N. Moran, J. Mccutcheon, and A. Nakabachi, Genomics and Evolution of Heritable Bacterial Symbionts, Annual Review of Genetics, vol.42, issue.1, pp.165-90, 2008.
DOI : 10.1146/annurev.genet.41.110306.130119

A. Moya, J. Pereto, R. Gil, and A. Latorre, Learning how to live together: genomic insights into prokaryote???animal symbioses, Nature Reviews Genetics, vol.34, issue.3, pp.218-247, 2008.
DOI : 10.1038/nrg2319

M. Thao and P. Baumann, Evolutionary Relationships of Primary Prokaryotic Endosymbionts of Whiteflies and Their Hosts, Applied and Environmental Microbiology, vol.70, issue.6, pp.3401-3407, 2004.
DOI : 10.1128/AEM.70.6.3401-3406.2004

A. Wilson, P. Ashton, F. Calevro, H. Charles, S. Colella et al., Genomic insight into the amino acid relations of the pea aphid, Acyrthosiphon pisum, with its symbiotic bacterium Buchnera aphidicola, Insect Molecular Biology, vol.68, issue.2, pp.249-58, 2010.
DOI : 10.1111/j.1365-2583.2009.00942.x
URL : https://hal.archives-ouvertes.fr/hal-00539196

F. Husnik, N. Nikoh, R. Koga, L. Ross, R. Duncan et al., Horizontal Gene Transfer from Diverse Bacteria to an Insect Genome Enables a Tripartite Nested Mealybug Symbiosis, Cell, vol.153, issue.7, pp.1567-78, 2013.
DOI : 10.1016/j.cell.2013.05.040
URL : http://doi.org/10.1016/j.cell.2013.05.040

D. Sloan, A. Nakabachi, S. Richards, J. Qu, S. Murali et al., Parallel Histories of Horizontal Gene Transfer Facilitated Extreme Reduction of Endosymbiont Genomes in Sap-Feeding Insects, Molecular Biology and Evolution, vol.31, issue.4, pp.857-71, 2014.
DOI : 10.1093/molbev/msu004

S. Shigenobu, H. Watanabe, M. Hattori, Y. Sakaki, and H. Ishikawa, Genome sequence of the endocellular bacterial symbiont of aphids Buchnera sp, APS Nature, vol.407, pp.81-87, 2000.

V. Perez-brocal, R. Gil, S. Ramos, A. Lamelas, M. Postigo et al., A Small Microbial Genome: The End of a Long Symbiotic Relationship?, Science, vol.314, issue.5797, pp.312-315, 2006.
DOI : 10.1126/science.1130441

D. Sloan and N. Moran, Genome Reduction and Co-evolution between the Primary and Secondary Bacterial Symbionts of Psyllids, Molecular Biology and Evolution, vol.29, issue.12, pp.3781-92, 2012.
DOI : 10.1093/molbev/mss180

D. Sloan and N. Moran, Endosymbiotic bacteria as a source of carotenoids in whiteflies, Biology Letters, vol.330, issue.6007, pp.986-995, 2012.
DOI : 10.1126/science.1195463

D. Sloan and N. Moran, The Evolution of Genomic Instability in the Obligate Endosymbionts of Whiteflies, Genome Biology and Evolution, vol.5, issue.5, pp.783-93, 2013.
DOI : 10.1093/gbe/evt044

D. Santos-garcia, P. Farnier, F. Beitia, E. Zchori-fein, F. Vavre et al., Complete Genome Sequence of "Candidatus Portiera aleyrodidarum" BT-QVLC, an Obligate Symbiont That Supplies Amino Acids and Carotenoids to Bemisia tabaci, Journal of Bacteriology, vol.194, issue.23, pp.6654-6659, 2012.
DOI : 10.1128/JB.01793-12
URL : https://hal.archives-ouvertes.fr/hal-00763436

