E. Rosenberg and I. Zilber-rosenberg, Symbiosis and development: the hologenome concept, Birth Defects Res C Embryo Today, vol.93, issue.1, pp.56-66, 2011.

R. Dillon and K. Charnley, Mutualism between the desert locust Schistocerca gregaria and its gut microbiota, Res Microbiol, vol.153, pp.503-539, 2002.

R. J. Dillon and V. M. Dillon, The gut bacteria of insects: nonpathogenic interactions, Annu Rev Entomol, vol.49, pp.71-92, 2004.

G. Sharon, D. Segal, J. M. Ringo, A. Hefetz, I. Zilber-rosenberg et al., Commensal bacteria play a role in mating preference of Drosophila melanogaster, Proc Natl Acad Sci, vol.107, issue.46, pp.20051-20056, 2010.

T. Tsuchida, R. Koga, M. Horikawa, T. Tsunoda, T. Maoka et al., Symbiotic bacterium modifies aphid body color, vol.330, pp.1102-1104, 2010.
URL : https://hal.archives-ouvertes.fr/hal-02667907

H. Toju and T. Fukatsu, Diversity and infection prevalence of endosymbionts in natural populations of the chestnut weevil: relevance of local climate and host plants, Mol Ecol, vol.20, pp.853-868, 2011.

V. J. Pidiyar, K. Jangid, M. S. Patole, and Y. S. Shouche, Studies on cultured and uncultured microbiota of wild Culex quinquefasciatus mosquito midgut based on 16 s ribosomal RNA gene analysis, AmJTrop Med Hyg, vol.70, pp.597-603, 2004.

A. Rani, A. Sharma, R. Rajagopal, T. Adak, and R. K. Bhatnagar, Bacterial diversity analysis of larvae and adult midgut microflora using culture-dependent and culture-independent methods in lab-reared and field-collected Anopheles stephensi-an Asian malarial vector, BMC Microbiol, vol.19, issue.9, p.96, 2009.

D. S. Gusmão, A. V. Santos, D. C. Marini, M. Bacci, M. A. Berbert-molina et al., Culture-dependent and culture-independent characterization of microorganisms associated with Aedes aegypti (Diptera: Culicidae) (L.) and dynamics of bacterial colonization in the midgut, Acta Trop, vol.115, pp.275-281, 2010.

A. R. Chavshin, M. A. Oshaghi, H. Vatandoost, M. R. Pourmand, A. Raeisi et al., Identification of bacterial microflora in the midgut of the larvae and adult of wild caught Anopheles stephensi: a step toward finding suitable paratransgenesis candidates, Acta Trop, vol.121, pp.129-134, 2012.

D. Djadid, N. Jazayeri, H. Raz, A. Favia, G. Ricci et al., Identification of the midgut microbiota of An. stephensi and An. maculipennis for their application as a paratransgenic tool against malaria, PLoS One, vol.6, p.28484, 2011.

K. Zouache, F. N. Raharimalala, V. Raquin, V. Tran-van, L. Raveloson et al., Bacterial diversity of field-caught mosquitoes, Aedes albopictus and Aedes aegypti, from different geographic regions of Madagascar, FEMS Microbiol Ecol, vol.75, pp.377-389, 2011.
URL : https://hal.archives-ouvertes.fr/halsde-00724643

W. R. Streit and R. A. Schmitz, Metagenomics-the key to the uncultured microbes, Curr Opin Microbiol, vol.7, issue.5, pp.492-498, 2004.

A. Boissière, M. T. Tchioffo, D. Bachar, L. Abate, M. A. Nsango et al., Midgut microbiota of the malaria mosquito vector Anopheles gambiae and interactions with Plasmodium falciparum infection, PLoS Patho, vol.8, issue.5, p.1002742, 2012.

A. Schäfer, R. Konrad, T. Kuhnigk, P. Kämpfer, H. Hertel et al., Hemicellulosedegrading bacteria and yeasts from the termite gut, J Appl Bacteriol, vol.80, issue.5, pp.471-478, 1996.

Y. Watanabe, N. Shinzato, and T. Fukatsu, Isolation of actinomycetes from termites' guts, Biosci Biotechnol Biochem, vol.7, issue.8, pp.1797-1801, 2003.

N. A. Moran and P. Baumann, Bacterial endosymbionts in animals, Curr Opin Microbiol, vol.3, issue.3, pp.270-275, 2000.

A. A. Pinto-tomás, M. A. Anderson, G. Suen, D. M. Stevenson, F. S. Chu et al., Symbiotic nitrogen fixation in the fungus gardens of leaf-cutter ants, Science, vol.326, issue.5956, pp.1120-1123, 2009.

