Taylor Steve M, Parobek Christian M, DeConti Derrick K, Kayentao Kassoum, Coulibaly Sheick Oumar, Greenwood Brian M, Tagbor Harry, Williams John, Bojang Kalifa, Njie Fanta, Desai Meghna, Kariuki Simon, Gutman Julie, Mathanga Don P, Mårtensson Andreas, Ngasala Billy, Conrad Melissa D, Rosenthal Philip J, Tshefu Antoinette K, Moormann Ann M, Vulule John M, Doumbo Ogobara K, Ter Kuile Feiko O, Meshnick Steven R, Bailey Jeffrey A, Juliano Jonathan J
Division of Infectious Diseases, Department of Medicine Duke Global Health Institute, Duke University Medical Center, Durham Department of Epidemiology, Gillings School of Global Public Health.
Curriculum in Genetics and Molecular Biology.
J Infect Dis. 2015 Mar 1;211(5):680-8. doi: 10.1093/infdis/jiu467. Epub 2014 Sep 1.
Plasmodium falciparum parasites that are resistant to artemisinins have been detected in Southeast Asia. Resistance is associated with several polymorphisms in the parasite's K13-propeller gene. The molecular epidemiology of these artemisinin resistance genotypes in African parasite populations is unknown. We developed an assay to quantify rare polymorphisms in parasite populations that uses a pooled deep-sequencing approach to score allele frequencies, validated it by evaluating mixtures of laboratory parasite strains, and then used it to screen P. falciparum parasites from >1100 African infections collected since 2002 from 14 sites across sub-Saharan Africa. We found no mutations in African parasite populations that are associated with artemisinin resistance in Southeast Asian parasites. However, we observed 15 coding mutations, including 12 novel mutations, and limited allele sharing between parasite populations, consistent with a large reservoir of naturally occurring K13-propeller variation. Although polymorphisms associated with artemisinin resistance in P. falciparum in Southeast Asia are not prevalent in sub-Saharan Africa, numerous K13-propeller coding polymorphisms circulate in Africa. Although their distributions do not support a widespread selective sweep for an artemisinin-resistant phenotype, the impact of these mutations on artemisinin susceptibility is unknown and will require further characterization. Rapid, scalable molecular surveillance offers a useful adjunct in tracking and containing artemisinin resistance.
在东南亚已检测到对青蒿素耐药的恶性疟原虫。耐药性与该寄生虫K13螺旋桨基因中的几种多态性有关。非洲寄生虫种群中这些青蒿素耐药基因型的分子流行病学尚不清楚。我们开发了一种用于量化寄生虫种群中罕见多态性的检测方法,该方法采用混合深度测序方法来计算等位基因频率,通过评估实验室寄生虫菌株的混合物对其进行验证,然后用它来筛查自2002年以来从撒哈拉以南非洲14个地点收集的1100多例非洲感染病例中的恶性疟原虫。我们在非洲寄生虫种群中未发现与东南亚寄生虫中与青蒿素耐药性相关的突变。然而,我们观察到15个编码突变,包括12个新突变,且寄生虫种群之间的等位基因共享有限,这与大量自然存在的K13螺旋桨变异库一致。尽管东南亚恶性疟原虫中与青蒿素耐药性相关的多态性在撒哈拉以南非洲并不普遍,但非洲存在大量K13螺旋桨编码多态性。尽管它们的分布不支持对青蒿素耐药表型进行广泛的选择性清除,但这些突变对青蒿素敏感性的影响尚不清楚,需要进一步表征。快速、可扩展的分子监测为追踪和控制青蒿素耐药性提供了一种有用的辅助手段。