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Characterization of drug resistance genes in Indian Plasmodium falciparum and Plasmodium vivax field isolates
被引:1
|作者:
Narang, Geetika
[1
,2
]
Jakhan, Jahnvi
[1
,2
]
Tamang, Suman
[1
,2
]
Yadav, Karmveer
[1
]
Singh, Vineeta
[1
,2
]
机构:
[1] ICMR Natl Inst Malaria Res NIMR, Sect 8, New Delhi 110077, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
来源:
关键词:
Malaria;
Plasmodium falciparum;
Plasmodium vivax;
Drug resistance markers;
Genotyping;
India;
SULFADOXINE-PYRIMETHAMINE RESISTANCE;
CHLOROQUINE-RESISTANCE;
DIHYDROPTEROATE SYNTHASE;
PFCRT GENE;
DIHYDROFOLATE-REDUCTASE;
MOLECULAR MARKER;
PFMDR1;
GENE;
ARTEMISININ RESISTANCE;
THERAPEUTIC-EFFICACY;
PROGRESSIVE INCREASE;
D O I:
10.1016/j.actatropica.2024.107218
中图分类号:
R38 [医学寄生虫学];
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
100103 ;
摘要:
One of the major challenges for malaria control and elimination is the spread and emergence of antimalarial drug resistance. Mutations in Plasmodium falciparum (Pf) and Plasmodium vivax (Pv) field isolates for five drug resistance genes viz. crt, mdr1, dhps, dhfr and kelch known to confer resistance to choloroquine (CQ), sulfadoxinepyrimethamine (SP) and artemisinin (ART) and its derivatives were analyzed. A total of 342 symptomatic isolates of P. falciparum (Pf) and P. vivax (Pv) from 1993 to 2014 were retrieved from malaria parasite repository at National Institute of Malaria Research (NIMR). Sample DNA was extracted from dried blood spots and various targeted single nucleotide polymorphisms (SNPs) associated with antimalarial drug resistance were analysed for these isolates. 72S (67.7%) and 76T (83.8%) mutations along with SVMNT haplotype (67.7%) predominated the study population for Pfcrt. The most prevalent SNPs were 108N (73.2%) and 437G (24.8%) and the most prevalent haplotypes were ACNRNI (51.9%) and SAKAA (74.5%) in Pfdhfr and Pfdhps respectively. Only two mutations in Pfmdr1, 86Y (26.31%) and 184F (56.26%), were seen frequently in our study population. No mutations associated with Pfk13 were observed. For Pv, all the studied isolates showed two Pvdhps mutations, 383G and 553G, and two Pfdhfr mutations, 58R and 117N. Similarly, three mutations, viz. 958M, 908L and 1076L were found in Pvmdr1. No variations were observed in Pvcrt-o and Pvk12 genes. Overall, our study demonstrates an increase in mutations associated with SP resistance in both Pf and Pv, however, no single nucleotide polymorphisms (SNPs) associated with ART resistance have been observed for either species. Various SNPs associated with CQ resistance were seen in Pf; whereas only Pvmdr1 associated resistant SNPs were observed in Pv. Therefore, molecular characterization of drug resistance genes is essential for timely monitoring and prevention of malaria by identifying the circulating drug resistant parasites in the country.
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