J. Mccutcheon and C. Von-dohlen, An Interdependent Metabolic Patchwork in the Nested Symbiosis of Mealybugs, Current Biology, vol.21, issue.16, pp.1366-72, 2011.
DOI : 10.1016/j.cub.2011.06.051

S. Lopez-madrigal, A. Latorre, M. Porcar, A. Moya, and R. Gil, Mealybugs nested endosymbiosis: going into the ???matryoshka??? system in Planococcus citri in depth, BMC Microbiology, vol.13, issue.1, p.74, 2013.
DOI : 10.1093/nar/gkf436

E. Zchori-fein and K. Bourtzis, Manipulative tenants: bacteria associated with arthropods, Boca Raton, 2012.

S. Sintupachee, J. Milne, S. Poonchaisri, V. Baimai, and P. Kittayapong, Closely Related Wolbachia Strains within the Pumpkin Arthropod Community and the Potential for Horizontal Transmission via the Plant, Microbial Ecology, vol.265, issue.3, pp.294-301, 2006.
DOI : 10.1007/s00248-006-9036-x

E. Chiel, E. Zchori-fein, M. Inbar, Y. Gottlieb, T. Adachi-hagimori et al., Almost There: Transmission Routes of Bacterial Symbionts between Trophic Levels, PLoS ONE, vol.36, issue.3, p.4767, 2009.
DOI : 10.1371/journal.pone.0004767.g007

P. Degnan, Y. Yu, N. Sisneros, R. Wing, and N. Moran, Hamiltonella defensa, genome evolution of protective bacterial endosymbiont from pathogenic ancestors, Proceedings of the National Academy of Sciences, vol.18, issue.3, pp.9063-9071, 2009.
DOI : 10.1093/bioinformatics/18.3.502
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690004

A. Lamelas, M. Gosalbes, A. Manzano-marin, J. Pereto, A. Moya et al., Serratia symbiotica from the Aphid Cinara cedri: A Missing Link from Facultative to Obligate Insect Endosymbiont, PLoS Genetics, vol.5, issue.11, p.1002357, 2011.
DOI : 10.1371/journal.pgen.1002357.s006

D. Wu, S. Daugherty, S. Van-aken, G. Pai, K. Watkins et al., Metabolic Complementarity and Genomics of the Dual Bacterial Symbiosis of Sharpshooters, PLoS Biology, vol.33, issue.6, pp.1079-92, 2006.
DOI : 10.1371/journal.pbio.0040188.st002

J. Mccutcheon, B. Mcdonald, and N. Moran, Convergent evolution of metabolic roles in bacterial co-symbionts of insects, Proceedings of the National Academy of Sciences, vol.94, issue.22, pp.15394-15403, 2009.
DOI : 10.1073/pnas.94.22.11819

J. Mccutcheon and N. Moran, Functional convergence in reduced genomes of bacterial symbionts spanning 200 My of evolution, Genome Biol Evol, vol.2, pp.708-726, 2010.

G. Bennett and N. Moran, Small, Smaller, Smallest: The Origins and Evolution of Ancient Dual Symbioses in a Phloem-Feeding Insect, Genome Biology and Evolution, vol.5, issue.9, pp.1675-88, 2013.
DOI : 10.1093/gbe/evt118

J. Ferrari and F. Vavre, Bacterial symbionts in insects or the story of communities affecting communities, Philosophical Transactions of the Royal Society B: Biological Sciences, vol.326, issue.5949, pp.1389-400, 2011.
DOI : 10.1126/science.1177531
URL : https://hal.archives-ouvertes.fr/hal-00784710

E. Vautrin and F. Vavre, Interactions between vertically transmitted symbionts: cooperation or conflict? Trends in Microbiol, pp.95-104, 2009.

