pv. tomato populations on tomato plants, Journal of Plant Pathology, vol.88, pp.245-251, 2006.

V. Poinsot, M. A. Carpéné, and F. Couderc, Coupled Mass Spectrometric Strategies for the Determination of Carbohydrates at Very Low Concentrations : The Case of Polysaccharides Involved in the Molecular Dialogue Between Plants and Rhizobia. The Complex World of Polysaccharides, 2012.

A. G. Portaliou, K. C. Tsolis, M. S. Loos, V. Zorzini, and A. Economou, Type III Secretion: Building and Operating a Remarkable Nanomachine, Trends in Biochemical Sciences, vol.41, pp.175-189, 2016.

D. Posada and K. A. Crandall, Evaluation of methods for detecting recombination from DNA sequences: Computer simulations, Proceedings of the National Academy of Sciences, vol.98, pp.13757-13762, 2001.

N. Potnis, K. Krasileva, V. Chow, N. F. Almeida, P. B. Patil et al., Comparative genomics reveals diversity among xanthomonads infecting tomato and pepper, BMC Genomics, vol.12, p.146, 2011.

P. Pottinger, L. B. Reller, and K. J. Ryan, Sherris Medical Microbiology, 2004.

N. V. Punina, A. N. Ignatov, E. S. Pekhtereva, K. P. Kornev, E. V. Matveeva et al., Occurrence of Xanthomonas campestris pv. raphani on tomato plants in the Russian Federation, Acta Horticulturae, vol.808, pp.287-290, 2009.

A. Purcell, Paradigms: Examples from the Bacterium Xylella fastidiosa, Annual Review of Phytopathology, vol.51, pp.339-356, 2013.

J. Qi, H. Luo, and B. Hao, CVTree: A phylogenetic tree reconstruction tool based on whole genomes, Nucleic Acids Research, vol.32, pp.45-47, 2004.

W. Qian, Y. Jia, S. Ren, Y. He, J. Feng et al., Comparative and functional genomic analyses of the pathogenicity of phytopathogen, Genome Research, vol.15, pp.757-767, 2005.

E. Quevillon, V. Silventoinen, S. Pillai, N. Harte, N. Mulder et al., InterProScan: Protein domains identifier, Nucleic Acids Research, vol.33, pp.116-120, 2005.

J. Rademaker, B. Hoste, F. J. Louws, K. Kersters, J. Swings et al., Comparison of AFLP and rep-PCR genomic fingerprinting with DNA -DNA homology studies : Xanthomonas as a model system, International Journal of Systematic and Evolutionary Microbiology, vol.50, pp.665-677, 2000.

J. Rademaker, F. J. Louws, M. H. Schultz, U. Rossbach, L. Vauterin et al., A comprehensive species to strain taxonomic framework for Xanthomonas, Phytopathology, vol.95, pp.1098-1111, 2005.

R. Rivera, N. G. García-salinas, C. Aragão, F. , D. De-la-garza et al., Metabolic engineering of folate and its precursors in Mexican common bean (Phaseolus vulgaris L.), Plant Biotechnology Journal, vol.14, pp.2021-2032, 2016.

F. A. Ran, P. D. Hsu, C. Lin, J. S. Gootenberg, S. Konermann et al., Double Nicking by RNAGuided CRISPR Cas9 for Enhanced Genome Editing Specificity, Cell, vol.154, pp.1380-1389, 2013.

A. R. Records and D. C. Gross, Sensor kinases RetS and LadS regulate Pseudomonas syringae Type VI secretion and virulence factors, Journal of Bacteriology, vol.192, pp.3584-3596, 2010.

M. Richter and R. Rosselló-móra, Shifting the genomic gold standard for the prokaryotic species definition, Proceedings of the National Academy of Sciences of the United States of America, vol.106, pp.19126-19157, 2009.

A. Richter, J. Streubel, C. Blücher, B. Szurek, M. Reschke et al., A TAL effector repeat architecture for frameshift binding, Nature communications, vol.5, p.3447, 2014.

F. C. Rinaldi, L. A. Doyle, B. L. Stoddard, and A. J. Bogdanove, The effect of increasing numbers of repeats on TAL effector DNA binding specificity, Nucleic Acids Research, vol.45, pp.6960-6970, 2017.

I. Robène, S. Bolot, O. Pruvost, M. Arlat, L. Noël et al., High-Quality Draft Genome Sequences of Two Xanthomonas Pathotype Strains Infecting Aroid Plants, Genome announcements, vol.4, pp.902-918, 2016.

. Rodriguez-r-lm, A. Grajales, M. Arrieta-ortiz, C. Salazar, S. Restrepo et al., Genomes-based phylogeny of the genus Xanthomonas, BMC Microbiology, vol.12, pp.1-14, 2012.

P. Römer, S. Hahn, T. Jordan, T. Strauss, U. Bonas et al., Plant pathogen recognition mediated by promoter activation of the pepper Bs3 resistance gene, Science, vol.318, pp.645-648, 2007.

