M. Turell, Horizontal and vertical transmission of viruses by insect and tick vectors The Arboviruses: Epidemiology and Ecology, Boca Raton, pp.127-152, 1988.

C. Paquet, I. Quatresous, J. Solet, D. Sissoko, and P. Renault, Chikungunya outbreak in Reunion: epidemiology and surveillance, Euro Surveill, vol.11, pp.60202-060203, 2005.
DOI : 10.2807/esw.11.05.02891-en

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

URL : https://hal.archives-ouvertes.fr/pasteur-01659363

H. Delatte, C. Paupy, J. Dehecq, J. Thiria, and A. Failloux, , vecteur des virus du chikungunya et de la dengue ?? la R??union : biologie et contr??le, Parasite, vol.15, issue.1, pp.3-13, 2008.
DOI : 10.1051/parasite/2008151003

URL : http://www.parasite-journal.org/articles/parasite/pdf/2008/01/parasite2008151p3.pdf

H. Delatte, J. Dehecq, J. Thiria, C. Domerg, and C. Paupy, (Diptera: Culicidae) During a Chikungunya Epidemic Event, Vector-Borne and Zoonotic Diseases, vol.8, issue.1, pp.25-34, 2008.
DOI : 10.1089/vbz.2007.0649

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

J. Hemingway, N. Hawkes, L. Mccarroll, and H. Ranson, The molecular basis of insecticide resistance in mosquitoes, Insect Biochemistry and Molecular Biology, vol.34, issue.7, pp.653-665, 2004.
DOI : 10.1016/j.ibmb.2004.03.018

S. Aksoy, Transgenesis and the management of vector-borne disease. Preface, Adv Exp Med Biol, vol.627, p.vii?viii, 2008.

P. Buchner, Endosymbiosis of animals with plant microorganisms, 1965.

C. Montllor, A. Maxmen, and A. Purcell, Facultative bacterial endosymbionts benefit pea aphids Acyrthosiphon pisum under heat stress, Ecological Entomology, vol.254, issue.2, pp.189-195, 2002.
DOI : 10.1006/jipa.2000.4927

URL : http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2311.2002.00393.x/pdf

H. Dunbar, A. Wilson, N. Ferguson, and N. Moran, Aphid Thermal Tolerance Is Governed by a Point Mutation in Bacterial Symbionts, PLoS Biology, vol.12, issue.5, p.96, 2007.
DOI : 10.1371/journal.pbio.0050096.sg001

C. Scarborough, J. Ferrari, and H. Godfray, Aphid Protected from Pathogen by Endosymbiont, Science, vol.310, issue.5755, p.1781, 2005.
DOI : 10.1126/science.1120180

L. Hedges, J. Brownlie, O. Neill, S. Johnson, and K. , Wolbachia and Virus Protection in Insects, Science, vol.148, issue.5772, p.702, 2008.
DOI : 10.1126/science.1125694

L. Hedges and K. Johnson, Induction of host defence responses by Drosophila C virus, Journal of General Virology, vol.89, issue.6, pp.1497-1501, 2008.
DOI : 10.1099/vir.0.83684-0

E. Schnepf, N. Crickmore, J. Van-rie, D. Lereclus, and J. Baum, Bacillus thuringiensis and its pesticidal crystal proteins, Microbiol Mol Biol Rev, vol.62, pp.775-806, 1998.

K. Min and S. Benzer, Wolbachia, normally a symbiont of Drosophila, can be virulent, causing degeneration and early death, Proceedings of the National Academy of Sciences, vol.171, issue.8, pp.10792-10796, 1997.
DOI : 10.1128/jb.171.8.4202-4206.1989

S. Zabalou, M. Riegler, M. Theodorakopoulou, C. Stauffer, and C. Savakis, Wolbachia-induced cytoplasmic incompatibility as a means for insect pest population control, Proceedings of the National Academy of Sciences, vol.116, issue.1, pp.15042-15045, 2004.
DOI : 10.1023/A:1020951407069

URL : http://www.pnas.org/content/101/42/15042.full.pdf

E. Zchori-fein, Y. Gottlieb, S. Kelly, J. Brown, and J. Wilson, A newly discovered bacterium associated with parthenogenesis and a change in host selection behavior in parasitoid wasps, Proceedings of the National Academy of Sciences, vol.28, issue.1438, pp.12555-12560, 2001.
DOI : 10.1007/BF02981799