E. Vautrin, S. Genieys, S. Charles, and F. Vavre, Do vertically transmitted symbionts co-existing in a single host compete or cooperate? A modelling approach, Journal of Evolutionary Biology, vol.95, issue.1, pp.145-61, 2008.
DOI : 10.1111/j.1420-9101.2007.01460.x
URL : https://hal.archives-ouvertes.fr/hal-00428181

A. Dinsdale, L. Cook, C. Riginos, Y. Buckley, and P. Barro, Refined Global Analysis of <I>Bemisia tabaci</I> (Hemiptera: Sternorrhyncha: Aleyrodoidea: Aleyrodidae) Mitochondrial Cytochrome Oxidase 1 to Identify Species Level Genetic Boundaries, Annals of the Entomological Society of America, vol.103, issue.2, pp.196-208, 2010.
DOI : 10.1603/AN09061.s1

D. Barro, P. Liu, S. Boykin, L. Dinsdale, and A. , : A Statement of Species Status, Annual Review of Entomology, vol.56, issue.1, pp.1-19, 2011.
DOI : 10.1146/annurev-ento-112408-085504

J. Hu, D. Barro, P. Zhao, H. Wang, J. Nardi et al., An Extensive Field Survey Combined with a Phylogenetic Analysis Reveals Rapid and Widespread Invasion of Two Alien Whiteflies in China, PLoS ONE, vol.99, issue.1), p.16061, 2011.
DOI : 10.1371/journal.pone.0016061.s002

Y. Gottlieb, M. Ghanim, G. Gueguen, S. Kontsedalov, F. Vavre et al., Inherited intracellular ecosystem: symbiotic bacteria share bacteriocytes in whiteflies, The FASEB Journal, vol.22, issue.7, pp.2591-2600, 2008.
DOI : 10.1096/fj.07-101162
URL : https://hal.archives-ouvertes.fr/hal-00428116

P. Baumann, BIOLOGY OF BACTERIOCYTE-ASSOCIATED ENDOSYMBIONTS OF PLANT SAP-SUCKING INSECTS, Annual Review of Microbiology, vol.59, issue.1, pp.155-89, 2005.
DOI : 10.1146/annurev.micro.59.030804.121041

A. Mahadav, D. Gerling, Y. Gottlieb, H. Czosnek, and M. Ghanim, Parasitization by the wasp Eretmocerus mundus induces transcription of genes related to immune response and symbiotic bacteria proliferation in the whitefly Bemisia tabaci, BMC Genomics, vol.9, issue.1, p.342, 2008.
DOI : 10.1186/1471-2164-9-342

M. Brumin, S. Kontsedalov, and M. Ghanim, Rickettsia influences thermotolerance in the whitefly Bemisia tabaci B biotype, Insect Science, vol.398, issue.273, pp.57-66, 2011.
DOI : 10.1111/j.1744-7917.2010.01396.x

M. Ghanim and S. Kontsedalov, is correlated with bacterial symbiont densities, Pest Management Science, vol.60, issue.9, pp.939-981, 2009.
DOI : 10.1002/ps.1795

X. Bing, J. Yang, E. Zchori-fein, X. Wang, and S. Liu, Characterization of a Newly Discovered Symbiont of the Whitefly Bemisia tabaci (Hemiptera: Aleyrodidae), Applied and Environmental Microbiology, vol.79, issue.2
DOI : 10.1128/AEM.03030-12

Q. Su, W. Xie, S. Wang, Q. Wu, B. Liu et al., The Endosymbiont Hamiltonella Increases the Growth Rate of Its Host Bemisia tabaci during Periods of Nutritional Stress, PLoS ONE, vol.70, issue.2, p.89002, 2014.
DOI : 10.1371/journal.pone.0089002.s001

Q. Rao, C. Luo, H. Zhang, X. Guo, and G. Devine, Distribution and dynamics of Bemisia tabaci invasive biotypes in central China, Bulletin of Entomological Research, vol.48, issue.01, pp.81-89, 2011.
DOI : 10.1111/j.1744-7917.2008.00191.x