P. Römer, S. Recht, T. Strauss, J. Elsaesser, S. Schornack et al., Promoter elements of rice susceptibility genes are bound and activated by specific TAL effectors from the bacterial blight pathogen, Xanthomonas oryzae pv. oryzae, New Phytologist, vol.187, pp.1048-1057, 2010.

O. Romero-arenas, D. Huato, M. A. , R. Tapia, J. A. Báez et al., The Nutritional value of Beans (Phaseolus vulgaris L.) and its importance for Feeding of Rural communities in Puebla-Mexico, International Research Journal of Biological Sciences, vol.2, pp.59-65, 2013.

P. Roumagnac, O. Pruvost, F. Chiroleu, and G. Hughes, Spatial and Temporal Analyses of Bacterial Blight of Onion Caused by Xanthomonas axonopodis pv. allii, Phytopathology, vol.94, pp.138-184, 2004.

C. Rousseau, E. Belin, E. Bove, D. Rousseau, F. Fabre et al., High throughput quantitative phenotyping of plant resistance using chlorophyll fluorescence image analysis, Plant methods, vol.9, p.17, 2013.
URL : https://hal.archives-ouvertes.fr/inserm-00837088

C. Rousseau, G. Hunault, S. Gaillard, J. Bourbeillon, G. Montiel et al., Phenoplant: a web resource for the exploration of large chlorophyll fluorescence image datasets, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01218602

B. Roux, S. Bolot, E. Guy, N. Denancé, M. Lautier et al., , 2015.

, Genomics and transcriptomics of Xanthomonas campestris species challenge the concept of core type III effectome, BMC genomics, vol.16

M. Ruh, M. Briand, S. Bonneau, M. Jacques, and N. Chen, Xanthomonas adaptation to common bean is associated with horizontal transfers of genes encoding TAL effectors, BMC Genomics, vol.18, p.670, 2017.

M. Ruh, M. Briand, S. Bonneau, M. Jacques, and N. Chen, First Complete Genome Sequences of Xanthomonas citri pv. vignicola Strains CFBP7111, CFBP7112, and CFBP7113 Obtained Using Long-Read Technology, Genome Announcements, vol.5, pp.813-830, 2017.

R. P. Ryan, F. Vorhölter, N. Potnis, J. B. Jones, V. Sluys et al., Pathogenomics of Xanthomonas: understanding bacterium-plant interactions, Nature Reviews Microbiology, vol.9, pp.344-355, 2011.

A. W. Saettler, C. R. Cafati, and D. M. Weller, Nonoverwintering of Xanthomonas Bean Blight Bacteria in Michigan, Plant Disease, vol.70, pp.285-287, 1986.

E. Sallet, J. Gouzy, and T. Schiex, EuGene-PP: A next-generation automated annotation pipeline for prokaryotic genomes, Bioinformatics, vol.30, pp.2659-2661, 2014.

S. L. Salzberg, D. D. Sommer, M. C. Schatz, A. M. Phillippy, P. D. Rabinowicz et al.,

, Genome sequence and rapid evolution of the rice pathogen Xanthomonas oryzae pv. oryzae PXO99A, BMC Genomics, vol.9, p.204

M. Sandkvist, Biology of type II secretion, Molecular Microbiology, vol.40, pp.271-283, 2001.

M. Santalla, A. P. Rodiño, and A. M. De-ron, Allozyme evidence supporting southwestern Europe as a secondary center of genetic diversity for the common bean, Theoretical and Applied Genetics, vol.104, pp.934-944, 2002.

M. Santalla, A. M. De-ron, L. De, and M. Fuente, Integration of genome and phenotypic scanning gives evidence of genetic structure in Mesoamerican common bean (Phaseolus vulgaris L.) landraces from the southwest of, Europe. Theoretical and Applied Genetics, vol.120, pp.1635-1651, 2010.

C. L. Santini, B. Ize, A. Chanal, M. Müller, G. Giordano et al., A novel Sec-independent periplasmic protein translocation pathway in Escherichia coli, EMBO Journal, vol.17, pp.101-112, 1998.

A. S. Santos, R. E. Bressan-smith, M. G. Pereira, R. Rodrigues, and C. F. Ferreira, Genetic linkage map of Phaseolus vulgaris and identification of QTLs responsible for resistance to Xanthomonas axonopodis pv. phaseoli, Fitopatologia Brasileira, vol.28, pp.5-10, 2003.

S. F. Sarkar and D. S. Guttman, Evolution of the Core Genome of Pseudomonas syringae , a Highly Clonal, Endemic Plant Pathogen. Applied and Environmental Microbiology, vol.70, pp.1999-2012, 2004.

S. C. Sati and S. Joshi, Antibacterial activities of Ginkgo biloba L. leaf extracts, TheScientificWorldJournal, vol.11, pp.2237-2279, 2011.

S. Sato, Y. Nakamura, T. Kaneko, E. Asamizu, T. Kato et al., Genome structure of the legume, Lotus japonicus, DNA Research, vol.15, pp.227-239, 2008.

