Polymorphism Analysis of <i>pfmdr1</i> and <i>pfcrt </i>from <i>Plasmodium falciparum </i>Isolates in Northwestern Nigeria Revealed the Major Markers Associated with Antimalarial Resistance

Suspicion of failure in the effectiveness of artemisinin-based combination therapies (currently the first-line treatment of malaria, worldwide) is leading to the unofficial use of alternative antimalarials, including chloroquine and sulfadoxine/pyrimethamine, across northern Nigeria. To facilitate e...

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Main Authors: Ruqayya Adam, Muhammad M. Mukhtar, Umar F. Abubakar, Hajara A. Damudi, Abdullahi Muhammad, Sulaiman S. Ibrahim
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Diseases
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Online Access:https://www.mdpi.com/2079-9721/9/1/6
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spelling doaj-b277766f27ba4dccb0ddd00c91e0a8152021-01-05T00:02:51ZengMDPI AGDiseases2079-97212021-01-0196610.3390/diseases9010006Polymorphism Analysis of <i>pfmdr1</i> and <i>pfcrt </i>from <i>Plasmodium falciparum </i>Isolates in Northwestern Nigeria Revealed the Major Markers Associated with Antimalarial ResistanceRuqayya Adam0Muhammad M. Mukhtar1Umar F. Abubakar2Hajara A. Damudi3Abdullahi Muhammad4Sulaiman S. Ibrahim5Department of Biological Sciences, Federal University Dutsinma, Katsina PMB 5001, NigeriaDepartment of Biochemistry, Bayero University, Kano PMB 3011, NigeriaLaboratory Department, Public Health and Diagnostic Institute, Yusuf Maitama Sule University, Kwanar Dawaki, Kano PMB 3220, NigeriaDepartment of Biochemistry, Bayero University, Kano PMB 3011, NigeriaCentre for Biotechnology Research, Bayero University, Kano PMB 3011, NigeriaDepartment of Biochemistry, Bayero University, Kano PMB 3011, NigeriaSuspicion of failure in the effectiveness of artemisinin-based combination therapies (currently the first-line treatment of malaria, worldwide) is leading to the unofficial use of alternative antimalarials, including chloroquine and sulfadoxine/pyrimethamine, across northern Nigeria. To facilitate evidence-based resistance management, antimalarial resistance mutations were investigated in <i>Plasmodium falciparum multidrug resistance-1</i> (<i>pfmdr1</i>) and <i>chloroquine resistance transporter</i> (<i>pfcrt</i>), in isolates from Kano, northwestern Nigeria. Out of the 88 samples genotyped for <i>pfmdr1</i>N86Y mutation using PCR/restriction fragment length polymorphism, one sample contained the 86Y mutation (86Y<sub>frequency</sub> = 1.14%). The analysis of 610 bp fragments of <i>pfmdr1</i> from 16 isolates revealed two polymorphic sites and low haplotype diversity (H<sub>d</sub> = 0.492), with only 86 Y mutations in one isolate, and 184 F replacements in five isolates (184F<sub>frequency</sub> = 31.25%). The analysis of 267 bp fragments of <i>pfcrt</i> isolates revealed high polymorphism (H<sub>d</sub> = 0.719), with six haplotypes and seven non-synonymous polymorphic sites. Eleven isolates (61.11%) were chloroquine-resistant, CQR (C<sub>72</sub>V<sub>73</sub>I<sub>74</sub>E<sub>75</sub>T<sub>76 </sub>haplotype), two of which had an additional mutation, D<sup>57</sup>E. An additional sequence was CQR, but of the C<sub>72</sub>V<sub>73</sub>M<sub>74</sub>E<sub>75</sub>T<sub>76</sub> haplotype, while the rest of the sequences (33.33%) were chloroquine susceptible (C<sub>72</sub>V<sub>73</sub>M<sub>74</sub>N<sub>75</sub>K<sub>76</sub> haplotype). The findings of these well characterized resistance markers should be considered when designing resistance management strategies in the northwestern Nigeria.https://www.mdpi.com/2079-9721/9/1/6<i>Plasmodium falciparum</i>pfmdr1pfcrtmutation, antimalarialresistanceNigeria
collection DOAJ
language English
format Article
sources DOAJ
author Ruqayya Adam
Muhammad M. Mukhtar
Umar F. Abubakar
Hajara A. Damudi
