1. Geographical emergence of sulfadoxine-pyrimethamine drug resistance-associated P. falciparum and P. malariae alleles in co-existing Anopheles mosquito and asymptomatic human populations across Cameroon.
- Author
-
Nkemngo FN, Raissa LW, Nguete DN, Ndo C, Fru-Cho J, Njiokou F, Wanji S, and Wondji CS
- Subjects
- Animals, Humans, Pyrimethamine pharmacology, Pyrimethamine therapeutic use, Sulfadoxine pharmacology, Sulfadoxine therapeutic use, Alleles, Cameroon epidemiology, Drug Combinations, Plasmodium falciparum, Drug Resistance genetics, Tetrahydrofolate Dehydrogenase genetics, Anopheles genetics, Antimalarials pharmacology, Antimalarials therapeutic use, Malaria, Falciparum drug therapy, Malaria, Falciparum epidemiology, Malaria, Falciparum genetics, Malaria drug therapy, Malaria epidemiology, Malaria genetics
- Abstract
Malaria molecular surveillance remains critical in detecting and tracking emerging parasite resistance to anti-malarial drugs. The current study employed molecular techniques to determine Plasmodium species prevalence and characterize the genetic diversity of Plasmodium falciparum and Plasmodium malariae molecular markers of sulfadoxine-pyrimethamine resistance in humans and wild Anopheles mosquito populations in Cameroon. Anopheles mosquito collections and parasitological survey were conducted in villages to determine Plasmodium species infection, and genomic phenotyping of anti-folate resistance was accomplished by sequencing the dihydrofolate-reductase ( dhfr ) and dihydropteroate-synthase ( dhps ) genes of naturally circulating P. falciparum and P. malariae isolates. The malaria prevalence in Elende was 73.5% with the 5-15 years age group harboring significant P. falciparum (27%) and P. falciparum + P. malariae (19%) infections. The polymorphism breadth of the pyrimethamine-associated Pfdhfr marker revealed a near fixation (94%) of the triple-mutant -A
16 I51 R59 N108 I164 . The Pfdhps backbone mediating sulfadoxine resistance reveals a high frequency of the V431 A436 G437 K540 A581 A613 alleles (20.8%). Similarly, the Pmdhfr N50 K55 L57 R58 S59 S114 F168 I170 haplotype (78.4%) was predominantly detected in the asexual blood stage. In contrast, the Pmdhps - S436 A437 occured at 37.2% frequency. The combined quadruple N50 K55 L57 R58 S59 S114 F168 I170 infection. Interventions directed at reducing malaria transmission such as the scaling-up of SP are favoring the emergence and spread of multiple drug-resistant alleles between the human and mosquito host systems.S436 G437 K540 A581 A613 (31.9%) was the major circulating haplotype with similar frequency in humans and mosquitoes. This study highlights the increasing frequency of the P. malariae parasite mostly common in asymptomatic individuals with apparent P. falciparum infection. Interventions directed at reducing malaria transmission such as the scaling-up of SP are favoring the emergence and spread of multiple drug-resistant alleles between the human and mosquito host systems., Competing Interests: The authors declare no conflict of interest.- Published
- 2023
- Full Text
- View/download PDF