G. Baldridge, N. Burkhardt, J. Simser, T. Kurtti, and U. Munderloh, Sequence and Expression Analysis of the ompA Gene of Rickettsia peacockii, an Endosymbiont of the Rocky Mountain Wood Tick, Dermacentor andersoni, Applied and Environmental Microbiology, vol.70, issue.11, pp.6628-6636, 2004.
DOI : 10.1128/AEM.70.11.6628-6636.2004

C. Beard, O. Neill, S. Tesh, R. Richards, F. Aksoy et al., Modification of arthropod vector competence via symbiotic bacteria, Parasitology Today, vol.9, issue.5, pp.179-183, 1993.
DOI : 10.1016/0169-4758(93)90142-3

C. Beard, E. Dotson, P. Pennington, S. Eichler, and C. Cordon-rosales, Bacterial symbiosis and paratransgenic control of vector-borne Chagas disease, International Journal for Parasitology, vol.31, issue.5-6, pp.621-627, 2001.
DOI : 10.1016/S0020-7519(01)00165-5

R. Durvasula, A. Gumbs, A. Panackal, O. Kruglov, and S. Aksoy, Prevention of insect-borne disease: An approach using transgenic symbiotic bacteria, Proceedings of the National Academy of Sciences, vol.59, issue.1, pp.3274-3278, 1997.
DOI : 10.1016/0035-9203(94)90483-9

N. Moran, J. Mccutcheon, and A. Nakabachi, Genomics and Evolution of Heritable Bacterial Symbionts, Annual Review of Genetics, vol.42, issue.1, pp.165-190, 2008.
DOI : 10.1146/annurev.genet.41.110306.130119

J. Zhong, A. Jasinskas, and A. Barbour, Antibiotic Treatment of the Tick Vector Amblyomma americanum Reduced Reproductive Fitness, PLoS ONE, vol.41, issue.5, p.405, 2007.
DOI : 10.1371/journal.pone.0000405.t001

H. Toh, B. Weiss, S. Perkin, A. Yamashita, and K. Oshima, Massive genome erosion and functional adaptations provide insights into the symbiotic lifestyle of Sodalis glossinidius in the tsetse host, Genome Research, vol.16, issue.2, pp.149-156, 2006.
DOI : 10.1101/gr.4106106

J. Allen, D. Reed, M. Perotti, and H. Braig, Evolutionary Relationships of "Candidatus Riesia spp.," Endosymbiotic Enterobacteriaceae Living within Hematophagous Primate Lice, Applied and Environmental Microbiology, vol.73, issue.5, pp.1659-1664, 2007.
DOI : 10.1128/AEM.01877-06

J. Chao and G. Wistreich, Microbial isolations from the midgut of Culex tarsalis Coquillett, J Insect Pathol, vol.1, pp.311-318, 1959.

J. Chao and G. Wistreich, Microorganisms from the midgut of larval and adult Culex quinquefasciatus Say, J Insect Pathol, vol.2, pp.220-224, 1960.

V. Vasanthi and S. Hoti, Microbial flora in gut of Culex quinquefasciatus breeding in cess pits, Southeast Asian J Trop Med Public Health, vol.23, pp.312-317, 1992.

S. Straif, C. Mbogo, A. Toure, E. Walker, and M. Kaufman, Midgut Bacteria in Anopheles gambiae and An. funestus (Diptera: Culicidae) from Kenya and Mali, Journal of Medical Entomology, vol.35, issue.3, pp.222-226, 1998.
DOI : 10.1093/jmedent/35.3.222

V. Pidiyar, A. Kaznowski, N. Narayan, M. Patole, and Y. Shouche, Aeromonas culicicola sp. nov., from the midgut of Culex quinquefasciatus, Int J Syst Evol Microbiol, vol.52, pp.1723-1728, 2002.

