Genetic variability in geographical populations of Culex quinquefasciatus Say (Diptera: Culicidae) from India based on random amplified polymorphic DNA analysis

Acta Tropica

Volumn 112, Issue 1, 2009, Pages 71-76

  Sharma, A K ^a   Mendki, M J ^a   Tikar, S N ^a   Chandel, K ^a   Sukumaran, D ^a   Parashar, B D ^a   Veer, Vijay ^a   Agarwal, O P ^b   Prakash, Shri ^a  

^a Entomology Division   (India)

^b JIWAJI UNIVERSITY   (India)

Author keywords

Culex quinquefasciatus; Genetic diversity; RAPD

Indexed keywords

GENOMIC DNA; MOLECULAR MARKER;

BIOMARKER; DISEASE TRANSMISSION; DISEASE VECTOR; DIVERSITY INDEX; DNA; ENVIRONMENTAL FACTOR; GENETIC VARIATION; MOSQUITO; POLYMORPHISM; POPULATION GENETICS;

ARTICLE; CONTROLLED STUDY; CULEX QUINQUEFASCIATUS; DISEASE TRANSMISSION; ENVIRONMENTAL FACTOR; FLY; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GEOGRAPHIC DISTRIBUTION; INDIA; NONHUMAN; POPULATION GENETICS; RANDOM AMPLIFIED POLYMORPHIC DNA; VECTOR CONTROL;

ANIMALS; CLUSTER ANALYSIS; CULEX; DNA FINGERPRINTING; DNA PRIMERS; FEMALE; GENETIC VARIATION; GEOGRAPHY; INDIA; RANDOM AMPLIFIED POLYMORPHIC DNA TECHNIQUE;

ASIA; EURASIA; INDIA; SOUTH ASIA;

CULEX PIPIENS QUINQUEFASCIATUS; CULICIDAE; DIPTERA;

EID: 68349111828     PISSN: 0001706X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.actatropica.2009.06.014     Document Type: Article

References (36)

