Wang Zenglei, Shrestha Sony, Li Xiaolian, Miao Jun, Yuan Lili, Cabrera Mynthia, Grube Caitlin, Yang Zhaoqing, Cui Liwang
Department of Entomology, The Pennsylvania State University, University Park, PA, 16802, USA.
Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan Province, 650500, China.
Malar J. 2015 Apr 18;14:168. doi: 10.1186/s12936-015-0672-9.
The recent emergence and spread of artemisinin resistance in the Greater Mekong Subregion poses a great threat to malaria control and elimination. A K13-propeller gene (K13), PF3D7_1343700, has been associated lately with artemisinin resistance both in vitro and in vivo. This study aimed to investigate the K13 polymorphisms in Plasmodium falciparum parasites from the China-Myanmar border area where artemisinin use has the longest history.
A total of 180 archived P. falciparum isolates containing 191 parasite clones, mainly collected in 2007-2012 from the China-Myanmar area, were used to obtain the full-length K13 gene sequences.
Seventeen point mutations were identified in 46.1% (88/191) parasite clones, of which seven were new. The F446I mutation predominated in 27.2% of the parasite clones. The C580Y mutation that is correlated with artemisinin resistance was detected at a low frequency of 1.6%. Collectively, 43.1% of the parasite clones contained point mutations in the kelch domain of the K13 gene. Moreover, there was a trend of increase in the frequency of parasites carrying kelch domain mutations through the years of sample collection. In addition, a microsatellite variation in the N-terminus of the K13 protein was found to have reached a high frequency (69.1%).
This study documented the presence of mutations in the K13 gene in parasite populations from the China-Myanmar border. Mutations present in the kelch domain have become prevalent (>40%). A predominant mutation F446I and a prevalent microsatellite variation in the N-terminus were identified, but their importance in artemisinin resistance remains to be elucidated.
近期,青蒿素抗性在大湄公河次区域出现并传播,这对疟疾控制和消除构成了巨大威胁。K13螺旋桨基因(K13,PF3D7_1343700)最近在体外和体内均与青蒿素抗性相关。本研究旨在调查来自青蒿素使用历史最长的中缅边境地区的恶性疟原虫寄生虫中的K13多态性。
共使用180株存档的恶性疟原虫分离株,包含191个寄生虫克隆,主要于2007 - 2012年从中缅地区收集,以获取K13基因全长序列。
在46.1%(88/191)的寄生虫克隆中鉴定出17个点突变,其中7个为新突变。F446I突变在27.2%的寄生虫克隆中占主导。与青蒿素抗性相关的C580Y突变检测频率较低,为1.6%。总体而言,43.1%的寄生虫克隆在K13基因的kelch结构域中存在点突变。此外,在样本收集的年份中,携带kelch结构域突变的寄生虫频率有上升趋势。另外,发现K13蛋白N端的微卫星变异频率较高(69.1%)。
本研究记录了中缅边境寄生虫群体中K13基因存在突变。kelch结构域中的突变已变得普遍(>40%)。鉴定出了占主导的F446I突变和N端普遍存在的微卫星变异,但其在青蒿素抗性中的重要性仍有待阐明。