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Investigation and Evaluation of Genetic Diversity of Plasmodium falciparum Kelch 13 Polymorphisms Imported From Southeast Asia and Africa in Southern China

机译:中国南方东南亚和非洲进口恶性疟原虫Kelch 13基因多态性的遗传多样性研究与评价

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>Objectives: In this study, we aimed to analyse the genetic diversity Kelch 13 (K13) propeller allele of the Plasmodium falciparum isolates mainly imported from Southeast Asia and Africa in southern China, including the provinces of Yunnan and Guangxi.>Methods: At enrolment, we collected blood samples from patients with confirmed cases of malaria infection between January 2012 and December 2017, for analysis. Individual patient information was obtained via a malaria surveillance system. The malaria infections and P. falciparum K13 mutations were diagnosed by using a nested polymerase chain reaction (PCR) method.>Results: The K13 mutations were identified in 283 P. falciparum isolates from 18 counties in Yunnan and 22 counties in Guangxi. Of Forty-six isolates (46/283, 16.3%) that harbored K13 mutant alleles were detected: 26.8% in Yunnan (33/123) and 8.1% in Guangxi (13/160). A total of 18 different K13 mutations were detected. Only the F446I mutation was detected in Yunnan isolates, and F446I was more frequent (20/46, 43.5%) than other alleles. Further, the temporal distribution of the F446I mutation ratio from 2012 to 2015 exhibited no significant difference in Yunnan Province (2012, 2/13, 15.4%; 2013, 7/40, 17.5%; 2014, 7/33, 21.2%; 2015, 4/37, 10.8%, p = 0.121). A578S allele was the main K13 mutation (5/283, 1.8%) from Africa. The K13 mutants were present in 33.3% of indigenous isolates, 27.4% of isolates from Southeast Asia, and 7.9% of isolates from Africa. The analysis of 10 neutral microsatellite loci of 60 isolates showed that at the TAA109 locus, the expected heterozygosity of F446I (He = 0.112 ± 0.007) was much lower than that of wild type and other mutation types in Myanmar isolates. With respect to geographic distribution, TAA109 also exhibited a significant difference between isolates from Southeast Asia (He = 0.139 ± 0.012) and those from Africa (He = 0.603 ± 0.044).>Conclusions: The present findings on the geographic diversity of K13 mutant alleles in P. falciparum may provide a basis for routine molecular surveillance and risk assessment, to monitor artemisinin resistance (ART) in China. Our results will be helpful for enriching the artemisinin resistance database in China during the elimination and post-elimination phases.
机译:>目的:本研究旨在分析主要从东南亚和非洲(包括云南和广西)进口的恶性疟原虫分离株的Kelch 13(K13)螺旋桨等位基因的遗传多样性。>方法:在入学时,我们从2012年1月至2017年12月期间确诊疟疾患者的血液样本中进行分析。个体患者信息是通过疟疾监测系统获得的。通过巢式聚合酶链反应(PCR)方法诊断出疟疾感染和恶性疟原虫K13突变。>结果:在云南18个县和22个县的283例恶性疟原虫中分离出K13突变。广西各县。在包含K13突变等位基因的46种分离株中(46/283,16.3%)被检测到:云南(26/8%)(33/123)和广西(8.1 / 13)。总共检测到18个不同的K13突变。在云南分离物中仅检测到F446I突变,并且F446I比其他等位基因更频繁(20/46,43.5%)。此外,2012年至2015年F446I突变率的时间分布在云南省没有显着差异(2012,2/13,15.4%; 2013,7/40,17.5%; 2014,7/33,21.2%; 2015 ,4 / 37,10.8%,p = 0.121)。 A578S等位基因是来自非洲的主要K13突变(5 / 283,1.8%)。 K13突变体存在于33.3%的本地分离株,27.4%的东南亚分离株和7.9%的非洲分离株中。对60个分离株的10个中性微卫星基因座进行的分析表明,在TAA109位点,F446I的预期杂合度(He = 0.112±0.007)远低于缅甸分离株的野生型和其他突变型。就地理分布而言,TAA109在东南亚分离株(He = 0.139±0.012)和非洲分离株(He = 0.603±0.044)之间也表现出显着差异。>结论:恶性疟原虫K13突变等位基因的地理多样性可能为常规分子监测和风险评估提供基础,以监测中国的青蒿素耐药性。我们的结果将有助于在消除和消除后阶段丰富中国的青蒿素耐药性数据库。

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