J. Malhotra, A. Dua, A. Saxena, N. Sangwan, U. Mukherjee et al., Genome sequence of Acinetobacter sp. strain HA, isolated from the gut of the polyphagous insect pest Helicoverpa armigera, J Bacteriol, vol.194, issue.18, p.5156, 2012.

I. V. Coutinho-abreu, K. Y. Zhu, and M. Ramalho-ortigao, Transgenesis and paratransgenesis to control insect-borne diseases: current status and future challenges, Parasitol Int, vol.59, pp.1-8, 2010.

G. Favia, I. Ricci, M. Marzorati, I. Negri, A. A. Sacchi et al., Bacteria of the genus Asaia: a potential paratransgenic weapon against malaria, Adv Exp Med Biol, vol.27, pp.49-59, 2008.

D. C. Bisi and D. J. Lampe, Secretion of anti-Plasmodium effector proteins from a natural Pantoea agglomerans isolate by using PelB and HlyA secretion signals, Appl Environ Microbiol, vol.77, pp.4669-4675, 2011.

L. Lambrechts, T. W. Scott, and D. J. Gubler, Consequences of the expanding global distribution of Aedes albopictus for dengue virus transmission, PLoS Negl Trop Dis, vol.25, issue.5, p.646, 2010.
URL : https://hal.archives-ouvertes.fr/pasteur-02011027

M. Ratsitorahina, J. Harisoa, J. Ratovonjato, S. Biacabe, J. M. Reynes et al., Outbreak of dengue and Chikungunya fevers, vol.14, pp.1135-1137, 2006.
URL : https://hal.archives-ouvertes.fr/pasteur-01835629

P. Renault, E. Balleydier, D. 'ortenzio, E. Bâville, M. Filleul et al., Epidemiology of chikungunya infection on Reunion Island, Mayotte, and neighboring countries, Med Mal Infect, vol.42, pp.93-101, 2012.

G. Minard, F. H. Tran, F. N. Raharimalala, E. Hellard, P. Ravelonandro et al., Valiente Moro C: Prevalence, genomic and metabolic profiles of Acinetobacter and Asaia associated with field-caught Aedes albopictus from Madagascar, FEMS Microbiol Ecol, vol.83, pp.63-73, 2013.

F. N. Raharimalala, L. H. Ravaomanarivo, P. Ravelonandro, L. S. Rafarasoa, K. Zouache et al., Biogeography of the two major arbovirus mosquito vectors, Aedes aegypti and Aedes albopictus, vol.5, p.56, 2012.
URL : https://hal.archives-ouvertes.fr/pasteur-00700521

C. Ravaonjanahary, . Madagascar, and . France, Travaux et documents de 1?ORSTOM, 1978.

P. Bouvet, M. L. Joly-guillou, J. Acinetobacter-;-freney, F. Renaud, W. Hansen et al., Précis de bactériologie Clinique, pp.1239-1258, 2000.

A. D. Mandel, K. Wright, and J. M. Mckinnon, Selective medium for isolation of Mima and Herellea organisms, J Bacteriol, vol.88, pp.1524-1525, 1964.

P. Listiyanti, H. Kawasaki, T. Seki, Y. Yamoda, T. Chimura et al., Identification of Acetobacter Strains isolated from Indonesian sources, and proposals of Acetobacter syzygii sp. nov., Acetobacter Cibinongensis sp.nov. Acetobacter cibinongensis sp. nov., and Acetobacter orientalis sp, J Gen Appl Microbiol, vol.47, pp.119-131, 2001.

B. Chouaia, P. Rossi, M. Montagna, I. Ricci, E. Crotti et al., Molecular evidence for multiple infections as revealed by typing of Asaia bacterial symbionts of four mosquito species, Appl Environ Microbiol, vol.76, pp.7444-7450, 2010.

T. A. Hall, BioEdit: a user-friendly biological sequence alignment editor and analysis program for windows 95/98/NT, Nucleic Acids Symp Ser, vol.41, pp.95-98, 1999.

D. C. Schwartz and C. R. Cantor, Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis, Cell, vol.37, pp.67-75, 1984.

T. Eckhardt, A rapid method for the identification of plasmid desoxyribonucleic acid in bacteria, Plasmid, vol.1, pp.584-588, 1978.