Q. Rao, Y. Xu, C. Luo, H. Zhang, C. Jones et al., Characterisation of Neonicotinoid and Pymetrozine Resistance in Strains of Bemisia tabaci (Hemiptera: Aleyrodidae) from China, Journal of Integrative Agriculture, vol.11, issue.2, pp.321-327, 2012.
DOI : 10.1016/S2095-3119(12)60016-1

G. Gueguen, F. Vavre, O. Gnankine, M. Peterschmitt, D. Charif et al., Endosymbiont metacommunities, mtDNA diversity and the evolution of the Bemisia tabaci (Hemiptera: Aleyrodidae) species complex, Molecular Ecology, vol.95, issue.19, pp.4365-78, 2010.
DOI : 10.1111/j.1365-294X.2010.04775.x
URL : https://hal.archives-ouvertes.fr/hal-00746855

J. Sandstrom, J. Russell, J. White, and N. Moran, Independent origins and horizontal transfer of bacterial symbionts of aphids, Molecular Ecology, vol.16, issue.1, pp.217-245, 2001.
DOI : 10.1006/viro.1999.9902

N. Moran, J. Russell, R. Koga, and T. Fukatsu, Evolutionary Relationships of Three New Species of Enterobacteriaceae Living as Symbionts of Aphids and Other Insects, Applied and Environmental Microbiology, vol.71, issue.6, pp.3302-3312, 2005.
DOI : 10.1128/AEM.71.6.3302-3310.2005

A. Nakabachi, A. Yamashita, H. Toh, H. Ishikawa, H. Dunbar et al., The 160-Kilobase Genome of the Bacterial Endosymbiont Carsonella, Science, vol.314, issue.5797, p.267, 2006.
DOI : 10.1126/science.1134196

J. Mccutcheon, B. Mcdonald, and N. Moran, Origin of an Alternative Genetic Code in the Extremely Small and GC???Rich Genome of a Bacterial Symbiont, PLoS Genetics, vol.4, issue.7, p.1000565, 2009.
DOI : 10.1371/journal.pgen.1000565.s003

Z. Sabree, C. Huang, A. Okusu, N. Moran, and B. Normark, , an endosymbiont of armoured scale insects, Environmental Microbiology, vol.65, issue.Suppl. 1, pp.1988-99, 2013.
DOI : 10.1111/1462-2920.12058

Z. Jiang, F. Xia, K. Johnson, E. Bartom, J. Tuteja et al., Comparison of the Genome Sequences of "Candidatus Portiera aleyrodidarum" Primary Endosymbionts of the Whitefly Bemisia tabaci B and Q Biotypes, Applied and Environmental Microbiology, vol.79, issue.5, pp.6678-6687, 2012.
DOI : 10.1128/AEM.02976-12

R. Tatusov, E. Koonin, and D. Lipman, A Genomic Perspective on Protein Families, Science, vol.278, issue.5338, pp.631-638, 1997.
DOI : 10.1126/science.278.5338.631

I. Tamas, J. Wernegreen, B. Nystedt, S. Kauppinen, A. Darby et al., Endosymbiont gene functions impaired and rescued by polymerase infidelity at poly(A) tracts, Proceedings of the National Academy of Sciences, vol.53, issue.13, pp.14934-14943, 2008.
DOI : 10.1186/1471-2148-4-18
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567471

X. Wang, J. Luan, J. Li, Y. Bao, C. Zhang et al., De novo characterization of a whitefly transcriptome and analysis of its gene expression during development, BMC Genomics, vol.11, issue.1, p.400, 2010.
DOI : 10.1186/1471-2164-11-400

M. Lopez-sanchez, A. Neef, J. Pereto, R. Patino-navarrete, M. Pignatelli et al., Evolutionary Convergence and Nitrogen Metabolism in Blattabacterium strain Bge, Primary Endosymbiont of the Cockroach Blattella germanica, PLoS Genetics, vol.15, issue.11, p.1000721, 2009.
DOI : 10.1371/journal.pgen.1000721.s005