N. W. Schaad and J. C. Dianese, Cruciferous weeds as sources of inoculum of Xanthomonas campestris in black rot crucifers, Phytopathology, vol.71, pp.1215-1220, 1981.

N. W. Schaad, E. Postnikova, G. H. Lacy, A. Sechler, I. Agarkova et al., Reclassification of Xanthomonas campestris pv. citri (ex Hasse 1915) Dye 1978 forms A, B/C/D, and E as X. smithii subsp. citri (ex Hasse) sp. nov. nom. rev. comb. nov., X. fuscans subsp. aurantifolii (ex Gabriel 1989) sp. nov. nom. rev. comb. nov., and X, Systematic and applied microbiology, vol.28, pp.494-518, 2005.

J. Schmutz, S. B. Cannon, J. Schlueter, J. Ma, T. Mitros et al., Genome sequence of the palaeopolyploid soybean, Nature, vol.463, pp.178-83, 2010.

J. Schmutz, P. E. Mcclean, S. Mamidi, G. A. Wu, S. B. Cannon et al., A reference genome for common bean and genome-wide analysis of dual domestications, Nature genetics, vol.46, pp.707-720, 2014.

T. D. Schneider and R. M. Stephens, Sequence logos: A new way to display consensus sequences, Nucleic Acids Research, vol.18, p.6097, 1990.

H. Scholze and J. Boch, TAL effectors are remote controls for gene activation, Current Opinion in Microbiology, vol.14, pp.47-53, 2011.

S. Schornack, A. Ballvora, D. Gürlebeck, J. Peart, M. Ganal et al., The tomato resistance protein Bs4 is a predicted non-nuclear TIR-NB-LRR protein that mediates defense responses to severely truncated derivatives of AvrBs4 and overexpressed AvrBs3, Plant Journal, vol.37, pp.46-60, 2004.

S. Schornack, G. V. Minsavage, R. E. Stall, J. B. Jones, and T. Lahaye, Characterization of AvrHah1, a novel AvrBs3-like effector from Xanthomonas gardneri with virulence and avirulence activity, New Phytologist, vol.179, pp.546-556, 2008.

S. Schornack, M. J. Moscou, E. R. Ward, and D. M. Horvath, Engineering Plant Disease Resistance Based on TAL Effectors, Annual Review of Phytopathology, vol.51, pp.383-406, 2013.

S. Schornack, K. Peter, U. Bonas, and T. Lahaye, Expression levels of avrBs3-like genes affect recognition specificity in tomato Bs4-but not in pepper Bs3-mediated perception, Molecular plant-microbe interactions : MPMI, vol.18, pp.1215-1225, 2005.

T. Schreiber and U. Bonas, Repeat 1 of TAL effectors affects target specificity for the base at position zero, Nucleic Acids Research, vol.42, pp.7160-7169, 2014.

T. Schultz and R. L. Gabrielson, Xanthomonas campestris pv. campestris in western washington cricifer seed fields: occurrence and survival, Phytopathology, vol.76, pp.1306-1309, 1986.

M. L. Schuster and D. P. Coyne, Survival Mechanisms of Phytopathogenic Bacteria, Annual Review of Phytopathology, vol.12, pp.199-221, 1974.

M. L. Schuster, D. P. Coyne, and B. Hoff, Comparative Virulence of Xanthomonas phaseoli Strains from Uganda, Colombia, and Nebrasca, Plant Disease Reporter, vol.57, pp.74-75, 1973.

A. R. Schwartz, R. Morbitzer, T. Lahaye, and B. J. Staskawicz, TALE-induced bHLH transcription factors that activate a pectate lyase contribute to water soaking in bacterial spot of tomato, Proceedings of the National Academy of Sciences of the United States of America, vol.114, pp.897-903, 2017.

A. R. Schwartz, N. Potnis, S. Timilsina, M. Wilson, J. Patané et al., Phylogenomics of Xanthomonas field strains infecting pepper and tomato reveals diversity in effector repertoires and identifies determinants of host specificity, Frontiers in Microbiology, vol.6, pp.1-17, 2015.

M. Senthil-kumar and K. S. Mysore, Nonhost Resistance Against Bacterial Pathogens: Retrospectives and Prospects, Annual Review of Phytopathology, vol.51, pp.407-427, 2013.

A. Shade, M. A. Jacques, and M. Barret, Ecological patterns of seed microbiome diversity, transmission, and assembly, Current Opinion in Microbiology, vol.37, pp.15-22, 2017.

A. Shelton and J. Hunter, Evaluation of the potential of the flea beetle Phyllotreta cruciferae to transmit Xanthomonas campestris pv. campestris, causal agent of black rot of crucifers, Canadian Journal of Plant Pathology, vol.7, pp.308-310, 1985.

C. Shi, S. Chaudhary, K. Yu, S. J. Park, A. Navabi et al., Identification of candidate genes associated with CBB resistance in common bean HR45 (Phaseolus vulgaris L.) using cDNA-AFLP, Molecular Biology Reports, vol.38, pp.75-81, 2011.

