| Literature DB >> 32386321 |
Justin Gibbons1, Junling Qin2, Pallavi Malla2, Zenglei Wang3, Awtum Brashear2, Chengqi Wang1, Jun Miao1,2, John H Adams1, Kami Kim1,2, Rays Jiang1, Liwang Cui1,2.
Abstract
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.Entities:
Keywords: zzm321990 Plasmodium falciparumzzm321990 ; zzm321990 pfhrp2 deletion; Southeast Asia; clonal expansion; genome
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Year: 2020 PMID: 32386321 PMCID: PMC7529045 DOI: 10.1093/infdis/jiaa250
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226