The spread of artemisinin-resistant Plasmodium falciparum in the Greater Mekong subregion: a molecular epidemiology observational study

被引:1
|
作者
Imwong, Mallika [1 ,2 ]
Suwannasin, Kanokon [2 ]
Kunasol, Chanon [2 ]
Sutawong, Kreepol [3 ,4 ]
Mayxay, Mayfong [5 ]
Rekol, Huy [7 ]
Smithuis, Frank M. [6 ,8 ,9 ]
Hlaing, Tin Maung [10 ]
Tun, Kyaw M. [8 ,10 ]
van der Pluijm, Rob W. [2 ,6 ]
Tripura, Rupam [2 ]
Miotto, Olivo [2 ]
Menard, Didier [11 ]
Dhorda, Mehul [12 ]
Day, Nicholas P. J. [2 ,6 ]
White, Nicholas J. [2 ]
Dondorp, Arjen M.
机构
[1] Mahidol Univ, Dept Mol Trop Med & Genet, Bangkok, Thailand
[2] Mahidol Univ, Mahidol Oxford Trop Med Res Unit, Fac Trop Med, Bangkok 10400, Thailand
[3] Buntharik Hosp, Bangkok, Thailand
[4] Lao Oxford Mahosot Hosp Wellcome Trust Res Unit, Viangchan, Laos
[5] Univ Hlth Sci, Fac Postgrad Studies, Viangchan, Laos
[6] Univ Oxford, Ctr Trop Med & Global Hlth, Oxford, England
[7] Ctr Parasitol Entomol & Malaria Control CNM, Phnom Penh, Cambodia
[8] Myanmar Oxford Clin Res Unit, Yangon, Myanmar
[9] Med Act Myanmar, Yangon, Myanmar
[10] Def Serv Med Res Ctr, Naypyitaw, Myanmar
[11] Inst Pasteur Cambodia, Malaria Mol Epidemiol Unit, Phnom Penh, Cambodia
[12] Worldwide Antimalarial Resistance Network WWARN, Bangkok, Thailand
来源
LANCET INFECTIOUS DISEASES | 2017年 / 17卷 / 05期
基金
英国惠康基金;
关键词
DIHYDROARTEMISININ-PIPERAQUINE FAILURE; MALARIA; CAMBODIA; MYANMAR; ASSOCIATION; INFECTIONS; THAILAND; MARKERS; COHORT; ASIA;
D O I
10.1016/S1473-3099(17)30048-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Evidence suggests that the PfKelch13 mutations that confer artemisinin resistance in falciparum malaria have multiple independent origins across the Greater Mekong subregion, which has motivated a regional malaria elimination agenda. We aimed to use molecular genotyping to assess antimalarial drug resistance selection and spread in the Greater Mekong subregion. Methods In this observational study, we tested Plasmodium falciparum isolates from Myanmar, northeastern Thailand, southern Laos, and western Cambodia for PfKelch13 mutations and for Pfplasmepsin2 gene amplification (indicating piperaquine resistance). We collected blood spots from patients with microscopy or rapid test confirmed uncomplicated falciparum malaria. We used microsatellite genotyping to assess genetic relatedness. Findings As part of studies on the epidemiology of artemisinin-resistant malaria between Jan 1, 2008, and Dec 31, 2015, we collected 434 isolates. In 2014-15, a single long PfKelch13 C580Y haplotype (-50 to +31.5 kb) lineage, which emerged in western Cambodia in 2008, was detected in 65 of 88 isolates from northeastern Thailand, 86 of 111 isolates from southern Laos, and 14 of 14 isolates from western Cambodia, signifying a hard transnational selective sweep. Pfplasmepsin2 amplification occurred only within this lineage, and by 2015 these closely related parasites were found in ten of the 14 isolates from Cambodia and 15 of 15 isolates from northeastern Thailand. C580Y mutated parasites from Myanmar had a different genetic origin. Interpretation Our results suggest that the dominant artemisinin-resistant P falciparum C580Y lineage probably arose in western Cambodia and then spread to Thailand and Laos, outcompeting other parasites and acquiring piperaquine resistance. The emergence and spread of fit artemisinin-resistant P falciparum parasite lineages, which then acquire partner drug resistance across the Greater Mekong subregion, threatens regional malaria control and elimination goals. Elimination of falciparum malaria from this region should be accelerated while available antimalarial drugs still remain effective. Copyright The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY license.
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收藏
页码:491 / 497
页数:7
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