C. Shi, A. Navabi, and K. Yu, Association mapping of common bacterial blight resistance QTL in Ontario bean breeding populations, 2011.

, BMC Plant Biology, vol.11, pp.1-11

C. Shi, K. Yu, W. Xie, G. Perry, A. Navabi et al., Development of candidate gene markers associated to common bacterial blight resistance in common bean, Theoretical and Apllied Genetic, vol.125, pp.1525-1562, 2012.

A. Da-silva, J. A. Ferro, F. C. Reinach, C. S. Farah, L. R. Furlan et al., Comparison of the genomes of two Xanthomonas pathogens with differing host specificities, Nature, vol.417, pp.459-463, 2002.

A. Simpson, F. Reinach, P. Arruda, F. Abreu, M. Acencio et al., The genome sequence of the plant pathogen Xylella fastidiosa, Nature, vol.406, pp.151-157, 2000.

S. P. Singh, Broadening the genetic base of common bean cultivars: A review, Crop Science, vol.41, pp.1659-1675, 2001.

S. P. Singh and C. G. Muñoz, Resistance to Common Bacterial Blight among Phaseolus Species and Common Bean Improvement, Crop Science, vol.39, pp.80-89, 1999.

S. P. Singh and H. F. Schwartz, Breeding common bean for resistance to diseases: A review, Crop Science, vol.50, pp.2199-2223, 2010.

M. Van-sluys, M. De-oliveira, C. Monteiro-vitorello, C. Miyaki, L. Furlan et al.,

, Comparative Analyses of the Complete Genome Sequences of Pierce's Disease and Citrus Variegated Chlorosis Strains of Xylella fastidiosa, Journal of bacteriology, vol.185, pp.1018-1026

J. M. Smith, Analyzing the mosaic structure of genes, Journal of Molecular Evolution, vol.34, pp.126-129, 1992.

J. J. Smith, D. R. Jones, E. Karamura, G. Blomme, and F. L. Turyagyenda, An analysis of the risk from Xanthomonas campestris pv . musacearum to banana cultivation in Eastern , Central and Southern Africa, Bioversity International, 2008.

M. Solé, F. Scheibner, A. K. Hoffmeister, N. Hartmann, G. Hause et al., , 2015.

, Xanthomonas campestris pv. vesicatoria secretes proteases and xylanases via the Xps type II secretion system and outer membrane vesicles, Journal of Bacteriology, vol.197, pp.2879-2893

M. Sory, A. Boland, I. Lambermont, and G. R. Cornelis, Identification of the YopE and YopH domains required for secretion and internalization into the cytosol of macrophages, using the cyaA gene fusion approach, Microbiology, vol.92, pp.11998-12002, 1995.

S. M. Soucy, J. Huang, and J. P. Gogarten, Horizontal gene transfer: building the web of life, Nature Reviews Genetics, vol.16, pp.472-482, 2015.

F. R. Spago, I. Mauro, C. S. Oliveira, A. G. Beranger, J. Cely et al.,

J. Mello, Pseudomonas aeruginosa produces secondary metabolites that have biological activity against plant pathogenic Xanthomonas species, Crop Protection, vol.62, pp.46-54, 2014.

S. Stella, R. Molina, C. Bertonatti, A. Juillerrat, and G. Montoya, Expression, purification, crystallization and preliminary X-ray diffraction analysis of the novel modular DNA-binding protein BurrH in its apo form and in complex with its target DNA, Acta Crystallographica Section F Structural Biology Communications, vol.70, pp.87-91, 2014.

V. Stewart, The HAMP signal-conversion domain: Static two-state or dynamic three-state?, Molecular Microbiology, vol.91, pp.853-857, 2014.

P. Stoodley, K. Sauer, D. G. Davies, and J. W. Costerton, Biofilms as complex differentiated communities, Annual Review of Microbiology, vol.56, pp.187-209, 2002.

T. Strauß, R. Van-poecke, A. Strauss, P. Römer, G. Minsavage et al., RNA-seq pinpoints a Xanthomonas TAL-effector activated resistance gene in a large-crop genome, Proceedings of the National Academy of Sciences of the United States of America, vol.109, pp.19480-19485, 2012.

J. Streubel, C. Blücher, A. Landgraf, and J. Boch, TAL effector RVD specificities and efficiencies, Nature Biotechnology, vol.30, pp.593-595, 2012.

J. Streubel, C. Pesce, M. Hutin, R. Koebnik, J. Boch et al., Five phylogenetically close rice SWEET genes confer TAL effectormediated susceptibility to Xanthomonas oryzae pv. oryzae, New Phytologist, vol.200, pp.808-819, 2013.

D. J. Studholme, E. Kemen, D. Maclean, S. Schornack, V. Aritua et al., Genome-wide sequencing data reveals virulence factors implicated in banana Xanthomonas wilt, FEMS Microbiology Letters, vol.310, pp.182-192, 2010.

D. J. Studholme, A. Wasukira, K. Paszkiewicz, V. Aritua, R. Thwaites et al., Draft genome sequences of xanthomonas sacchari and two banana-associated xanthomonads reveal insights into the xanthomonas group 1 clade, Genes, vol.2, pp.1050-1065, 2011.

