Diversities of Anopheles gambiae ss and Plasmodium falciparum in Minna, Nigeria

http://dx.doi.org/10.4314/njpar.v40i2.2

Authors

  • I. C. J. Omalu Department of Animal Biology, Federal University of Technology, Minna 2Department of Biochemistry, Federal University of Technology, Minna
  • S. S. Eke Department of Animal Biology, Federal University of Technology, Minna
  • I. K. Olayemi Department of Animal Biology, Federal University of Technology, Minna
  • E. C. Egwim Department of Biochemistry, Federal University of Technology, Minna
  • H. U. Yamman Department of Animal Biology, Federal University of Technology, Minna
  • I. M. Ocha Department of Animal Biology, Federal University of Technology, Minna
  • M. T. Ogunniyi Department of Animal Biology, Federal University of Technology, Minna
  • O. S. Ajibaye Malaria Research Laboratory, Biochemistry Division, Nigeria Institute of Medical Research
  • C. A. Otuu Department of Zoology, University of Nigeria, Nsukka
  • C. I. Nnaji National Biotechnology Development Agency, Abuja
  • P.U. Inyama Abt Associates, USAID/PMI Vector Link Project, Nigeria

Keywords:

malaria control strategy, Genetic veriabilities

Abstract

Genetic diversities of Anopheles gambiae ss and Plasmodium falciparum is a major challenge in malaria control as it affects the vector, treatment and production of a vaccine. The aim of the study is to identify the genetic variabilities of A. gambiae ss using the A. gambiae species-specific multiplex Polymerase Chain Reaction (PCR) and P. falciparum using merozoite surface protein (msp2) as antigenic marker. Results revealed that the A. gambiaes ss identified were of the M-forms and the two families of msp-2, FC27 and 3D7 were observed among the isolates of P. falciparum. Eleven (11) number of genotypes were recorded with FC27 having the highest frequency of 8(26.67%) while 3D7 had the least number of genotypes encountered with 3(10%). The allelic frequency of FC27 type was higher 29(96.67%) than 3D7 alleles with 26 (86.67%). There is no significant difference found in the distribution of FC27 alleles and 3D7 alleles in the study populations (p>0.05). The observed population genetics of A. gambiae ss and P.falciparum is likely to be a consequence of the high transmission intensity. This has important implications for malaria control strategies and vaccine production.

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References

Nigerian Malaria Indicator Survey, 2010.

Cohuet, A., Simard, F., Toto, J., Kengne, P., Coetzee, M. and Didier, F. 2003. Species identification within the Anopheles funestus group of malaria vectors in Cameroon and evidence for a new species. Am. J. Trop. Med. Hyg., 69(2): 200-205.

Omalu, I. C. J., Olayemi, I. K., Otuu, C. A., Hassan, S. C., Eke, S. S., Paul, S. and Uzoaga, G. O. 2015. Entomological and parasitological indices of malaria transmission in Minna, Niger State, North Central Nigeria. Advances in Research, 3(2): 181-188.

Toure,Y.T.,Petrarca, V.,Traore, S. F.,Coulibaly, A., Maiga, H. M., Sankare, O., Sow, M., Di Deco, M. A. and Coluzzi, M. 1994. The ecological requirements of Savannah and Mopti forms of Anopheles gambiae sensu strict. Genetica, 94(2-3): 213-223.

Coetzee, M., Hunt, R. H., Wilkerson, R., Torre, A. D., Coulibaly, M. B. and Besansky, N. J. 2015. Anopheles coluzzii and Anopheles amharicus, new members of the Anopheles gambiae complex. Zootaxa, 3619(3): 246- 274.

Lehmann, T.and Diabate, A. 2008. The molecular forms of Anopheles gambiae: A phenotypic perspective. Infect. Genet. Evol., 8(5): 737-746.

Onyabe, D. Y., Vajime, C. G., Nock, I. H., Ndams, I. S., Akpa, A. U., Alaribe, A. A. and Conn, J. E. 2003. The distribution of M and S molecular forms of Anopheles gambiae in Nigeria. Transaction of the Royal Society of Tropical Medicine and Hygiene, 97(5), 605-608.

Kemp, D.J., Cowman, A.F. and Walliker, D. 1990. Genetic diversity in Plasmodium falciparum. Advance. Parasitol., 29, 75-149.

World Health Organizations. 2002. Malaria entomology and vector control, learner’s Guide. Social mobilization and training control, prevention and eradication department, communicable diseases cluster, World Health Organization, Geneva. WHO/CDS/MAL/2012.

Gillies, M. T.and De Meillon, B. 1968. The Anophelinae of Africa South of the Sahara (Ethiopian Zoogeographical Region). Johannesburg: South African Institute for Medical Research, 51, 248-252.

Gillies, M. T. and Coetzee, M. 1987. A supplement to the anophelinae of Africa South of the Sahara (Afrotropical Region). Publications of the South African Institute for Medical Research, No. 55.

