Drug resistance markers in Plasmodium vivax isolates from a Kanchanaburi province, Thailand between January to May 2023

被引:1
作者
Sridapan, Thanawat [1 ]
Rattanakoch, Paweesuda [1 ]
Kijprasong, Kaewkanha [2 ]
Srisutham, Suttipat [1 ]
机构
[1] Chulalongkorn Univ, Fac Allied Hlth Sci, Dept Clin Microscopy, Bangkok, Thailand
[2] Satan Prabaramee Hosp, Kanchanaburi, Thailand
关键词
DIHYDROFOLATE-REDUCTASE GENE; DIHYDROPTEROATE SYNTHASE; SULFADOXINE-PYRIMETHAMINE; MALARIA PARASITES; CLINICAL-EFFICACY; CHLOROQUINE; MUTATIONS; PVMDR1; POLYMORPHISMS; SENSITIVITY;
D O I
10.1371/journal.pone.0304337
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Plasmodium vivax has become the predominant species in the border regions of Thailand. The emergence and spread of antimalarial drug resistance in P. vivax is one of the significant challenges for malaria control. Continuous surveillance of drug resistance is therefore necessary for monitoring the development of drug resistance in the region. This study aims to investigate the prevalence of the mutation in the P. vivax multidrug resistant 1 (Pvmdr1), dihydrofolate reductase (Pvdhfr), and dihydropteroate synthetase (Pvdhps) genes conferred resistance to chloroquine (CQ), pyrimethamine (P) and sulfadoxine (S), respectively. Method 100 P. vivax isolates were obtained between January to May 2023 from a Kanchanaburi province, western Thailand. Nucleotide sequences of Pvmdr1, Pvdhfr, and Pvdhps genes were amplified and sequenced. The frequency of single nucleotide polymorphisms (SNPs)-haplotypes of drug-resistant alleles was assessed. The linkage disequilibrium (LD) tests were also analyzed. Results In Pvmdr1, T958M, Y976F, and F1076L, mutations were detected in 100%, 21%, and 23% of the isolates, respectively. In Pvdhfr, the quadruple mutant allele (I57R58M61T117) prevailed in 84% of the samples, followed by (L57R58M61T117) in 11%. For Pvdhps, the double mutant allele (G383G553) was detected (48%), followed by the triple mutant allele (G383M512G553) (47%) of the isolates. The most prevalent combination of Pvdhfr (I57R58M61T117) and Pvdhps (G383G553) alleles was sextuple mutated haplotypes (48%). For LD analysis, the association in the SNPs pairs was found between the intragenic and intergenic regions of the Pvdhfr and Pvdhps genes. Conclusion The study has recently updated the high prevalence of three gene mutations associated with CQ and SP resistance. Genetic monitoring is therefore important to intensify in the regions to further assess the spread of drug resistant. Our data also provide evidence on the distribution of drug resistance for the early warning system, thereby threatening P. vivax malaria treatment policy decisions at the national level.
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相关论文
共 71 条
[1]   Similar trends of pyrimethamine resistance-associated mutations in Plasmodium vivax and P. falciparum [J].
Alam, Mohammad Tauqeer ;
Bora, Hema ;
Bharti, Praveen K. ;
Saifi, Muheet A. ;
Das, Manoj K. ;
Dev, Vas ;
Kumar, Ashwani ;
Singh, Neeru ;
Dash, Aditya P. ;
Das, Brahmananda ;
Wajihullah ;
Sharma, Yagya D. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (03) :857-863
[2]   Polymorphisms in genes associated with drug resistance of Plasmodium vivax in India [J].
Anantabotla, Vamsi Mohan ;
Antony, Hiasindh Ashmi ;
Parija, Subhash Chandra ;
Rajkumari, Nonika ;
Kini, Jyoti R. ;
Manipura, Radhakrishna ;
Nag, Vijaya Lakshmi ;
Gadepalli, R. ;
Chayani, Nirupama ;
Patro, Somi .
PARASITOLOGY INTERNATIONAL, 2019, 70 :92-97
[3]  
[Anonymous], 2004, STRATEGIC FRAMEWORK
[4]  
[Anonymous], World Malaria Report 2011
[5]   Distribution of Plasmodium vivax pvdhfr and pvdhps alleles and their association with sulfadoxine-pyrimethamine treatment outcomes in Indonesia [J].
Asih, Puji B. S. ;
Marantina, Sylvia S. ;
Nababan, Rodiah ;
Lobo, Neil F. ;
Rozi, Ismail E. ;
Sumarto, Wajio ;
Dewi, Rita M. ;
Tuti, Sekar ;
Taufik, Ahmad S. ;
Mulyanto ;
Sauerwein, Robert W. ;
Syafruddin, Din .
MALARIA JOURNAL, 2015, 14
[6]   Defining the Role of Mutations in Plasmodium vivax Dihydrofolate Reductase-Thymidylate Synthase Gene Using an Episomal Plasmodium falciparum Transfection System [J].
Auliff, Alyson M. ;
Adams, John H. ;
O'Neil, Michael T. ;
Cheng, Qin .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (09) :3927-3932
[7]   Resistance to Therapies for Infection by Plasmodium vivax [J].
Baird, J. Kevin .
CLINICAL MICROBIOLOGY REVIEWS, 2009, 22 (03) :508-534
[8]   RESISTANCE TO CHLOROQUINE BY PLASMODIUM-VIVAX IN IRIAN-JAYA, INDONESIA [J].
BAIRD, JK ;
BASRI, H ;
PURNOMO ;
BANGS, MJ ;
SUBIANTO, B ;
PATCHEN, LC ;
HOFFMAN, SL .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1991, 44 (05) :547-552
[9]   Plasmodium vivax Resistance to Chloroquine in Madagascar: Clinical Efficacy and Polymorphisms in pvmdr1 and pvcrt-o Genes [J].
Barnadas, Celine ;
Ratsimbasoa, Arsene ;
Tichit, Magali ;
Bouchier, Christiane ;
Jahevitra, Martial ;
Picot, Stephane ;
Menard, Didier .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (12) :4233-4240
[10]   Plasmodium vivax dhfr and dhps mutations in isolates from Madagascar and therapeutic response to sulphadoxine-pyrimethamine [J].
Barnadas, Celine ;
Tichit, Magali ;
Bouchier, Christiane ;
Ratsimbasoa, Arsene ;
Randrianasolo, Laurence ;
Raherinjafy, Rogelin ;
Jahevitra, Martial ;
Picot, Stephane ;
Menard, Didier .
MALARIA JOURNAL, 2008, 7 (1)