C. Lo, A. Stahl, P. D. Raposo, and G. , Extracellular vesicles shuffling intercellular messages: for good or for bad

, Curr Opin Cell Biol, vol.35, pp.69-77, 2015.

S. Maas, X. O. Breakefield, and A. M. Weaver, Extracellular Vesicles: Unique Intercellular Delivery Vehicles, Trends Cell Biol, vol.27, pp.172-88, 2017.

G. Coakley, R. M. Maizels, and A. H. Buck, Exosomes and Other Extracellular Vesicles: The New Communicators in Parasite Infections, Trends Parasitol, vol.31, pp.477-89, 2015.

D. Toro, J. Herschlik, L. Waldner, C. Mongini, and C. , Emerging Roles of Exosomes in Normal and Pathological Conditions: New Insights for Diagnosis and Therapeutic Applications, Front Immunol, vol.6, pp.1-12, 2015.

G. Coakley, J. L. Mccaskill, J. G. Borger, F. Simbari, E. Robertson et al., Extracellular Vesicles from a Helminth Parasite Suppress Macrophage Activation and Constitute an Effective Vaccine for Protective Immunity, Cell Reports, vol.19, pp.1545-57, 2017.

Y. Ofir-birin, M. Heidenreich, and N. Regev-rudzki, Pathogen-derived extracellular vesicles coordinate social behaviour and host manipulation, Semin Cell Dev Biol, vol.67, pp.83-90, 2017.

H. Godfray and . Parasitoids, , 1994.

Y. Carton, M. Poirié, and A. J. Nappi, Insect immune resistance to parasitoids, Insect Science, vol.15, issue.1, pp.67-87, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00319495

J. L. Gatti, A. Schmitz, D. Colinet, and M. Poirié, Diversity of virus-like particles in parasitoids' venom: viral or cellular origin, Parasitoid Viruses, Symbionts and Pathogens, pp.181-192, 2012.

D. B. Stoltz, S. B. Vinson, and E. A. Mackinnon, Baculovirus-like particles in the reproductive tracts of female parasitoid wasps, Can J Microbiol, vol.22, pp.1013-1036, 1976.

J. Gauthier, J. Drezen, and E. A. Herniou, The recurrent domestication of viruses: major evolutionary transitions in parasitic wasps, Parasitology, vol.3457, pp.1-13, 2017.
URL : https://hal.archives-ouvertes.fr/hal-02140632

R. M. Rizki and T. M. Rizki, Parasitoid virus-like particles destroy Drosophila cellular immunity, Proc Natl Acad Sci, vol.87, pp.8388-92, 1990.

S. Dupas, M. Brehelin, F. Frey, and Y. Carton, Immune suppressive virus-like particles in a Drosophila parasitoid: significance of their intraspecific morphological variations, Parasitology, vol.113, pp.207-219, 1996.

C. Labrosse, Y. Carton, A. Dubuffet, J. M. Drezen, and M. Poirie, Active suppression of D. melanogaster immune response by long gland products of the parasitic wasp Leptopilina boulardi, J Insect Physiol, vol.49, pp.513-535, 2003.

J. Morales, H. Chiu, T. Oo, R. Plaza, S. Hoskins et al., Biogenesis, structure, and immune-suppressive effects of virus-like particles of a Drosophila parasitoid, Leptopilina victoriae, vol.51, 2005.

H. Chiu, J. Morales, and S. Govind, Identification and immuno-electron microscopy localization of p40, a protein component of immunosuppressive virus-like particles from Leptopilina heterotoma, a virulent parasitoid wasp of Drosophila, J Gen Virol, vol.87, pp.461-70, 2006.

R. Ferrarese, J. Morales, D. Fimiarz, B. A. Webb, and S. Govind, A supracellular system of actin-lined canals controls biogenesis and release of virulence factors in parasitoid venom glands, J Exp Biol, vol.212, pp.2261-2269, 2009.

G. Gueguen, R. Rajwani, I. Paddibhatla, J. Morales, and S. Govind, VLPs of Leptopilina boulardi share biogenesis and overall stellate morphology with VLPs of the heterotoma clade, Virus Res, vol.2011, pp.1-7

A. J. Nappi, Cellular immunity and pathogen strategies in combative interactions involving Drosophila hosts and their endoparasitic wasps, Invertebrate Survival Journal, vol.7, 2010.

H. Chiu and S. Govind, Natural infection of D. melanogaster by virulent parasitic wasps induces apoptotic depletion of hematopoietic precursors, Cell Death Differ, vol.9, pp.1379-81, 2002.

S. Dupas, Y. Carton, and M. Poirié, Genetic dimension of the coevolution of virulence-resistance in Drosophilaparasitoid wasp relationships, Heredity, vol.90, pp.84-93, 2003.

A. Dubuffet, S. Dupas, F. Frey, J. Drezen, M. Poirié et al., Genetic interactions between the parasitoid wasp Leptopilina boulardi and its Drosophila hosts, Heredity, vol.98, pp.21-28, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00193317

A. Dubuffet, D. Colinet, C. Anselme, S. Dupas, Y. Carton et al., Variation of Leptopilina boulardi success in Drosophila hosts: what is inside the black box?, Advances in Parasitology, vol.70, pp.70006-70011, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00410262

D. Colinet, E. Deleury, C. Anselme, D. Cazes, J. Poulain et al., Extensive inter-and intraspecific venom variation in closely related parasites targeting the same host: The case of Leptopilina parasitoids of Drosophila, Insect Biochemistry and Molecular Biology, vol.43, pp.601-612, 2013.

C. Labrosse, K. Stasiak, J. Lesobre, A. Grangeia, E. Huguet et al., A RhoGAP protein as a main immune suppressive factor in the Leptopilina boulardi (Hymenoptera, Figitidae)-Drosophila melanogaster interaction, Insect Biochemistry and Molecular Biology, vol.35, pp.93-103, 2005.

D. Colinet, A. Schmitz, D. Depoix, D. Crochard, and M. Poirié, Convergent use of RhoGAP toxins by eukaryotic parasites and bacterial pathogens, PLOS Pathogens, vol.3, p.203, 2007.
URL : https://hal.archives-ouvertes.fr/hal-02337684

D. Colinet, A. Schmitz, D. Cazes, J. Gatti, and M. Poirié, The origin of intraspecific variation of virulence in an eukaryotic immune suppressive parasite, PLOS Pathogens, vol.6, p.1001206, 2010.

D. Colinet, A. Dubuffet, D. Cazes, S. Moreau, J. Drezen et al., A serpin from the parasitoid wasp Leptopilina boulardi targets the Drosophila phenoloxidase cascade, Dev Comp Immunol, vol.33, pp.681-690, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00435637

J. Goecks, N. T. Mortimer, J. A. Mobley, G. J. Bowersock, J. Taylor et al., Integrative Approach Reveals Composition of Endoparasitoid Wasp Venoms, PLoS ONE, vol.8, p.64125, 2013.

J. Russo, M. Brehélin, and Y. Carton, Haemocyte changes in resistant and susceptible strains of D. melanogaster caused by virulent and avirulent strains of the parasitic wasp Leptopilina boulardi, J Insect Physiol, vol.47, pp.167-72, 2001.

V. Honti, E. Kurucz, G. Csordás, B. Laurinyecz, R. Márkus et al., In vivo detection of lamellocytes in Drosophila melanogaster, Immunol Lett, vol.126, p.84, 2009.

R. Márkus, B. Laurinyecz, E. Kurucz, V. Honti, I. Bajusz et al., Sessile hemocytes as a hematopoietic compartment in Drosophila melanogaster, Proceedings of the National Academy of Sciences, vol.106, pp.4805-4814, 2009.

M. Rizki, Melanotic tumor formation in drosophila, J Morphol, vol.106, pp.147-57, 1960.

H. Luo, W. P. Hanratty, and C. R. Dearolf, An amino acid substitution in the Drosophila hopTum-l Jak kinase causes leukemia-like hematopoietic defects, Embo J, vol.14, pp.1412-1432, 1995.

S. Dupas, M. Poirie, F. Frey, and Y. Carton, Is parasitoid virulence against multiple hosts adaptive or constrained by phylogeny? A study of Leptopilina spp, Hymenoptera: Figitidae)/Drosophila (Diptera: Drosophilidae) interactions

, International Journal of Entomology, vol.49, pp.222-253, 2013.

B. Z. Kacsoh and T. A. Schlenke, High Hemocyte Load Is Associated with Increased Resistance against Parasitoids in Drosophila suzukii, a Relative of D. melanogaster, PLoS ONE, vol.7, p.34721, 2012.

S. Chabert, R. Allemand, M. Poyet, P. Eslin, and P. Gibert, Ability of European parasitoids (Hymenoptera) to control a new invasive Asiatic pest, Drosophila suzukii, Biological Control, vol.63, pp.40-47, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01917394

M. Brehélin, Immunity in invertebrates. Cells, molecules and defense reactions, 1986.

M. Suzuki and T. Tanaka, Virus-like particles in venom of Meteorus pulchricornis induce host hemocyte apoptosis, J Insect Physiol, vol.52, pp.602-615, 2006.

R. Allemand, C. Lemaitre, F. Frey, M. Boulétreau, F. Vavre et al., Phylogeny of six African Leptopilina species (Hymenoptera: Cynipoidea, Figitidae), parasitoids of Drosophila, with description of three new species, Annales De La Société Entomologique De France, vol.38, pp.319-351, 2002.

R. M. Rizki and T. M. Rizki, Selective destruction of a host blood cell type by a parasitoid wasp, Proc Natl Acad Sci, vol.81, pp.6154-6162, 1984.

M. O. Fauvarque and M. J. Williams, Drosophila cellular immunity: a story of migration and adhesion, J Cell Sci, vol.124, pp.1373-82, 2011.

M. J. Williams, I. Andó, and D. Hultmark, Drosophila melanogaster Rac2 is necessary for a proper cellular immune response, Genes Cells, vol.10, pp.813-836, 2005.

C. J. Sampson, S. Valanne, M. Fauvarque, D. Hultmark, M. Rämet et al., The RhoGEF Zizimin-related acts in the Drosophila cellular immune response via the Rho GTPases Rac2 and Cdc42, Dev Comp Immunol, vol.38, pp.160-168, 2012.

D. Colinet, L. Kremmer, S. Lemauf, C. Rebuf, J. Gatti et al., Development of RNAi in a Drosophila endoparasitoid wasp and demonstration of its efficiency in impairing venom protein production, J Insect Physiol, vol.63, pp.56-61, 2014.

A. Ertürk, K. Becker, N. Jährling, C. P. Mauch, C. D. Hojer et al., Three-dimensional imaging of solventcleared organs using 3DISCO, Nat Protoc, vol.7, pp.1983-95, 2012.

J. C. Akers, D. Gonda, R. Kim, B. S. Carter, and C. C. Chen, Biogenesis of extracellular vesicles (EV): Exosomes, microvesicles, retrovirus-like vesicles, and apoptotic bodies, J Neurooncol, vol.113, pp.1-11, 2013.

M. Bastiani and R. G. Parton, Caveolae at a glance, J Cell Sci, vol.123, pp.3831-3836, 2010.

R. J. Botelho and S. Grinstein, Phagocytosis. Curr Biol, vol.21, pp.533-538, 2011.

C. Braicu, C. Tomuleasa, P. Monroig, A. Cucuianu, and I. Berindan-neagoe, Exosomes as divine messengers: are they the Hermes of modern molecular oncology?, Cell Death Differ, vol.22, pp.34-45, 2015.

Y. Carton and H. Kitano, Changes in the hemocyte population of Drosophila larvae after single and multiple parasitization by Cothonaspis (Parasitic Cynipidae), J Invertebr Pathol, vol.34, pp.88-89, 1979.

Y. Carton, M. Poirié, and A. J. Nappi, Insect immune resistance to parasitoids, Insect Sci, vol.15, pp.67-87, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00319495

P. T. Caswell, S. Vadrevu, and J. C. Norman, Integrins: masters and slaves of endocytic transport, Nat Rev Mol Cell Biol, vol.10, pp.843-853, 2009.

D. Colinet, A. Schmitz, D. Cazes, J. Gatti, and M. Poirié, The origin of intraspecific variation of virulence in an eukaryotic immune suppressive parasite, PLoS Pathog, vol.6, p.1001206, 2010.

D. Colinet, A. Schmitz, D. Depoix, D. Crochard, and M. Poirié, Convergent use of RhoGAP toxins by eukaryotic parasites and bacterial pathogens, PLoS Pathog, vol.3, p.203, 2007.
URL : https://hal.archives-ouvertes.fr/hal-02337684

D. Colinet, E. Deleury, C. Anselme, D. Cazes, and J. Poulain, Extensive inter-and intraspecific venom variation in closely related parasites targeting the same host: The case of Leptopilina parasitoids of Drosophila, Insect Biochem Mol Biol, vol.43, pp.601-611, 2013.

C. Verdera, H. Gitz-francois, J. J. Schiffelers, R. M. Vader, and P. , Cellular uptake of extracellular vesicles is mediated by clathrin-independent endocytosis and macropinocytosis, J Control Release, vol.266, pp.100-108, 2017.

B. Charroux and J. Royet, Elimination of plasmatocytes by targeted apoptosis reveals their role in multiple aspects of the Drosophila immune response, Proc Natl Acad Sci, vol.106, pp.9797-9802, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00429491

A. Clayton, Adhesion and signaling by B cell-derived exosomes: the role of integrins, FASEB J, vol.22, pp.1-22, 2004.

G. J. Doherty and H. T. Mcmahon, Mechanisms of Endocytosis, Annu Rev Biochem, vol.78, pp.857-902, 2009.

J. G. Donaldson, D. L. Johnson, and D. Dutta, Rab and Arf G proteins in endosomal trafficking and cell surface homeostasis, Small GTPases, vol.7, pp.247-251, 2016.

S. Dupas, M. Brehelin, F. Frey, and Y. Carton, Immune suppressive virus-like particles in a Drosophila parasitoid: significance of their intraspecific morphological variations, Parasitology, vol.113, pp.207-212, 1996.

S. Dupas and M. Boscaro, Geographic Variation and Evolution of Immunosuppressive Genes in a Drosophila Parasitoid Geographic variation and evolution of immunosuppressive genes in a Drosophila parasitoid, Ecography (Cop), vol.22, pp.284-291, 1999.

A. Dubuffet, D. Colinet, C. Anselme, S. Dupas, Y. Carton et al., Variation of Leptopilina boulardi success in Drosophila hosts: what is inside the black box, Adv Parasitol, vol.70, pp.147-188, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00410262

M. Fauvarque and M. J. Williams, Drosophila cellular immunity: a story of migration and adhesion, J Cell Sci, vol.124, pp.1373-1382, 2011.

B. Février and G. Raposo, Exosomes: Endosomal-derived vesicles shipping extracellular messages, Curr Opin Cell Biol, vol.16, pp.415-421, 2004.

D. Feng, W. L. Zhao, Y. Y. Ye, X. C. Bai, and R. Q. Liu, Cellular internalization of exosomes occurs through phagocytosis, Traffic, vol.11, pp.675-687, 2010.