J. Su, X. Zou, L. Huang, T. Bai, S. Liu et al., DgcA, a diguanylate cyclase from Xanthomonas oryzae pv. oryzae regulates bacterial pathogenicity on rice, Scientific reports, vol.6, p.25978, 2016.

A. Sugio, B. Yang, T. Zhu, and F. F. White, Two type III effector genes of Xanthomonas oryzae pv. oryzae control the induction of the host genes OsTFIIAgamma1 and OsTFX1 during bacterial blight of rice, Proceedings of the National Academy of Sciences of the United States of America, vol.104, pp.10720-10725, 2007.

G. W. Sundin, Genomic Insights into the Contribution of Phytopathogenic Bacterial Plasmids to the Evolutionary History of Their Hosts, Annual Review of Phytopathology, vol.45, pp.129-151, 2007.

P. Sung and H. Klein, Mechanism of homologous recombination: mediators and helicases take on regulatory functions, Nature reviews. Molecular cell biology, vol.7, pp.739-750, 2006.

D. Svetleva, M. Velcheva, and G. Bhowmik, Biotechnology as a useful tool in common bean, 2003.

, Euphytica, vol.131, pp.189-200

B. Szurek, E. Marois, U. Bonas, G. Van-ackerveken, and . Den, Eukaryotic features of the Xanthomonas type III effector AvrBs3: Protein domains involved in transcriptional activation and the interaction with nuclear import receptors from pepper, Plant Journal, vol.26, p.523, 2001.

B. Szurek, O. Rossier, G. Hause, and U. Bonas, Type III-dependent translocation of the Xanthomonas AvrBs3 protein into the plant cell, Molecular Microbiology, vol.46, pp.13-23, 2002.

S. Taghavi, C. Garafola, S. Monchy, L. Newman, A. Hoffman et al., Genome survey and characterization of endophytic bacteria exhibiting a beneficial effect on growth and development of poplar trees, Applied and Environmental Microbiology, vol.75, pp.748-757, 2009.

H. Tang, V. Krishnakumar, S. Bidwell, B. Rosen, A. Chan et al., An improved genome release (version Mt4.0) for the model legume Medicago truncatula, BMC genomics, vol.15, p.312, 2014.

F. Tao, S. Swarup, and L. H. Zhang, Quorum sensing modulation of a putative glycosyltransferase gene cluster essential for Xanthomonas campestris biofilm formation, Environmental Microbiology, vol.12, pp.3159-3170, 2010.

L. Tayi, S. Kumar, R. Nathawat, A. S. Haque, R. Maku et al., , 2017.

D. Teper, D. Burstein, D. Salomon, M. Gershovitz, T. Pupko et al., Identification of novel Xanthomonas euvesicatoria type III effector proteins by a machine-learning approach, Molecular Plant Pathology, vol.17, pp.398-411, 2016.

F. Thieme, R. Koebnik, T. Bekel, C. Berger, J. Boch et al., Insights into genome plasticity and pathogenicity of the plant pathogenic bacterium Xanthomonas campestris pv. vesicatoria revealed by the complete genome sequence, Journal of bacteriology, vol.187, pp.7254-7266, 2005.

B. Thomma, T. Nürnberger, and M. Joosten, Of PAMPs and effectors: the blurred PTI-ETI dichotomy, The Plant cell, vol.23, p.4, 2011.

N. Tochio, K. Umehara, J. Uewaki, H. Flechsig, M. Kondo et al., , 2016.

B. Todorovi?, I. Poto?nik, E. Rekanovi?, M. Stepanovi?, M. Kosti? et al., Toxicity of twenty-two plant essential oils against pathogenic bacteria of vegetables and mushrooms, Journal of environmental science and health, vol.51, p.832, 2016.

I. K. Toth, L. J. Hyman, R. Taylor, and P. Birch, PCR-based detection of Xanthomonas campestris pv. phaseoli var. fuscans in plant material and its differentiation from X. c. pv. phaseoli, Journal of Applied Microbiology, vol.85, pp.327-336, 1998.

W. Tushemereirwe, A. Kangire, F. Ssekiwoko, L. C. Offord, J. Crozier et al., First report of Xanthomonas campestris pv. musacearum on banana in Uganda, Plant Pathology, vol.53, p.802, 2004.

G. J. Vandemark, D. Fourie, and P. N. Miklas, Genotyping with real-time PCR reveals recessive epistasis between independent QTL conferring resistance to common bacterial blight in dry bean, Theoretical and Applied Genetics, vol.117, pp.513-522, 2008.

R. K. Varshney, C. Song, R. K. Saxena, S. Azam, S. Yu et al., Draft genome sequence of chickpea (Cicer arietinum) provides a resource for trait improvement, Nature Biotechnology, vol.31, pp.240-246, 2013.

L. Vauterin, B. Hoste, K. Kersters, and J. Swings, Reclassification of Xanthomonas, International Journal of Systematic Bacteriology, vol.45, pp.472-489, 1995.

