Quantitative genetics of Aedes aegypti vector competence for dengue viruses: Towards a new paradigm?

Trends in Parasitology

Volumn 27, Issue 3, 2011, Pages 111-114

  Lambrechts, Louis ^a  

^a INSTITUT PASTEUR   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AEDES AEGYPTI; DENGUE VIRUS; GENE FREQUENCY; GENE INTERACTION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HOST PARASITE INTERACTION; NONHUMAN; PARASITE TRANSMISSION; PARASITE VECTOR; REVIEW; VIRUS ISOLATION; VIRUS TRANSMISSION; VIRUS VIRULENCE;

AEDES; ANIMALS; DENGUE VIRUS; GENOTYPE; HOST-PATHOGEN INTERACTIONS; INSECT VECTORS; SPECIES SPECIFICITY;

AEDES AEGYPTI; DENGUE VIRUS GROUP;

EID: 79952101584     PISSN: 14714922     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pt.2010.12.001     Document Type: Review

References (54)

1. Beerntsen B.T., et al. Genetics of mosquito vector competence. Microbiol. Mol. Biol. Rev. 2000, 64:115-137.
2. Billingsley P.F., Sinden R.E. Determinants of malaria-mosquito specificity. Parasitol. Today 1997, 13:297-301.
3. Leake C.J. Arbovirus-mosquito interactions and vector specificity. Parasitol. Today 1992, 8:123-128.
4. Rosenberg R. Inability of Plasmodium knowlesi sporozoites to invade Anopheles freeborni salivary glands. Am. J. Trop. Med. Hyg. 1985, 34:687-691.
5. Vaughan J.A., et al. Sporogonic development of Plasmodium yoelii in five anopheline species. J. Parasitol. 1994, 80:674-681.
6. Harris C., et al. Polymorphisms in Anopheles gambiae immune genes associated with natural resistance to Plasmodium falciparum. PLoS Pathog. 2010, 6:e1001112.
7. Lambrechts L., et al. Host genotype by parasite genotype interactions underlying the resistance of anopheline mosquitoes to Plasmodium falciparum. Malar. J. 2005, 4:3.
8. Lambrechts L., et al. Genetic specificity and potential for local adaptation between dengue viruses and mosquito vectors. BMC Evol. Biol. 2009, 9:160.
9. Lambrechts L. Dissecting the genetic architecture of host-pathogen specificity. PLoS Pathog. 2010, 6:e1001019.
10. Carius H.J., et al. Genetic variation in a host-parasite association: potential for coevolution and frequency-dependent selection. Evolution 2001, 55:1136-1145.
11. de Roode J.C., Altizer S. Host-parasite genetic interactions and virulence-transmission relationships in natural populations of monarch butterflies. Evolution 2009, 64:502-514.
12. Salvaudon L., et al. Genotype-specific interactions and the trade-off between host and parasite fitness. BMC Evol. Biol. 2007, 7:189.
13. Schmid-Hempel P., et al. Dynamic and genetic consequences of variation in horizontal transmission for a microparasitic infection. Evolution 1999, 53:426-434.
14. Schulenburg H., Ewbank J.J. Diversity and specificity in the interaction between Caenorhabditis elegans and the pathogen Serratia marcescens. BMC Evol. Biol. 2004, 4:49.
15. Webster J.P., Woolhouse M.E.J. Selection and strain specificity of compatibility between snail intermediate hosts and their parasitic schistosomes. Evolution 1998, 52:1627-1634.
16. Armstrong P.M., Rico-Hesse R. Differential susceptibility of Aedes aegypti to infection by the American and Southeast Asian genotypes of dengue type 2 virus. Vector Borne Zoonotic Dis. 2001, 1:159-168.
17. Rosen L., et al. Comparative susceptibility of mosquito species and strains to oral and parenteral infection with dengue and Japanese encephalitis viruses. Am. J. Trop. Med. Hyg. 1985, 34:603-615.
18. Holmes E.C., Twiddy S.S. The origin, emergence and evolutionary genetics of dengue virus. Infect. Genet. Evol. 2003, 3:19-28.
19. Apostol B.L., et al. Population genetics with RAPD-PCR markers: the breeding structure of Aedes aegypti in Puerto Rico. Heredity 1996, 76:325-334.
20. Bosio C.F., et al. Genetic structure of Aedes aegypti populations in Thailand using mitochondrial DNA. Am. J. Trop. Med. Hyg. 2005, 72:434-442.
21. Hemme R.R., et al. Influence of urban landscapes on population dynamics in a short-distance migrant mosquito: evidence for the dengue vector Aedes aegypti. PLoS Negl. Trop. Dis. 2010, 4:e634.
22. Chevillon C., Failloux A.B. Questions on viral population biology to complete dengue puzzle. Trends Microbiol. 2003, 11:415-421.
23. Flor H.H. The complementary genetic systems in flax and flax rust. Adv. Genet. 1956, 8:29-54.
