Center for Global Health and Infectious Diseases Research, College of Public Health, University of South Florida, Tampa, Florida, USA.
Department of Internal Medicine, Morsani College of Medicine, University of South Florida, Tampa, Florida, USA.
J Infect Dis. 2020 Oct 1;222(9):1561-1569. doi: 10.1093/infdis/jiaa250.
Deletion of the pfhrp2 gene in Plasmodium falciparum can lead to false-negative rapid diagnostic test (RDT) results, constituting a major challenge for evidence-based malaria treatment. Here we analyzed the whole genome sequences of 138 P. falciparum clinical samples collected from the China-Myanmar boarder for pfhrp2 and pfhrp3 gene deletions. We found pfhrp2 and pfhrp3 deletions in 9.4% and 3.6% of samples, respectively, with no samples harboring deletions of both genes. The pfhrp2 deletions showed 2 distinct breakpoints, representing 2 different chromosomal deletion events. A phylogenetic analysis performed using genome-wide single-nucleotide polymorphisms revealed that the 2 pfhrp2 breakpoint groups as well as all the pfhrp3-negative parasites formed separate clades, suggesting they might have resulted from clonal expansion of pfhrp2- and pfhrp3-negative parasites. These findings highlight the need for urgent surveys to determine the prevalence of pfhrp2-negative parasites causing false-negative RDT results and a plan for switching of RDTs pending the survey results.
疟原虫 falciparum 中 pfhrp2 基因的缺失可能导致快速诊断检测(RDT)的假阴性结果,这是基于证据的疟疾治疗的一个主要挑战。在这里,我们分析了从中国-缅甸边境采集的 138 个疟原虫临床样本的全基因组序列,以研究 pfhrp2 和 pfhrp3 基因缺失情况。我们发现,pfhrp2 和 pfhrp3 缺失的比例分别为 9.4%和 3.6%,没有同时缺失这两个基因的样本。pfhrp2 缺失显示出 2 个不同的断点,代表 2 个不同的染色体缺失事件。使用全基因组单核苷酸多态性进行的系统发育分析表明,2 个 pfhrp2 断点组以及所有 pfhrp3 阴性寄生虫形成了单独的分支,表明它们可能是由 pfhrp2 和 pfhrp3 阴性寄生虫的克隆扩张引起的。这些发现强调了迫切需要进行调查,以确定导致 RDT 假阴性结果的 pfhrp2 阴性寄生虫的流行率,并在调查结果出来之前制定 RDT 转换计划。