J. Woodring, S. Higgs, and B. Beaty, Natural cycles of vector-borne pathogens The biology of disease vectors, pp.51-72, 1996.

. Black-wct, K. Bennett, N. Gorrochotegui-escalante, C. Barillas-mury, and I. Fernandez-salas, Flavivirus Susceptibility in Aedes aegypti, Archives of Medical Research, vol.33, issue.4, pp.379-388, 2002.
DOI : 10.1016/S0188-4409(02)00373-9

T. Lefevre, J. Koella, F. Renaud, H. Hurd, and D. Biron, New Prospects for Research on Manipulation of Insect Vectors by Pathogens, PLoS Pathogens, vol.266, issue.7, p.72, 2006.
DOI : 0962-8452(1999)266[1729:TEOPYN]2.0.CO;2

M. Fernandez-garcia, M. Mazzon, M. Jacobs, and A. A. , Pathogenesis of Flavivirus Infections: Using and Abusing the Host Cell, Cell Host & Microbe, vol.5, issue.4, pp.318-328, 2009.
DOI : 10.1016/j.chom.2009.04.001
URL : https://hal.archives-ouvertes.fr/pasteur-00429869

X. Guo, Y. Xu, G. Bian, A. Pike, and Y. Xie, Response of the mosquito protein interaction network to dengue infection, BMC Genomics, vol.11, issue.1, p.380, 2010.
DOI : 10.1186/1471-2164-11-380

V. Nene, J. Wortman, D. Lawson, B. Haas, and C. Kodira, Genome Sequence of Aedes aegypti, a Major Arbovirus Vector, Science, vol.316, issue.5832, pp.1718-1723, 2007.
DOI : 10.1126/science.1138878
URL : https://hal.archives-ouvertes.fr/hal-00156214

S. Blandin and E. Levashina, Curing mosquitoes to control malaria?, Med Sci, vol.20, pp.740-742, 2004.

H. Sanders, B. Foy, A. Evans, L. Ross, and B. Beaty, Sindbis virus induces transport processes and alters expression of innate immunity pathway genes in the midgut of the disease vector, Aedes aegypti, Insect Biochemistry and Molecular Biology, vol.35, issue.11, pp.1293-1307, 2005.
DOI : 10.1016/j.ibmb.2005.07.006

O. Baron, R. Ursic-bedoya, C. Lowenberger, and C. Ocampo, , Infected with Dengue-2 Virus, Journal of Insect Science, vol.10, issue.41, p.41, 2010.
DOI : 10.1673/031.010.4101

O. Sessions, N. Barrows, J. Souza-neto, T. Robinson, and C. Hershey, Discovery of insect and human dengue virus host factors, Nature, vol.27, issue.7241, pp.1047-1050, 2009.
DOI : 10.1038/nature07967

V. Choumet, A. Carmi-leroy, C. Laurent, P. Lenormand, and J. Rousselle, The salivary glands and saliva ofAnopheles gambiae as an essential step in thePlasmodium life cycle: A global proteomic study, PROTEOMICS, vol.61, issue.8, pp.3384-3394, 2007.
DOI : 10.1002/pmic.200700334

J. Vennestrom and P. Jensen, Ixodes ricinus: The potential of two-dimensional gel electrophoresis as a tool for studying host???vector???pathogen interactions, Experimental Parasitology, vol.115, issue.1, pp.53-58, 2007.
DOI : 10.1016/j.exppara.2006.05.008

L. Brennan, B. Keddie, H. Braig, and H. Harris, The Endosymbiont Wolbachia pipientis Induces the Expression of Host Antioxidant Proteins in an Aedes albopictus Cell Line, PLoS ONE, vol.279, issue.5, p.2083, 2008.
DOI : 10.1371/journal.pone.0002083.t001

A. Popova-butler and D. Dean, Proteomic analysis of the mosquito Aedes aegypti midgut brush border membrane vesicles, Journal of Insect Physiology, vol.55, issue.3, pp.264-272, 2009.
DOI : 10.1016/j.jinsphys.2008.12.008

L. Wasinpiyamongkol, S. Patramool, N. Luplertlop, P. Surasombatpattana, and S. Doucoure, Blood-feeding and immunogenic Aedes aegypti saliva proteins, PROTEOMICS, vol.2, issue.10, pp.1906-1916, 2009.
DOI : 10.1002/pmic.200900626
URL : https://hal.archives-ouvertes.fr/hal-00820653

H. Dieng, M. Boots, J. Higashihara, T. Okada, and K. Kato, Effects of blood and virus-infected blood on protein expression in the midgut of the dengue vector Aedes albopictus, Medical and Veterinary Entomology, vol.16, issue.Suppl, pp.278-283, 2007.
DOI : 10.1111/j.1365-2915.2007.00693.x