H. Charles, S. Balmand, A. Lamelas, L. Cottret, V. Perez-brocal et al., A Genomic Reappraisal of Symbiotic Function in the Aphid/Buchnera Symbiosis: Reduced Transporter Sets and Variable Membrane Organisations, PLoS ONE, vol.327, issue.12, p.29096, 2011.
DOI : 10.1371/journal.pone.0029096.s004
URL : https://hal.archives-ouvertes.fr/hal-00850377

A. Hansen and N. Moran, The impact of microbial symbionts on host plant utilization by herbivorous insects, Molecular Ecology, vol.4, issue.Suppl 2, pp.1473-96, 2014.
DOI : 10.1111/mec.12421

C. Russell, S. Bouvaine, P. Newell, and A. Douglas, Shared Metabolic Pathways in a Coevolved Insect-Bacterial Symbiosis, Applied and Environmental Microbiology, vol.79, issue.19, pp.6117-6140, 2013.
DOI : 10.1128/AEM.01543-13

A. Douglas, Phloem-sap feeding by animals: problems and solutions, Journal of Experimental Botany, vol.57, issue.4, pp.747-54, 2006.
DOI : 10.1093/jxb/erj067
URL : http://jxb.oxfordjournals.org/cgi/content/short/57/4/747

N. Moran and T. Jarvik, Lateral Transfer of Genes from Fungi Underlies Carotenoid Production in Aphids, Science, vol.105, issue.46, pp.624-631, 2010.
DOI : 10.1073/pnas.0804968105

Q. Ren and I. Paulsen, Comparative Analyses of Fundamental Differences in Membrane Transport Capabilities in Prokaryotes and Eukaryotes, PLoS Computational Biology, vol.95, issue.3, p.27, 2005.
DOI : 10.1371/journal.pcbi.0010027.st001

D. Price, H. Feng, J. Baker, S. Bavan, C. Luetje et al., Aphid amino acid transporter regulates glutamine supply to intracellular bacterial symbionts, Proceedings of the National Academy of Sciences, vol.59, issue.1, pp.320-325, 2014.
DOI : 10.1369/jhc.2010.956920
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890774

B. Wallace, Y. Yang, J. Hong, and D. Lum, Cloning and sequencing of a gene encoding a glutamate and aspartate carrier of Escherichia coli K-12., Journal of Bacteriology, vol.172, issue.6, pp.3214-3234, 1990.
DOI : 10.1128/jb.172.6.3214-3220.1990

M. Nandineni and J. Gowrishankar, Evidence for an Arginine Exporter Encoded by yggA (argO) That Is Regulated by the LysR-Type Transcriptional Regulator ArgP in Escherichia coli, Journal of Bacteriology, vol.186, issue.11, pp.3539-3585, 2004.
DOI : 10.1128/JB.186.11.3539-3546.2004

V. Martin and W. Mohn, Genetic Investigation of the Catabolic Pathway for Degradation of Abietane Diterpenoids by Pseudomonas abietaniphila BKME-9, Journal of Bacteriology, vol.182, issue.13
DOI : 10.1128/JB.182.13.3784-3793.2000

D. Barro, P. Driver, and F. , Use of RAPD PCR to Distinguish the B Biotype from Other Biotypes of Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae), Australian Journal of Entomology, vol.38, issue.2, pp.149-52, 1997.
DOI : 10.1007/BF00554731

Y. Gottlieb, M. Ghanim, E. Chiel, D. Gerling, V. Portnoy et al., Identification and Localization of a Rickettsia sp. in Bemisia tabaci (Homoptera: Aleyrodidae), Applied and Environmental Microbiology, vol.72, issue.5, pp.3646-52, 2006.
DOI : 10.1128/AEM.72.5.3646-3652.2006

