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Synergism between Pfcrt and Pfmdr1 genes could account for the slow recovery of chloroquine sensitive Plasmodium falciparum strains in Ghana after chloroquine withdrawal

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dc.contributor.author Asare, Kwame K.
dc.contributor.author Boampong, Johnson N.
dc.contributor.author Duah, Nancy O.
dc.contributor.author Afoakwah, Richmond
dc.contributor.author Sehgal, Rakesh
dc.contributor.author Quashie, Neils B.
dc.date.accessioned 2021-07-05T15:01:01Z
dc.date.available 2021-07-05T15:01:01Z
dc.date.issued 2015
dc.identifier.issn 23105496
dc.identifier.uri http://hdl.handle.net/123456789/5593
dc.description 10p:, ill. en_US
dc.description.abstract Summary Unlike other countries, the chloroquine resistant marker Pfcrt T76 mutant has remained fairly stable in Ghana several years after official disuse of chloroquine. Certain mutations inPfmdr1may potentiate Pfcrt T76, offering a possible explanation for this observation. To understand the phenomenon, the coexistence of mutations in Pfmdr1 with Pfcrt T76 in Ghanaian Plasmodium falciparum isolates was studied. The reported presence of parasites with reduced sensitivity to amodiaquine and quinine in the country was also studied. Blood samples collected from confirmed malaria patients presenting at health facilities in two distinct ecological zones were analyzed. The prevalence of Pfcrt K76T and the five point mutations in Pfmdr1were determined using nested PCR followed by RFLP analysis. The association between genes was determined by chisquare analysis, and synergism between the two genes was ascertained using the Jonckheere—Terptra (J—T) test followed by Monte Carlo simulation (MCS). Nearly fifty-four percent (53.7%)of the P.falciparum isolates examined had the Pfcrt T76 gene, out of which18.3% had bothK76 and T76 alleles. Mutations at codon86, 184, 1034, 1042 and 1246 of the Pfmdr1 gene were detected in36.0%,87.9%,71.0%,91.6% and 8.4% of the isolates, respectively. The haplotypes of Pfmdr1 present were NFCDD(43.46%),YFCDD(27.57%),NFSDD(7.48%), NYSNY (5.14%)and YFSDD(4.67%). Pfcrt T76 was significantly associated with a double mutation at codon86 and 184 of Pfmdr1 (YF;2 = 8.045, = .006). associations were observed between Pfcrt K76T and Pfmdr1triple mutation at codons 86,184 and 1034 (NFC;2 = 3.770, = .032 and YFC; = 1.489, p= 0011). Te J—T test showed significant synergism between Pfcrt 76 and Pfmdr1polymorphisms (p <0.0001), which was confirmed by MCS at 99% CI.Synergism between Pfcrt and Pfmdr1mutant genes could account for the slow recovery of chloroquine sensitive P.falciparum in Ghana. The same phenomenon could explain resistance to amodiaquine and quinine. The outcomes of this study also indicated a possible emergence of artemether-lumefantrine resistance in Ghana en_US
dc.language.iso en en_US
dc.publisher University of Cape Coast en_US
dc.subject Malaria en_US
dc.subject Drug resistance en_US
dc.subject Haplotype en_US
dc.subject Recovery en_US
dc.subject Synergism en_US
dc.subject Gene en_US
dc.subject Plasmodium falciparum en_US
dc.subject Chloroquine en_US
dc.subject Amodiaquine en_US
dc.subject Quinine en_US
dc.subject Pfcrt en_US
dc.subject Pfmdr1 en_US
dc.title Synergism between Pfcrt and Pfmdr1 genes could account for the slow recovery of chloroquine sensitive Plasmodium falciparum strains in Ghana after chloroquine withdrawal en_US
dc.type Article en_US


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