M. Solignat, B. Gay, S. Higgs, L. Briant, and C. Devaux, Replication cycle of chikungunya: A re-emerging arbovirus, Virology, vol.393, issue.2, pp.183-197, 2009.
DOI : 10.1016/j.virol.2009.07.024
URL : https://hal.archives-ouvertes.fr/hal-00420502

R. Bartenschlager and S. Miller, Molecular aspects of Dengue virus replication, Future Microbiology, vol.3, issue.2, pp.155-165, 2008.
DOI : 10.2217/17460913.3.2.155

M. Kielian, Class II virus membrane fusion proteins, Virology, vol.344, issue.1, pp.38-47, 2006.
DOI : 10.1016/j.virol.2005.09.036
URL : http://doi.org/10.1016/j.virol.2005.09.036

S. Mukhopadhyay, R. Kuhn, and M. Rossmann, A structural perspective of the flavivirus life cycle, Nature Reviews Microbiology, vol.55, issue.1, pp.13-22, 2005.
DOI : 10.1080/096876899294706

K. Stiasny and F. Heinz, Flavivirus membrane fusion, Journal of General Virology, vol.87, issue.10, pp.2755-2766, 2006.
DOI : 10.1099/vir.0.82210-0
URL : https://hal.archives-ouvertes.fr/hal-00167646

M. Dubrulle, L. Mousson, S. Moutailler, M. Vazeille, and A. Failloux, Chikungunya Virus and Aedes Mosquitoes: Saliva Is Infectious as soon as Two Days after Oral Infection, PLoS ONE, vol.4, issue.6, p.5895, 2009.
DOI : 10.1371/journal.pone.0005895.g005
URL : https://hal.archives-ouvertes.fr/pasteur-00395262

M. Salazar, J. Richardson, I. Sanchez-vargas, K. Olson, and B. Beaty, Dengue virus type 2: replication and tropisms in orally infected Aedes aegypti mosquitoes, BMC Microbiology, vol.7, issue.1, p.9, 2007.
DOI : 10.1186/1471-2180-7-9

R. Mercado-curiel and B. Wct, A dengue receptor as possible genetic marker of vector competence in Aedes aegypti, BMC Microbiology, vol.8, issue.1, p.118, 2008.
DOI : 10.1186/1471-2180-8-118

D. Friedman, S. Hoving, and R. Westermeier, Chapter 30 Isoelectric Focusing and Two-Dimensional Gel Electrophoresis, Methods Enzymol, vol.463, pp.515-540, 2009.
DOI : 10.1016/S0076-6879(09)63030-5

K. Mohankumar and P. Ramasamy, Activities of membrane bound phosphatases, transaminases and mitochondrial enzymes in white spot syndrome virus infected tissues of Fenneropenaeus indicus, Virus Research, vol.118, issue.1-2, pp.130-135, 2006.
DOI : 10.1016/j.virusres.2005.12.002

D. Suresh, V. Annam, K. Pratibha, and B. Prasad, Total antioxidant capacity ??? a novel early bio-chemical marker of oxidative stress in HIV infected individuals, Journal of Biomedical Science, vol.16, issue.1, p.61, 2009.
DOI : 10.1186/1423-0127-16-61

V. Finnerty and G. Johnson, Post-Translational Modification as a Potential Explanation of High Levels of Enzyme Polymorphism: Xanthine Dehydrogenase and Aldehyde Oxidase in Drosophila Melanogaster, Genetics, vol.91, pp.695-722, 1979.

M. Corona and G. Robinson, Genes of the antioxidant system of the honey bee: annotation and phylogeny, Insect Molecular Biology, vol.144, issue.5, pp.687-701, 2006.
DOI : 10.1016/0531-5565(83)90026-8

S. Radyuk, V. Klichko, B. Spinola, R. Sohal, and W. Orr, The peroxiredoxin gene family in drosophila melanogaster, Free Radical Biology and Medicine, vol.31, issue.9, pp.1090-1100, 2001.
DOI : 10.1016/S0891-5849(01)00692-X

F. Missirlis, S. Rahlfs, N. Dimopoulos, H. Bauer, and K. Becker, A Putative Glutathione Peroxidase of Drosophila Encodes a Thioredoxin Peroxidase That Provides Resistance against Oxidative Stress But Fails to Complement a Lack of Catalase Activity, Biological Chemistry, vol.384, issue.3, pp.463-472, 2003.
DOI : 10.1515/BC.2003.052