24. Flor H.H. Current satus of the gene-for-gene concept. Annu. Rev. Phytopathol. 1971, 9:275-296.
25. Thompson J.N., Burdon J.J. Gene-for-gene coevolution between plants and parasites. Nature 1992, 360:121-126.
26. Frank S.A. Coevolutionary genetics of plants and pathogens. Evol. Ecol. 1993, 7:45-75.
27. Sasaki A. Host-parasite coevolution in a multilocus gene-for-gene system. Proc. Biol. Sci. 2000, 267:2183-2188.
28. Segarra J. Stable polymorphisms in a two-locus gene-for-gene system. Phytopathology 2005, 95:728-736.
29. Agrawal A., Lively C.M. Infection genetics: gene-for-gene versus matching-alleles models and all points in between. Evol. Ecol. Res. 2002, 4:79-90.
30. Frank S.A. Specificity versus detectable polymorphism in host-parasite genetics. Proc. Biol. Sci. 1993, 254:191-197.
31. Grosberg R.K., Hart M.W. Mate selection and the evolution of highly polymorphic self/nonself recognition genes. Science 2000, 289:2111-2114.
32. Hamilton W.D. Sex versus non-sex versus parasite. Oikos 1980, 35:282-290.
33. Hamilton W.D., et al. Sexual reproduction as an adaptation to resist parasites (a review). Proc. Natl. Acad. Sci. U. S. A. 1990, 87:3566-3573.
34. Theron A., Coustau C. Are Biomphalaria snails resistant to Schistosoma mansoni?. J. Helminthol. 2005, 79:187-191.
35. Bennett K.E., et al. Quantitative trait loci that control dengue-2 virus dissemination in the mosquito Aedes aegypti. Genetics 2005, 170:185-194.
36. Bosio C.F., et al. Quantitative trait loci that control vector competence for dengue-2 virus in the mosquito Aedes aegypti. Genetics 2000, 156:687-698.
37. Gomez-Machorro C., et al. Quantitative trait loci affecting dengue midgut infection barriers in an advanced intercross line of Aedes aegypti. Insect. Mol. Biol. 2004, 13:637-648.
38. Wilfert L., Schmid-Hempel P. The genetic architecture of susceptibility to parasites. BMC Evol. Biol. 2008, 8:187.
39. Brault A.C., et al. Venezuelan equine encephalitis emergence: enhanced vector infection from a single amino acid substitution in the envelope glycoprotein. Proc. Natl. Acad. Sci. U. S. A. 2004, 101:11344-11349.
40. Moudy R.M., et al. A newly emergent genotype of West Nile virus is transmitted earlier and more efficiently by Culex mosquitoes. Am. J. Trop. Med. Hyg. 2007, 77:365-370.
41. Tsetsarkin K.A., et al. A single mutation in chikungunya virus affects vector specificity and epidemic potential. PLoS Pathog. 2007, 3:e201.
42. Vazeille M., et al. Two Chikungunya isolates from the outbreak of La Reunion (Indian Ocean) exhibit different patterns of infection in the mosquito, Aedes albopictus. PLoS ONE 2007, 2:e1168.
43. Black W.C., et al. Flavivirus susceptibility in Aedes aegypti. Arch. Med. Res. 2002, 33:379-388.
44. Thomas M.B., Blanford S. Thermal biology in insect-parasite interactions. Trends Ecol. Evol. 2003, 18:344-350.
45. Lambrechts L., et al. Shifting priorities in vector biology to improve control of vector-borne disease. Trop. Med. Int. Health 2009, 14:1505-1514.
46. Schneider D.J., Collmer A. Studying plant-pathogen interactions in the genomics era: beyond molecular Koch's postulates to systems biology. Annu. Rev. Phytopathol. 2010, 48:457-479.
47. Lawson D., et al. VectorBase: a data resource for invertebrate vector genomics. Nucleic Acids Res. 2009, 37:D583-587.
48. Yang J., et al. Mapping interspecific genetic architecture in a host-parasite interaction system. Genetics 2008, 178:1737-1743.
49. Phillips P.C. Epistasis--the essential role of gene interactions in the structure and evolution of genetic systems. Nat. Rev. Genet. 2008, 9:855-867.
50. Nene V., et al. Genome sequence of Aedes aegypti, a major arbovirus vector. Science 2007, 316:1718-1723.
51. Bian G., et al. The endosymbiotic bacterium Wolbachia induces resistance to dengue virus in Aedes aegypti. PLoS Pathog. 2010, 6:e1000833.
52. Dong Y., et al. Implication of the mosquito midgut microbiota in the defense against malaria parasites. PLoS Pathog. 2009, 5:e1000423.
53. Moreira L.A., et al. A Wolbachia symbiont in Aedes aegypti limits infection with dengue, Chikungunya, and Plasmodium. Cell 2009, 139:1268-1278.
54. Xi Z., et al. The Aedes aegypti toll pathway controls dengue virus infection. PLoS Pathog. 2008, 4:e1000098.