T. Woyke, D. Tighe, K. Mavromatis, A. Clum, A. Copeland et al., One Bacterial Cell, One Complete Genome, PLoS ONE, vol.5, issue.4, p.10314, 2010.
DOI : 10.1371/journal.pone.0010314.s005
URL : http://doi.org/10.1371/journal.pone.0010314

E. Zchori-fein and J. Brown, Diversity of Prokaryotes Associated with <I>Bemisia tabaci</I> (Gennadius) (Hemiptera: Aleyrodidae), Annals of the Entomological Society of America, vol.95, issue.6, pp.711-719, 2002.
DOI : 10.1603/0013-8746(2002)095[0711:DOPAWB]2.0.CO;2

M. Ghanim, I. Sobol, M. Ghanim, and H. Czosnek, Horizontal transmission of begomoviruses between Bemisia tabaci biotypes, Arthropod-Plant Interactions, vol.72, issue.3, pp.195-204, 2007.
DOI : 10.1007/s11829-007-9018-z

E. Lerat and H. Ochman, Recognizing the pseudogenes in bacterial genomes, Nucleic Acids Research, vol.33, issue.10, pp.3125-3157, 2005.
DOI : 10.1093/nar/gki631
URL : https://hal.archives-ouvertes.fr/hal-00427776

K. Lagesen, P. Hallin, E. Rodland, H. Staerfeldt, T. Rognes et al., RNAmmer: consistent and rapid annotation of ribosomal RNA genes, Nucleic Acids Research, vol.35, issue.9, pp.3100-3108, 2007.
DOI : 10.1093/nar/gkm160
URL : http://doi.org/10.1093/nar/gkm160

P. Schattner, A. Brooks, and T. Lowe, The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs, Nucleic Acids Research, vol.33, issue.Web Server, pp.686-689, 2005.
DOI : 10.1093/nar/gki366

F. Silva, E. Belda, and S. Talens, Differential annotation of tRNA genes with anticodon CAT in bacterial genomes, Nucleic Acids Research, vol.34, issue.20, pp.6015-6037, 2006.
DOI : 10.1093/nar/gkl739

Y. Moriya, M. Itoh, S. Okuda, A. Yoshizawa, and M. Kanehisa, KAAS: an automatic genome annotation and pathway reconstruction server, Nucleic Acids Research, vol.35, issue.Web Server, pp.182-185, 2007.
DOI : 10.1093/nar/gkm321
URL : http://doi.org/10.1093/nar/gkm321

P. Karp, S. Paley, and P. Romero, The Pathway Tools software, Bioinformatics, vol.18, issue.Suppl 1, pp.225-232, 2002.
DOI : 10.1093/bioinformatics/18.suppl_1.S225
URL : http://bioinformatics.oxfordjournals.org/cgi/content/short/18/suppl_1/S225

L. Cottret, D. Wildridge, F. Vinson, M. Barrett, H. Charles et al., MetExplore: a web server to link metabolomic experiments and genome-scale metabolic networks, Nucleic Acids Research, vol.38, issue.Web Server, pp.132-137, 2010.
DOI : 10.1093/nar/gkq312
URL : https://hal.archives-ouvertes.fr/hal-00690651

M. Smoot, K. Ono, J. Ruscheinski, P. Wang, and T. Ideker, Cytoscape 2.8: new features for data integration and network visualization, Bioinformatics, vol.27, issue.3, pp.431-433, 2011.
DOI : 10.1093/bioinformatics/btq675

E. Borenstein, M. Kupiec, M. Feldman, and E. Ruppin, Large-scale reconstruction and phylogenetic analysis of metabolic environments, Proceedings of the National Academy of Sciences, vol.13, issue.10, pp.14482-14489, 2008.
DOI : 10.1101/gr.1589103