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

J. 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, Applied and Environmental Microbiology, vol.71, issue.11, pp.7217-7223, 2005.
DOI : 10.1128/AEM.71.11.7217-7223.2005

G. Favia, I. Ricci, C. Damiani, N. Raddadi, and E. Crotti, Bacteria of the genus Asaia stably associate with Anopheles stephensi, an Asian malarial mosquito vector, Proceedings of the National Academy of Sciences, vol.70, issue.5, pp.9047-9051, 2007.
DOI : 10.1128/AEM.70.5.2596-2602.2004

O. Terenius, C. De-oliveira, W. Pinheiro, W. Tadei, and A. James, 16S rRNA Gene Sequences from Bacteria Associated with Adult Anopheles darlingi (Diptera: Culicidae) Mosquitoes, Journal of Medical Entomology, vol.113, issue.1, pp.172-175, 2008.
DOI : 10.1016/S0166-6851(00)00387-X

J. Demaio, C. Pumpuni, M. Kent, and J. Beier, The Midgut Bacterial Flora of Wild Aedes triseriatus, Culex pipiens, and Psorophora columbiae Mosquitoes, The American Journal of Tropical Medicine and Hygiene, vol.54, issue.2, pp.219-223, 1996.
DOI : 10.4269/ajtmh.1996.54.219

P. Luxananil, H. Atomi, S. Panyim, and T. Imanaka, Isolation of bacterial strains colonizable in mosquito larval guts as novel host cells for mosquito control, Journal of Bioscience and Bioengineering, vol.92, issue.4, 2001.
DOI : 10.1016/S1389-1723(01)80237-1

D. Gusmao, A. Santos, D. Marini, R. Ede, S. Peixoto et al., First isolation of microorganisms from the gut diverticulum of Aedes aegypti (Diptera: Culicidae): new perspectives for an insect-bacteria association, Mem??rias do Instituto Oswaldo Cruz, vol.69, issue.8, pp.919-924, 2007.
DOI : 10.1016/j.femsyr.2004.10.008

S. Yoshida, D. Ioka, H. Matsuoka, H. Endo, and A. Ishii, Bacteria expressing single-chain immunotoxin inhibit malaria parasite development in mosquitoes, Molecular and Biochemical Parasitology, vol.113, issue.1, 2001.
DOI : 10.1016/S0166-6851(00)00387-X

M. Riehle and M. Jacobs-lorena, Using bacteria to express and display anti-parasite molecules in mosquitoes: current and future strategies, Insect Biochemistry and Molecular Biology, vol.35, issue.7, pp.699-707, 2005.
DOI : 10.1016/j.ibmb.2005.02.008

M. Riehle, C. Moreira, D. Lampe, C. Lauzon, and M. Jacobs-lorena, Using bacteria to express and display anti-Plasmodium molecules in the mosquito midgut, International Journal for Parasitology, vol.37, issue.6, pp.595-603, 2007.
DOI : 10.1016/j.ijpara.2006.12.002

P. Kittayapong, K. Baisley, V. Baimai, O. Neill, and S. , Distribution and Diversity of <I>Wolbachia</I> Infections in Southeast Asian Mosquitoes (Diptera: Culicidae), Journal of Medical Entomology, vol.37, issue.3, pp.340-345, 2000.
DOI : 10.1098/rspb.1998.0324

P. Kittayapong, V. Baimai, O. Neill, and S. , Field prevalence of Wolbachia in the mosquito vector Aedes albopictus., The American Journal of Tropical Medicine and Hygiene, vol.66, issue.1, pp.108-111, 2002.
DOI : 10.4269/ajtmh.2002.66.108

S. Sinkins, H. Braig, O. Neill, and S. , Wolbachia Superinfections and the Expression of Cytoplasmic Incompatibility, Proceedings of the Royal Society B: Biological Sciences, vol.261, issue.1362, pp.325-330, 1995.
DOI : 10.1098/rspb.1995.0154

S. Sinkins, H. Braig, O. Neill, and S. , Wolbachia pipientis: Bacterial Density and Unidirectional Cytoplasmic Incompatibility between Infected Populations of Aedes albopictus, Experimental Parasitology, vol.81, issue.3, pp.284-291, 1995.
DOI : 10.1006/expr.1995.1119

S. Dobson, E. Marsland, and W. Rattanadechakul, <I>Wolbachia</I>-Induced Cytoplasmic Incompatibility in Single- and Superinfected <I>Aedes albopictus</I> (Diptera: Culicidae), Journal of Medical Entomology, vol.38, issue.3, pp.382-387, 2001.
DOI : 10.1098/rspb.1998.0324

S. Dobson, E. Marsland, and W. Rattanadechakul, Mutualistic Wolbachia infection in Aedes: accelerating cytoplasmic drive, Genetics, vol.160, pp.1087-1094, 2002.

