Evolutionary ideas about genetically manipulated mosquitoes and malaria control

Trends in Parasitology

Volumn 19, Issue 1, 2003, Pages 32-38

  Boëte, Christophe ^a   Koella, Jacob C ^a  

^a SORBONNE UNIVERSITÉ   (France)

Author keywords

[No Author keywords available]

Indexed keywords

COST; GENE IDENTIFICATION; GENETIC LINKAGE; GENETIC MANIPULATION; IMMUNE RESPONSE; MALARIA; MOLECULAR EVOLUTION; MOSQUITO; NONHUMAN; PLASMODIUM FALCIPARUM; PLASMODIUM MALARIAE; REVIEW; THEORETICAL MODEL; TRANSPOSON;

ANIMALS; ANOPHELES; COST-BENEFIT ANALYSIS; DECISION SUPPORT TECHNIQUES; DNA TRANSPOSABLE ELEMENTS; EVOLUTION; INSECT VECTORS; MALARIA, FALCIPARUM; PLASMODIUM FALCIPARUM;

ARACHNIDA; HEXAPODA; PLASMODIUM FALCIPARUM; PLASMODIUM MALARIAE;

EID: 0037213419     PISSN: 14714922     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1471-4922(02)00003-X     Document Type: Review

References (48)

1. The World Health Report 1999. 1999;World Health Organization.
2. Manfredi C. Can the resurgence of malaria be partially attributed to structural adjustment programmes? Parassitologia. 41:1999;389-390.
3. Sachs J., Malaney P. The economic and social burden of malaria. Nature. 415:2002;680-685.
4. Aultmann K.S., et al. Genetically manipulated vectors of human disease: a practical overview. Trends Parasitol. 17:2001;507-509.
5. Dimopoulos G., et al. Innate immune defense against malaria infection in the mosquito. Curr. Opin. Immunol. 13:2001;79-88.
6. Barillas-Mury C., et al. Mosquito immune responses and malaria transmission: lessons from insect model systems and implications for vertebrate innate immunity and vaccine development. Insect Biochem. Mol. Biol. 30:2000;429-442.
7. Dimopoulos G., et al. Anopheles gambiae pilot gene discovery project: identification of mosquito innate immunity genes from expressed sequence tags generated from immune-competent cell lines. Proc. Natl Acad. Sci. USA. 97:2000;6619-6624.
8. Oduol F., et al. Genes identified by an expression screen of the vector mosquito Anopheles gambiae display differential molecular immune response to malaria parasites and bacteria. Proc. Natl Acad. Sci. USA. 97:2000;11397-11402.
9. Gorman M.J., et al. Mapping a quantitative trait locus involved in melanotic encapsulation of foreign bodies in the malaria vector, Anopheles gambiae. Genetics. 146:1997;965-971.
10. Zheng L., et al. Quantitative trait loci for refractoriness of Anopheles gambiae to Plasmodium cynomolgi B. Science. 276:1997;425-428.
11. Collins F.H., et al. Genetic selection of a Plasmodium-refractory strain of the malaria vector Anopheles gambiae. Science. 234:1986;607-610.
12. de Lara-Capurro M., et al. Virus-expressed, recombinant single-chain antibody blocks sporozoite infection of salivary glands in Plasmodium gallinaceum-infected Aedes aegypti. Am. J. Trop. Med. Hyg. 62:2000;427-433.
13. Ito J., et al. Transgenic anopheline mosquitoes impaired in transmission of a malaria parasite. Nature. 417:2002;452-455.
14. Catteruccia F., et al. Stable germline transformation of the malaria mosquito Anopheles stephensi. Nature. 405:2000;959-962.
15. Boëte C., Koella J.C. A theoretical approach to predicting the success of genetic manipulation of malaria mosquitoes in malaria control. Malaria J. 1:2002;3.
16. Kiszewski A.E., Spielman A. Spatially explicit model of transposon-based genetic drive mechanisms for displacing fluctuating populations of anopheline vector mosquitoes. J. Med. Entomol. 35:1998;584-590.
17. Ribeiro J.M.C., Kidwell M.G. Transposable elements as population drive mechanisms: specification of critical parameter values. J. Med. Entomol. 31:1994;10-15.
18. Hogg J.C., Hurd H. Plasmodium yoelii nigeriensis: the effect of high and low intensity of infection upon the egg production and bloodmeal size of Anopheles stephensi during three gonotrophic cycles. Parasitology. 111:1995;555-562.
19. Hogg J.C., Hurd H. Malaria-induced reduction of fecundity during the first gonotrophic cycle of Anopheles stephensi mosquitoes. Med. Vet. Entomol. 9:1995;176-180.
20. Hogg J.C., Hurd H. The effects of natural Plasmodium falciparum infection on the fecundity and mortality of Anopheles gambiae in north east Tanzania. Parasitology. 114:1997;325-331.
21. Jahan N., Hurd H. Effect of Plasmodium yoelii nigeriensis (Haemosporidia: Plasmodiidae) on Anopheles stephensi (Diptera: Culicidae) vitellogenesis. J. Med. Entomol. 35:1998;956-961.