J. A. Fischer, S. H. Eun, and B. T. Doolan, Endocytosis, Endosome Trafficking, and the Regulation of Drosophila Development, Annu Rev Cell Dev Biol, vol.22, pp.181-206, 2006.

J. Gatti, A. Schmitz, D. Colinet, and M. Poirié, Diversity of Virus-Like Particles in Parasitoids' Venom: Viral or Cellular Origin?, Parasitoid viruses: symbionts or pathogens, 2012.

, , pp.181-192

F. Galbiati, D. Volonté, J. S. Goltz, Z. Steele, and J. Sen, Identification, sequence and developmental expression of invertebrate flotillins from Drosophila melanogaster, Gene, vol.210, pp.229-237, 1998.

J. Gauthier, J. Drezen, and E. Herniou, The recurrent domestication of viruses: major evolutionary transitions in parasitic wasps, Parasitology, pp.1-13, 2017.
URL : https://hal.archives-ouvertes.fr/hal-02140632

J. Goecks, N. T. Mortimer, J. A. Mobley, G. J. Bowersock, and J. Taylor, Integrative Approach Reveals Composition of Endoparasitoid Wasp Venoms, PLoS One, vol.8, pp.1-14, 2013.

M. Gray and R. J. Botelho, Phagocytosis and Phagosomes, p.1519, 2017.

A. Guha, shibire mutations reveal distinct dynamin-independent and -dependent endocytic pathways in primary cultures of Drosophila hemocytes, J Cell Sci, vol.116, pp.3373-3386, 2003.

A. Guha, V. Sriram, K. S. Krishnan, and S. Mayor, Shibire mutations reveal distinct dynamin-independent and -dependent endocytic pathways in primary cultures of Drosophila hemocytes, J Cell Sci, vol.116, pp.3373-3386, 2003.

G. Gueguen, R. Rajwani, I. Paddibhatla, J. Morales, and S. Govind, VLPs of Leptopilina boulardi share biogenesis and overall stellate morphology with VLPs of the heterotoma clade, Virus Res, vol.160, pp.159-165, 2011.

W. P. Hanratty and C. R. Dearolf, The Drosophila Tumorous lethal hematopoietic oncogene is a dominant mutation in the hopscotch locus, Mol Gen Genet, vol.238, pp.33-37, 1993.

M. E. Heavner, J. Ramroop, G. Gueguen, G. Ramrattan, and G. Dolios, Novel Organelles with Elements of Bacterial and Eukaryotic Secretion Systems Weaponize Parasites of Drosophila, Curr Biol, vol.27, pp.2869-2877, 2017.

A. Hemalatha, C. Prabhakara, and S. Mayor, Endocytosis of Wingless via a dynamin-independent pathway is necessary for signaling in Drosophila wing discs, Proc Natl Acad Sci, vol.113, pp.6993-7002, 2016.

V. Honti, G. Csordás, É. Kurucz, R. Márkus, and I. Andó, The cell-mediated immunity of Drosophila melanogaster: Hemocyte lineages, immune compartments, microanatomy and regulation, Dev Comp Immunol, vol.42, pp.47-56, 2014.

A. Hijazi, W. Masson, B. Auge, L. Waltzer, M. Haenlin et al., boudin is required for septate junction organisation in Drosophila and codes for a diffusible protein of the Ly6 superfamily, Development, vol.136, pp.2199-2209, 2009.

P. Irving, J. Ubeda, D. Doucet, L. Troxler, M. Lagueux et al., New insights into Drosophila larval haemocyte functions through genome-wide analysis, Cell Microbiol, vol.7, pp.335-350, 2005.
URL : https://hal.archives-ouvertes.fr/hal-00093694

M. Kirkham and R. G. Parton, Clathrin-independent endocytosis: New insights into caveolae and non-caveolar lipid raft carriers, Biochim Biophys Acta -Mol Cell Res, vol.1745, pp.273-286, 2005.

S. Kumari, . Mg-s, and S. Mayor, Endocytosis unplugged: multiple ways to enter the cell, Cell Res, vol.20, pp.256-275, 2010.

C. Labrosse, Y. Carton, A. Dubuffet, J. Drezen, and M. Poirie, Active suppression of D. melanogaster immune response by long gland products of the parasitic wasp Leptopilina boulardi, J Insect Physiol, vol.49, pp.513-522, 2003.

C. Labrosse, K. Stasiak, J. Lesobre, . Grangeia-a, and E. Huguet, A RhoGAP protein as a main immune suppressive factor in the Leptopilina boulardi (Hymenoptera, Figitidae)-Drosophila melanogaster interaction, Insect Biochem Mol Biol, vol.35, pp.93-103, 2005.

P. Y. Lee, J. X. Wang, E. Parisini, C. C. Dascher, and P. A. Nigrovic, Ly6 family proteins in neutrophil biology, J Leukoc Biol, vol.94, pp.585-594, 2013.

J. P. Lim and P. A. Gleeson, Macropinocytosis: an endocytic pathway for internalising large gulps, Immunol Cell Biol, vol.89, pp.836-843, 2011.

H. Luo, P. Rose, T. Roberts, and C. Dearolf, The Hopscotch Jak kinase requires the Raf pathway to promote blood cell activation and differentiation in Drosophila, Mol Genet Genomics, vol.267, pp.57-63, 2002.

L. Maldonado-báez, C. Williamson, and J. G. Donaldson, Clathrin-independent endocytosis: A cargocentric view, Exp Cell Res, vol.319, pp.2759-2769, 2013.

S. Mayor, R. G. Parton, and J. G. Donaldson, Clathrin-independent pathways of endocytosis, Cold Spring Harb Perspect Biol, vol.6, 2014.

S. Mathivanan, H. Ji, and R. J. Simpson, Exosomes: Extracellular organelles important in intercellular communication, J Proteomics, vol.73, pp.1907-1920, 2010.

A. J. Mackrell, B. Blumberg, S. R. Haynes, and J. H. Fessler, The lethal myospheroid gene of Drosophila encodes a membrane protein homologous to vertebrate integrin beta subunits, Proc Natl Acad Sci, vol.85, pp.2633-2637, 1988.

M. Meister and R. Tikkanen, Endocytic trafficking of membrane-bound cargo: A flotillin point of view, Membranes (Basel), vol.4, pp.356-371, 2014.

M. Mettlen, D. Loerke, D. Yarar, G. Danuser, and S. L. Schmid, Cargo-and adaptor-specific mechanisms regulate clathrin-mediated endocytosis, J Cell Biol, vol.188, pp.919-933, 2010.

H. T. Mcmahon and E. Boucrot, Molecular mechanism and physiological functions of clathrin-mediated endocytosis, Nat Rev Mol Cell Biol, vol.12, pp.517-533, 2011.

J. Morales, H. Chiu, T. Oo, R. Plaza, and S. Hoskins, Biogenesis, structure, and immune-suppressive effects of virus-like particles of a Drosophila parasitoid, Leptopilina victoriae, J Insect Physiol, vol.51, pp.181-195, 2005.

L. A. Mulcahy, R. C. Pink, and D. Carter, Routes and mechanisms of extracellular vesicle uptake, J Extracell Vesicles, vol.3, pp.1-14, 2014.

R. Narayanan and M. Ramaswami, Endocytosis in Drosophila: Progress, Possibilities, Prognostications. Exp Cell Res, vol.271, pp.28-35, 2001.

A. Nilton, K. Oshima, F. Zare, S. Byri, U. Nannmark et al., Crooked, Coiled and Crimpled are three Ly6-like proteins required for proper localization of septate junction components, Development, vol.137, pp.2427-2437, 2010.

N. R. Paul, G. Jacquemet, and P. T. Caswell, Endocytic Trafficking of Integrins in Cell Migration, Curr Biol, vol.25, 2015.

R. G. Parton and B. M. Collins, Unraveling the architecture of caveolae, Proc Natl Acad Sci, vol.113, pp.14170-14172, 2016.

M. Poirié, Y. Carton, and A. Dubuffet, Virulence strategies in parasitoid Hymenoptera as an example of adaptive diversity, C R Biol, vol.332, pp.311-320, 2009.

E. Puklin-faucher and M. P. Sheetz, The mechanical integrin cycle, J Cell Sci, vol.122, pp.575-575, 2009.

B. Qualmann and H. Mellor, Regulation of endocytic traffic by Rho GTPases, Biochem J, vol.371, pp.233-241, 2003.

C. Ribeiro and M. Brehélin, Insect haemocytes: What type of cell is that?, J Insect Physiol, vol.52, pp.417-429, 2006.

J. Russo, S. Dupas, F. Frey, Y. Carton, and M. Brehelin, Insect immunity: early events in the encapsulation process of parasitoid (Leptopilina boulardi) eggs in resistant and susceptible strains of Drosophila, Parasitology, vol.112, pp.135-142, 1996.

E. Smythe and K. R. Ayscough, Actin regulation in endocytosis, J Cell Sci, vol.119, pp.4589-4598, 2006.

M. Simons and G. Raposo, Exosomes--vesicular carriers for intercellular communication, Curr Opin Cell Biol, vol.21, pp.575-581, 2009.

H. Stenmark, Rab GTPases as coordinators of vesicle traffic, Nat Rev Mol Cell Biol, vol.10, pp.513-525, 2009.

M. R. Strand and G. R. Burke, Polydnavirus-wasp associations: Evolution, genome organization, and function, Curr Opin Virol, vol.3, pp.587-594, 2013.

M. H. Syed, A. Krudewig, D. Engelen, T. Stork, and C. Klambt, The CD59 Family Member Leaky/Coiled Is Required for the Establishment of the Blood-Brain Barrier in Drosophila, J Neurosci, vol.31, pp.7876-7885, 2011.

K. Tanaka, Y. Diekmann, A. Hazbun, A. Hijazi, B. Vreede et al., Multispecies Analysis of Expression Pattern Diversification in the Recently Expanded Insect Ly6 Gene Family, Mol Biol Evol, vol.32, pp.1730-1747, 2015.

H. A. Watson, M. Zastrow, . Von, and B. Wendland, Endocytosis. Encyclopedia of Molecular Cell Biology and Molecular Medicine, 2006.

B. Wan, E. Goguet, M. Ravallec, O. Pierre, S. Lemauf et al., Atypical extracellular vesicles as interspecies communicasomes involved in host specificity: the case of a parasitoid wasp of Drosophila, 2017.

M. J. Williams, Rac1 signalling in the Drosophila larval cellular immune response, J Cell Sci, vol.119, 2006.

D. B. Williams, Beyond lectins: the calnexin/calreticulin chaperone system of the endoplasmic reticulum, J Cell Sci, vol.119, pp.615-623, 2006.

Y. Wurm, J. Wang, O. Riba-grognuz, M. Corona, and S. Nygaard, The genome of the fire ant Solenopsis invicta, Proc Natl Acad Sci U S A, vol.108, pp.5679-5684, 2011.

M. J. Xavier and M. J. Williams, The Rho-family GTPase Rac1 regulates integrin localization in Drosophila immunosurveillance cells, PLoS One, vol.6, 2011.

J. M. Yang and S. J. Gould, The cis-acting signals that target proteins to exosomes and microvesicles, Biochem Soc Trans, vol.41, pp.277-282, 2013.

J. C. Maynard, T. Pham, T. Zheng, A. Jockheck-clark, H. B. Rankin et al., the Drosophila GRP94 ortholog, is required for gut epithelial homeostasis and nutrient assimilation-coupled growth control, Dev. Biol, vol.2010, issue.2, pp.295-306

C. Morales and Z. Li, Drosophila canopy-b is a cochaperone of glycoprotein-93, J. Biol. Chem. y;?, 2017.

M. J. Xavier and M. J. Williams, The Rho-family GTPase Rac1 regulates integrin localization in Drosophila immunosurveillance cells, PLoS ONE, vol.6, issue.5, p.19504, 2011.

J. Shen, X. Chen, L. Hendershot, and R. Prywes, ER stress regulation of ATF6 localization by dissociation of BiP/GRP78 binding and unmasking of Golgi localization signals, Dev Cell, vol.3, issue.1, pp.99-111, 2002.

H. Ham, A. R. Woolery, C. Tracy, D. Stenesen, H. Krämer et al., Unfolded Protein Response-regulated DrosophilaFic (dFic) Protein Reversibly AMPylates BiP Chaperone during Endoplasmic Reticulum Homeostasis, J Biol Chem, vol.289, issue.52, pp.36059-69, 2014.

J. P. Dudzic, S. Kondo, R. Ueda, C. M. Bergman, and B. Lemaitre, Drosophila innate immunity: regional and functional specialization of prophenoloxidases, BMC Biol, vol.29, pp.1-16, 2015.

V. Uytterhoeven, E. Lauwers, I. Maes, K. Miskiewicz, M. N. Melo et al., Hsc70-4 Deforms Membranes to Promote Synaptic Protein Turnover by Endosomal Microautophagy, Neuron, vol.88, issue.4, pp.735-783, 2015.

P. Bronk, J. J. Wenniger, K. Dawson-scully, X. Guo, S. Hong et al., Drosophila Hsc70-4 Is Critical for Neurotransmitter Exocytosis In Vivo, Neuron, vol.30, issue.2, pp.475-88, 2001.

K. I. Brackley and J. Grantham, Activities of the chaperonin containing TCP-1 (CCT): implications for cell cycle progression and cytoskeletal organisation. Cell Stress and Chaperones, vol.14, pp.23-31, 2008.

C. Tsai, A. Chao, S. Jung, C. Tsai, C. Lin et al., Stress-induced phosphoprotein-1 maintains the stability of JAK2 in cancer cells, Oncotarget, vol.7, pp.50548-63, 2016.

P. A. Bond and J. H. Sang, Glutamate dehydrogenase of Drosophila larvae, J Insect Physiol, vol.14, issue.3, pp.341-59, 1968.

A. K. Tiwari, P. Panda, and J. S. Purohit, Evaluation of sub-cellular distribution of glutamate dehydrogenase (GDH) in Drosophila melanogaster larvae, Acta Histochem, vol.116, issue.2, pp.297-303, 2014.

P. Irving, J. Ubeda, D. Doucet, L. Troxler, M. Lagueux et al., New insights into Drosophila larval haemocyte functions through genome-wide analysis, Cell Microbiol, vol.7, issue.3, pp.335-50, 2005.
URL : https://hal.archives-ouvertes.fr/hal-00093694

K. Kim, S. Kim, J. Kim, H. Kim, and J. Yim, Glutathione S-Transferase Omega 1 Activity Is Sufficient to Suppress Neurodegeneration in a Drosophila Model of Parkinson Disease, J Biol Chem, vol.287, issue.9, pp.6628-6669, 2012.

C. S. Ricard, J. M. Jakubowski, J. W. Verbsky, M. A. Barbieri, W. M. Lewis et al., Drosophila rab GDI mutants disrupt development but have normal Rab membrane extraction, Genesis, vol.31, issue.1, pp.17-29, 2001.

A. N. Sasikumar, W. B. Perez, and T. G. Kinzy, The many roles of the eukaryotic elongation factor 1 complex, WIREs RNA, vol.3, issue.4, pp.543-55, 2012.