L. Vauterin, J. Rademaker, and J. Swings, Synopsis on the taxonomy of the genus Xanthomonas, Phytopathology, vol.90, pp.677-682, 2000.

V. Cruz, C. M. Bai, J. , O. I. Leung, H. Nelson et al., Predicting durability of a disease resistance gene based on an assessment of the fitness loss and epidemiological consequences of avirulence gene mutation, Proceedings of the National Academy of Sciences of the United States of America, vol.97, pp.13500-13505, 2000.

J. G. Vicente and E. B. Holub, Xanthomonas campestris pv. Campestris (cause of black rot of crucifers) in the genomic era is still a worldwide threat to brassica crops, Molecular Plant Pathology, vol.14, pp.2-18, 2013.

B. A. Vinatzer, C. L. Monteil, and C. R. Clarke, Harnessing Population Genomics to Understand How Bacterial Pathogens Emerge, Adapt to Crop Hosts, and Disseminate, Annual Review of Phytopathology, vol.52, pp.19-43, 2014.

N. Vladimirov and V. Sourjik, Chemotaxis: How bacteria use memory, Biological Chemistry, vol.390, pp.1097-1104, 2009.

F. Vorhölter, S. Schneiker, A. Goesmann, L. Krause, T. Bekel et al., The genome of Xanthomonas campestris pv. campestris B100 and its use for the reconstruction of metabolic pathways involved in xanthan biosynthesis, Journal of Biotechnology, vol.134, pp.33-45, 2008.

F. Vorhölter, H. Wiggerich, H. Scheidle, V. K. Sidhu, K. Mrozek et al., Involvement of bacterial TonB-dependent signaling in the generation of an oligogalacturonide damage-associated molecular pattern from plant cell walls exposed to Xanthomonas campestris pv. campestris pectate lyases, BMC Microbiology, vol.12, p.239, 2012.

D. F. Voytas and J. K. Joung, DNA binding made easy, Science, vol.326, pp.1491-1492, 2009.

G. H. Wadhams and J. P. Armitage, Making sense of it all: bactrial chemotaxis, Nature reviews. Molecular cell biology, vol.5, pp.1024-1037, 2004.

R. R. Walcott, R. D. Gitaitis, C. , and C. , Role of Blossoms in Watermelon Seed Infestation by Acidovorax avenae subsp. citrulli, Phytopathology, vol.93, pp.528-534, 2003.

T. S. Walker, H. P. Bais, E. De, H. P. Schweizer, L. G. Rahme et al., , 2004.

. Pathogenicity, Biofilm Formation, and Root Exudation, Plant Physiology, vol.134, pp.320-331

K. Wallden, A. Rivera-calzada, and G. Waksman, Type IV secretion systems: versatility and diversity in function, Cellular Microbiology, vol.12, pp.1203-1212, 2010.

L. Wang, F. C. Rinaldi, P. Singh, E. L. Doyle, Z. E. Dubrow et al., TAL effectors drive transcription bidirectionally in plants, Molecular Plant, vol.10, pp.285-296, 2017.

L. Wang, E. V. Vinogradov, and A. J. Bogdanove, Requirement of the lipopolysaccharide O-chain biosynthesis gene wxocB for type III secretion and virulence of Xanthomonas oryzae pv, Oryzicola. Journal of Bacteriology, vol.195, pp.1959-1969, 2013.

C. Wang, X. Zhang, Y. Fan, Y. Gao, Q. Zhu et al., XA23 Is an executor r protein and confers broad-spectrum disease resistance in rice, Molecular Plant, vol.8, pp.290-302, 2015.

A. Wasukira, J. Tayebwa, R. Thwaites, K. Paszkiewicz, V. Aritua et al., Genome-wide sequencing reveals two major sub-lineages in the genetically monomorphic pathogen Xanthomonas campestris pathovar musacearum, Genes, vol.3, pp.361-377, 2012.

E. Weber, R. Gruetzner, S. Werner, C. Engler, and S. Marillonnet, Assembly of designer tal effectors by golden gate cloning, PLoS ONE, vol.6, 2011.

D. M. Weller and A. W. Saetller, Evaluation of Seedborne Xanthomonas phaseoli and X. phaseoli var. fuscans as Primary Inocula in Bean Blights, Phytopathology, vol.70, pp.148-152, 1980.

K. Wengelnik, G. Van-den-ackerveken, and U. Bonas, HrpG, a key hrp regulatory protein of Xanthomonas campestris pv. vesicatoria is homologous to two-component response regulators, Molecular plant-microbe interactions : MPMI, vol.9, pp.704-712, 1996.

K. Wengelnik and U. Bonas, HrpXv, an AraC-type regulator, activates expression of five of the six loci in the hrp cluster of Xanthomonas campestris pv. vesicatoria, Journal of Bacteriology, vol.178, pp.3462-3469, 1996.

F. Wichmann, F. Vorhölter, L. Hersemann, F. Widmer, J. Blom et al., The noncanonical type III secretion system of Xanthomonas translucens pv. graminis is essential for forage grass infection, Molecular Plant Pathology, vol.14, pp.576-588, 2013.