22. Hopwood J.A., et al. Malaria-induced apoptosis in mosquito ovaries: a mechanism to control vector egg production. J. Exp. Biol. 204:2001;2773-2780.
23. Anderson R.A., et al. The effect of Plasmodium yoelii nigeriensis infection on the feeding persistence of Anopheles stephensi Liston throughout the sporogonic cycle. Proc. R. Soc. Lond. Ser. B. 266:1999;1729-1733.
24. Koella J.C., et al. Stage-specific manipulation of a mosquito's host-seeking behavior by the malaria parasite Plasmodium gallinaceum. Behav. Ecol. Sociobiol. 2002;. in press.
25. Ferguson H.M. Why is the impact of malaria parasites on mosquito survival still unresolved? Trends Parasitol. 18:2002;256-261.
26. Anderson R.A., et al. Plasmodium falciparum sporozoites increase feeding-associated mortality of their mosquito hosts Anopheles gambiae s.l. Parasitology. 120:2000;329-333.
27. Koella J.C., et al. The malaria parasite Plasmodium falciparum increases the frequency of multiple feeding of its mosquito vector Anopheles gambiae. Proc. R. Soc. Lond. Ser. B. 265:1998;763-768.
28. Kraaijeveld A.R., Godfray H.C. Trade-off between parasitoid resistance and larval competitive ability in Drosophila melanogaster. Nature. 389:1997;278-280.
29. Moret Y., Schmid-Hempel P. Survival for immunity: the price of immune system activation for bumblebee workers. Science. 290:2000;1166-1168.
30. Siva-Jothy M.T., et al. Decreased immune response as a proximate cost of copulation and oviposition in a damselfly. Physiol. Entomol. 23:1998;274-277.
31. McKean K.A., Nunney L. Increased sexual activity reduces male immune function in Drosophila melanogaster. Proc. Natl Acad. Sci. USA. 98:2001;7904-7909.
32. Koella J.C., Boëte C. A genetic correlation between age at pupation and melanisation immune response of the yellow fever mosquito Aedes aegypti. Evolution. 56:2002;1074-1079.
33. Ahmed A.M., et al. The costs of mounting an immune response are reflected in the reproductive fitness of the mosquito Anopheles gambiae. Oikos. 97:2002;371-377.
34. Schwartz A., Koella J.C. Melanization of Plasmodium falciparum and C-25 Sephadex beads by field caught Anopheles gambiae (Diptera: Culicidae) from Southern Tanzania. J. Med. Entomol. 39:2002;84-88.
35. Macdonald G. The Epidemiology and Control of Malaria. 1957;Oxford University Press.
36. Brey P.T. The impact of stress on insect immunity. Bull. Inst. Pasteur. 92:1994;101-118.
37. Suwanchaichinda C., Paskewitz S.M. Effects of larval nutrition, adult body size, and adult temperature on the ability of Anopheles gambiae (Diptera: Culicidae) to melanize beads. J. Med. Entomol. 35:1998;157-161.
38. Chun J., et al. Effect of mosquito age and reproductive status on melanization of sephadex beads in Plasmodium-refractory and -susceptible strains of Anopheles gambiae. J. Invertebr. Pathol. 66:1995;11-17.
39. Boëte C., et al. Reduced efficacy of the immune melanisation response in mosquitoes infected by malaria parasites. Parasitology. 125:2002;93-98.
40. Lyimo E.O., Koella J.C. Relationship between body size of adult Anopheles gambiae s.l. and infection with the malaria parasite Plasmodium falciparum. Parasitology. 104:1992;233-237.
41. Strand M.R., Pech L. Immunological basis for compatibility in parasitoid-host relationships. Annu. Rev. Entomol. 40:1995;31-56.
42. Beckage N.E. Modulation of immune responses to parasitoids by polydnaviruses. Parasitology. 116:1998;S57-S64.
43. Vinson S.B. How parasitoids deal with the immune system of their host: an overview. Arch. Insect Biochem. Physiol. 13:1990;3-27.
44. Rizki R.M., Rizki T.M. Parasitoid virus-like particle destroy Drosophila cellular immunity. Proc. Natl Acad. Sci. USA. 87:1990;8388-8392.
45. Boemare N., et al. Symbiosis and pathogenicity of nematode-bacterium complexes. Symbiosis. 22:1997;21-45.
46. Wang Y.I., Gaugler R. Steinernema glaseri surface coat protein suppresses the immune response of Popillia japonica (Coleoptera: Scarabaeidae) larvae. Biological Control. 14:1999;45-50.
47. Gouagna L.C., et al. The early sporogonic cycle of Plasmodium falciparum in laboratory-infected Anopheles gambiae: an estimation of parasite efficacy. Trop. Med. Int. Health. 3:1998;21-28.
48. Koella J.C., Sørensen F.L. Effect of adult nutrition on the melanization immune response of Anopheles stephensi (Diptera: Culicidae). Med. Vet. Entomol. 16:2002;1-5.