E. A. Fyrberg, J. W. Mahaffey, B. J. Bond, and N. Davidson, Transcripts of the six Drosophila actin genes accumulate in a stage- and tissue-specific manner, Cell, vol.33, issue.1, pp.115-138, 1983.

M. A. Siddiq, D. W. Loehlin, K. L. Montooth, and J. W. Thornton, Experimental test and refutation of a classic case of molecular adaptation in Drosophila melanogaster, Nat Ecol Evol, vol.1, pp.1-6, 2017.

K. Fong, F. Au, Y. Jia, S. Yang, L. Zhou et al., Microtubule plus-end tracking of end-binding protein 1 (EB1) is regulated by CDK5 regulatory subunit-associated protein 2, J. Biol. Chem, vol.292, issue.18, pp.7675-87, 2017.

Y. S. Ng, A. Sorvina, C. A. Bader, F. Weiland, A. F. Lopez et al., Proteome Analysis of DrosophilaMutants Identifies a Regulatory Role for 14-3-3? in Metabolic Pathways, J Proteome Res, vol.16, issue.5, pp.1976-87, 2017.

T. P. Le, L. T. Vuong, A. Kim, Y. Hsu, and K. Choi, 14-3-3 proteins regulate Tctp-Rheb interaction for organ growth in Drosophila, Nat. Commun.;?, pp.1-10, 2016.

D. R. Adams, D. Ron, and P. A. Kiely, RACK1, A multifaceted scaffolding protein: Structure and function, Cell Commun. Signal, vol.9, issue.1, p.22, 2011.

S. Mishra, L. C. Murphy, and L. J. Murphy, The Prohibitins: emerging roles in diverse functions, J Cell Mol Med, vol.10, issue.2, pp.353-63, 2006.

S. R. Ande, K. H. Nguyen, B. Nyomba, and S. Mishra, Prohibitin in Adipose and Immune Functions, Trends Endocrinol Metab, vol.27, issue.8, pp.531-572, 2016.

J. Park, Y. Kim, S. Choi, H. Koh, S. Lee et al., Drosophila Porin/VDAC affects mitochondrial morphology, PLoS ONE, vol.5, p.13151, 2010.

R. Garcia-mata, E. Boulter, and K. Burridge, The "invisible hand": regulation of RHO GTPases by RHOGDIs, Nat Rev Mol Cell Biol, vol.12, issue.8, pp.493-504, 2011.

M. Degennaro, T. R. Hurd, D. E. Siekhaus, B. Biteau, H. Jasper et al., Peroxiredoxin Stabilization of DE-Cadherin Promotes Primordial Germ Cell Adhesion, Dev Cell, vol.20, issue.2, pp.233-276, 2011.

C. Tu, B. Akgül, and S. Drosophila-glutathione, Gluthione Transferases and Gamma-Glutamyl Transpeptidases, vol.401, pp.204-230, 2005.

V. Muñoz-soriano, A. Domingo-muelas, T. Li, E. Gamero, A. Bizy et al., Evolutionary conserved role of eukaryotic translation factor eIF5A in the regulation of actin-nucleating formins, Sci Rep, vol.7, p.9580, 2017.

L. Salazar-jaramillo, K. M. Jalvingh, A. De-haan, K. Kraaijeveld, H. Buermans et al., Inter- and intra-species variation in genome-wide gene expression of Drosophila in response to parasitoid wasp attack, BMC Genomics, vol.18, p.331, 2017.

M. Ignesti, M. Barraco, G. Nallamothu, J. A. Woolworth, S. Duchi et al., Notch signaling during development requires the function of awd, the Drosophila homolog of human metastasis suppressor gene Nm23, BMC Biol, vol.12, issue.1, pp.1-18, 2014.

E. M. Verheyen and L. Cooley, Profilin mutations disrupt multiple actin-dependent processes during Drosophila development, Development, vol.120, issue.4, pp.717-745, 1994.

, Bien que cette liste fournisse déjà un certain nombre d'informations, nous avons analysé

. Cependant, en particulier bien que nous ayons retrouvé des protéines à ancre GPI, nous n'avons pas retrouvé les flotillines alors qu'elles sont présentes dans l'analyse globale des cellules par 2D. Cette absence peut s'expliquer par la méthode d'extraction (Beta-octylglucopyranoside) qui n'est peut-être pas capable de solubiliser les radeaux lipidiques contenant la flotilline

, D'autres détergeants pourraient être mieux appropriés

, Je n'ai pas eu le temps durant la fin de ma thèse d'effectuer cette expérience, mais si le récepteur des vénosomes est localisé comme il semblerait dans ces domaines, il faudra les purifier et les analyser pour l'identifier

, Cette thèse, bien qu'à plus long terme, ouvre aussi sur des aspects appliqués

, Les citoyens s'inquiètent de plus en plus de la qualité et de l

A. Dobson, K. D. Lafferty, A. M. Kuris, R. F. Hechinger, and W. Jetz, Homage to Linnaeus: How many parasites? How many hosts?, Proceedings of the National Academy of Sciences, vol.105, pp.11482-11489, 2008.

L. Van-valen, A new evolutionary law. Evolutionary Theory. 1973. pp. 1-30

P. Eggleton and K. J. Gaston, Pmasitoid " species and assemblages : convenient deJiniabns or misleading compromises ?, Oikos, vol.59, pp.417-421, 1990.

P. Eggleton and R. Belshaw, Insect Parasitoids: An Evolutionary Overview, Philosophical Transactions of the Royal Society B: Biological Sciences, vol.337, pp.1-20, 1992.

J. O. Stireman, Community ecology of the "other" parasitoids. Current Opinion in Insect Science, vol.14, pp.87-93, 2016.

H. Godfray, Parasitoids: behavioral and evolutionary ecology, 1994.

H. Godfray and M. Shimada, Parasitoids: a model system to answer questions in behavioral, evolutionary and population ecology. Researches on Population Ecology, vol.41, pp.3-10, 1999.

E. E. Grissell, Hymenopteran biodiversity: some alien notions, Am Entomol, vol.45, pp.235-244, 1999.

R. S. Peters, L. Krogmann, C. Mayer, A. Donath, S. Gunkel et al., Evolutionary History of the Hymenoptera, Current Biology. Elsevier Ltd, vol.27, pp.1013-1018, 2017.

D. Quicke, The Braconid and Ichneumonid Parasitoid Wasps: Biology, Systematics, Evolution and Ecology, 2015.

H. Godfray, Four decades of parasitoid science, Entomologia Experimentalis et Applicata, vol.159, pp.135-146, 2016.

D. Quicke, Parasitic wasps. London: Chapman & Hall Ltd, 1997.

B. Lemaitre and J. Hoffmann, The Host Defense of Drosophila melanogaster, Annual Review of Immunology, vol.25, pp.697-743, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00167467

J. A. Hoffmann and J. Reichhart, Drosophila innate immunity: an evolutionary perspective, Nature Immunology, vol.3, pp.121-126, 2002.

P. Tzou, D. Gregorio, E. Lemaitre, and B. , How Drosophila combats microbial infection: A model to study innate immunity and host-pathogen interactions, Current Opinion in Microbiology, vol.5, pp.102-110, 2002.

L. Wang, I. Kounatidis, and P. Ligoxygakis, Drosophila as a model to study the role of blood cells in inflammation, innate immunity and cancer, Frontiers in Cellular and Infection Microbiology, vol.3, 2014.

B. Arefin, M. Kunc, R. Krautz, and U. Theopold, The Immune Phenotype of Three Drosophila Leukemia Models, Genes Genomes Genetics, pp.2139-2149, 2017.

P. Michel and M. Solignac, Molecular Phylogeny of Drosophila Based on Ribosomal RNA Sequences, Journal of Molecular Evolution, pp.525-543, 1993.

A. G. Clark, M. B. Eisen, D. R. Smith, C. M. Bergman, B. Oliver et al., Evolution of genes and genomes on the Drosophila phylogeny, Nature, vol.450, pp.203-218, 2007.

K. Van-der-linde, D. Houle, G. S. Spicer, and S. J. Steppan, A supermatrix-based molecular phylogeny of the family Drosophilidae, Genetics Research, vol.92, p.25, 2010.

T. A. Markow, O. Grady, and P. M. , Drosophila : a guide to species identification and use, 2005.

H. L. Carson, University of Hawaii Foundation Lyon Arboretum Fund, 1971.

T. Okada, Bleeding Sap Preference of the Drosophilid Flies, Japanese journal of applied entomology and zoology, vol.6, pp.216-229, 1962.

T. A. Markow, The secret lives of Drosophila flies, eLife, vol.4, pp.1-9, 2015.

J. Atallah, L. Teixeira, R. Salazar, G. Zaragoza, and A. Kopp, The making of a pest: the evolution of a fruitpenetrating ovipositor in Drosophila suzukii and related species, Proceedings of the Royal Society B: Biological Sciences, vol.281, pp.20132840-20132840, 2014.

M. K. Asplen, G. Anfora, A. Biondi, D. S. Choi, D. Chu et al., Invasion biology of spotted wing Drosophila (Drosophila suzukii): a global perspective and future priorities, Journal of Pest Science, vol.88, pp.469-494, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01921732

D. Lachaise, M. Cariou, J. R. David, F. Lemeunier, L. Tsacas et al., Historical Biogeography of the Drosophila melanogaster Species Subgroup, Evolutionary Biology, pp.159-225, 1988.

J. R. David and P. Capy, Genetic variation of Drosophila melanogaster natural populations, Trends in Genetics, vol.4, pp.106-111, 1988.

D. B. Roberts, Drosophila-a versatile model in biology & medicine. Materials Today, Applicata, vol.121, pp.190-195, 2006.

E. S. Keebaugh and T. A. Schlenke, Insights from natural host-parasite interactions: The Drosophila model, Developmental and Comparative Immunology. Elsevier Ltd, vol.42, pp.111-123, 2014.

R. Warrington, W. Watson, H. L. Kim, and F. Antonetti, An introduction to immunology and immunopathology, Asthma & Clinical Immunology, vol.7, p.1, 2011.

G. Eberl, Immunity by equilibrium, Nature Reviews Immunology. Nature Publishing Group, vol.16, pp.524-532, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01402375

K. Buchmann, Rizki MT, Rizki RM. Functional significance of the crystal cells in the larva of Drosophila melanogaster, The Journal of biophysical and biochemical cytology, vol.5, pp.235-240, 1959.

T. M. Rizki, The circulatory system and associated cells and tissues. The Genetics and Biology of Drosophila, pp.397-452, 1978.

M. Brehelin, D. Zachary, and J. A. Hoffmann, A comparative ultrastructural study of blood cells from nine insect orders, Cell and Tissue Research, vol.195, pp.45-57, 1978.

M. Brehelin, Comparative study of structure and function of blood cells from two Drosophila species, Cell Tissue Res, vol.221, pp.607-615, 1982.

M. Fauvarque and M. J. Williams, Drosophila cellular immunity: a story of migration and adhesion, Journal of cell science, vol.124, pp.1373-1382, 2011.

A. S. Gandhe, S. H. John, J. Nagaraju, and . Noduler, A Novel Immune Up-Regulated Protein Mediates Nodulation Response in Insects, The Journal of Immunology, vol.179, pp.6943-6951, 2007.

I. Vallet-gely, B. Lemaitre, and F. Boccard, Bacterial strategies to overcome insect defences, Nature Reviews Microbiology, vol.6, pp.302-313, 2008.

D. Im, K. Na, G. Vv, and R. Na, Encapsulation and nodulation in insects, Isj, vol.13, pp.229-246, 2016.

T. M. Rizki, Hemocyte Encapsulation of Streptococci in Drosophila, JOURAL OF INVERTEBHATE PATHOLOGY, vol.12, pp.339-343, 1968.

Y. Carton, M. Poirie, and A. J. Nappi, Insect immune resistance to parasitoids, Insect Science, vol.15, pp.67-87, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00319495

I. Anderl, L. Vesala, T. O. Ihalainen, L. M. Vanha-aho, I. Ando et al., Transdifferentiation and Proliferation in Two Distinct Hemocyte Lineages in Drosophila melanogaster Larvae after Wasp Infection, PLoS Pathogens, vol.12, pp.1-34, 2016.

T. Lebestky, J. S. Banerjee, and U. Serrate,

, Genes & Development, vol.17, pp.348-353, 2003.

C. Ribeiro and M. Brehelin, Insect haemocytes: What type of cell is that, Journal of Insect Physiology, vol.52, pp.417-429, 2006.

A. J. Nappi, Defense reactions of Drosophila euronotus larvae against the hymenopterous parasite Pseudeucoila bochei, Journal of Invertebrate Pathology, vol.16, pp.90160-90166, 1970.

J. C. De-roode and T. Lefevre, Behavioral immunity in insects. Insects, vol.3, pp.789-820, 2012.

P. Gross, Insect Behavioral and Morphological Defenses Against Parasitoids, Annual Review of Entomology, vol.38, pp.251-274, 1993.

R. Y. Hwang, L. Zhong, Y. Xu, T. Johnson, F. Zhang et al., Nociceptive Neurons Protect Drosophila Larvae from Parasitoid Wasps, Current Biology, vol.17, pp.2105-2116, 2007.

N. F. Milan, B. Z. Kacsoh, T. A. Schlenke, Z. R. Lynch, T. A. Schlenke et al., Ethanol confers differential protection against generalist and Specialist parasitoids of Drosophila melanogaster, Current Biology. Elsevier Ltd, vol.22, pp.1-19, 2012.

B. Z. Kacsoh, Z. R. Lynch, N. T. Mortimer, T. A. Schlenke, J. Bouletreau-merle et al., Sexually Dimorphic Response to Host Habitat Toxicity in Drosophila Parasitic Wasps, Evolution, vol.339, pp.395-399, 1981.

Z. R. Lynch, T. A. Schlenke, and J. C. De-roode, Evolution of behavioural and cellular defences against parasitoid wasps in the Drosophila melanogaster subgroup, Journal of Evolutionary Biology, vol.29, pp.1016-1029, 2016.

T. Lefevre, J. C. De-roode, B. Z. Kacsoh, and T. A. Schlenke, Defence strategies against a parasitoid wasp in Drosophila: fight or flight?, Biology Letters, vol.8, pp.230-233, 2012.

S. Ebrahim, H. Dweck, J. Stokl, J. E. Hofferberth, F. Trona et al., Drosophila Avoids Parasitoids by Sensing Their Semiochemicals via a Dedicated Olfactory Circuit, PLoS Biology, vol.13, pp.1-18, 2015.

A. Janssen, G. Driessen, M. De-haan, and N. Roodbol, The Impact of Parasitoids On Natural Populations of Temperate Woodland Drosophila, Netherlands Journal of Zoology, vol.38, pp.61-73, 1988.

J. Rouault, Role des parasites entomophages dans la competition entre especes jumelles de Drosophiles: approche experimentale. C R Acad Sc Paris, vol.289, pp.1-4, 1979.

Y. Carton, M. Bouletreau, J. Van-alphen, and J. C. Van-lenteren, The Drosophila Parasitic Wasps. The Genetics and Biology of Drosophila, pp.347-394, 1986.
URL : https://hal.archives-ouvertes.fr/hal-00410269

H. Mitsui, K. Van-achterberg, G. Nordlander, and M. T. Kimura, Geographical distributions and host associations of larval parasitoids of frugivorous Drosophilidae in Japan, Journal of Natural History, vol.41, pp.1731-1738, 2007.