P. Ferree, H. Frydman, J. Li, J. Cao, and E. Wieschaus, Wolbachia Utilizes Host Microtubules and Dynein for Anterior Localization in the Drosophila Oocyte, PLoS Pathogens, vol.128, issue.2, p.14, 2005.
DOI : 10.1371/journal.ppat.0010014.sv002

V. Corby-harris, A. Pontaroli, L. Shimkets, J. Bennetzen, and K. Habel, Geographical Distribution and Diversity of Bacteria Associated with Natural Populations of Drosophila melanogaster, Applied and Environmental Microbiology, vol.73, issue.11, pp.3470-3479, 2007.
DOI : 10.1128/AEM.02120-06

M. Curley, C. Brodie, E. Lechner, M. Purcell, and A. , Exploration for facultative endosymbionts of Glass-Winged Sharpshooter (Hemiptera:Cicadellidae), 2007.

G. Favia, I. Ricci, M. Marzorati, I. Negri, and A. Alma, Bacteria of the Genus Asaia: A Potential Paratransgenic Weapon Against Malaria, Adv Exp Med Biol, vol.627, pp.49-59, 2008.
DOI : 10.1007/978-0-387-78225-6_4

R. Dillon and V. Dillon, : Nonpathogenic Interactions, Annual Review of Entomology, vol.49, issue.1, pp.71-92, 2004.
DOI : 10.1146/annurev.ento.49.061802.123416

Y. Kikuchi, T. Hosokawa, and T. Fukatsu, Insect-Microbe Mutualism without Vertical Transmission: a Stinkbug Acquires a Beneficial Gut Symbiont from the Environment Every Generation, Applied and Environmental Microbiology, vol.73, issue.13, pp.4308-4316, 2007.
DOI : 10.1128/AEM.00067-07

T. Fukatsu and T. Hosokawa, Capsule-Transmitted Gut Symbiotic Bacterium of the Japanese Common Plataspid Stinkbug, Megacopta punctatissima, Applied and Environmental Microbiology, vol.68, issue.1, pp.389-396, 2002.
DOI : 10.1128/AEM.68.1.389-396.2002

J. Lee, K. Lee, K. Kim, I. Hwang, and C. Jang, Acinetobacter antiviralis sp. nov., from Tobacco Plant Roots, Journal of Microbiology and Biotechnology, vol.19, issue.3, pp.250-256, 2009.
DOI : 10.4014/jmb.0901.083

O. Neill, S. Gooding, R. Aksoy, and S. , Phylogenetically distant symbiotic microorganisms reside in Glossina midgut and ovary tissues, Medical and Veterinary Entomology, vol.21, issue.4, pp.377-383, 1993.
DOI : 10.1016/0022-2011(81)90109-9

J. Werren, Wolbachia run amok, Proceedings of the National Academy of Sciences, vol.173, issue.2, pp.11154-11155, 1997.
DOI : 10.1128/jb.173.2.697-703.1991

URL : http://www.pnas.org/content/94/21/11154.full.pdf

M. Taylor and A. Hoerauf, Wolbachia Bacteria of Filarial Nematodes, Parasitology Today, vol.15, issue.11, pp.437-442, 1999.
DOI : 10.1016/S0169-4758(99)01533-1

Y. Otsuka and H. Takaota, Elimination of Wolbachia pipientis from Aedes albopictus, Medical Entomology and Zoology, vol.48, issue.3, pp.257-260, 1997.
DOI : 10.7601/mez.48.257

S. Dobson, W. Rattanadechakul, and E. Marsland, Fitness advantage and cytoplasmic incompatibility in Wolbachia single- and superinfected Aedes albopictus, Heredity, vol.265, issue.2, pp.135-142, 2004.
DOI : 10.1098/rspb.1998.0324