Collins, W. E and Jeffery, G. M. 2007. Plasmodium malariae: Parasite and disease. Clinical Microbiology Review, 20(4), 579-592.

Scott, J. A., Brogdon, W. G. and Collins, F. H. 1993. Identification of single specimens of the Anopheles gambiae complex by the polymerase chain reaction. American Journal of Tropical Medicine and Hygiene, 49, 520-529.

Greenwood, B.M., Armstrong, J.R., 1991. Comparison of two simple methods for determining malaria parasite density. Trans. R. Soc. Trop. Med. Hyg., 85(2), 186- 188.

Snounou, G., Beck, H. P. 1998. The use of PCR genotyping in the assessment of recrudescence or reinfection after antimalarial drug treatment. Parasitol. Today, 14, 462-467.

Hughes, A. L. 1992. Positive selection and interallelic recombination at the merozoite surface antigen-1 (MSA-1) locus of Plasmodium falciparum. Molecul. Bio. Evol., 9, 381-393.

Oyedeji, S. I., Awobode, H. O., Anumudu, C., JÜrgen, K. 2013. Genetic diversity of Plasmodium falciparum isolates from naturally infected children in Northcentral Nigeria using the merozoite surface protein-2 as molecular marker. Asian, Pac. J. Trop. Med., 589-594

Oyebola, M. K., Emmanuel, I. T.,Yetunde, O.A., Chimere, A. O., Olusola, A. O., Monday, T. and Adetoro, O. 2014. Genetic Diversity and Complexity of Plasmodium falciparum infections in Lagos, Nigeria. Journal of Bacteriology and Parasitology, 5, 4.

Magesa, S. M., Mdira, K. Y., Babiker, H. A., Alifrangis, M., Farnert, A., Simonsen, P. E. 2002. Diversity of Plasmodium falciparum clones infecting children living in a holoendemic area in north-eastern Tanzania.Acta. Tropica, 84(2), 83-92.

Fluck, C., Schopflin, S., Smith, T., Genton, B., Alpers, M. P.and Beck, H. P.2007. Effect of the malaria vaccine

Combination B on merozoite surface antigen 2 diversity. Infect, Gen. Evol., 7(1), 44-51.

Falk, N., Maire, N., Sama, W., Owusu-Agyei, S., Smith, T. and Beck, H. P.2006. Comparison of PCR-RFLP and Genescan-based genotyping for analyzing infection dynamics of Plasmodium falciparum. Ams. J. T. Med. Hyg., 74(6), 944-950

Peyerl-Hoffmann, G., Jelinek, T., Kilian, A., Kabagambe, G., Metzger, W. G., Von Sonnenburg, F. 2001. Genetic diversity of Plasmodium falciparum and its relationship to parasite density in an area with different malaria endemicities in West Uganda. Trop. Med. Inter. Health, 6, 607-13. Citation Omalu, I. C. J., Eke, S. S., Olayemi, I. K., Egwim, E. C., Yamman, H. U., Ocha, I. M., Ogunniyi, M. T., Ajibaye, O. S., Otuu, C. A., Nnaji, C. I. and Inyama, P.U.

Diversities of Anopheles gambiae ss and Plasmodium falciparum in Minna, Nigeria, pages 135-140. http://dx.doi.org/10.4314/njpar.v40i2.2 Nigerian Journal of Parasitology ISSN 1117 4145, Volume 40[2] September 2019

Ghanchi, N. K., Martensson, A., Ursing, J., Jafri, S., Bereczky, S., Hussain, R. and Beg, M. A. 2010. Genetic diversity among Plasmodium falciparum field isolates in Pakistan measured with PCR genotyping of the merozoite surface protein 1 and 2. Mal. J. 9, 1.

Gomez, D., Chaparro, J., Rubiano, C., Rojas, M. O., Wasserman, M. 2002. Genetic diversity of Plasmodium falciparum field samples from an isolated Colombian village. Ams. J. Trop.Med. Hyg., 67, 611-6.

Atroosh, W. M., Al-Mekhlafi, H. M., Mahdy, M. A, SaifAli, R., Al-Mekhlafi, A. M. and Surin, J. 2011. Genetic diversity of Plasmodium falciparum isolates from Pahang, Malaysia based on MSP-1 and MSP-2 genes. Para. Vec., 4, 233.

Published

2019-05-01

How to Cite

Omalu, I. C. J., Eke, S. S., Olayemi, I. K., Egwim, E. C., Yamman, H. U., Ocha, I. M., … Inyama, P. (2019). Diversities of Anopheles gambiae ss and Plasmodium falciparum in Minna, Nigeria: http://dx.doi.org/10.4314/njpar.v40i2.2. Nigerian Journal of Parasitology, 40(2), 135–140. Retrieved from https://njpar.com.ng/index.php/home/article/view/28

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