P. Mavingui, M. Flores, X. Guo, G. Dávila, X. Perret et al., Dynamics of genome architecture in Rhizobium sp. strain NGR234, J Bacteriol, vol.184, pp.171-176, 2002.
URL : https://hal.archives-ouvertes.fr/hal-02573533

H. Seifert, B. Boullion, A. Schulze, and G. Pulverer, Plasmid DNA profiles of Acinetobacter baumannii: clinical application in a complex endemic setting, Infect Control Hosp Epidemiol, vol.15, pp.520-528, 1994.

J. Caballero-mellado, L. López-reyes, and R. Bustillos, Presence of 16S rRNA Genes in Multiple Replicons in Azospirillum brasilense, FEMS Microbial Lett, vol.178, pp.283-288, 1999.

F. Wisniewski-dyé, K. Borziak, G. Khalsa-moyers, A. , G. Sukharnikov et al., Azospirillum genomes reveal transition of bacteria from aquatic to terrestrial environments, PLoS Genet, vol.7, p.1002430, 2011.

. Development-core, Team: R: A Language and Environment for Statistical computing. R Foundation for Statistical Computing, 2009.

J. M. Lindh, O. Terenius, and F. I. , 16S rRNA gene-based identification of midgut bacteria from field-caught Anopheles gambiae sensu lato and A. funestus mosquitoes reveals new species related to known insect symbionts, Appl Environ Microbiol, vol.71, pp.7217-7223, 2005.

O. Terenius, J. M. Lindh, K. Eriksson-gonzales, L. Bussière, A. T. Laugen et al., Midgut bacterial dynamics in Aedes aegypti, FEMS Microbiol Ecol, vol.80, pp.556-565, 2012.

G. C. Müller, R. D. Xue, and Y. Schlein, Differential attraction of Aedes albopictus in the field to flowers, fruits and honeydew, Acta Trop, vol.118, pp.45-49, 2011.

S. Alvarez-pérez, C. M. Herrera, and C. De-vega, Zooming-in on floral nectar: a first exploration of nectar-associated bacteria in wild plant communities, FEMS Microbiol Ecol, vol.80, pp.591-602, 2012.

K. Gneiding, R. Frodl, and G. Funke, Identities of Microbacterium spp. encountered in human clinical specimens, J Clin Microbiol, vol.46, pp.3646-3652, 2008.

L. O. Helsel, D. Hollis, A. G. Steigerwalt, R. E. Morey, J. Jordan et al., Identification of "Haematobacter" a new genus of aerobic Gram-negative rods isolated from clinical specimens, and reclassification of Rhodobacter massiliensis as "Haematobacter massiliensis comb. nov, J Clin Microbiol, vol.45, pp.1238-1243, 2007.

C. Brady, I. Cleenwerck, S. Venter, M. Vancanneyt, J. Swings et al., Phylogeny and identification of Pantoea species associated with plants, humans and the natural environment based on multilocus sequence analysis (MLSA), Syst Appl Microbiol, vol.31, issue.6-8, pp.447-460, 2008.

E. J. De-vries, G. Jacobs, and J. A. Breeuwer, Growth and transmission of gut bacteria in the Western flower thrips. Frankliniella occidentalis, J Invertebr Pathol, vol.77, issue.2, pp.129-137, 2001.

S. C. Straif, C. N. Mbogo, A. M. Toure, E. D. Walker, M. Kaufman et al., Midgut bacteria in Anopheles gambiae and An. funestus (Diptera: Culicidae) from Kenya and Mali, J Med Entomol, vol.35, pp.222-226, 1998.

M. A. Riehle, C. K. Moreira, D. Lampe, C. Lauzon, and M. Jacobs-lorena, Using bacteria to express and display anti-Plasmodium molecules in the mosquito midgut, Int J Parasitol, vol.37, pp.595-603, 2007.

J. D. Joyce, J. R. Nogueira, A. A. Bales, K. E. Pittman, and J. R. Anderson, Interactions between La Crosse virus and bacteria isolated from the digestive tract of Aedes albopictus (Diptera: Culicidae), J Med Entomol, vol.48, issue.2, pp.389-94, 2011.

V. Moro, Submit your next manuscript to BioMed Central and take full advantage of: ? Convenient online submission ? Thorough peer review ? No space constraints or color figure charges ? Immediate publication on acceptance ? Inclusion in PubMed, CAS, Scopus and Google Scholar ? Research which is freely available for redistribution, BMC Microbiology, vol.13, p.70, 2013.