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Allelic frequencies of mutants of the Plasmodium falciparum, quinoline and folate metabolizing genes in the west region of Cameroon.
Ali, Innocent Mbulli; Tchuenkam, Valery Pacome Kom; Tagomo, Sandra Sob; Mawamba, Hornela; Moyeh, Marcel Nyuylam; Nfor, Emmanuel Nfor; Nji, Akindeh Mbuh; Fomboh, Calvino Tah; Nana, William Dorian; Kengne, Jean-Paul Chedjou; Niba, Peter Thelma Ngwa; Ekoyol, Germaine Ekobo; Achu, Dorothy Fosah; Bigoga, Jude Daiga; Mbacham, Wilfred Fon.
Afiliación
  • Ali IM; MARCAD Program, The Biotechnology Centre, University of Yaoundé 1, BP 8094, Yaoundé, Centre Region, Cameroon.
  • Tchuenkam VPK; Department of Biochemistry, Faculty of Science, BP 67, University of Dschang, Dschang, West Region, Cameroon.
  • Tagomo SS; Department of Biochemistry, Faculty of Science, BP 67, University of Dschang, Dschang, West Region, Cameroon.
  • Mawamba H; Department of Biochemistry, Faculty of Science, BP 67, University of Dschang, Dschang, West Region, Cameroon.
  • Moyeh MN; Department of Biochemistry, Faculty of Science, BP 67, University of Dschang, Dschang, West Region, Cameroon.
  • Nfor EN; Department of Biochemistry and Molecular Biology, Faculty of Science, Uni-versity of Buea, BP 63, Buea, South West Region, Cameroon.
  • Nji AM; Malaria Program, Cameroon Baptist Convention Health Services, BP 01, Nkwen, Bamenda, North West Region, Cameroon.
  • Fomboh CT; MARCAD Program, The Biotechnology Centre, University of Yaoundé 1, BP 8094, Yaoundé, Centre Region, Cameroon.
  • Nana WD; MARCAD Program, The Biotechnology Centre, University of Yaoundé 1, BP 8094, Yaoundé, Centre Region, Cameroon.
  • Kengne JC; MARCAD Program, The Biotechnology Centre, University of Yaoundé 1, BP 8094, Yaoundé, Centre Region, Cameroon.
  • Niba PTN; MARCAD Program, The Biotechnology Centre, University of Yaoundé 1, BP 8094, Yaoundé, Centre Region, Cameroon.
  • Ekoyol GE; MARCAD Program, The Biotechnology Centre, University of Yaoundé 1, BP 8094, Yaoundé, Centre Region, Cameroon.
  • Achu DF; National Malaria Control Program, Ministry of Public Health, Yaoundé, BP 14386, Centre Region, Cameroon.
  • Bigoga JD; National Malaria Control Program, Ministry of Public Health, Yaoundé, BP 14386, Centre Region, Cameroon.
  • Mbacham WF; MARCAD Program, The Biotechnology Centre, University of Yaoundé 1, BP 8094, Yaoundé, Centre Region, Cameroon.
Heliyon ; 8(11): e11861, 2022 Nov.
Article en En | MEDLINE | ID: mdl-36451747
ABSTRACT
The emergence and spread of Plasmodium falciparum (P.f) drug resistance is still a major concern in Sub-Saharan Africa and warrants that its evolution be monitored continuously. The present study aimed at determining the distribution of key P.f drug resistance-mediating alleles in circulating malaria parasites in the West region of Cameroon. A cross sectional hospital-based study was conducted in Dschang and Ngounso in the West region of Cameroon. The Pfcrt, Pfmdr1, and the Pfdhps genes were amplified through nested PCR in 208 malaria-infected samples of the 301 febrile outpatients enrolled. The presence or absence of mutations in the K76T, N86Y, A437G and A581G codons of these P.f. genes respectively were determined through restriction digestion analysis. The proportion of different alleles were estimated as percentages and compared between two study sites using the Chi square test. A p value <0.05 was considered significant. A high prevalence (75.6%) of the 437G allele was observed. It was significantly different between Dschang and Ngounso (62% vs. 89.2%, X2 = 19.6, P = 0.00005). Equally observed was a 19.2% (95%CI 13.3-25.6) of the dhps-581G mutant allele. Furthermore, we observed the Pfcrt-76T, Pfmdr1-N86 mutations in 73.0% (67.5-79.7) and 87.2% (83.2-91.9), and 3.0% (0.0-9.6) and 12.8% was observed for the Pfcrt-K76T and Pfmdr1-N86Y respectively. When biallelic haplotypes were constructed from alleles of the three genes, same pattern was seen. Overall, 73% and 87% of circulating P. falciparum isolates carried wild type alleles at Pfmdr1-N86Y and Pfcrt-K76T. On the other hand, we found more parasites with mutant alleles at dhps (437G and 581G) loci which may reflect possible drug-related selection of this mutant in the parasite population. Continuous monitoring of these mutations is recommended to pre-empt a loss in sulphadoxine-pyrimethamine efficacy in malaria chemoprevention programs.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Heliyon Año: 2022 Tipo del documento: Article País de afiliación: Camerún

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Heliyon Año: 2022 Tipo del documento: Article País de afiliación: Camerún