Abdullahi Muhammad
Sulaiman S. Ibrahim
spellingShingle Ruqayya Adam
Muhammad M. Mukhtar
Umar F. Abubakar
Hajara A. Damudi
Abdullahi Muhammad
Sulaiman S. Ibrahim
Polymorphism Analysis of <i>pfmdr1</i> and <i>pfcrt </i>from <i>Plasmodium falciparum </i>Isolates in Northwestern Nigeria Revealed the Major Markers Associated with Antimalarial Resistance
Diseases
<i>Plasmodium falciparum</i>
pfmdr1
pfcrt
mutation, antimalarial
resistance
Nigeria
author_facet Ruqayya Adam
Muhammad M. Mukhtar
Umar F. Abubakar
Hajara A. Damudi
Abdullahi Muhammad
Sulaiman S. Ibrahim
author_sort Ruqayya Adam
title Polymorphism Analysis of <i>pfmdr1</i> and <i>pfcrt </i>from <i>Plasmodium falciparum </i>Isolates in Northwestern Nigeria Revealed the Major Markers Associated with Antimalarial Resistance
title_short Polymorphism Analysis of <i>pfmdr1</i> and <i>pfcrt </i>from <i>Plasmodium falciparum </i>Isolates in Northwestern Nigeria Revealed the Major Markers Associated with Antimalarial Resistance
title_full Polymorphism Analysis of <i>pfmdr1</i> and <i>pfcrt </i>from <i>Plasmodium falciparum </i>Isolates in Northwestern Nigeria Revealed the Major Markers Associated with Antimalarial Resistance
title_fullStr Polymorphism Analysis of <i>pfmdr1</i> and <i>pfcrt </i>from <i>Plasmodium falciparum </i>Isolates in Northwestern Nigeria Revealed the Major Markers Associated with Antimalarial Resistance
title_full_unstemmed Polymorphism Analysis of <i>pfmdr1</i> and <i>pfcrt </i>from <i>Plasmodium falciparum </i>Isolates in Northwestern Nigeria Revealed the Major Markers Associated with Antimalarial Resistance
title_sort polymorphism analysis of <i>pfmdr1</i> and <i>pfcrt </i>from <i>plasmodium falciparum </i>isolates in northwestern nigeria revealed the major markers associated with antimalarial resistance
publisher MDPI AG
series Diseases
issn 2079-9721
publishDate 2021-01-01
description Suspicion of failure in the effectiveness of artemisinin-based combination therapies (currently the first-line treatment of malaria, worldwide) is leading to the unofficial use of alternative antimalarials, including chloroquine and sulfadoxine/pyrimethamine, across northern Nigeria. To facilitate evidence-based resistance management, antimalarial resistance mutations were investigated in <i>Plasmodium falciparum multidrug resistance-1</i> (<i>pfmdr1</i>) and <i>chloroquine resistance transporter</i> (<i>pfcrt</i>), in isolates from Kano, northwestern Nigeria. Out of the 88 samples genotyped for <i>pfmdr1</i>N86Y mutation using PCR/restriction fragment length polymorphism, one sample contained the 86Y mutation (86Y<sub>frequency</sub> = 1.14%). The analysis of 610 bp fragments of <i>pfmdr1</i> from 16 isolates revealed two polymorphic sites and low haplotype diversity (H<sub>d</sub> = 0.492), with only 86 Y mutations in one isolate, and 184 F replacements in five isolates (184F<sub>frequency</sub> = 31.25%). The analysis of 267 bp fragments of <i>pfcrt</i> isolates revealed high polymorphism (H<sub>d</sub> = 0.719), with six haplotypes and seven non-synonymous polymorphic sites. Eleven isolates (61.11%) were chloroquine-resistant, CQR (C<sub>72</sub>V<sub>73</sub>I<sub>74</sub>E<sub>75</sub>T<sub>76 </sub>haplotype), two of which had an additional mutation, D<sup>57</sup>E. An additional sequence was CQR, but of the C<sub>72</sub>V<sub>73</sub>M<sub>74</sub>E<sub>75</sub>T<sub>76</sub> haplotype, while the rest of the sequences (33.33%) were chloroquine susceptible (C<sub>72</sub>V<sub>73</sub>M<sub>74</sub>N<sub>75</sub>K<sub>76</sub> haplotype). The findings of these well characterized resistance markers should be considered when designing resistance management strategies in the northwestern Nigeria.
topic <i>Plasmodium falciparum</i>
pfmdr1
pfcrt
mutation, antimalarial
resistance
Nigeria
url https://www.mdpi.com/2079-9721/9/1/6
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