URL : http://www.nature.com/hdy/journal/v93/n2/pdf/6800458a.pdf

Z. Xi, C. Khoo, and S. Dobson, Wolbachia Establishment and Invasion in an Aedes aegypti Laboratory Population, Science, vol.310, issue.5746, pp.326-328, 2005.
DOI : 10.1126/science.1117607

S. Sinkins and I. Hastings, Male-specific insecticide resistance and mosquito transgene dispersal, Trends in Parasitology, vol.20, issue.9, pp.413-416, 2004.
DOI : 10.1016/j.pt.2004.07.003

S. Sinkins and H. Godfray, Use of Wolbachia to drive nuclear transgenes through insect populations, Proceedings of the Royal Society B: Biological Sciences, vol.271, issue.1546, pp.1421-1426, 1546.
DOI : 10.1098/rspb.2004.2740

Q. Cheng, T. Ruel, W. Zhou, S. Moloo, and P. Majiwa, Tissue distribution and prevalence of Wolbachia infections in tsetse flies, Glossina spp., Medical and Veterinary Entomology, vol.21, issue.1, pp.44-50, 2000.
DOI : 10.1098/rspb.1998.0324

H. Frydman, J. Li, D. Robson, and E. Wieschaus, Somatic stem cell niche tropism in Wolbachia, Nature, vol.18, issue.7092, pp.509-512, 2006.
DOI : 10.1089/104454999315178

S. Dobson, K. Bourtzis, H. Braig, B. Jones, and W. Zhou, Wolbachia infections are distributed throughout insect somatic and germ line tissues, Insect Biochemistry and Molecular Biology, vol.29, issue.2, pp.153-160, 1999.
DOI : 10.1016/S0965-1748(98)00119-2

N. Kondo, N. Ijichi, M. Shimada, and T. Fukatsu, Prevailing triple infection with Wolbachia in Callosobruchus chinensis (Coleoptera: Bruchidae), Molecular Ecology, vol.51, issue.2, pp.167-180, 2002.
DOI : 10.1098/rspb.1998.0324

J. Hotopp, M. Clark, D. Oliveira, J. Foster, and P. Fischer, Widespread Lateral Gene Transfer from Intracellular Bacteria to Multicellular Eukaryotes, Science, vol.267, issue.1, pp.1753-1756, 2007.
DOI : 10.1146/annurev.ento.42.1.587

URL : http://www.rifters.com/real/articles/Science_Wolbachia.pdf

N. Nikoh, K. Tanaka, F. Shibata, N. Kondo, and M. Hizume, Wolbachia genome integrated in an insect chromosome: Evolution and fate of laterally transferred endosymbiont genes, Genome Research, vol.18, issue.2, pp.272-280, 2008.
DOI : 10.1101/gr.7144908

W. Chen, K. Tsai, S. Cheng, C. Huang, and W. Wu, Using In Situ Hybridization to Detect Endosymbiont Wolbachia in Dissected Tissues of Mosquito Host, Journal of Medical Entomology, vol.265, issue.2, pp.120-124, 2005.
DOI : 10.1098/rspb.1998.0324

K. Tsai, C. Huang, W. Wu, C. Chuang, and C. Lin, Parallel Infection of Japanese Encephalitis Virus and <I>Wolbachia</I> within Cells of Mosquito Salivary Glands, Journal of Medical Entomology, vol.43, issue.4, pp.752-756, 2006.
DOI : 10.1016/0022-2011(73)90141-9

Z. Xi, L. Gavotte, Y. Xie, and S. Dobson, Genome-wide analysis of the interaction between the endosymbiotic bacterium Wolbachia and its Drosophila host, BMC Genomics, vol.9, issue.1, p.1, 2008.
DOI : 10.1186/1471-2164-9-1

C. Braquart-varnier, M. Lachat, J. Herbiniere, M. Johnson, and Y. Caubet, Wolbachia Mediate Variation of Host Immunocompetence, PLoS ONE, vol.7, issue.5, p.3286, 2008.
DOI : 10.1371/journal.pone.0003286.g005