G. Toba and T. Aigaki, Disruption of the Microsomal glutathione S-transferase-like gene reduces life span of Drosophila melanogaster, Gene, vol.253, issue.2, pp.179-187, 2000.
DOI : 10.1016/S0378-1119(00)00246-8

N. Lumjuan, B. Stevenson, L. Prapanthadara, P. Somboon, and P. Brophy, The Aedes aegypti glutathione transferase family, Insect Biochemistry and Molecular Biology, vol.37, issue.10, pp.1026-1035, 2007.
DOI : 10.1016/j.ibmb.2007.05.018

S. Kanzok, A. Fechner, H. Bauer, J. Ulschmid, and H. Muller, Substitution of the Thioredoxin System for Glutathione Reductase in Drosophila melanogaster, Science, vol.291, issue.5504, pp.643-646, 2001.
DOI : 10.1126/science.291.5504.643

Z. Xi, J. Ramirez, and G. Dimopoulos, The Aedes aegypti Toll Pathway Controls Dengue Virus Infection, PLoS Pathogens, vol.19, issue.7, p.1000098, 2008.
DOI : 10.1371/journal.ppat.1000098.s008

G. Jaramillo-gutierrez, J. Rodrigues, G. Ndikuyeze, M. Povelones, and A. Molina-cruz, Mosquito immune responses and compatibility between Plasmodium parasites and anopheline mosquitoes, BMC Microbiology, vol.9, issue.1, p.154, 2009.
DOI : 10.1186/1471-2180-9-154
URL : http://doi.org/10.1186/1471-2180-9-154

J. Kim and C. Dang, Multifaceted roles of glycolytic enzymes, Trends in Biochemical Sciences, vol.30, issue.3, pp.142-150, 2005.
DOI : 10.1016/j.tibs.2005.01.005

T. Ogino, T. Yamadera, T. Nonaka, S. Imajoh-ohmi, and K. Mizumoto, Enolase, a Cellular Glycolytic Enzyme, Is Required for Efficient Transcription of Sendai Virus Genome, Biochemical and Biophysical Research Communications, vol.285, issue.2, pp.447-455, 2001.
DOI : 10.1006/bbrc.2001.5160

M. Courageot, M. Frenkiel, D. Santos, C. Deubel, V. Despres et al., alpha -Glucosidase Inhibitors Reduce Dengue Virus Production by Affecting the Initial Steps of Virion Morphogenesis in the Endoplasmic Reticulum, Journal of Virology, vol.74, issue.1, pp.564-572, 2000.
DOI : 10.1128/JVI.74.1.564-572.2000

S. Wu, C. Lee, C. Liao, R. Dwek, and N. Zitzmann, Antiviral Effects of an Iminosugar Derivative on Flavivirus Infections, Journal of Virology, vol.76, issue.8, pp.3596-3604, 2002.
DOI : 10.1128/JVI.76.8.3596-3604.2002

C. Charrier, G. Duncan, M. Reid, G. Rucklidge, and D. Henderson, A novel class of CoA-transferase involved in short-chain fatty acid metabolism in butyrate-producing human colonic bacteria, Microbiology, vol.152, issue.1, pp.179-185, 2006.
DOI : 10.1099/mic.0.28412-0

M. Samsa, J. Mondotte, N. Iglesias, I. Assuncao-miranda, and G. Barbosa-lima, Dengue Virus Capsid Protein Usurps Lipid Droplets for Viral Particle Formation, PLoS Pathogens, vol.230, issue.7, p.1000632, 2009.
DOI : 10.1371/journal.ppat.1000632.t001

N. Darby, M. Van-straaten, E. Penka, R. Vincentelli, and J. Kemmink, Identifying and characterizing a second structural domain of protein disulfide isomerase, FEBS Letters, vol.5, issue.1, pp.167-172, 1999.
DOI : 10.1016/S0014-5793(99)00374-9

X. Jiang, M. Fitzgerald, C. Grant, and P. Hogg, Redox Control of Exofacial Protein Thiols/Disulfides by Protein Disulfide Isomerase, Journal of Biological Chemistry, vol.274, issue.4, pp.2416-2423, 1999.
DOI : 10.1074/jbc.274.4.2416

P. Klappa, H. Hawkins, and R. Freedman, Interactions Between Protein Disulphide Isomerase and Peptides, European Journal of Biochemistry, vol.265, issue.1, pp.37-42, 1997.
DOI : 10.1074/jbc.270.52.31046

R. Yocupicio-monroy, F. Medina, R. Valle, J. Angel, and R. , Cellular Proteins from Human Monocytes Bind to Dengue 4 Virus Minus-Strand 3' Untranslated Region RNA, Journal of Virology, vol.77, issue.5, pp.3067-3076, 2003.
DOI : 10.1128/JVI.77.5.3067-3076.2003

