Ex vivo piperaquine resistance developed rapidly in Plasmodium falciparum isolates in northern Cambodia compared to Thailand

被引:31
作者
Chaorattanakawee, Suwanna [1 ,2 ]
Lon, Chanthap [1 ,3 ]
Jongsakul, Krisada [1 ]
Gawee, Jariyanart [4 ]
Sok, Somethy [5 ]
Sundrakes, Siratchana [1 ]
Kong, Nareth [6 ]
Thamnurak, Chatchadaporn [1 ]
Chann, Soklyda [3 ]
Chattrakarn, Sorayut [1 ]
Praditpol, Chantida [1 ]
Buathong, Nillawan [1 ]
Uthaimongkol, Nichapat [1 ]
Smith, Philip [1 ]
Sirisopana, Narongrid [4 ]
Huy, Rekol
Prom, Satharath [5 ]
Fukuda, Mark M. [1 ]
Bethell, Delia [1 ]
Walsh, Douglas S. [1 ]
Lanteri, Charlotte [1 ,7 ]
Saunders, David [1 ]
机构
[1] US Army Med Component Armed Forces Res Inst Med S, Bangkok, Thailand
[2] Mahidol Univ, Dept Parasitol & Entomol, Fac Publ Hlth, Bangkok, Thailand
[3] USAMC AFRIMS, Phnom Penh, Cambodia
[4] Royal Thai Army, Bangkok, Thailand
[5] Royal Cambodian Armed Forces, Phnom Penh, Cambodia
[6] Natl Ctr Parasitol Entomol & Malaria Control, Phnom Penh, Cambodia
[7] Brooke Army Med Ctr, Dept Pathol & Area Lab Serv, Microbiol Sect, San Antonio, TX USA
关键词
Malaria; Drug resistance; Piperaquine; Mefloquine; Cambodia; Thailand; DIHYDROARTEMISININ-PIPERAQUINE; IN-VITRO; UNCOMPLICATED FALCIPARUM; WESTERN CAMBODIA; POPULATION PHARMACOKINETICS; ARTEMISININ RESISTANCE; ATOVAQUONE-PROGUANIL; MALARIA; COMBINATION; CHILDREN;
D O I
10.1186/s12936-016-1569-y
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: The recent dramatic decline in dihydroartemisinin-piperaquine (DHA-PPQ) efficacy in northwestern Cambodia has raised concerns about the rapid spread of piperaquine resistance just as DHA-PPQ is being introduced as first-line therapy in neighbouring countries. Methods: Ex vivo parasite susceptibilities were tracked to determine the rate of progression of DHA, PPQ and mefloquine (MQ) resistance from sentinel sites on the Thai-Cambodian and Thai-Myanmar borders from 2010 to 2015. Immediate ex vivo (IEV) histidine-rich protein 2 (HRP-2) assays were used on fresh patient Plasmodium falciparum isolates to determine drug susceptibility profiles. Results: IEV HRP-2 assays detected the precipitous emergence of PPQ resistance in Cambodia beginning in 2013 when 40 % of isolates had an IC90 greater than the upper limit of prior years, and this rate doubled to 80 % by 2015. In contrast, Thai-Myanmar isolates from 2013 to 14 remained PPQ-sensitive, while northeastern Thai isolates appeared to have an intermediate resistance profile. The opposite trend was observed for MQ where Cambodian isolates appeared to have a modest increase in overall sensitivity during the same period, with IC50 declining to median levels comparable to those found in Thailand. A significant association between increased PPQ IC50 and IC90 among Cambodian isolates with DHA-PPQ treatment failure was observed. Nearly all Cambodian and Thai isolates were deemed artemisinin resistant with a > 1 % survival rate for DHA in the ring-stage assay (RSA), though there was no correlation among isolates to indicate cross-resistance between PPQ and artemisinins. Conclusions: Clinical DHA-PPQ failures appear to be associated with declines in the long-acting partner drug PPQ, though sensitivity appears to remain largely intact for now in western Thailand. Rapid progression of PPQ resistance associated with DHA-PPQ treatment failures in northern Cambodia limits drugs of choice in this region, and urgently requires alternative therapy. The temporary re-introduction of artesunate AS-MQ is the current response to PPQ resistance in this area, due to inverse MQ and PPQ resistance patterns. This will require careful monitoring for re-emergence of MQ resistance, and possible simultaneous resistance to all three drugs (AS, MQ and PPQ).
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