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Accueil Tous les numéros Volume 27 / Numéro 11 (Novembre 2011) Med Sci (Paris), 27 11 (2011) 953-958 Références
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Numéro
Med Sci (Paris)
Volume 27, Numéro 11, Novembre 2011
Page(s) 953 - 958
Section M/S Revues
DOI https://doi.org/10.1051/medsci/20112711010
Publié en ligne 30 novembre 2011
  1. Backhed F, Ley R, Sonnenburg J, et al. Host-bacterial mutualism in the human intestine. Science 2005 ; 307 : 1915–1920. [CrossRef] [PubMed] [Google Scholar]
  2. Ley R, Peterson D, Gordon J. Ecological and evolutionary forces shaping microbial diversity in the human intestine. Cell 2006 ; 124 : 837–848. [CrossRef] [PubMed] [Google Scholar]
  3. Swynghedauw B. L’évolution biologique : grande oubliée de l’enseignement médical et base rationnelle d’une politique de santé. Med Sci (Paris) 2010 ; 26 : 526–528. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  4. Moran NA, Wernegreen JJ. Lifestyle evolution in symbiotic bacteria: insights from genomics. Trends Ecol Evol 2000 ; 15 : 321–326. [NASA ADS] [CrossRef] [EDP Sciences] [MathSciNet] [PubMed] [Google Scholar]
  5. Hilgenboecker K, Hammerstein P, Schlattmann P, et al. How many species are infected with Wolbachia? A statistical analysis of current data. Fems Microbiol Lett 2008 ; 281 : 215–220. [CrossRef] [PubMed] [Google Scholar]
  6. Baumann P. Biology of bacteriocyte-associated endosymbionts of plant sap-sucking insects. Annu Rev Microbiol 2005 ; 59 : 155–189. [CrossRef] [PubMed] [Google Scholar]
  7. Engelstädter J, Hurst GDD. The ecology and evolution of microbes that manipulate host reproduction. Annu Rev Ecol Evol Syst 2009 ; 40 : 127–149. [CrossRef] [Google Scholar]
  8. Brownlie JC, Johnson KN. Symbiont-mediated protection in insect hosts. Trends Microbiol 2009 ; 17 : 348–354. [CrossRef] [PubMed] [Google Scholar]
  9. Aksoy S. Tsetse: a haven for microorganisms. Parasitol Today 2000 ; 16 : 114–118. [CrossRef] [PubMed] [Google Scholar]
  10. Taylor MJ, Bandi C, Hoerauf A. Wolbachia bacterial endosymbionts of filarial nematodes. Adv Parasitol 2005 ; 60 : 245–284. [CrossRef] [PubMed] [Google Scholar]
  11. Langworthy NG, Renz A, Mackenstedt U, et al. Macrofilaricidal activity of tetracycline against the filarial nematode Onchocerca ochengi: elimination of Wolbachia precedes worm death and suggests a dependent relationship. Proc R S Lond S B Biol Sci 2000 ; 267 : 1063–1069. [CrossRef] [Google Scholar]
  12. Foster J, Ganatra M, Kamal I, et al. The Wolbachia genome of Brugia malayi: Endosymbiont evolution within a human pathogenic nematode. PLoS Biol 2005 ; 3 : e121. [CrossRef] [PubMed] [Google Scholar]
  13. Sironi M, Bandi C, Sacchi L, et al. Molecular evidence for a close relative of the arthropod endosymbiont Wolbachia in a filarial worm. Mol Biochem Parasitol 1995 ; 74 : 223–227. [CrossRef] [PubMed] [Google Scholar]
  14. Saint Andre AV, Blackwell NM, Hall LR, et al. The role of endosymbiotic Wolbachia bacteria in the pathogenesis of river blindness. Science 2002 ; 295 : 1892–1895. [CrossRef] [PubMed] [Google Scholar]
  15. Taylor MJ, Makunde WH, McGarry HF, et al. Macrofilaricidal activity after doxycycline treatment of Wuchereria bancrofti: a double-blind, randomised placebo-control led trial. Lancet 2005 ; 365 : 2116–2121. [CrossRef] [PubMed] [Google Scholar]
  16. Hoerauf A, Specht S, Buttner M, et al. Wolbachia endobacteria depletion by doxycycline as antifilarial therapy has macrofilaricidal activity in onchocerciasis: a randomized placebo-controlled study. Med Microbiol Immunol 2008 ; 197 : 295–311. [CrossRef] [PubMed] [Google Scholar]
  17. Debrah A, Mand S, Marfo-Debrekyei Y, et al. Macrofilaricidal effect of 4 weeks of treatment with doxycycline on Wuchereria bancrofti. Trop Med Int Health 2007 ; 12 : 1433–1441. [NASA ADS] [CrossRef] [EDP Sciences] [MathSciNet] [PubMed] [Google Scholar]
  18. Taylor M, Hoerauf A, Bockarie M. Lymphatic filariasis and onchocerciasis. Lancet 2010 ; 376 : 1175–1185. [CrossRef] [PubMed] [Google Scholar]
  19. Moran NA, Degnan PH, Santos SR, et al. The players in a mutualistic symbiosis: insects, bacteria, viruses, and virulence genes. Proc Natl Acad Sci USA 2005 ; 102 : 16919–16926. [CrossRef] [Google Scholar]
  20. Oliver KM, Degnan PH, Hunter MS, Moran NS. Bacteriophages encode factors required for protection in a symbiotic mutualism. Science 2009 ; 325 : 992–994. [CrossRef] [PubMed] [Google Scholar]