J. Wiedenbeck and F. M. Cohan, Origins of bacterial diversity through horizontal genetic transfer and adaptation to new ecological niches, FEMS Microbiology Reviews, vol.35, pp.957-976, 2011.

K. E. Wilkins, N. J. Booher, L. Wang, and A. J. Bogdanove, TAL effectors and activation of predicted host targets distinguish Asian from African strains of the rice pathogen Xanthomonas oryzae pv. oryzicola while strict conservation suggests universal importance of five TAL effectors, Frontiers in Plant Science, vol.6, pp.1-15, 2015.

P. H. Williams, Black rot: A continuing Threat to World Crucifers, Plant disease, vol.64, pp.736-742, 1980.

C. S. Wortmann, R. A. Kirkby, C. A. Eledu, and D. J. Allen, Atlas of common bean (Phaseolus vulgaris L.) production in Africa, Centro Internacional de Agricultura Tropical (CIAT), vol.297, p.133, 1998.

L. Wu, M. L. Goh, C. Sreekala, and Z. Yin, XA27 depends on an amino-terminal signal-anchor-like sequence to localize to the apoplast for resistance to Xanthomonas oryzae pv oryzae, Plant physiology, vol.148, pp.1497-1509, 2008.

X. M. Wu, Y. R. Li, L. F. Zou, and G. Y. Chen, Gene-for-gene relationships between rice and diverse avrBs3/pthA avirulence genes in Xanthomonas oryzae pv. oryzae, Plant Pathology, vol.56, pp.26-34, 2007.

Y. Wu, D. Zhang, J. Y. Chu, P. Boyle, Y. Wang et al., The Arabidopsis NPR1 Protein Is a Receptor for the Plant Defense Hormone Salicylic Acid, Cell Reports, vol.1, pp.639-647, 2012.

K. Wuichet, R. P. Alexander, and I. B. Zhulin, Comparative Genomic and Protein Sequence Analyses of a Complex System Controlling Bacterial Chemotaxis, Methods in Enzymology, vol.422, pp.1-24, 2007.

K. Wuichet and I. B. Zhulin, Molecular evolution of sensory domains in cyanobacterial chemoreceptors, Trends Microbiology, vol.11, p.200, 2003.

Y. Xia, H. Suzuki, J. Borevitz, J. Blount, Z. Guo et al., An Extracellular Aspartic Protease Functions in Arabidopsis Disease Resistance Signaling, EMBO Journal, vol.23, pp.980-988, 2004.

G. Xie, C. A. Bonner, T. Brettin, R. Gottardo, N. O. Keyhani et al., Lateral gene transfer and ancient paralogy of operons containing redundant copies of tryptophan-pathway genes in Xylella species and in heterocystous cyanobacteria, Genome biology, vol.4, p.14, 2003.

X. Xin, K. Nomura, K. Aung, A. C. Velásquez, J. Yao et al., Bacteria establish an aqueous living space in plants crucial for virulence, Nature, vol.539, pp.524-529, 2016.

B. El-yacoubi, A. M. Brunings, Q. Yuan, S. Shankar, and D. W. Gabriel, In planta horizontal transfer of a major pathogenicity effector gene, Applied and Environmental Microbiology, vol.73, pp.1612-1621, 2007.

K. Yamaguchi, Y. Nakamura, K. Ishikawa, Y. Yoshimura, S. Tsuge et al., Suppression of rice immunity by Xanthomonas oryzae type III effector Xoo2875, Bioscience, biotechnology, and biochemistry, vol.77, pp.796-801, 2013.

Y. Yang and D. W. Gabriel, Xanthomonas avirulence/pathogenicity gene family encodes functional plant nuclear targeting signals, Molecular plant-microbe interactions : MPMI, vol.8, pp.627-631, 1995.

Y. Yang and D. W. Gabriel, Intragenic recombination of a single plant pathogen gene provides a mechanism for the evolution of new host specificities . These include : Intragenic Recombination of a Single Plant Pathogen Gene Provides a Mechanism for the Evolution of New Host Specifi, Journal of Bacteriology, vol.177, pp.4963-4968, 1995.

C. Yang, M. Gavilanes-ruiz, Y. Okinaka, R. Vedel, I. Berthuy et al., hrp genes of Erwinia chrysanthemi 3937 are important virulence factors, Molecular plant-microbe interactions : MPMI, vol.15, pp.472-480, 2002.

B. Yang, A. Sugio, and F. F. White, Os8N3 is a host disease-susceptibility gene for bacterial blight of rice, Proceedings of the National Academy of Sciences of the United States of America, vol.103, pp.10503-10511, 2006.

K. Yang, Z. Tian, C. Chen, L. Luo, B. Zhao et al., Genome sequencing of adzuki bean (Vigna angularis) provides insight into high starch and low fat accumulation and domestication, Proceedings of the National Academy of Sciences of the United States of America, vol.112, pp.13213-13221, 2015.