C. Le-lann, B. Visser, M. Meriaux, J. Moiroux, J. Van-baaren et al., Rising temperature reduces divergence in resource use strategies in coexisting parasitoid species, Oecologia, vol.174, pp.967-977, 2014.
URL : https://hal.archives-ouvertes.fr/hal-00906723

L. Kaiser, C. Bartheye, V. Kerguelen, and M. H. Pham-delegue, Odour conditioning of ovipositor probing in a parasitic wasp, Ethology Ecology and Evolution, vol.7, pp.245-255, 1995.

M. E. Lof, M. De-gee, M. Dicke, G. Gort, and L. Hemerik, Exploitation of Chemical Signaling by Parasitoids: Impact on Host Population Dynamics, Journal of Chemical Ecology, vol.39, pp.752-763, 2013.

I. Weiss, T. Rossler, J. Hofferberth, M. Brummer, J. Ruther et al., A nonspecific defensive compound evolves into a competition avoidance cue and a female sex pheromone, Nature Communications, vol.4, 2013.

M. Ne-goubault, L. Krespi, G. Boivin, D. Poinsot, J. Nenon et al., Intraspecific Variations in Host Discrimination Behavior in the Pupal Parasitoid Pachycrepoideus vindemmiae Rondani (Hymenoptera: Pteromalidae), Environ Entomol, vol.33, pp.362-369, 2004.

R. Romani, N. Isidoro, F. Bin, and S. B. Vinson, Host recognition in the pupal parasitoid Trichopria drosophilae: A morpho-functional approach, Entomologia Experimentalis et Applicata, vol.105, pp.119-128, 2002.

W. Chen, Z. He, X. L. Ji, S. T. Tang, and H. Y. Hu, Hyperparasitism in a generalist ectoparasitic pupal parasitoid, Pachycrepoideus vindemmiae (Hymenoptera: Pteromalidae), on its own conspecifics: When the lack of resource lead to cannibalism, PLoS ONE, vol.10, pp.1-16, 2015.

F. Fleury, P. Gibert, N. Ris, and R. Allemand, Ecology and Life History Evolution of Frugivorous Drosophila Parasitoids, Advances in Parasitology, vol.70, pp.3-44, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00539382

Y. Carton and H. Kitano, Journal of Invertebrate Pathology (USA). 1979. 73. Streams FA. Defense Reactions of Drosophila Species (Diptera: Drosophilidae) to the Parasite Pseudeucoila bochei (Hymenoptera: Cynipidae), Annals of the Entomological Society of America, vol.61, pp.158-164, 1963.

E. Schlegel-oprecht, Versuche Zur Auslösung Von Mutationen Bei Der Zoophagen Cynipide Pseudeucoila Bochei Weld Und Befunde Über Die Stammspezifische Abwehrreaktion Des Wirtes Drosophila Melanogaster. Zeitschrift für Induktive Abstammungs-und Vererbungslehre, vol.85, pp.245-281, 1953.

Z. Meig, Beitrah Zur Morphologie Und Biologie Der Cynipide Pseudeucolia Bochei Weld, Eines Larvenparasiten Von Drosophila Melanogaster, Acta Zoologica, 1951.

R. D. Boche, Studies on hymenopteran parasitism of drosophila, 1938.

G. Nordlander, Revision of the genus Leptopilina Forster, 1869, with notes on the status of some other genera (Hymenoptera, Cynipoidea: Eucoilidae), Entomologica Scandinavica, vol.11, pp.428-453, 1980.

R. Allemand, C. Lemaitre, F. Frey, M. Bouletreau, F. Vavre et al., Phylogeny of six African Leptopilina species, Ann Soc Entomol, vol.38, pp.319-332, 2002.
URL : https://hal.archives-ouvertes.fr/hal-00427243

M. Fellowes, H. Godfray, H. A. Orr, and S. Irving, The genetics of adaptation: the genetic basis of resistance to wasp parasitism in Drosophila melanogaster, Evolution, vol.84, pp.1877-1885, 1997.

A. Dubuffet, S. Dupas, F. Frey, J. Drezen, M. Poirie et al., Genetic interactions between the parasitoid wasp Leptopilina boulardi and its Drosophila hosts, Heredity, vol.98, pp.21-27, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00193317

S. Dupas, M. Poirie, F. Frey, and Y. Carton, Is parasitoid virulence against multiple hosts adaptive or constrained by phylogeny? A study of Leptopilina spp. (Hymenoptera: Figitidae)/Drosophila (Diptera: Drosophilidae) interactions. Annales de la Societe Entomologique de France, vol.49, pp.222-231, 2013.

S. Dupas and Y. Carton, Two non-linked genes for specific virulence of Leptopilina boulardi against Drosophila melanogaster and D. yakuba, Evolutionary Ecology, vol.13, pp.211-220, 1999.

T. M. Rizki, R. M. Rizki, Y. Carton, L. Leptopilina, and . Boulardi, Nappi AJ. Cellular immunity and pathogen strategies in combative interactions involving Drosophila hosts and their endoparasitic wasps, Invertebrate Survival Journal, vol.70, pp.198-210, 1990.

M. Poirie, Y. Carton, and A. Dubuffet, Virulence strategies in parasitoid Hymenoptera as an example of adaptive diversity, Comptes Rendus -Biologies. Elsevier Masson SAS, vol.332, pp.311-320, 2009.

R. M. Rizki and T. M. Rizki, Selective destruction of a host blood cell type by a parasitoid wasp, Proceedings of the National Academy of Sciences of the United States of America, vol.81, pp.6154-6158, 1984.

G. Prevost, P. Eslin, G. Doury, S. Moreau, and G. S. Asobara, braconid parasitoids of Drosophila larvae: Unusual strategies to avoid encapsulation without VLPs, Journal of Insect Physiology, vol.51, pp.171-179, 2005.
URL : https://hal.archives-ouvertes.fr/hal-00015126

P. Eslin, P. Giordanengo, Y. Fourdrain, and G. Prevost, Avoidance of encapsulation in the absence of VLP by a braconid parasitoid of Drosophila larvae: An ultrastructural study, Canadian Journal of Zoology-Revue Canadienne De Zoologie, vol.74, pp.2193-2198, 1996.

R. M. Rizki and T. M. Rizki, Effects of lammellolysin from a parasitoid wasp on Drosophila blood cells in vitro, Journal of Experimental Zoology, vol.257, pp.236-244, 1991.

H. Chiu and S. Govind, Natural infection of D. melanogaster by virulent parasitic wasps induces apoptotic depletion of hematopoietic precursors, Cell death and differentiation, vol.9, pp.1379-1381, 2002.

A. Dubuffet, D. Colinet, C. Anselme, S. Dupas, Y. Carton et al., Variation of Leptopilina boulardi Success in Drosophila Hosts. What is Inside the Black Box?, Advances in Parasitology, vol.70, pp.147-188, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00410262

J. L. Gatti, A. Schmitz, D. Colinet, and M. Poirie, Diversity of Virus-Like Particles in Parasitoids' Venom: Viral or Cellular Origin? Parasitoid Viruses: Symbionts and Pathogens, pp.181-192, 2012.

M. R. Strand and G. R. Burke, Polydnaviruses: Nature's Genetic Engineers, Annu Rev Virol, vol.1, pp.333-54, 2014.

M. R. Strand and G. R. Burke, Polydnaviruses: From discovery to current insights, pp.393-402, 2015.

J. Gauthier, J. Drezen, and E. A. Herniou, The recurrent domestication of viruses: major evolutionary transitions in parasitic wasps, Parasitology, pp.1-13, 2017.
URL : https://hal.archives-ouvertes.fr/hal-02140632

A. Pichon, A. Bezier, S. Urbach, J. Aury, V. Jouan et al., Recurrent DNA virus domestication leading to different parasite virulence strategies, Science advances, vol.1, p.1501150, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01318262

M. Poirie, D. Colinet, and J. L. Gatti, Insights into function and evolution of parasitoid wasp venoms, Current Opinion in Insect Science, vol.6, pp.52-60, 2014.

D. Colinet, E. Deleury, C. Anselme, D. Cazes, J. Poulain et al., Extensive inter-and intraspecific venom variation in closely related parasites targeting the same host: The case of Leptopilina parasitoids of Drosophila, Insect Biochemistry and Molecular Biology. Elsevier Ltd, vol.43, pp.601-611, 2013.

J. Goecks, N. T. Mortimer, J. Mobley, G. J. Bowersock, J. Taylor et al., Integrative Approach Reveals Composition of Endoparasitoid Wasp Venoms, PLoS ONE, vol.8, pp.1-14, 2013.

D. Colinet, A. Dubuffet, D. Cazes, S. Moreau, J. M. Drezen et al., A serpin from the parasitoid wasp Leptopilina boulardi targets the Drosophila phenoloxidase cascade, Developmental and Comparative Immunology, vol.33, pp.681-689, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00435637

A. Dubuffet, G. Doury, C. Labrousse, J. M. Drezen, Y. Carton et al., Variation of success of Leptopilina boulardi in Drosophila yakuba: The mechanisms explored, Developmental and Comparative Immunology, vol.32, pp.597-602, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00315871

R. M. Rizki and T. M. Rizki, Parasitoid virus-like particles destroy Drosophila cellular immunity, Proceedings of the National Academy of Sciences of the United States of America, vol.87, pp.8388-8392, 1990.

T. M. Rizki and R. M. Rizki, Parasitoid--Induced Cellular Immune Deficiency in Drosophila, Annals of the New York Academy of Sciences, vol.712, pp.178-194, 1994.

C. Labrosse, Y. Carton, D. A. Drezen, J. M. Poirie, and M. , Active suppression of D. melanogaster immune response by long gland products of the parasitic wasp Leptopilina boulardi, Journal of Insect Physiology, vol.49, pp.513-522, 2003.

D. Colinet, A. Schmitz, D. Cazes, J. L. Gatti, and M. Poirie, The origin of intraspecific variation of virulence in an eukaryotic immune suppressive parasite, PLoS Pathogens, vol.6, 2010.

H. Chiu, J. Morales, and S. Govind, Identification and immuno-electron microscopy localization of p40, a protein component of immunosuppressive virus-like particles from Leptopilina heterotoma, a virulent parasitoid wasp of Drosophila, Journal of General Virology, vol.87, pp.461-470, 2006.

C. Labrosse, K. Stasiak, J. Lesobre, A. Grangeia, E. Huguet et al., A RhoGAP protein as a main immune suppressive factor in the Leptopilina boulardi (Hymenoptera, Figitidae)-Drosophila melanogaster interaction, Insect Biochemistry and Molecular Biology, vol.35, pp.93-103, 2005.

D. Colinet, A. Schmitz, D. Depoix, D. Crochard, and M. Poirie, Convergent use of RhoGAP toxins by eukaryotic parasites and bacterial pathogens, PLoS Pathogens, vol.3, pp.2029-2037, 2007.
URL : https://hal.archives-ouvertes.fr/hal-02337684

M. J. Williams, I. Ando, and D. Hultmark, Drosophila melanogaster Rac2 is necessary for a proper cellular immune response, Genes to Cells, vol.10, pp.813-823, 2005.

M. J. Williams, Rac1 signalling in the Drosophila larval cellular immune response, Journal of Cell Science, vol.119, pp.2015-2024, 2006.

M. J. Xavier and M. J. Williams, The Rho-family GTPase Rac1 regulates integrin localization in Drosophila immunosurveillance cells, PLoS ONE, vol.6, 2011.

Y. J. Yoon, O. Y. Kim, and Y. S. Gho, Extracellular vesicles as emerging intercellular communicasomes, BMB Reports, vol.47, pp.531-539, 2014.

V. Ricci, M. Giannouli, M. Romano, and R. Zarrilli, Helicobacter pylori gamma-glutamyl transpeptidase and its pathogenic role, World Journal of Gastroenterology, vol.20, pp.630-638, 2014.

A. J. Szempruch, L. Dennison, R. Kieft, J. M. Harrington, and S. L. Hajduk, Sending a message: extracellular vesicles of pathogenic protozoan parasites, Nature Reviews Microbiology, vol.14, pp.669-675, 2016.

A. H. Kopelman and P. C. Chabora, Aspects of the reproductive biology of Leptopilina boulardi (Hymenoptera: Eucoilidae), Annals of the Entomological Society of America, vol.79, pp.808-813, 1986.

Y. Carton, P. Capy, and A. J. Nappi, Genetic variability of host-parasite relationship traits: utilization of isofemale lines in a Drosophila simulans parasitic wasp, Genetics Selection Evolution, vol.21, pp.437-446, 1989.
URL : https://hal.archives-ouvertes.fr/hal-00893814

Y. Carton, J. Rouault, and . Kh, Susceptibility of the seven sibling species of subgroup melanogaster infected with a cynipide parasite, Drosophila Inf Serv, vol.364, 1981.

Y. Carton and H. Kitano, Evolutionary relationships to parasitism by seven species of the Drosophila melanogaster subgroup, Biological Journal of the Linnean Society, vol.16, pp.227-241, 1981.

S. Dupas and M. Boscaro, Geographic variation and evolution of immunosuppressive genes in a Drosophila parasitoid, Ecography, vol.22, pp.284-291, 1999.

S. Dupas, Y. Carton, and M. Poirie, Genetic dimension of the coevolution of virulence-resistance in Drosophilaparasitoid wasp relationships, Heredity, vol.90, pp.84-89, 2003.

S. Dupas, F. Frey, and Y. Carton, A single parasitoid segregating factor controls immune suppression in Drosophila, Journal of Heredity, vol.89, pp.306-311, 1998.

M. Bouletreau and P. Fouillet, Variabilité génétique intrapopulation de l'aptitude de Drosophila melanogaster à permettre le développement d'un hyménoptère parasite, CR Acad Sci, vol.295, pp.775-778, 1982.

Y. Carton and F. Frey, Analyse expérimentale de trois niveaux d'interactions entre Drosophila melanogaster et le parasite Leptopilina boulardi (sympatrie, allopatrie, xénopatrie), Genet Sel Evol, vol.16, pp.417-430, 1984.

Y. Carton and M. Bouletreau, Encapsulation ability of Drosophila melanogaster: A genetic analysis, Developmental and Comparative Immunology, vol.9, pp.211-219, 1985.

E. Vass and A. Nappi, Fruit Fly Immunity, Bioscience, vol.51, pp.529-536, 2001.

T. Hita, M. Poirié, M. Leblanc, N. Lemeunier, F. Lutcher et al., Genetic Localization of a Drosophila melanogaster Resistance Gene to a Parasitoid Wasp and Physical Mapping of the Region. Genome research, 1999.

M. Poirie, F. Frey, M. Hita, E. Huguet, F. Lemeunier et al., Drosophila resistance genes to parasitoids: chromosomal location and linkage analysis, Proceedings of the Royal Society of London Series B-Biological Sciences, vol.267, pp.1417-1421, 2000.

