Carter Tamar E, Boulter Alexis, Existe Alexandre, Romain Jean R, St Victor Jean Yves, Mulligan Connie J, Okech Bernard A
Genetics and Genomics Program, University of Florida, Gainesville, Florida; Department of Anthropology, University of Florida, Gainesville, Florida; Genetics Institute, University of Florida, Gainesville, Florida; National Public Health Laboratory, Ministry of Public Health and the Population, Port-au-Prince, Haiti; Hospital Saint Croix, Leogane, Haiti; Blanchard Clinic, Terre Noire, Haiti; Emerging Pathogens Institute, University of Florida, Gainesville, Florida; Department of Environmental and Global Health, University of Florida, Gainesville, Florida
Genetics and Genomics Program, University of Florida, Gainesville, Florida; Department of Anthropology, University of Florida, Gainesville, Florida; Genetics Institute, University of Florida, Gainesville, Florida; National Public Health Laboratory, Ministry of Public Health and the Population, Port-au-Prince, Haiti; Hospital Saint Croix, Leogane, Haiti; Blanchard Clinic, Terre Noire, Haiti; Emerging Pathogens Institute, University of Florida, Gainesville, Florida; Department of Environmental and Global Health, University of Florida, Gainesville, Florida.
Am J Trop Med Hyg. 2015 Mar;92(3):552-4. doi: 10.4269/ajtmh.14-0664. Epub 2015 Feb 2.
Antimalarial drugs are a key tool in malaria elimination programs. With the emergence of artemisinin resistance in southeast Asia, an effort to identify molecular markers for surveillance of resistant malaria parasites is underway. Non-synonymous mutations in the kelch propeller domain (K13-propeller) in Plasmodium falciparum have been associated with artemisinin resistance in samples from southeast Asia, but additional studies are needed to characterize this locus in other P. falciparum populations with different levels of artemisinin use. Here, we sequenced the K13-propeller locus in 82 samples from Haiti, where limited government oversight of non-governmental organizations may have resulted in low-level use of artemisinin-based combination therapies. We detected a single-nucleotide polymorphism (SNP) at nucleotide 1,359 in a single isolate. Our results contribute to our understanding of the global genomic diversity of the K13-propeller locus in P. falciparum populations.
抗疟药物是疟疾消除计划中的关键工具。随着东南亚地区青蒿素耐药性的出现,目前正在努力寻找监测耐药疟原虫的分子标记。恶性疟原虫中kelch螺旋桨结构域(K13螺旋桨)的非同义突变与东南亚样本中的青蒿素耐药性有关,但需要更多研究来表征其他不同青蒿素使用水平的恶性疟原虫群体中的该位点。在此,我们对来自海地的82个样本中的K13螺旋桨位点进行了测序,海地政府对非政府组织的监管有限,可能导致基于青蒿素的联合疗法使用水平较低。我们在一个分离株的第1359位核苷酸处检测到一个单核苷酸多态性(SNP)。我们的结果有助于我们了解恶性疟原虫群体中K13螺旋桨位点的全球基因组多样性。