URL : https://hal.archives-ouvertes.fr/hal-00325528

B. Pannebakker, B. Loppin, C. Elemans, L. Humblot, and F. Vavre, Parasitic inhibition of cell death facilitates symbiosis, Proceedings of the National Academy of Sciences, vol.5, issue.3, pp.213-215, 2007.
DOI : 10.1002/1097-0169(200103)48:3<224::AID-CM1011>3.0.CO;2-O

URL : https://hal.archives-ouvertes.fr/hal-00180908

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

K. Zouache, D. Voronin, T. Van, and P. Mavingui, Composition of Bacterial Communities Associated with Natural and Laboratory Populations of Asobara tabida Infected with Wolbachia, Applied and Environmental Microbiology, vol.75, issue.11, pp.3755-3764, 2009.
DOI : 10.1128/AEM.02964-08

A. Heddi, A. Grenier, C. Khatchadourian, H. Charles, and P. Nardon, Four intracellular genomes direct weevil biology: Nuclear, mitochondrial, principal endosymbiont, and Wolbachia, Proceedings of the National Academy of Sciences, vol.35, issue.5, pp.6814-6819, 1999.
DOI : 10.1007/BF00171817

URL : http://www.pnas.org/content/96/12/6814.full.pdf

H. Sanguin, A. Herrera, C. Oger-desfeux, A. Dechesne, and P. Simonet, Development and validation of a prototype 16S rRNA-based taxonomic microarray for Alphaproteobacteria, Environmental Microbiology, vol.51, issue.2, pp.289-307, 2006.
DOI : 10.1016/S0038-0717(03)00124-X

URL : https://hal.archives-ouvertes.fr/hal-00124522

M. Wagner, R. Erhart, W. Manz, R. Amann, and H. Lemmer, Development of an rRNA-targeted oligonucleotide probe specific for the genus Acinetobacter and its application for in situ monitoring in activated sludge, Appl Environ Microbiol, vol.60, pp.792-800, 1994.

T. Kenzaka, N. Yamaguchi, K. Tani, and M. Nasu, rRNA-targeted fluorescent in situ hybridization analysis of bacterial community structure in river water, Microbiology, vol.144, issue.8, pp.2085-2093, 1998.
DOI : 10.1099/00221287-144-8-2085

K. Bruce, W. Hiorns, J. Hobman, A. Osborn, and P. Strike, Amplification of DNA from native populations of soil bacteria by using the polymerase chain reaction, Appl Environ Microbiol, vol.58, pp.3413-3416, 1992.

G. Muyzer, E. De-waal, and A. Uitterlinden, Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA, Appl Environ Microbiol, vol.59, pp.695-700, 1993.

O. Neill, S. Giordano, R. Colbert, A. Karr, T. Robertson et al., 16S rRNA phylogenetic analysis of the bacterial endosymbionts associated with cytoplasmic incompatibility in insects., Proceedings of the National Academy of Sciences, vol.89, issue.7, pp.2699-2702, 1992.
DOI : 10.1073/pnas.89.7.2699

H. Braig, W. Zhou, S. Dobson, O. Neill, and S. , Cloning and characterization of a gene encoding the major surface protein of the bacterial endosymbiont Wolbachia pipientis, J Bacteriol, vol.180, pp.2373-2378, 1998.

W. Zhou, F. Rousset, O. Neil, and S. , Phylogeny and PCR-based classification of Wolbachia strains using wsp gene sequences, Proceedings of the Royal Society B: Biological Sciences, vol.265, issue.1395, pp.509-515, 1998.
DOI : 10.1098/rspb.1998.0324

F. Widmer, R. Seidler, P. Gillevet, L. Watrud, D. Giovanni et al., A highly selective PCR protocol for detecting 16S rRNA genes of the genus Pseudomonas (sensu stricto) in environmental samples, Appl Environ Microbiol, vol.64, pp.2545-2553, 1998.

P. Mavingui, V. Van, E. Labeyrie, E. Rances, and F. Vavre, Efficient Procedure for Purification of Obligate Intracellular Wolbachia pipientis and Representative Amplification of Its Genome by Multiple-Displacement Amplification, Applied and Environmental Microbiology, vol.71, issue.11, pp.6910-6917, 2005.
DOI : 10.1128/AEM.71.11.6910-6917.2005

URL : https://hal.archives-ouvertes.fr/hal-00427783