M. Hita, E. Espagne, F. Lemeunier, L. Pascual, Y. Carton et al., Mapping candidate genes for Drosophila melanogaster resistance to the parasitoid wasp Leptopilina boulardi, Genetical research, vol.88, pp.81-91, 2006.
URL : https://hal.archives-ouvertes.fr/hal-00113518

T. Yamada, M. Okabe, and Y. Hiromi, EDL/MAE regulates EGF-mediated induction by antagonizing Ets transcription factor Pointed, Development, vol.130, pp.4085-4096, 2003.

L. Vet, J. Alphen, and . Van, A comparative functional approach to the host detection behavior of parasitic wasps. 1. A qualitative study on Eucoilinae and Alysiinae, Oikos, vol.44, pp.478-486, 1985.

J. L. Robertson, A. Tsubouchi, and W. D. Tracey, Larval Defense against Attack from Parasitoid Wasps Requires Nociceptive Neurons, PLoS ONE, vol.8, pp.1-9, 2013.

S. Moreau and S. Asgari, Venom proteins from parasitoid wasps and their biological functions, Toxins, vol.7, pp.2385-2412, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01316572

J. L. Robertson, Leptopilina Parasitoid Wasps, Ion Channels, and Dendritic Morphology in Drosophila Nociception Paradigms, 2013.

Y. Tokusumi, T. Tokusumi, and R. A. Schulz, The nociception genes painless and Piezo are required for the cellular immune response of Drosophila larvae to wasp parasitization. Biochemical and Biophysical Research Communications, vol.486, pp.893-897, 2017.

A. Capilla, D. Karachentsev, R. A. Patterson, A. Hermann, M. T. Juarez et al., Toll pathway is required for wound-induced expression of barrier repair genes in the Drosophila epidermis, Proceedings of the National Academy of Sciences, vol.114, pp.2682-2688, 2017.

M. T. Abreu-blanco, J. M. Verboon, and S. M. Parkhurst, Cell wound repair in Drosophila occurs through three distinct phases of membrane and cytoskeletal remodeling, Journal of Cell Biology, vol.193, pp.455-464, 2011.

T. J. Shaw and P. Martin, Wound repair at a glance, Journal of Cell Science, vol.122, pp.3209-3213, 2009.

W. Razzell, I. R. Evans, P. Martin, and W. Wood, Calcium flashes orchestrate the wound inflammatory response through duox activation and hydrogen peroxide release, Current Biology. Elsevier Ltd, vol.23, pp.424-429, 2013.

J. M. Verboon and S. M. Parkhurst, Rho family GTPase functions in Drosophila epithelial wound repair, Small GTPases, vol.6, pp.28-35, 2015.

R. Krautz, B. Arefin, and U. Theopold, Damage signals in the insect immune response, Frontiers in Plant Science, vol.5, 2014.

M. J. Galko and M. A. Krasnow, Cellular and genetic analysis of wound healing in Drosophila larvae, PLoS Biology, vol.2, 2004.

W. Wood and P. Martin, Macrophage Functions in Tissue Patterning and Disease: New Insights from the Fly. Developmental Cell, vol.40, pp.221-233, 2017.

C. Scherfer, C. Karlsson, O. Loseva, G. Bidla, and A. Goto, Isolation and Characterization of Hemolymph Clotting Factors in Drosophila melanogaster by a Pullout Method Christoph, Current Biology, vol.14, pp.25-29, 2004.

M. S. Dushay, Insect hemolymph clotting, Cellular and Molecular Life Sciences, vol.66, pp.2643-2650, 2009.

T. G. Loof, O. Schmidt, H. Herwald, and U. Theopold, Coagulation systems of invertebrates and vertebrates and their roles in innate immunity: The same side of two coins, Journal of Innate Immunity, vol.3, pp.34-40, 2011.

R. A. Patterson, M. T. Juarez, A. Hermann, R. Sasik, G. Hardiman et al., Serine Proteolytic Pathway Activation Reveals an Expanded Ensemble of Wound Response Genes in Drosophila, PLoS ONE, vol.8, 2013.

Z. Wang, C. Wilhelmsson, P. Hyrsl, T. G. Loof, P. Dobes et al., Pathogen entrapment by transglutaminase -A conserved early innate immune mechanism, PLoS Pathogens, vol.6, 2010.

C. Karlsson, A. M. Korayem, C. Scherfer, O. Loseva, M. S. Dushay et al., Proteomic analysis of the Drosophila larval hemolymph clot, Journal of Biological Chemistry, vol.279, pp.52033-52041, 2004.

A. Goto, T. Kadowaki, and Y. Kitagawa, Drosophila hemolectin gene is expressed in embryonic and larval hemocytes and its knock down causes bleeding defects 1, vol.264, pp.582-591, 2003.

O. Binggeli, C. Neyen, M. Poidevin, and B. Lemaitre, Prophenoloxidase Activation Is Required for Survival to Microbial Infections in Drosophila, PLoS Pathogens, vol.10, 2014.

R. Márkus, É. Kurucz, F. Rus, and I. Andó, Sterile wounding is a minimal and sufficient trigger for a cellular immune response in Drosophila melanogaster, Immunology Letters, vol.101, pp.108-111, 2005.

S. Ruschioni, J. Van-loon, H. M. Smid, and J. C. Van-lenteren, Insects can count: Sensory basis of host discrimination in parasitoid wasps revealed, PLoS ONE, vol.10, pp.3-7, 2015.

K. Bakker, M. E. Visser, and P. Peulet, The Ability To Distinguish Between Hosts Containing Different Numbers of Parasitoid Eggs By the Solitary Parasitoid Leptopilina Heterotoma (Thomson) (Hym

, Netherlands Journal of Zoology, vol.40, pp.514-520, 1990.

T. Ahmed, T. T. Zhang, K. L. He, S. X. Bai, and Z. Y. Wang, Sense organs on the ovipositor of Macrocentrus cingulum Brischke (Hymenoptera: Braconidae): Cheir probable role in stinging, oviposition and host selection process, Journal of Asia-Pacific Entomology. The Authors, vol.16, pp.343-348, 2013.

M. L. Buffington, The occurrence and phylogenetic implications of the ovipositor clip within the Figitidae (Insecta: Hymenoptera: Cynipoidea), Journal of Natural History, vol.41, pp.2267-2282, 2007.

A. G. De-la-filia, S. A. Bain, and L. Ross, Haplodiploidy and the reproductive ecology of Arthropods, Current Opinion in Insect Science, vol.9, pp.36-43, 2015.

A. Mabiala-moundoungou, G. Doury, P. Eslin, A. Cherqui, and G. Prévost, Deadly venom of Asobara japonica parasitoid needs ovarian antidote to regulate host physiology, Journal of Insect Physiology, vol.56, pp.35-41, 2010.

J. Nakhleh, L. El-moussawi, and M. A. Osta, The Melanization Response in Insect Immunity, Advances in Insect Physiology. Elsevier Ltd, 2017.

H. Jiang, A. Vilcinskas, and M. Kanost, Advances in experimental medicine and biology, 2010.

M. Grigorian and V. Hartenstein, Hematopoiesis and hematopoietic organs in arthropods, Development Genes and Evolution, vol.223, pp.103-115, 2013.

C. D. Price and N. A. Ratcliffe, A reappraisal of insect haemocyte classification by the examination of blood from fifteen insect orders. Zeitschrift für Zellforschung und mikroskopische Anatomie, vol.147, pp.537-549, 1974.

D. G. Perez and C. S. Fontanetti, Hemocitical responses to environmental stress in invertebrates: A review, Environmental Monitoring and Assessment, vol.177, pp.437-447, 2011.

M. R. Strand, Insect Hemocytes and Their Role in Immunity, Insect Immunology, vol.32, pp.25-47, 2008.

M. A. Choma, M. J. Suter, B. J. Vakoc, B. E. Bouma, and G. J. Tearney, Physiological homology between Drosophila melanogaster and vertebrate cardiovascular systems, Disease Models & Mechanisms, vol.4, pp.411-420, 2011.

S. Ghosh, A. Singh, S. Mandal, and L. Mandal, Active Hematopoietic Hubs in Drosophila Adults Generate Hemocytes and Contribute to Immune Response, Developmental Cell. The Authors, vol.33, pp.478-488, 2015.

E. Ramond, M. Meister, and B. Lemaitre, From Embryo to Adult: Hematopoiesis along the Drosophila Life Cycle, Developmental Cell. Elsevier Inc, vol.33, pp.367-368, 2015.

A. B. Leitão and É. Sucena, Drosophila sessile hemocyte clusters are true hematopoietic tissues that regulate larval blood cell differentiation. eLife, vol.2015, pp.1-38, 2015.

C. J. Evans, T. Liu, and U. Banerjee, Drosophila hematopoiesis: Markers and methods for molecular genetic analysis, Methods. Elsevier Inc, vol.68, pp.242-251, 2014.

I. Morin-poulard, A. Vincent, and M. Crozatier, The Drosophila JAK-STAT pathway in blood cell formation and immunity, Jak-Stat, vol.2, p.25700, 2013.

K. Makhijani and K. Brückner, Of blood cells and the nervous system: hematopoiesis in the Drosophila larva, Fly, vol.6, pp.254-260, 2012.

M. Crozatier and A. Vincent, Drosophila: a model for studying genetic and molecular aspects of haematopoiesis and associated leukaemias, Disease Models & Mechanisms, vol.4, pp.439-445, 2011.

J. Krzemien, M. Crozatier, and A. Vincent, Ontogeny of the Drosophila larval hematopoietic organ, hemocyte homeostasis and the dedicated cellular immune response to parasitism, International Journal of Developmental Biology, vol.54, pp.1117-1125, 2010.

K. S. Gold and K. Brückner, Drosophila as a model for the two myeloid blood cell systems in vertebrates, Experimental Hematology, vol.42, pp.717-727, 2014.

W. Wood and J. A. , Drosophila melanogaster embryonic haemocytes: masters of multitasking, Nature Reviews Molecular Cell Biology, vol.8, pp.542-551, 2007.

A. Holz, The two origins of hemocytes in Drosophila, Development, vol.130, pp.4955-4962, 2003.

U. Tepass, L. I. Fessler, A. Aziz, and V. Hartenstein, Embryonic origin of hemocytes and their relationship to cell death in Drosophila, Development, vol.120, pp.1829-1837, 1994.

P. Spahn, S. Huelsmann, K. P. Rehorn, S. Mischke, M. Mayer et al., Multiple regulatory safeguards confine the expression of the GATA factor serpent to the hemocyte primordium within the drosophila mesoderm, Developmental Biology, vol.386, pp.272-279, 2014.

L. Waltzer, G. Ferjoux, L. Bataillé, and M. Haenlin, Cooperation between the GATA and RUNX factors Serpent and Lozenge during Drosophila hematopoiesis, EMBO Journal, vol.22, pp.6516-6525, 2003.
URL : https://hal.archives-ouvertes.fr/hal-00170569

M. J. Williams, Drosophila Hemopoiesis and Cellular Immunity, The Journal of Immunology, vol.178, pp.4711-4716, 2007.

J. Krzemie?, L. Dubois, R. Makki, M. Meister, A. Vincent et al., Control of blood cell homeostasis in Drosophila larvae by the posterior signalling centre, Nature, vol.446, pp.325-328, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00169818

A. I. Munier, D. Doucet, E. Perrodou, D. Zachary, M. Meister et al., PVF2, a PDGF/VEGF-like growth factor, induces hemocyte proliferation in Drosophila larvae, EMBO Reports, vol.3, pp.1195-1200, 2002.

B. P. Lazzaro, Adenosine Signaling and the Energetic Costs of Induced Immunity, PLoS Biology, vol.13, pp.1-6, 2015.

J. Krzemien, J. Oyallon, M. Crozatier, and A. Vincent, Hematopoietic progenitors and hemocyte lineages in the Drosophila lymph gland, Developmental Biology, vol.346, pp.310-319, 2010.

B. Benmimoun, C. Polesello, L. Waltzer, and M. Haenlin, Dual role for Insulin/TOR signaling in the control of hematopoietic progenitor maintenance in Drosophila, Development, vol.139, pp.1713-1717, 2012.

H. Luo, W. P. Hanratty, and C. R. Dearolf, An amino acid substitution in the Drosophila hopTum-l Jak kinase causes leukemia-like hematopoietic defects, The EMBO journal, vol.14, pp.1412-1432, 1995.

E. Gateff, Tumor--Suppressor Genes, Hematopoietic Malignancies and Other Hematopoietic Disorders of Drosophila melanogaster, Annals of the New York Academy of Sciences, vol.712, pp.260-279, 1994.

W. P. Hanratty and C. R. Dearolf, The Drosophila Tumorous lethal hematopoietic oncogene is a dominant mutation in the hopscotch locus, MGG Molecular & General Genetics, vol.238, pp.33-37, 1993.

Y. Hao and L. H. Jin, Dual role for Jumu in the control of hematopoietic progenitors in the Drosophila lymph gland, vol.6, pp.1-27, 2017.

T. A. Reimels and C. M. Pfleger, Drosophila Rabex-5 restricts Notch activity in hematopoietic cells and maintains hematopoietic homeostasis, Journal of Cell Science, vol.128, pp.4512-4525, 2015.

M. R. Schmid, I. Anderl, L. Vesala, L. M. Vanha-aho, X. J. Deng et al., Control of Drosophila blood cell activation via toll signaling in the fat body, PLoS ONE, vol.9, pp.1-10, 2014.

G. B. Ferguson and J. A. Martinez-agosto, Yorkie and scalloped signaling regulates notch-dependent lineage specification during drosophila hematopoiesis, Current Biology. Elsevier Ltd, vol.24, pp.2665-2672, 2014.

S. Valanne, J. Wang, and M. Ramet, The Drosophila Toll Signaling Pathway, The Journal of Immunology, vol.186, pp.649-656, 2011.

H. Asha, I. Nagy, G. Kovacs, D. Stetson, I. Ando et al., Analysis of Ras-induced overproliferation in Drosophila hemocytes, Genetics, vol.163, pp.203-215, 2003.

A. J. Bretscher, V. Honti, O. Binggeli, O. Burri, M. Poidevin et al., The Nimrod transmembrane receptor Eater is required for hemocyte attachment to the sessile compartment in Drosophila melanogaster, Biology Open, vol.4, pp.355-363, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01207975

V. Honti, G. Csordás, É. Kurucz, R. Márkus, and I. Andó, The cell-mediated immunity of Drosophila melanogaster: Hemocyte lineages, immune compartments, microanatomy and regulation. Developmental and Comparative Immunology, vol.42, pp.47-56, 2014.

R. Lanot, D. Zachary, F. Holder, and M. Meister, Postembryonic hematopoiesis in Drosophila, Developmental biology, vol.230, pp.243-257, 2001.

K. Makhijani, B. Alexander, T. Tanaka, E. Rulifson, and K. Bruckner, The peripheral nervous system supports blood cell homing and survival in the Drosophila larva, Development, vol.138, pp.5379-5391, 2011.

R. Márkus, B. Laurinyecz, E. Kurucz, V. Honti, I. Bajusz et al., Sessile hemocytes as a hematopoietic compartment in Drosophila melanogaster, Proceedings of the National Academy of Sciences of the United States of America, vol.106, pp.4805-4809, 2009.

