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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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 |
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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 |
work_keys_str_mv |
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