Auburn Sarah, Serre David, Pearson Richard D, Amato Roberto, Sriprawat Kanlaya, To Sheren, Handayuni Irene, Suwanarusk Rossarin, Russell Bruce, Drury Eleanor, Stalker Jim, Miotto Olivo, Kwiatkowski Dominic P, Nosten Francois, Price Ric N
Global and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Australia.
Genomic Medicine Institute, Cleveland Clinic Lerner Research institute, Ohio.
J Infect Dis. 2016 Oct 15;214(8):1235-42. doi: 10.1093/infdis/jiw323. Epub 2016 Jul 24.
In regions of coendemicity for Plasmodium falciparum and Plasmodium vivax where mefloquine is used to treat P. falciparum infection, drug pressure mediated by increased copy numbers of the multidrug resistance 1 gene (pvmdr1) may select for mefloquine-resistant P. vivax Surveillance is not undertaken routinely owing in part to methodological challenges in detection of gene amplification. Using genomic data on 88 P. vivax samples from western Thailand, we identified pvmdr1 amplification in 17 isolates, all exhibiting tandem copies of a 37.6-kilobase pair region with identical breakpoints. A novel breakpoint-specific polymerase chain reaction assay was designed to detect the amplification. The assay demonstrated high sensitivity, identifying amplifications in 13 additional, polyclonal infections. Application to 132 further samples identified the common breakpoint in all years tested (2003-2015), with a decline in prevalence after 2012 corresponding to local discontinuation of mefloquine regimens. Assessment of the structure of pvmdr1 amplification in other geographic regions will yield information about the population-specificity of the breakpoints and underlying amplification mechanisms.
在恶性疟原虫和间日疟原虫共流行地区,若使用甲氟喹治疗恶性疟原虫感染,多药耐药1基因(pvmdr1)拷贝数增加介导的药物压力可能会筛选出对甲氟喹耐药的间日疟原虫。由于基因扩增检测存在方法学挑战,目前尚未常规开展监测。利用来自泰国西部的88份间日疟原虫样本的基因组数据,我们在17株分离株中鉴定出pvmdr1扩增,所有分离株均表现出一个37.6千碱基对区域的串联拷贝,且断点相同。设计了一种新型的断点特异性聚合酶链反应检测方法来检测扩增。该检测方法显示出高灵敏度,在另外13例多克隆感染中鉴定出扩增。应用于另外132份样本时,在所有检测年份(2003 - 2015年)均鉴定出了共同断点,2012年后患病率下降,这与当地停用甲氟喹治疗方案相对应。评估其他地理区域pvmdr1扩增的结构将产生有关断点的人群特异性和潜在扩增机制的信息。