S. Petraki, B. Alexander, and K. Brückner, Assaying Blood Cell Populations of the Drosophila melanogaster Larva, Journal of Visualized Experiments, pp.1-11, 2015.

C. Zettervall, I. Anderl, M. J. Williams, R. Palmer, E. Kurucz et al., A directed screen for genes involved in Drosophila blood cell activation, Proceedings of the National Academy of Sciences of the United States of America, vol.101, pp.14192-14199, 2004.

B. Wertheim, A. R. Kraaijeveld, E. Schuster, E. Blanc, M. Hopkins et al., Genome-wide gene expression in response to parasitoid attack in Drosophila, Genome biology. England, vol.6, p.94, 2005.

T. A. Schlenke, J. Morales, S. Govind, and A. G. Clark, Contrasting infection strategies in generalist and specialist wasp parasitoids of Drosophila melanogaster, PLoS Pathogens, vol.3, pp.1486-1501, 2007.

C. Coustau, Y. Carkion, A. Nappi, F. Shotkoski, and R. Ffrench-constant, Differential induction of antibacterial transcripts in Drosophila susceptible and resistant to parasitism by Leptopilina boulardi, Insect molecular biology. England, vol.5, pp.167-172, 1996.

A. J. Nappi and B. M. Christensen, Melanogenesis and associated cytotoxic reactions: Applications to insect innate immunity, Insect Biochemistry and Molecular Biology, vol.35, pp.443-459, 2005.

A. J. Nappi and E. Ottaviani, Cytotoxicity and cytotoxic molecules in invertebrates, BioEssays, vol.22, pp.469-480, 2000.

A. J. Nappi, E. Vass, D. Malagoli, and Y. Carton, The effects of parasite-derived immune-suppressive factors on the cellular innate immune and autoimmune responses of Drosophila melanogaster, Journal of Parasitology, vol.90, pp.1139-1149, 2004.

J. Russo, S. Dupas, F. Frey, Y. Carton, and M. Brehelin, Insect immunity: early events in the encapsulation process of parasitoid (Leptopilina boulardi) eggs in resistant and susceptible strains of Drosophila, Parasitology. University of Leeds, vol.112, pp.135-142, 1996.

M. Crozatier, J. M. Ubeda, A. Vincent, and M. Meister, Cellular immune response to parasitization in Drosophila requires the EBF orthologue collier, PLoS Biology, vol.2, 2004.
URL : https://hal.archives-ouvertes.fr/hal-00169831

E. Owusu-ansah and U. Banerjee, Reactive oxygen species prime Drosophila haematopoietic progenitors for differentiation. Nature, vol.461, pp.537-541, 2009.

C. Small, J. Ramroop, M. Otazo, L. H. Huang, S. Saleque et al., An unexpected link between notch signaling and ROS in restricting the differentiation of hematopoietic progenitors in Drosophila, Genetics, vol.197, pp.471-483, 2014.

I. Louradour, A. Sharma, I. Morin-poulard, M. Letourneau, A. Vincenta et al., Reactive oxygen species-dependent Toll / NF-Kappa B activation in the Drosophila hematopoietic niche confers resistance to wasp parasitism, 2017.

R. P. Sorrentino, J. P. Melk, and S. Govind, Genetic Analysis of Contributions of Dorsal Group and JAK-Stat92E Pathway Genes to Larval Hemocyte Concentration and the Egg Encapsulation Response in Drosophila, Genetics, vol.166, pp.1343-1356, 2004.

R. Shrestha and E. Gateff, Ultrastructure and Cytochemistry of the Cell-types in the Tumorous Hematopoietic Organs and the Hemolymph of the Mutant Lethal ( 1) Malignant Blood Neoplasm ( I ( 1 ) mbn) of Drosophila Melanogaster, Dev Growth & Differ, vol.24, pp.83-98, 1982.

R. Makki, M. Meister, D. Pennetier, J. M. Ubeda, A. Braun et al., A short receptor downregulates JAK/STAT signalling to control the Drosophila cellular immune response, PLoS Biology, vol.8, pp.33-34, 2010.

H. Weavers, J. Liepe, A. Sim, W. Wood, P. Martin et al., Systems Analysis of the Dynamic Inflammatory Response to Tissue Damage Reveals Spatiotemporal Properties of the Wound Attractant Gradient, Current Biology. The Authors, vol.26, pp.1975-1989, 2016.

L. M. Vanha-aho, I. Anderl, L. Vesala, D. Hultmark, S. Valanne et al., Edin Expression in the Fat Body Is Required in the Defense Against Parasitic Wasps in Drosophila melanogaster, PLoS Pathog, vol.11, p.1004895, 2015.

L. Howell, C. J. Sampson, M. J. Xavier, E. Bolukbasi, M. Heck et al., A directed miniscreen for genes involved in the Drosophila anti-parasitoid immune response, Immunogenetics, vol.64, pp.155-161, 2012.

M. J. Williams, The Drosophila cell adhesion molecule Neuroglian regulates Lissencephaly-1 localisation in circulating immunosurveillance cells, BMC immunology, vol.10, p.17, 2009.

C. J. Sampson, S. Valanne, M. O. Fauvarque, D. Hultmark, M. Rämet et al., The RhoGEF Ziziminrelated acts in the Drosophila cellular immune response via the Rho GTPases Rac2 and Cdc42. Developmental and Comparative Immunology, vol.38, pp.160-168, 2012.

B. Kari, G. Csordás, V. Honti, G. Cinege, M. J. Williams et al., The raspberry gene is involved in the regulation of the cellular immune response in drosophila melanogaster, PLoS ONE, vol.11, pp.1-13, 2016.

S. A. Freeman and S. Grinstein, Phagocytosis: receptors, signal integration, and the cytoskeleton, Immunological reviews, vol.262, pp.193-215, 2014.

I. Vlisidou and W. Wood, Drosophila blood cells and their role in immune responses, FEBS Journal, vol.282, pp.1368-1382, 2015.

A. Schmitz, Interactions immunité-parasitisme et immunité-symbiose chez les insectes : apport de deux modèles biologiques : drosophile-parasitoïde et puceron-symbiotes-parasitoïde, 2012.

V. Honti, É. Kurucz, G. Csordás, B. Laurinyecz, R. Márkus et al., In vivo detection of lamellocytes in Drosophila melanogaster, Immunology Letters, vol.126, pp.83-84, 2009.

P. Y. Lee, J. Wang, E. Parisini, C. C. Dascher, and P. A. Nigrovic, Ly6 family proteins in neutrophil biology, Journal of Leukocyte Biology, vol.94, pp.585-594, 2013.

C. Weinstock, M. Anliker, I. Von-zabern, and . Cd59, A long-known complement inhibitor has advanced to a blood group system, Immunohematology. United States, vol.31, pp.145-151, 2015.

K. Tanaka, Y. Diekmann, A. Hazbun, A. Hijazi, B. Vreede et al., Multispecies analysis of expression pattern diversification in the recently expanded insect Ly6 gene family, Molecular Biology and Evolution, vol.32, pp.1730-1747, 2015.

M. H. Syed, A. Krudewig, D. Engelen, T. Stork, and C. Klambt, The CD59 Family Member Leaky/Coiled Is Required for the Establishment of the Blood-Brain Barrier in Drosophila, Journal of Neuroscience, vol.31, pp.7876-7885, 2011.

A. Hijazi, M. Haenlin, L. Waltzer, and F. Roch, The Ly6 protein coiled is required for septate junction and blood brain barrier organisation in Drosophila, PLoS ONE, vol.6, 2011.

A. Nilton, K. Oshima, F. Zare, S. Byri, U. Nannmark et al., Crooked, coiled and crimpled are three Ly6-like proteins required for proper localization of septate junction components, Development, vol.137, pp.2427-2464, 2010.

J. P. Dudzic, S. Kondo, R. Ueda, C. M. Bergman, and B. Lemaitre, Drosophila innate immunity: regional and functional specialization of prophenoloxidases, BMC Biology. BMC Biology, vol.13, p.81, 2015.

P. Irving, J. M. Ubeda, D. Doucet, L. Troxler, M. Lagueux et al., New insights into Drosophila larval haemocyte functions through genome-wide analysis, Cellular Microbiology, vol.7, pp.335-350, 2005.
URL : https://hal.archives-ouvertes.fr/hal-00093694

A. Braun, J. A. Hoffmann, and M. Meister, Analysis of the Drosophila host defense in domino mutant larvae, which are devoid of hemocytes, Proceedings of the National Academy of Sciences, vol.95, pp.14337-14342, 1998.

J. C. Corbo and M. Levine, Characterization of an immunodeficiency mutant in Drosophila, Mechanisms of Development, vol.55, pp.211-220, 1996.

R. M. Rizki and T. M. Rizki, Encapsulation of parasitoid eggs in phenoloxidase-deficient mutants of Drosophila melanogaster, Journal of Insect Physiology, vol.36, pp.523-529, 1990.

T. M. Rizki, R. M. Rizki, and R. A. Bellotti, Genetics of a Drosophila phenoloxidase, Molecular & general genetics : MGG. Germany, vol.201, pp.7-13, 1985.

G. Bidla, M. S. Dushay, and U. Theopold, Crystal cell rupture after injury in Drosophila requires the JNK pathway, small GTPases and the TNF homolog Eiger, Journal of Cell Science, vol.120, pp.1209-1215, 2007.

M. D'ischia, A. Napolitano, A. Pezzella, P. Meredith, and T. Sarna, Chemical and structural diversity in eumelanins: Unexplored bio-optoelectronic materials, Angewandte Chemie -International Edition, vol.48, pp.3914-3921, 2009.

A. J. Nappi, E. Vass, F. Frey, and Y. Carton, Superoxide anion generation in Drosophila during melanotic encapsulation of parasites, European journal of cell biology. Germany, vol.68, pp.450-456, 1995.

A. J. Nappi, Y. Carton, and E. Vass, Reduced cellular immune competence of a temperature-sensitive dopa decarboxylase mutant strain of Drosophila melanogaster against the parasite Leptopilina boulardi. Comparative biochemistry and physiology B, Comparative biochemistry, vol.101, pp.453-460, 1992.

A. Lu, Q. Zhang, J. Zhang, B. Yang, K. Wu et al., Insect prophenoloxidase: the view beyond immunity, Frontiers in physiology. Switzerland, vol.5, p.252, 2014.

H. Nam, I. Jang, H. You, K. Lee, and W. Lee, Genetic evidence of a redox-dependent systemic wound response via Hayan protease-phenoloxidase system in Drosophila, The EMBO journal. England, vol.31, pp.1253-1265, 2012.

C. Castillejo-lopez and U. Hacker, The serine protease Sp7 is expressed in blood cells and regulates the melanization reaction in Drosophila. Biochemical and biophysical research communications. United States, vol.338, pp.1075-1082, 2005.

P. Ligoxygakis, N. Pelte, C. Ji, V. Leclerc, B. Duvic et al., A serpin mutant links Toll activation to melanization in the host defence of Drosophila, The EMBO journal. England, vol.21, pp.6330-6337, 2002.

D. Gregorio, E. Han, S. Lee, W. Baek, M. Osaki et al., An immune-responsive Serpin regulates the melanization cascade in Drosophila, Developmental cell. United States, vol.3, pp.581-592, 2002.

H. Tang, Z. Kambris, B. Lemaitre, and C. Hashimoto, Two proteases defining a melanization cascade in the immune system of Drosophila, The Journal of biological chemistry. United States, vol.281, pp.28097-28104, 2006.
URL : https://hal.archives-ouvertes.fr/hal-00133103

O. Schmidt, K. Soderhall, U. Theopold, and F. I. , Role of adhesion in arthropod immune recognition, Annual review of entomology. United States, vol.55, pp.485-504, 2010.

C. An, J. Ishibashi, E. J. Ragan, H. Jiang, and M. R. Kanost, Functions of Manduca sexta hemolymph proteinases HP6 and HP8 in two innate immune pathways, The Journal of biological chemistry. United States, vol.284, pp.19716-19726, 2009.

S. Asgari, Venom proteins from polydnavirus-producing endoparasitoids: their role in host-parasite interactions. Archives of insect biochemistry and physiology, vol.61, pp.146-156, 2006.

S. Asgari and D. B. Rivers, Venom proteins from endoparasitoid wasps and their role in host-parasite interactions, Annual review of entomology. United States, vol.56, pp.313-335, 2011.

Z. Yan, Q. Fang, L. Wang, J. Liu, Y. Zhu et al., Insights into the venom composition and evolution of an endoparasitoid wasp by combining proteomic and transcriptomic analyses, Scientific reports. England, vol.6, 2016.

Z. Teng, S. Xiong, G. Xu, S. Gan, C. X. Stanley et al., Protein Discovery: Combined Transcriptomic and Proteomic Analyses of Venom from the Endoparasitoid Cotesia chilonis (Hymenoptera: Braconidae), Toxins. Switzerland, p.9, 2017.

D. Colinet, D. Cazes, M. Belghazi, J. Gatti, and M. Poirie, Extracellular superoxide dismutase in insects: characterization, function, and interspecific variation in parasitoid wasp venom, The Journal of biological chemistry. United States, vol.286, pp.40110-40121, 2011.

Q. Coulette, S. Lemauf, D. Colinet, G. Prevost, C. Anselme et al., Biochemical characterization and comparison of aspartylglucosaminidases secreted in venom of the parasitoid wasps Asobara tabida and Leptopilina heterotoma, PloS ONE. United States, vol.12, p.181940, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01608182

P. Falabella, L. Riviello, P. Caccialupi, T. Rossodivita, T. Valente et al., A gamma-glutamyl transpeptidase of Aphidius ervi venom induces apoptosis in the ovaries of host aphids, Insect biochemistry and molecular biology. England, vol.37, pp.453-465, 2007.

M. C. Digilio, N. Isidoro, E. Tremblay, and F. Pennacchio, Host castration by Aphidius ervi venom proteins, Journal of insect physiology. England, vol.46, pp.1041-1050, 2000.

G. R. Burke and M. R. Strand, Polydnaviruses of Parasitic Wasps: Domestication of Viruses To Act as, Gene Delivery Vectors. Insects. Switzerland, vol.3, pp.91-119, 2012.

G. R. Burke, K. Walden, J. B. Whitfield, H. M. Robertson, and M. R. Strand, Widespread genome reorganization of an obligate virus mutualist, PLoS genetics. United States, vol.10, p.1004660, 2014.

N. Beckage, J. Drezen, and . Parasitoid, Viruses Symbionts and Pathogens, pp.115-125, 2012.

A. Volkoff, M. Ravallec, J. Bossy, P. Cerutti, J. Rocher et al., The replication of Hyposoter didymator polydnavirus: Cytopathology of the calyx cells in the parasitoid, Biology of the Cell, vol.83, pp.89926-89932, 1995.

D. B. Stoltz, S. B. Vinson, and E. A. Mackinnon, Baculovirus-like particles in the reproductive tracts of female parasitoid wasps, Canadian journal of microbiology. Canada, vol.22, pp.1013-1023, 1976.

W. N. Norton, S. B. Vinson, and D. B. Stoltz, Nuclear secretory particles associated with the calyx cells of the ichneumonid parasitoid Campoletis sonorensis (Cameron). Cell and tissue research, vol.162, pp.195-208, 1975.