G. Csardi and T. Nepusz, The igraph software package for complex network research, Complex Systems: Inter Journal, 2012.

Q. Rao, S. Wang, Y. Su, X. Bing, S. Liu et al., Draft Genome Sequence of "Candidatus Hamiltonella defensa," an Endosymbiont of the Whitefly Bemisia tabaci, Journal of Bacteriology, vol.194, issue.13, p.3558, 2012.
DOI : 10.1128/JB.00069-12

H. Ogata, L. Scola, B. Audic, S. Renesto, P. Blanc et al., Genome Sequence of Rickettsia bellii Illuminates the Role of Amoebae in Gene Exchanges between Intracellular Pathogens, PLoS Genetics, vol.36, issue.5, p.76, 2006.
DOI : 10.1371/journal.pgen.0020076.st008

M. Wu, L. Sun, J. Vamathevan, M. Riegler, R. Deboy et al., Phylogenomics of the Reproductive Parasite Wolbachia pipientis wMel: A Streamlined Genome Overrun by Mobile Genetic Elements, PLoS Biology, vol.265, issue.3, p.69, 2004.
DOI : 10.1371/journal.pbio.0020069.st009

A. Nakabachi, R. Ueoka, K. Oshima, R. Teta, A. Mangoni et al., Defensive Bacteriome Symbiont with a Drastically Reduced Genome, Current Biology, vol.23, issue.15, pp.1478-84, 2013.
DOI : 10.1016/j.cub.2013.06.027
URL : http://doi.org/10.1016/j.cub.2013.06.027

F. Blattner, G. Plunkett-3rd, C. Bloch, N. Perna, V. Burland et al., The Complete Genome Sequence of Escherichia coli K-12, Science, vol.277, issue.5331, pp.1453-62, 1997.
DOI : 10.1126/science.277.5331.1453

H. Toh, B. Weiss, S. Perkin, A. Yamashita, K. Oshima et al., 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.149-56, 2006.
DOI : 10.1101/gr.4106106

P. Degnan, A. Lazarus, and J. Wernegreen, Genome sequence of Blochmannia pennsylvanicus indicates parallel evolutionary trends among bacterial mutualists of insects, Genome Research, vol.15, issue.8, pp.1023-1056, 2005.
DOI : 10.1101/gr.3771305

R. Gil, F. Silva, E. Zientz, F. Delmotte, F. Gonzalez-candelas et al., The genome sequence of Blochmannia floridanus: Comparative analysis of reduced genomes, Proceedings of the National Academy of Sciences, vol.182, issue.3, pp.9388-93, 2003.
DOI : 10.1006/jtbi.1996.0168

J. Mccutcheon and N. Moran, Parallel genomic evolution and metabolic interdependence in an ancient symbiosis, Proceedings of the National Academy of Sciences, vol.5, issue.22, pp.19392-19399, 2007.
DOI : 10.1093/nar/22.22.4673

E. Zientz, T. Dandekar, and R. Gross, Metabolic Interdependence of Obligate Intracellular Bacteria and Their Insect Hosts, Microbiology and Molecular Biology Reviews, vol.68, issue.4, pp.745-70, 2004.
DOI : 10.1128/MMBR.68.4.745-770.2004

L. Cottret, P. Milreu, V. Acuña, A. Marchetti-spaccamela, L. Stougie et al., Graph-Based Analysis of the Metabolic Exchanges between Two Co-Resident Intracellular Symbionts, Baumannia cicadellinicola and Sulcia muelleri, with Their Insect Host, Homalodisca coagulata, PLoS Computational Biology, vol.106, issue.9, p.1000904, 2010.
DOI : 10.1371/journal.pcbi.1000904.s030
URL : https://hal.archives-ouvertes.fr/hal-00690650

H. Lin, B. Lou, J. Glynn, H. Doddapaneni, E. Civerolo et al., The Complete Genome Sequence of ???Candidatus Liberibacter solanacearum???, the Bacterium Associated with Potato Zebra Chip Disease, PLoS ONE, vol.10, issue.4, p.19135, 2011.
DOI : 10.1371/journal.pone.0019135.s013