1. Apostol B.L., Black W.C.IV., Reiter P., and Miller B.R. Use of randomly amplified polymorphic DNA amplified by polymerase chain reaction markers to estimate the number of Aedes aegypti families at oviposition sites in San Juan, Puerto Rico. Am. J. Trop. Med. Hyg. 51 (1994) 89-97
2. Ayres C.E.J., Melo-Santos M.A.V., Solé-Cava A.M., and Furtado A.F. Genetic differentiation of Aedes aegypti (Diptera: Culicidae), the major dengue vector in Brazil. J. Med. Entomol. 40 (2003) 430-435
3. Ayres C.E.J., Melo-Santos M.A.V., Prota J.R.M., Solé-Cava A.M., Regis L., and Furtado A.F. Genetic structure of natural populations of Aedes aegypti at the micro- and macro-geographic levels in Brazil. J. Am. Mosq. Control Assoc. 20 (2004) 350-356
4. Ballinger-Crabtree M.E., Black W.C., and Miller B.R. Use of genetic polymorphisms detected by the random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) for differentiation and identification of Aedes aegypti subspecies and populations. Am. J. Trop. Med. Hyg. 47 (1992) 893-901
5. Bosio C.F., Fulton R.E., Salasek M.L., Beaty B.J., and Black W.C. Quantitative trait loci that control vector competence for dengue-2 virus in the mosquito Aedes aegypti. Genetics 156 (2000) 687-698
6. Coen E.S., Stracha T., and Dover G. Dynamics of concerted evolution of ribosomal DNA and histone gene families in the melanogaster species subgroup of Drosophila. J. Mol. Biol. 158 (1982) 7-35
7. Cornel A.J., Mcabee R.D., Rasgon J., Mathew A., Scott T.W., and Coetzee M. Differences in extent of genetic introgression between sympatric Culex pipiens and Culex quinquefasciatus (Diptera: Culicide) in California and South Africa. J. Med. Entomol. 40 (2003) 36-51
8. de Souza G.B., Blanco A., and Gardenal C.N. Genetic relationships among Aedes aegypti 9 Diptera: Culicidae) populations from Argentina using random amplified polymorphic DNA polymerase chain reaction markers. J. Med. Entomol. 38 (2001) 371-375
9. Failloux A.B., Darius H., and Pasteur N. Genetic differentiation of Aedes aegypti, the vector of Dengue virus in French Polynesia. J. Am. Mosq. Control Assoc. 11 (1995) 457-462
10. Farid H.A., Gad A.M., and Speilman A. A genetic similarity among Egyptian populations of Culex pipiens (Diptera: Culicidae). J. Med. Entomol. 28 (1991) 198-204
11. Gomez-Machorro C., Bennett K.E., de Lourdes Munoz M., and Black W.C. Quantitative trait loci affecting dengue midgut infection barriers in an advanced intercross line of Aedes aegypti. Insect Mol. Biol. 13 (2004) 637-648
12. Gooding R.H. Genetic variation in arthropod vectors of disease causing organisms: obstacles and opportunities. Clin. Microbiol. Rev. 3 (1996) 301-320
13. Gorrochotegui-Escalante N., Munoz M.L., Fernandez-Salas I., Beaty B.J., and Black W.C. Genetic isolation by distance among Aedes aegypti populations along the northeastern coast of Mexico. Am. J. Trop. Med. Hyg. 62 (2000) 200-209
14. Graham D.H., Holmes J.L., Beaty B.J., and Black W.C. Quantitative trait loci conditioning vertical transmission of La Crosse virus in the eastern tree hole mosquito, Ochlerotatus triseriatus. Insect Mol. Biol. 12 (2003) 307-318
15. Herrera F., Urdaneta L.R.J., Zoghbi N., Ruiz J., Carrasquel G., Martinez J.A., Pernalete M., Villeges P., Montoya A., Palis Rubia Y., and Rojas E. Population genetic structure of the dengue mosquito Aedes aegypti in Venezuela. Mem. Inst. Oswaldo Cruz 101 (2006) 625-633
16. Hill S.M., and Compton J.M. DNA based methods for the identification of insect vectors. Ann. Trop. Med. Parasitol. 88 (1994) 227-250
17. Kent R.J., Harrington L.C., and Norris D.E. Genetic difference between Culex pipiens f. molestus and Culex pipiens pipiens (Diptera: Culicidae) in New York. J. Med. Entomol. 44 (2007) 50-59
18. Komalamisra N. Genetic variability in isozymes of Anopheles minimus group from various localities from Thailand. Jpn. J. Sanit. Zool. 40 (1989) 69-80
19. Kumar P., Prajapati P.B., Saxena D., Kavishwar A.B., and Kurian G. An evaluation of coverage and compliance of Mass Drug Administration 2006 for elimination of Lymphatic filariasis in endemic areas of Gujrat. Ind. J. Commun. Med. 33 (2008) 38-42
20. Lynch M., and Milligan B.G. Analysis of population genetic structure with RAPD markers. Mol. Ecol. 3 (1994) 91-99
21. Menge D.M., Zhong D., Guda T., Gouagna L., Githure J., Beier J., and Yan G. Quantitative trait loci controlling refractoriness to Plasmodium falciparum in natural Anopheles gambiae mosquitoes from a malaria-endemic region in western Kenya. Genetics 173 (2006) 235-241
22. Bockaire M.J., Pederson E.M., White G.B., and Michael E. Role of vector control in global programe to eliminate lymphatic filariasis. Ann. Rev. Entomol. 54 (2008) 469-487
23. NAVBDCP, 2008. http://www.navbdcp.gov.in/filariasis.
24. Nei M. Genetic distance between populations. Am. Nat. 106 (1972) 283-292
25. Ocampo C.B., and Wesson D.M. Population dynamics of Aedes aegypti from a dengue hyperendemic urban setting in Colombia. Am. J. Trop. Med. Hyg. 71 (2004) 506-513
26. Paduan K.S., Araujo-Junior J.P., and Ribolla Paulo E.M. Genetic variability in geographical populations of Aedes aegypti (Diptera Culicidae) in Brazil elucidated by molecular markers. Genet. Mol. Biol. 29 (2006) 391-395
27. Paupy C., Vazeille-Falcoz M., Mousson L., Rodhain F., and Failloux A.B. Aedes aegypti in Tahiti and Moorea (French Polynesia): isoenzyme differentiation in the mosquito population according to human population density. Am. J. Trop. Med. Hyg. 62 (2000) 217-224
28. Riehle M.M., Markianos K., Niare O., et al. Natural malaria infection in Anopheles gambiae is regulated by a single genomic control region. Science 312 (2006) 577-579
29. Sambrook J., Fritsch E.F., and Maniats T. Molecular Cloning: A Laboratory Manual. 2nd ed. (1989), Cold Spring Harbor Laboratory, Cold Spring Harbor, NY
30. Shouche Y.S., and Patole M.S. Sequence analysis of mitochondrial 16S ribosomal RNA gene fragment from seven mosquito species. J. Biosci. 25 (2000) 361-366
31. Tikar S.N., Mendki M.J., Sukumaran D., Sharma A.K., Chandel K., Seenivasagan T., Parashar B.D., and Prakash S. Insecticide resistance in Culex quinquefasciatus from Rajasthan. 9th International Symposium on Vector and Vector Borne Diseases. Puri, India, 15-17 February (2008)
32. Welsh J., and McClelland M. Fingerprinting genome using PCR with arbitrary primers. Nucl. Acids Res. 18 (1990) 7213-7218
33. World Health Organization (WHO), 2002. Lymphatic filariasis-The Disease and its Control. Technical Report 71, WHO, Geneva.
34. WHO/UNICEF and NNDP/World Bank/WHO/TDR "Research on rapid geographical assessment of Bancroftian Filariasis" July, 1997.
35. Williams J.G., Kubelik A.R., and Livak K.J. DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. Nucl. Acids Res. 18 (1990) 6531-6535
36. Zheng L., Wang S., Romans P., Zhao H., Luna C., and Benedict M.Q. Quantitative trait loci in Anopheles gambiae controlling the encapsulation response against Plasmodium cynomolgi Ceylon. BMC Genet. 4 (2003) 16