D. Gundersen-rindal, C. Dupuy, E. Huguet, and J. Drezen, Parasitoid polydnaviruses: evolution, pathology and applications: Dedicated to the memory of Nancy E, Beckage. Biocontrol Science and Technology, 2013.

A. Bezier, M. Annaheim, J. Herbiniere, C. Wetterwald, G. Gyapay et al., Polydnaviruses of braconid wasps derive from an ancestral nudivirus, Science. United States, vol.323, pp.926-930, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00402741

A. Volkoff, V. Jouan, S. Urbach, S. Samain, M. Bergoin et al., Analysis of virion structural components reveals vestiges of the ancestral ichnovirus genome, PLoS pathogens. United States, vol.6, p.1000923, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00551112

C. Dupuy, E. Huguet, and J. Drezen, Unfolding the evolutionary story of polydnaviruses, Virus research. Netherlands, vol.117, pp.81-89, 2006.
URL : https://hal.archives-ouvertes.fr/hal-00080679

M. R. Strand and G. R. Burke, Polydnavirus-wasp associations: evolution, genome organization, and function. Current opinion in virology. Netherlands, vol.3, pp.587-594, 2013.

B. A. Federici and Y. Bigot, Origin and evolution of polydnaviruses by symbiogenesis of insect DNA viruses in endoparasitic wasps, Journal of insect physiology. England, vol.49, pp.419-432, 2003.

J. B. Whitfield and S. Asgari, Virus or not? Phylogenetics of polydnaviruses and their wasp carriers, Journal of insect physiology. England, vol.49, pp.397-405, 2003.

M. Barat-houari, F. Hilliou, F. Jousset, L. Sofer, E. Deleury et al., Gene expression profiling of Spodoptera frugiperda hemocytes and fat body using cDNA microarray reveals polydnavirus-associated variations in lepidopteran host genes transcript levels, BMC genomics. England, vol.7, p.160, 2006.

J. A. Kroemer and B. A. Webb, Ikappabeta-related vankyrin genes in the Campoletis sonorensis ichnovirus: temporal and tissue-specific patterns of expression in parasitized Heliothis virescens lepidopteran hosts, Journal of virology. United States, vol.79, pp.7617-7628, 2005.

G. R. Burke and M. R. Strand, Systematic analysis of a wasp parasitism arsenal, Molecular ecology. England, vol.23, pp.890-901, 2014.

J. Song, X. Wang, D. Hou, H. Huang, X. Liu et al., The Host Specificities of Baculovirus per os Infectivity Factors, PloS ONE. United States, vol.11, p.159862, 2016.

T. Doremus, S. Urbach, V. Jouan, F. Cousserans, M. Ravallec et al., Venom gland extract is not required for successful parasitism in the polydnavirus-associated endoparasitoid Hyposoter didymator (Hym. Ichneumonidae) despite the presence of numerous novel and conserved venom proteins, Insect biochemistry and molecular biology. England, vol.43, pp.292-307, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01837249

R. Yu, Y. Chen, X. Chen, F. Huang, Y. Lou et al., Effects of venom/calyx fluid from the endoparasitic wasp Cotesia plutellae on the hemocytes of its host Plutella xylostella in vitro, Journal of insect physiology. England, vol.53, pp.22-29, 2007.

N. E. Beckage, . Parasitoids, . Polydnaviruses, and . Bioscience, , vol.48, pp.305-311, 1998.

I. Feddersen, K. Sander, and O. Schmidt, Virus-like particles with host protein-like antigenic determinants protect an insect parasitoid from encapsulation, Experientia, vol.42, pp.1278-1281, 1986.

O. Bedwin, An insect glycoprotein: a study of the particles responsible for the resistance of a parasitoid's egg to the defence reactions of its insect host, Proceedings of the Royal Society of London Series B, vol.205, pp.271-286, 1979.

A. Reineke, S. Asgari, and O. Schmidt, Evolutionary origin of Venturia canescens virus-like particles. Archives of insect biochemistry and physiology, vol.61, pp.123-133, 2006.

G. Salt, Experimental studies in insect parasitism XIII. The haemocytic reaction of a caterpillar to eggs of its habitual parasite, Proceedings of the Royal Society of London Series B Biological Sciences, vol.162, pp.303-318, 1965.

S. Rotheram, The surface of the egg of a parasitic insect. II. The ultrastructure of the particulate coat on the egg of Nemeritis, Proceedings of the Royal Society of London Series B Biological Sciences, vol.183, pp.195-204, 1973.

S. Rotheram, Immune surface of eggs of a parasitic insect, Nature. England, vol.214, p.700, 1967.

G. Gueguen, R. Rajwani, I. Paddibhatla, J. Morales, and S. Govind, VLPs of Leptopilina boulardi share biogenesis and overall stellate morphology with VLPs of the heterotoma clade, Virus research. Netherlands, vol.160, pp.159-165, 2011.

J. Morales, H. Chiu, T. Oo, R. Plaza, S. Hoskins et al., Biogenesis, structure, and immune-suppressive effects of virus-like particles of a Drosophila parasitoid, Leptopilina victoriae, Journal of Insect Physiology, vol.51, pp.181-195, 2005.

R. Ferrarese, J. Morales, D. Fimiarz, B. A. Webb, and S. Govind, A supracellular system of actin-lined canals controls biogenesis and release of virulence factors in parasitoid venom glands, The Journal of experimental biology, vol.212, pp.2261-2268, 2009.

S. Dupas, M. Brehelin, F. Frey, and Y. Carton, Immune suppressive virus-like particles in a Drosophila parasitoid: significance of their intraspecific morphological variations, Parasitology. England, vol.113, pp.207-212, 1996.

T. M. Rizki and R. M. Rizki, Lamellocyte differentiation in Drosophila larvae parasitized by Leptopilina, Developmental and Comparative Immunology, vol.16, pp.103-110, 1992.

M. E. Heavner, J. Ramroop, G. Gueguen, G. Ramrattan, G. Dolios et al., Novel Organelles with Elements of Bacterial and Eukaryotic Secretion Systems Weaponize Parasites of Drosophila, Current biology. England, vol.27, pp.2869-2877, 2017.

M. Samson-boshuizen, J. C. Van-lenteren, and K. Bakker, Success of Parasitization of Pseudeucoila Bochei Weld (Hym., Cynip.): a Matter of Experience, Netherlands Journal of Zoology, 1973.

S. Vinchon, S. Moreau, J. M. Drezen, G. Prevost, and A. Cherqui, Molecular and biochemical analysis of an aspartylglucosaminidase from the venom of the parasitoid wasp Asobara tabida (Hymenoptera: Braconidae). Insect biochemistry and molecular biology. England, vol.40, pp.38-48, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00550977

S. Moreau, A. Dingremont, G. Doury, and P. Giordanengo, Effects of parasitism by Asobara tabida (Hymenoptera: Braconidae) on the development, survival and activity of Drosophila melanogaster larvae, Journal of insect physiology. England, vol.48, pp.337-347, 2002.
URL : https://hal.archives-ouvertes.fr/hal-02140604

N. Enomaa, T. Heiskanen, R. Halila, R. Sormunen, R. Seppala et al., Human aspartylglucosaminidase. A biochemical and immunocytochemical characterization of the enzyme in normal and aspartylglucosaminuria fibroblasts, The Biochemical journal. England, vol.286, pp.613-618, 1992.

T. Noronkoski, I. B. Stoineva, D. D. Petkov, and I. Mononen, Recombinant human glycosylasparaginase catalyzes hydrolysis of L-asparagine, FEBS letters. England, vol.412, pp.149-152, 1997.

T. J. Ragan, A. P. Bailey, A. P. Gould, and P. C. Driscoll, Volume determination with two standards allows absolute quantification and improved chemometric analysis of metabolites by NMR from submicroliter samples, Analytical chemistry. United States, vol.85, pp.12046-12054, 2013.

B. S. Meldrum, Glutamate as a neurotransmitter in the brain: review of physiology and pathology, The Journal of nutrition. United States, vol.130, pp.1007-1022, 2000.

E. Kelo, T. Noronkoski, and I. Mononen, Depletion of L-asparagine supply and apoptosis of leukemia cells induced by human glycosylasparaginase, pp.1167-1171, 2009.

J. M. Reichhart, D. Gubb, and V. Leclerc, The Drosophila serpins: multiple functions in immunity and morphogenesis, Methods in enzymology. United States, vol.499, pp.205-225, 2011.
URL : https://hal.archives-ouvertes.fr/hal-02310176

F. Veillard, L. Troxler, and J. Reichhart, Drosophila melanogaster clip-domain serine proteases: Structure, function and regulation, Biochimie. France, vol.122, pp.255-269, 2016.

C. Labrosse, P. Eslin, G. Doury, J. M. Drezen, and M. Poirie, Haemocyte changes in D. Melanogaster in response to long gland components of the parasitoid wasp Leptopilina boulardi: a Rho-GAP protein as an important factor, Journal of insect physiology. England, vol.51, pp.161-170, 2005.

S. Chabert, R. Allemand, M. Poyet, P. Eslin, and P. Gibert, Ability of European parasitoids (Hymenoptera) to control a new invasive Asiatic pest, Drosophila suzukii, Biological Control, vol.63, pp.40-47, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01917394

B. Z. Kacsoh and T. A. Schlenke, High hemocyte load is associated with increased resistance against parasitoids in drosophila suzukii, a relative of D. melanogaster, PLoS ONE, vol.7, 2012.

J. Mercer, M. Schelhaas, and A. Helenius, Virus entry by endocytosis. Annual review of biochemistry. United States, vol.79, pp.803-833, 2010.

S. Kumari, S. Mg, and S. Mayor, Endocytosis unplugged: multiple ways to enter the cell, Cell research. England, vol.20, pp.256-275, 2010.

H. T. Mcmahon and E. Boucrot, Molecular mechanism and physiological functions of clathrin-mediated endocytosis, Nature reviews Molecular cell biology. England, vol.12, pp.517-533, 2011.

P. Luyet and J. Gruenberg, L'endocytose, cheval de Troie pour l'infection virale. médecine sciences, vol.21, pp.909-910, 2005.

G. J. Doherty and H. T. Mcmahon, Mechanisms of endocytosis. Annual review of biochemistry, vol.78, pp.857-902, 2009.

M. Miaczynska and H. Stenmark, Mechanisms and functions of endocytosis, The Journal of cell biology. United States, pp.7-11, 2008.

S. L. Schmid, A. Sorkin, and M. Zerial, Endocytosis: Past, present, and future. Cold Spring Harbor perspectives in biology, p.22509, 2014.

N. Popova, I. E. Deyev, and A. G. Petrenko, Clathrin-Mediated Endocytosis and Adaptor Proteins, Acta Naturae. A.I. Gordeyev, vol.5, pp.62-73, 2013.

E. Smythe and K. R. Ayscough, Actin regulation in endocytosis, Journal of cell science. England, vol.119, pp.4589-4598, 2006.

E. Sezgin, I. Levental, S. Mayor, and C. Eggeling, The mystery of membrane organization: composition, regulation and roles of lipid rafts, Nature reviews Molecular cell biology. England, vol.18, pp.361-374, 2017.

G. Gaibelet, F. Terce, S. Allart, C. Lebrun, X. Collet et al., Fluorescent probes for detecting cholesterol-rich ordered membrane microdomains: Entangled relationships between structural analogies in the membrane and functional homologies in the cell, AIMS Biophysics, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01600989

A. Ludwig, B. J. Nichols, and S. Sandin, Architecture of the caveolar coat complex, Journal of cell science. England, vol.129, pp.3077-3083, 2016.

R. G. Parton and B. M. Collins, Unraveling the architecture of caveolae, Proceedings of the National Academy of Sciences of the United States of America. United States, vol.113, pp.14170-14172, 2016.

A. Ludwig, G. Howard, C. Mendoza-topaz, T. Deerinck, M. Mackey et al., Molecular composition and ultrastructure of the caveolar coat complex, PLoS biology. United States, vol.11, 2013.

S. Mayor, R. G. Parton, and J. G. Donaldson, Clathrin-independent pathways of endocytosis. Cold Spring Harbor perspectives in biology, United States, vol.6, 2014.

C. G. Hansen and B. J. Nichols, Molecular mechanisms of clathrin-independent endocytosis, Journal of cell science. England, vol.122, pp.1713-1721, 2009.

T. Ait-slimane, R. Galmes, G. Trugnan, and M. M. , Basolateral internalization of GPI-anchored proteins occurs via a clathrin-independent flotillin-dependent pathway in polarized hepatic cells, Molecular biology of the cell. United States, vol.20, pp.3792-3800, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00579692

M. Meister and R. Tikkanen, Endocytic trafficking of membrane-bound cargo: a flotillin point of view, Membranes. Switzerland, vol.4, pp.356-371, 2014.

K. Riento, M. Frick, I. Schafer, and B. J. Nichols, Endocytosis of flotillin-1 and flotillin-2 is regulated by Fyn kinase, pp.912-918, 2009.

J. G. Donaldson, D. L. Johnson, and D. Dutta, Rab and Arf G proteins in endosomal trafficking and cell surface homeostasis, Small GTPases. United States, vol.7, pp.247-251, 2016.

J. K. Schweitzer, A. E. Sedgwick, D. Souza-schorey, and C. , ARF6-mediated endocytic recycling impacts cell movement, cell division and lipid homeostasis, Seminars in cell & developmental biology. England, vol.22, pp.39-47, 2011.

A. Llobet, J. L. Gallop, J. Burden, G. Camdere, P. Chandra et al., Endophilin drives the fast mode of vesicle retrieval in a ribbon synapse, The Journal of neuroscience : the official journal of the Society for Neuroscience. United States, vol.31, pp.8512-8519, 2011.

S. Watanabe and E. Boucrot, Fast and ultrafast endocytosis. Current opinion in cell biology, vol.47, pp.64-71, 2017.

J. Cendrowski, A. Maminska, and M. Miaczynska, Endocytic regulation of cytokine receptor signaling, Cytokine & growth factor reviews. England, vol.32, pp.63-73, 2016.

A. Guha, V. Sriram, K. S. Krishnan, and S. Mayor, Shibire mutations reveal distinct dynamin-independent anddependent endocytic pathways in primary cultures of Drosophila hemocytes, Journal of cell science. England, vol.116, pp.3373-3386, 2003.

D. Dutta and J. G. Donaldson, Search for inhibitors of endocytosis: Intended specificity and unintended consequences, Cellular Logistics. Landes Bioscience, vol.2, pp.203-208, 2012.

A. Hijazi, W. Masson, B. Auge, L. Waltzer, M. Haenlin et al., boudin is required for septate junction organisation in Drosophila and codes for a diffusible protein of the Ly6 superfamily, Development, vol.136, pp.2199-2209, 2009.

B. Wan, E. Goguet, M. Ravallec, O. Pierre, S. Lemauf et al., Atypical extracellular vesicles as interspecies communicasomes involved in host specificity: the case of a parasitoid wasp of Drosophila, 2017.

L. Cherbas, A. Willingham, D. Zhang, L. Yang, Y. Zou et al., The transcriptional diversity of 25 Drosophila cell lines, Genome research. United States, vol.21, pp.301-314, 2011.

