Distribution of pfmdr1 and pfcrt chloroquine drug resistance alleles in north-western Nigeria.

Abstract

BACKGROUND:

In Nigeria, decline in the sensitivity of Plasmodium falciparum to Artemisinin Combination Therapy (ACT) has prompted the unofficial use of chloroquine (CQ) for self-medication. This study was designed to determine the prevalence and distribution of CQ resistant/susceptible alleles of CQ resistance transporter (Pfcrt) and P. falciparum multidrug resistance gene 1 (Pfmdr1) in view of the possible re-introduction of CQ for malaria treatment.

MATERIALS AND METHODS:

Four hundred and sixty six (466) P. falciparum positive samples were randomly collected from five states of northwest Nigeria. The samples were amplified using RT- PCR at codon 76 for Pfcrt and codon 86 for Pfmdr1. Data was analysed using chi-square, odds ratios and paired t-tests.

RESULTS:

Drug susceptible alleles (N86) were most prevalent in the study population (47.9%; 223/466), followed by the drug resistance alleles 86Y (28.3%; 132/466), followed by the drug susceptible alleles K76 (17.4%; 81/466), the resistant alleles 76T (12.4%; 58/466) and finally the mixed infection mutation K76T (3.6%; 17/466). Differences between the distributions of the Pfmdr1 and Pfcrt alleles were significant (P<0.05). There were significant differences (P<0.05) between N86 and 86Y alleles, but no significant differences between K76 and 76T alleles, including the prevalence of the various alleles across the different age groups.

CONCLUSION:

The results of this study suggest the possibility of (re)introducing CQ for malaria treatment in north-western Nigeria and provide insight in the genetic background of P. falciparum in the study area.

• Authors: Ruqayyah H Muhammad, Ishaya H Nock, Iliya S Ndams, Jonathan B George, Yusuf Deeni
• Journal: MalariaWorld journal (Malariaworld J) Vol. 8 Pg. 15 ( 2017) ISSN: 2214-4374 [Electronic] Netherlands
• PMID: 34532238 (Publication Type: Journal Article)
• Copyright: Copyright © 2017 Muhammad et al.