  21. Zouache K, Voronin D, Tran-Van V, et al. Persistent Wolbachia and cultivable bacteria infection in the reproductive, somatic tissues of the mosquito vector Aedes albopictus. PLoS One 2009 ; 4 : e6388. [CrossRef] [PubMed] [Google Scholar]
  22. Moreira LA, Iturbe-Ormaetxe I, Jeffery JA, et al. A Wolbachia symbiont in Aedes aegypti limits infection with dengue, Chikungunya, and Plasmodium. Cell 2009 ; 139 : 1268–1278. [CrossRef] [PubMed] [Google Scholar]
  23. Wang JW, Wu YN, Yang GX, Aksoy S. Interactions between mutualist Wigglesworthia and tsetse peptidoglycan recognition protein (PGRP-LB) influence trypanosome transmission. Proc Natl Acad Sci USA 2009 ; 106 : 12133–12138. [CrossRef] [Google Scholar]
  24. McMeniman CJ, Lane RV, Cass BN, et al. Stable introduction of a life-shortening Wolbachia infection into the mosquito Aedes aegypti. Science 2009 ; 323 : 141–144. [CrossRef] [PubMed] [Google Scholar]
  25. Kambris Z, Cook PE, Phuc HK, Sinkins SP. Immune activation by life-shortening Wolbachia and reduced filarial competence in mosquitoes. Science 2009 ; 326 : 134–136. [CrossRef] [PubMed] [Google Scholar]
  26. Bian G, Xu Y, Lu P, et al. The endosymbiotic bacterium Wolbachia induces resistance to dengue virus in Aedes aegypti. PLoS Pathog 2010 ; 6 : e1000833. [CrossRef] [PubMed] [Google Scholar]
  27. Bourtzis K, Pettigrew MM, O’Neill SL. Wolbachia neither induces nor suppresses transcripts encoding antimicrobial peptides. Insect Mol Biol 2000 ; 9 : 635–639. [CrossRef] [PubMed] [Google Scholar]
  28. Mousson L, Martin E, Zouache K, et al. Wolbachia modulates Chikungunya replication in Aedes albopictus. Mol Ecol 2010 ; 19 : 1953–1964. [CrossRef] [PubMed] [Google Scholar]
  29. Teixeira L, Ferreira A, Ashburner M. The bacterial symbiont Wolbachia induces resistance to RNA viral infections in Drosophila melanogaster. PLoS Biol 2008 ; 6 : e1000002. [CrossRef] [Google Scholar]
  30. Hedges LM, Brownlie JC, O’Neill SL, Johnson KN. Wolbachia and virus protection in insects. Science 2008 ; 322 : 702. [CrossRef] [PubMed] [Google Scholar]
  31. Glaser R, Meola M. The native Wolbachia endosymbionts of Drosophila melanogaster and Culex quinquefasciatus increase host resistance to West Nile virus infection. PLoS One 2010 ; 5 : e11977. [CrossRef] [PubMed] [Google Scholar]
  32. Lanteri MC, Assal A, Norris PJ, Busch MP. Le virus West Nile. I. La conquête de l’Ouest. Med Sci (Paris) 2011 ; 27 : 375–381. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  33. Lanteri MC, Diamond MS, Norris PJ, Busch MP. Infection par le virus West Nile chez l’homme. II. Aspects physiopathologiques et réponses immunitaires. Med Sci (Paris) 2011 ; 27 : 382–386. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  34. Martinez J. Wolbachia: une nouvelle arme dans la lutte contre le virus de la dengue. Med Sci (Paris) 2011 ; 27 : 947. [Google Scholar]
  35. Kremer N, Charif D, Henri H, et al. A new case of Wolbachia dependence in the genus Asobara: evidence for parthenogenesis induction in Asobara japonica. Heredity 2009 ; 103 : 248–256. [CrossRef] [PubMed] [Google Scholar]
  36. Favia G, Ricci I, Damiani C, et al. Bacteria of the genus Asaia stably associate with Anopheles stephensi, an Asian malarial mosquito vector. Proc Natl Acad Sci USA 2007 ; 104 : 9047–9051. [CrossRef] [Google Scholar]
  37. Klassen W, Curtis C. History of the sterile insect technique. In : Dyck VA, Hendrichs J, Robinson AS, eds. Sterile insect technique. Principles and practice in area-wide integrated pest management. Dordrecht : Springer, 2005 : 3–31. [Google Scholar]
  38. Laven H. Eradication of Culex pipiens fatigans through cytoplasmic incompatibility. Nature 1967 ; 216 : 383–384. [CrossRef] [PubMed] [Google Scholar]
  39. Zabalou S, Riegler M, Theodorakopoulou M, et al. Wolbachia-induced cytoplasmic incompatibility as a means for insect pest population control. Proc Natl Acad Sci USA 2004 ; 101 : 15042–15045. [CrossRef] [Google Scholar]
  40. Brelsfoard C, St Clair W, Dobson S. Integration of irradiation with cytoplasmic incompatibility to facilitate a lymphatic filariasis vector elimination approach. Parasit Vectors 2009 ; 2 : 38. [NASA ADS] [CrossRef] [EDP Sciences] [MathSciNet] [PubMed] [Google Scholar]

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