K. C. Johansson, C. Metzendorf, and K. Soderhall, Microarray analysis of immune challenged Drosophila hemocytes, Experimental cell research. United States, vol.305, pp.145-155, 2005.

O. Loseva and Y. Engström, Analysis of signal-dependent changes in the proteome of Drosophila blood cells during an immune response, Molecular & cellular proteomics, vol.3, pp.796-808, 2004.

S. C. Piyankarage, H. Augustin, Y. Grosjean, D. E. Featherstone, and S. A. Shippy, Hemolymph amino acid analysis of individual Drosophila larvae, Analytical chemistry. United States, vol.80, pp.1201-1207, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00452130

P. Salmand, M. Iche-torres, and L. Perrin, Tissue-specific cell sorting from Drosophila embryos: application to gene expression analysis, Fly. United States, vol.5, pp.261-265, 2011.
URL : https://hal.archives-ouvertes.fr/hal-01619089

R. Tirouvanziam, C. J. Davidson, J. S. Lipsick, and L. A. Herzenberg, Fluorescence-activated cell sorting ( FACS ) of Drosophila hemocytes reveals important functional similarities to mammalian leukocytes, 2004.

T. Anggraeni and N. Ratcliffe, Studies on cell-cell co-operation during phagocytosis by purified haemocyte populations of the wax moth, Galleria mellonella, Journal of Insect Physiology, pp.90055-90060, 1991.

I. M. Huxham and A. M. Lackie, Behaviour in vitro of separated fractions of haemocytes of the locust Schistocerca gregaria, Cell and Tissue Research, vol.251, pp.677-684, 1988.

L. L. Pech, D. Trudeau, and M. R. Strand, Separation and behavior in vitro of hemoeytes from the moth , Pseudoplusia includens, Cell and Tissue Research, pp.159-167, 1994.

J. H. Morrissey, Silver stain for proteins in polyacrylamide gels: a modified procedure with enhanced uniform sensitivity, Analytical biochemistry, vol.117, pp.307-310, 1981.

H. Mathe-hubert, D. Colinet, E. Deleury, M. Belghazi, M. Ravallec et al., Comparative venomics of Psyttalia lounsburyi and P. concolor, two olive fruit fly parasitoids: a hypothetical role for a GH1 betaglucosidase, Scientific reports. England, vol.6, p.35873, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01473970

P. Syntin, F. Dacheux, X. Druart, J. L. Gatti, N. Okamura et al., Characterization and identification of proteins secreted in the various regions of the adult boar epididymis, Biology of reproduction. United States, vol.55, pp.956-974, 1996.

S. Markoutsa, U. Bahr, D. G. Papasotiriou, A. Hafner, M. Karas et al., Sulfo-NHS-SS-biotin derivatization: a versatile tool for MALDI mass analysis of PTMs in lysine-rich proteins, Proteomics. Germany, vol.14, pp.659-667, 2014.

B. Handke, I. Poernbacher, S. Goetze, C. H. Ahrens, U. Omasits et al., The Hemolymph Proteome of Fed and Starved Drosophila Larvae, PLoS ONE, vol.8, p.67208, 2013.

J. D. Sato and D. B. Roberts, Synthesis of larval serum proteins 1 and 2 of Drosophila melanogaster by third instar fat body, Insect Biochemistry, vol.13, pp.1-5, 1983.

N. Asada, G. Yokoyama, N. Kawamoto, S. Norioka, and T. Hatta, Prophenol Oxidase A3 in Drosophila melanogaster: Activation and the PCR-Based cDNA Sequence. Biochemical genetics, 2003.

V. E. Alatortsev, I. A. Kramerova, M. Frolov, S. A. Lavrov, and E. D. Westphal, Vinculin gene is non-essential in Drosophila melanogaster, FEBS letters. England, vol.413, pp.197-201, 1997.

B. J. Galletta, X. P. Niu, M. R. Erickson, and S. M. Abmayr, Identification of a Drosophila homologue to vertebrate Crk by interaction with MBC, Gene. Netherlands, vol.228, pp.243-252, 1999.

N. H. Brown, S. L. Gregory, W. L. Rickoll, L. I. Fessler, M. Prout et al., Talin is essential for integrin function in Drosophila, Developmental cell. United States, vol.3, pp.569-579, 2002.

R. B. Birge, C. Kalodimos, F. Inagaki, and S. Tanaka, Crk and CrkL adaptor proteins: networks for physiological and pathological signaling, Cell Communication and Signaling, vol.7, p.13, 2009.

S. H. Baek, Y. Kwon, H. Lee, and K. Choe, Rho-family small GTPases are required for cell polarization and directional sensing in Drosophila wound healing. Biochemical and biophysical research communications. United States, vol.394, pp.488-492, 2010.

L. M. Escudero, M. Bischoff, and M. Freeman, Myosin II regulates complex cellular arrangement and epithelial architecture in Drosophila. Developmental cell. United States, vol.13, pp.717-729, 2007.

J. W. Bloor and D. P. Kiehart, zipper Nonmuscle myosin-II functions downstream of PS2 integrin in Drosophila myogenesis and is necessary for myofibril formation, Developmental biology. United States, vol.239, pp.215-228, 2001.

K. Kawamura, T. Shibata, O. Saget, D. Peel, and P. J. Bryant, A new family of growth factors produced by the fat body and active on Drosophila imaginal disc cells, Development, vol.126, pp.211-219, 1999.

S. Nonaka, K. Nagaosa, T. Mori, A. Shiratsuchi, and Y. Nakanishi, Integrin alphaPS3/betanu-mediated phagocytosis of apoptotic cells and bacteria in Drosophila, The Journal of biological chemistry. United States, vol.288, pp.10374-10380, 2013.

U. Shokal and I. Eleftherianos, Evolution and Function of Thioester-Containing Proteins and the Complement System in the Innate Immune Response, Frontiers in immunology. Switzerland, vol.8, p.759, 2017.

S. Blandin and E. A. Levashina, Thioester-containing proteins and insect immunity, Molecular immunology. England, vol.40, pp.903-908, 2004.

A. Dostalova, S. Rommelaere, M. Poidevin, and B. Lemaitre, Thioester-containing proteins regulate the Toll pathway and play a role in Drosophila defence against microbial pathogens and parasitoid wasps, BMC biology. England, vol.15, p.79, 2017.
URL : https://hal.archives-ouvertes.fr/hal-02191707

A. M. Pearson, Scavenger receptors in innate immunity, Current opinion in immunology. England, vol.8, pp.20-28, 1996.

M. Ramet, A. Pearson, P. Manfruelli, X. Li, H. Koziel et al., Drosophila scavenger receptor CI is a pattern recognition receptor for bacteria, Immunity. United States, vol.15, pp.1027-1038, 2001.

A. Pearson, A. Lux, and M. Krieger, Expression cloning of dSR-CI, a class C macrophage-specific scavenger receptor from Drosophila melanogaster, Proceedings of the National Academy of Sciences of the United States of America. United States, vol.92, pp.4056-4060, 1995.

B. P. Lazzaro, Elevated polymorphism and divergence in the class C scavenger receptors of Drosophila melanogaster and D. simulans, Genetics. United States, vol.169, pp.2023-2034, 2005.

Q. Fang, L. Wang, Y. Zhu, D. W. Stanley, X. Chen et al., Pteromalus puparum venom impairs host cellular immune responses by decreasing expression of its scavenger receptor gene, Insect biochemistry and molecular biology. England, vol.41, pp.852-862, 2011.

K. Etebari, M. Hussain, and S. Asgari, Suppression of scavenger receptors transcription by parasitoid factors, Developmental & Comparative Immunology, vol.38, pp.517-524, 2012.

D. Ferrandon, J. Imler, C. Hetru, and J. A. Hoffmann, The Drosophila systemic immune response: sensing and signalling during bacterial and fungal infections, Nature reviews Immunology. England, vol.7, pp.862-874, 2007.

E. Kurucz, R. Markus, J. Zsamboki, K. Folkl-medzihradszky, Z. Darula et al., Nimrod, a putative phagocytosis receptor with EGF repeats in Drosophila plasmatocytes, Current biology. England, vol.17, pp.649-654, 2007.

N. C. Franc, J. L. Dimarcq, M. Lagueux, J. Hoffmann, and R. A. Ezekowitz, Croquemort, a novel Drosophila hemocyte/macrophage receptor that recognizes apoptotic cells, Immunity. United States, vol.4, pp.431-443, 1996.

M. Gottar, V. Gobert, A. A. Matskevich, J. Reichhart, C. Wang et al., Dual detection of fungal infections in Drosophila via recognition of glucans and sensing of virulence factors, Cell. United States, vol.127, pp.1425-1437, 2006.
URL : https://hal.archives-ouvertes.fr/hal-02393544

S. R. Kudumala, T. Penserga, J. Borner, O. Slipchuk, P. Kakad et al., Lissencephaly-1 dependent axonal retrograde transport of L1-type CAM Neuroglian in the adult drosophila central nervous system, PLoS ONE. United States, vol.12, p.183605, 2017.

N. Prevost, D. Woulfe, T. Tanaka, and L. F. Brass, Interactions between Eph kinases and ephrins provide a mechanism to support platelet aggregation once cell-to-cell contact has occurred, Proceedings of the National Academy of Sciences of the United States of America. United States, vol.99, pp.9219-9224, 2002.

M. Amit, S. J. Weisberg, M. Nadler-holly, E. A. Mccormack, E. Feldmesser et al., Equivalent mutations in the eight subunits of the chaperonin CCT produce dramatically different cellular and gene expression phenotypes, Journal of molecular biology. England, vol.401, pp.532-543, 2010.

C. Dekker, P. C. Stirling, E. A. Mccormack, H. Filmore, A. Paul et al., The interaction network of the chaperonin CCT, The EMBO journal. England, vol.27, pp.1827-1839, 2008.

S. Roh, M. Kasembeli, J. G. Galaz-montoya, M. Trnka, W. Lau et al., Chaperonin TRiC/CCT Modulates the Folding and Activity of Leukemogenic Fusion Oncoprotein AML1-ETO, The Journal of biological chemistry. United States, vol.291, pp.4732-4741, 2016.

A. Bajgar, K. Kucerova, L. Jonatova, A. Tomcala, I. Schneedorferova et al., Extracellular adenosine mediates a systemic metabolic switch during immune response, PLoS biology. United States, vol.13, p.1002135, 2015.

G. Raposo and W. Stoorvogel, Extracellular vesicles: Exosomes, microvesicles, and friends, Journal of Cell Biology, vol.200, pp.373-383, 2013.

S. M. Van-dommelen, P. Vader, S. Lakhal, S. Kooijmans, W. W. Van-solinge et al., Microvesicles and exosomes: opportunities for cell-derived membrane vesicles in drug delivery, Journal of controlled release : official journal of the Controlled Release Society. Netherlands, vol.161, pp.635-644, 2012.

M. A. Antonyak and R. A. Cerione, Emerging picture of the distinct traits and functions of microvesicles and exosomes, Proceedings of the National Academy of Sciences of the United States of America. United States, vol.112, pp.3589-3590, 2015.

R. A. Haraszti, M. Didiot, E. Sapp, J. Leszyk, S. A. Shaffer et al., High-resolution proteomic and lipidomic analysis of exosomes and microvesicles from different cell sources, Journal of extracellular vesicles. Sweden, vol.5, p.32570, 2016.

R. Crescitelli, C. Lasser, T. G. Szabo, A. Kittel, M. Eldh et al., Distinct RNA profiles in subpopulations of extracellular vesicles: apoptotic bodies, microvesicles and exosomes, Journal of extracellular vesicles. Sweden, issue.2, 2013.

J. Tissot, G. Canellini, O. Rubin, A. Angelillo-scherrer, J. Delobel et al., Blood microvesicles: From proteomics to physiology, Translational Proteomics, vol.1, pp.38-52, 2013.

M. Colombo, G. Raposo, and C. Thery, Biogenesis, secretion, and intercellular interactions of exosomes and other extracellular vesicles. Annual review of cell and developmental biology, vol.30, pp.255-289, 2014.

E. Cocucci and J. Meldolesi, Ectosomes and exosomes: shedding the confusion between extracellular vesicles, Trends in cell biology. England, vol.25, pp.364-372, 2015.

S. Mathivanan, H. Ji, and R. J. Simpson, Exosomes: extracellular organelles important in intercellular communication, Journal of proteomics. Netherlands, vol.73, pp.1907-1920, 2010.

B. Fevrier and G. Raposo, Exosomes: endosomal-derived vesicles shipping extracellular messages, Current opinion in cell biology. England, vol.16, pp.415-421, 2004.

D. M. Pegtel, K. Cosmopoulos, D. A. Thorley-lawson, M. Van-eijndhoven, E. S. Hopmans et al., Functional delivery of viral miRNAs via exosomes, Proceedings of the National Academy of Sciences of the United States of America. United States, vol.107, pp.6328-6333, 2010.

J. Kowal, M. Tkach, and C. Thery, Biogenesis and secretion of exosomes, Current opinion in cell biology. England, vol.29, pp.116-125, 2014.

C. Thery, L. Zitvogel, and S. Amigorena, Exosomes: composition, biogenesis and function, Nature reviews. Immunology. England, pp.569-579, 2002.

O. A. Sergeeva and F. G. Van-der-goot, Kicking Out Pathogens in Exosomes, Cell. United States, vol.161, pp.1241-1242, 2015.

G. Coakley, R. M. Maizels, and A. H. Buck, Exosomes and Other Extracellular Vesicles: The New Communicators in Parasite Infections, Trends in parasitology. England, vol.31, pp.477-489, 2015.

L. Gangoda, S. Boukouris, M. Liem, H. Kalra, and S. Mathivanan, Extracellular vesicles including exosomes are mediators of signal transduction: are they protective or pathogenic?, Proteomics. Germany, vol.15, pp.260-271, 2015.

J. S. Schorey, Y. Cheng, P. P. Singh, and V. L. Smith, Exosomes and other extracellular vesicles in host-pathogen interactions, EMBO reports, vol.16, pp.24-43, 2015.

B. Arefin, L. Kucerova, R. Krautz, H. Kranenburg, F. Parvin et al., Apoptosis in Hemocytes Induces a Shift in Effector Mechanisms in the Drosophila Immune System and Leads to a Pro-Inflammatory State, PloS ONE. United States, vol.10, p.136593, 2015.

J. C. Castillo, S. E. Reynolds, and I. Eleftherianos, Insect immune responses to nematode parasites, Trends in parasitology. England, vol.27, pp.537-547, 2011.

D. Colinet, L. Kremmer, S. Lemauf, C. Rebuf, J. Gatti et al., Development of RNAi in a Drosophila endoparasitoid wasp and demonstration of its efficiency in impairing venom protein production, Journal of insect physiology. England, vol.63, pp.56-61, 2014.

I. Levental, M. Grzybek, and K. Simons, Raft domains of variable properties and compositions in plasma membrane vesicles, Proceedings of the National Academy of Sciences of the United States of America. United States, vol.108, pp.11411-11416, 2011.

K. Simons and J. L. Sampaio, Cold Spring Harbor perspectives in biology, United States, vol.3, p.4697, 2011.