B. Yang and F. F. White, Diverse members of the AvrBs3/PthA family of type III effectors are major virulence determinants in bacterial blight disease of rice, Molecular plant-microbe interactions : MPMI, vol.17, pp.1192-200, 2004.

J. Yang, Y. Zhang, P. Yuan, Y. Zhou, C. Cai et al., Complete decoding of TAL effectors for DNA recognition, Cell research, vol.24, pp.628-659, 2014.

N. D. Young, F. Debellé, G. Oldroyd, R. Geurts, S. B. Cannon et al., , 2011.

, The Medicago genome provides insight into the evolution of rhizobial symbioses, Nature, vol.480, pp.520-524

J. M. Young, D. C. Park, H. M. Shearman, and E. Fargier, A multilocus sequence analysis of the genus Xanthomonas, Systematic and Applied Microbiology, vol.31, pp.366-377, 2008.

M. Yuan, Z. Chu, X. Li, C. Xu, and S. Wang, Pathogen-induced expressional loss of function is the key factor in race-specific bacterial resistance conferred by a recessive R gene xa13 in rice, Plant and Cell Physiology, vol.50, pp.947-955, 2009.

T. Yuan, X. Li, J. Xiao, and S. Wang, Characterization of xanthomonas oryzae-responsive cis-acting element in the promoter of rice race-specific susceptibility gene Xa13, Molecular Plant, vol.4, pp.300-309, 2011.

K. Yu, S. J. Park, and V. Poysa, Marker-assisted selection of common beans for resistance to common bacterial blight: Efficacy and economics, Plant Breeding, vol.119, pp.411-415, 2000.

Y. Yu, J. Streubel, S. Balzergue, A. Champion, J. Boch et al., Colonization of rice leaf blades by an african strain of Xanthomonas oryzae pv. oryzae depends on a new TAL effector that induces the rice nodulin-3 Os11N3 gene, Molecular Plant-Microbe Interactions, vol.24, pp.1102-1115, 2011.

H. H. Zahran, Rhizobium-legume symbiosis and nitrogen fixation under severe conditions and in an arid climate, Microbiology and molecular biology reviews : MMBR, vol.63, pp.968-89, 1999.

W. J. Zaumeyer, The bacterial blight of beans caused by Bacterium phaseoli, Technical Bulletin US Department of Agriculture, p.1, 1930.

X. Zeng, D. Tian, K. Gu, Z. Zhou, X. Yang et al., Genetic engineering of the Xa10 promoter for broad-spectrum and durable resistance to Xanthomonas oryzae pv. oryzae, Plant Biotechnology Journal, vol.13, pp.993-1001, 2015.

D. R. Zerbino and E. Birney, Velvet: Algorithms for de novo short read assembly using de Bruijn graphs, Genome Research, vol.18, p.821, 2008.

F. Zhang, L. Cong, S. Lodato, S. Kosuri, G. M. Church et al., Efficient construction of sequence-specific TAL effectors for modulating mammalian transcription, Nature Biotechnology, vol.29, pp.149-154, 2011.

Y. Zhang, N. Jalan, X. Zhou, E. Goss, J. B. Jones et al., Positive selection is the main driving force for evolution of citrus canker-causing Xanthomonas, The ISME Journal, vol.9, pp.2128-2166, 2015.

J. Zhang, Z. Yin, and F. White, TAL effectors and the executor R genes, Frontiers in Plant Science, vol.6, p.641, 2015.

J. Zhou, Z. Peng, J. Long, D. Sosso, B. Liu et al., Gene targeting by the TAL effector PthXo2 reveals cryptic resistance gene for bacterial blight of rice, Plant Journal, vol.82, pp.632-643, 2015.

C. Zipfel, Pattern-recognition receptors in plant innate immunity, Current Opinion in Immunology, vol.20, pp.10-16, 2008.

C. Zipfel, Early molecular events in PAMP-triggered immunity, Current Opinion in Plant Biology, vol.12, pp.414-420, 2009.

H. S. Zou, W. X. Zhao, X. F. Zhang, Y. C. Han, L. F. Zou et al., Identification of an avirulence gene, avrxa5, from the rice pathogen Xanthomonas oryzae pv. oryzae, Science China Life Sciences, vol.53, pp.1440-1449, 2010.

. École-doctorale-?-Écologie, A. Géosciences, (. Alimentation, . Egaal)-laboratoire-d'accueil-?-umr-inra-/-agrocampus, and . Ouest,

, UMR IRHS / présidente du jury Valérie GEFFROY Directrice de recherche Institute of Plant Sciences Paris Saclay / rapporteur Laurent NOËL Directeur de recherche CNRS, UMR LIPM / rapporteur Alia DELLAGI Maître de conférence AgroParisTech, UMR IJPB / examinateur Thomas GUILLEMETTE Professeur Université d'Angers, UMR IRHS / examinateur Boris SZUREK Chargé de recherche IRD, Déterminisme de la spécifi cité d'hôte et rôle des effecteurs TAL dans l'interaction Xanthomonas -haricot Mathilde BRIARD Professeure Agrocampus Ouest