Y. Padwad, K. Mishra, M. Jain, C. S. Karan, and D. , RNA interference mediated silencing of Hsp60 gene in human monocytic myeloma cell line U937 revealed decreased dengue virus multiplication, Immunobiology, vol.214, issue.6, pp.422-429, 2009.
DOI : 10.1016/j.imbio.2008.11.010

L. Stuart, J. Boulais, G. Charriere, E. Hennessy, and S. Brunet, A systems biology analysis of the Drosophila phagosome, Nature, vol.124, issue.7123, pp.95-101, 2007.
DOI : 10.1038/nature05380

Y. Fan, M. Schlierf, A. Gaspar, C. Dreux, and A. Kpebe, Drosophila Translational Elongation Factor-1?? Is Modified in Response to DOA Kinase Activity and Is Essential for Cellular Viability, Genetics, vol.184, issue.1, pp.141-154, 2010.
DOI : 10.1534/genetics.109.109553
URL : https://hal.archives-ouvertes.fr/hal-00677738

M. Adams, S. Celniker, R. Holt, C. Evans, and J. Gocayne, The Genome Sequence of Drosophila melanogaster, Science, vol.287, issue.5461, pp.2185-2195, 2000.
DOI : 10.1126/science.287.5461.2185

L. Hertel and E. Mocarski, Global Analysis of Host Cell Gene Expression Late during Cytomegalovirus Infection Reveals Extensive Dysregulation of Cell Cycle Gene Expression and Induction of Pseudomitosis Independent of US28 Function, Journal of Virology, vol.78, issue.21, pp.11988-12011, 2004.
DOI : 10.1128/JVI.78.21.11988-12011.2004

S. Weaver, T. Scott, L. Lorenz, K. Lerdthusnee, and W. Romoser, Togavirus-associated pathologic changes in the midgut of a natural mosquito vector, J Virol, vol.62, pp.2083-2090, 1988.

M. Shaw, K. Stone, C. Colangelo, E. Gulcicek, and P. Palese, Cellular Proteins in Influenza Virus Particles, PLoS Pathogens, vol.72, issue.4, p.1000085, 2008.
DOI : 10.1371/journal.ppat.1000085.s002

G. Smith and L. Enquist, Break Ins and Break Outs: Viral Interactions with the Cytoskeleton of Mammalian Cells, Annual Review of Cell and Developmental Biology, vol.18, issue.1, pp.135-161, 2002.
DOI : 10.1146/annurev.cellbio.18.012502.105920

K. Radtke, K. Dohner, and B. Sodeik, Viral interactions with the cytoskeleton: a hitchhiker's guide to the cell, Cellular Microbiology, vol.2, issue.3, pp.387-400, 2006.
DOI : 10.1128/JVI.79.2.800-811.2005

R. Jacob, M. Heine, J. Eikemeyer, N. Frerker, and K. Zimmer, Annexin II Is Required for Apical Transport in Polarized Epithelial Cells, Journal of Biological Chemistry, vol.279, issue.5, pp.3680-3684, 2004.
DOI : 10.1074/jbc.C300503200

I. Schuffenecker, I. Iteman, A. Michault, S. Murri, and L. Frangeul, Genome Microevolution of Chikungunya Viruses Causing the Indian Ocean Outbreak, PLoS Medicine, vol.105, issue.7, p.263, 2006.
DOI : 10.1371/journal.pmed.0030263.st005

M. Vazeille, S. Moutailler, D. Coudrier, C. Rousseaux, and H. Khun, Two Chikungunya Isolates from the Outbreak of La Reunion (Indian Ocean) Exhibit Different Patterns of Infection in the Mosquito, Aedes albopictus, PLoS ONE, vol.103, issue.11, p.1168, 2007.
DOI : 10.1371/journal.pone.0001168.t003
URL : https://hal.archives-ouvertes.fr/hal-00196860

M. Vazeille-falcoz, L. Mousson, F. Rodhain, E. Chungue, and A. Failloux, Variation in oral susceptibility to dengue type 2 virus of populations of Aedes aegypti from the islands of Tahiti and Moorea, French Polynesia, Am J Trop Med Hyg, vol.60, pp.292-299, 1999.

L. Reed and H. Muench, A simple method of estimating fifty percent endpoints, Am J Hyg, vol.27, pp.493-497, 1938.

J. Bancroft, . Ch, R. Stirling, and D. Turner, Manual of histological technics and their diagnostic applications, 1994.