Abstract

BackgroundPlasmodium vivax is the predominant species of human malaria parasites present in China. Although sulphadoxine-pyrimethamine (SP) and chloroquine (CQ) have been widely used for malaria treatment in China, the resistance profiles of these drugs are not available. Analysis of dihydrofolate reductase (dhfr), dihydropteroate synthase (dhps), and multidrug resistance (mdr-1) gene mutations in P. vivax isolates is a valuable molecular approach for mapping resistance to SP and CQ. This study investigates the prevalence of pvdhfr, pvdhps, and pvmdr-1 of P. vivax clinical isolates from China and provides baseline molecular epidemiologic data on SP- and CQ-associated resistance in P. vivax.MethodsPlasmodium vivax clinical isolates were collected from two malaria-endemic regions of China, subtropical (Xishuangbanna, Yunnan province) and temperate (Bozhou, Anhui province), from 2009 to 2012. All isolates were analysed for single nucleotide polymorphism haplotypes in pvdhfr, pvdhps, and pvmdr-1 using direct DNA sequencing.ResultsIn pvdhfr, 15% of Xishuangbanna isolates carried wild-type (WT) allele, whereas the majority of isolates carried mutant genes with substitutions at five codons. Eight mutant haplotypes of pvdhfr were detected, while limited polymorphism of pvdhfr was found in Bozhou isolates. A size polymorphism was present in pvdhfr, with the three-repeat type being the most predominate in both Xishuangbanna (79%) and Bozhou (97%) isolates. In pvdhps, mutations at four codons were detected in Xishuangbanna isolates leading to six haplotypes, including WT allele, single-mutation, double-mutation, and triple-mutation alleles. All Bozhou isolates carried WT pvhdps. In pvmdr-1, isolates from Xishuangbanna carried mutations at codons Y976F and F1076L, whereas all isolates from Bozhou had only a single mutation at codon F1076L.ConclusionsPlasmodium vivax isolates from subtropical and temperate zones of China are shown to have dramatically different frequencies and patterns of mutations in pvdhfr, pvdhps, and pvmdr-1. Whereas P. vivax populations in subtropical China are highly resistant to SP and CQ, those in the temperate zone may still be susceptible to SP and CQ. This information is useful for establishing treatment policy and provides a baseline for molecular surveillance of drug-resistant P. vivax in these areas.Electronic supplementary materialThe online version of this article (doi:10.1186/1475-2875-13-346) contains supplementary material, which is available to authorized users.

Highlights

  • Plasmodium vivax is the predominant species of human malaria parasites present in China

  • P. vivax malaria accounted for > 95% of all malaria cases reported in China in 2007 [5], having become the sole parasite species and responsible for more than 90% of re-emerged malaria cases reported in temperate zone of China in 2009 [6]

  • This study investigated the frequencies and patterns of mutations in pvdhfr, pvdhps, and pvmdr-1 linked to SP and CQ resistance in P. vivax isolates from Yunnan and Anhui provinces of China, and the results provide important information for molecular surveillance of drug-resistant P. vivax in these areas

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Summary

Introduction

Plasmodium vivax is the predominant species of human malaria parasites present in China. Sulphadoxine-pyrimethamine (SP) and chloroquine (CQ) have been widely used for malaria treatment in China, the resistance profiles of these drugs are not available. Malaria has been a significant public health problem in China until recently, predominantly in two areas of China: subtropical zone (Yunnan and Hainan provinces) and temperate zone (such as Anhui, Henan, Hunan, Hubei, and Jiangsu provinces). In subtropical China, Yunnan is one of the two provinces with year-round local transmission of P. vivax and Plasmodium falciparum and has suffered one of the highest malaria morbidity and mortality rates in China. In temperate zone of Central China, outbreaks of malaria have been reported in Anhui and Henan provinces.

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