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2
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Novel pfk13 polymorphisms in Plasmodium falciparum population in Ghana.加纳恶性疟原虫群体中新的 pfk13 多态性。
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本文引用的文献

1
A Worldwide Map of Plasmodium falciparum K13-Propeller Polymorphisms.恶性疟原虫K13螺旋桨多态性的全球地图。
N Engl J Med. 2016 Jun 23;374(25):2453-64. doi: 10.1056/NEJMoa1513137.
2
A Method for Amplicon Deep Sequencing of Drug Resistance Genes in Plasmodium falciparum Clinical Isolates from India.一种用于对来自印度的恶性疟原虫临床分离株中耐药基因进行扩增子深度测序的方法。
J Clin Microbiol. 2016 Jun;54(6):1500-1511. doi: 10.1128/JCM.00235-16. Epub 2016 Mar 23.
3
Advanced Molecular Detection of Malarone Resistance.甲氟喹耐药性的高级分子检测
Antimicrob Agents Chemother. 2016 May 23;60(6):3821-3. doi: 10.1128/AAC.00171-16. Print 2016 Jun.
4
Genomic epidemiology of artemisinin resistant malaria.青蒿素耐药性疟疾的基因组流行病学
Elife. 2016 Mar 4;5:e08714. doi: 10.7554/eLife.08714.
5
Independent Emergence of the Plasmodium falciparum Kelch Propeller Domain Mutant Allele C580Y in Guyana.圭亚那恶性疟原虫 Kelch 螺旋域突变等位基因 C580Y 的独立出现。
J Infect Dis. 2016 May 1;213(9):1472-5. doi: 10.1093/infdis/jiv752. Epub 2015 Dec 21.
6
Emergence of Mutations in the K13 Propeller Gene of Plasmodium falciparum Isolates from Dakar, Senegal, in 2013-2014.2013 - 2014年塞内加尔达喀尔恶性疟原虫分离株K13螺旋桨基因中突变的出现
Antimicrob Agents Chemother. 2015 Oct 26;60(1):624-7. doi: 10.1128/AAC.01346-15. Print 2016 Jan.
7
Genetic Analysis and Species Specific Amplification of the Artemisinin Resistance-Associated Kelch Propeller Domain in P. falciparum and P. vivax.恶性疟原虫和间日疟原虫中与青蒿素抗性相关的 Kelch 螺旋桨结构域的遗传分析及物种特异性扩增
PLoS One. 2015 Aug 20;10(8):e0136099. doi: 10.1371/journal.pone.0136099. eCollection 2015.
8
Antimalarial Drug Resistance: Literature Review and Activities and Findings of the ICEMR Network.抗疟药物耐药性:文献综述及ICEMR网络的活动与发现
Am J Trop Med Hyg. 2015 Sep;93(3 Suppl):57-68. doi: 10.4269/ajtmh.15-0007. Epub 2015 Aug 10.
9
Frequency-based haplotype reconstruction from deep sequencing data of bacterial populations.基于频率的细菌群体深度测序数据单倍型重建
Nucleic Acids Res. 2015 Sep 18;43(16):e105. doi: 10.1093/nar/gkv478. Epub 2015 May 18.
10
Selection and spread of artemisinin-resistant alleles in Thailand prior to the global artemisinin resistance containment campaign.在全球青蒿素抗药遏制行动之前泰国青蒿素抗药等位基因的选择与传播。
PLoS Pathog. 2015 Apr 2;11(4):e1004789. doi: 10.1371/journal.ppat.1004789. eCollection 2015 Apr.

塞内加尔恶性疟原虫kelch13基因突变的分子流行病学研究:基于靶向扩增子深度测序技术

Molecular Epidemiology of Plasmodium falciparum kelch13 Mutations in Senegal Determined by Using Targeted Amplicon Deep Sequencing.

作者信息

Talundzic Eldin, Ndiaye Yaye D, Deme Awa B, Olsen Christian, Patel Dhruviben S, Biliya Shweta, Daniels Rachel, Vannberg Fredrik O, Volkman Sarah K, Udhayakumar Venkatachalam, Ndiaye Daouda

机构信息

Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA

Atlanta Research and Education Foundation, VAMC, Atlanta, Georgia, USA.

出版信息

Antimicrob Agents Chemother. 2017 Feb 23;61(3). doi: 10.1128/AAC.02116-16. Print 2017 Mar.

DOI:10.1128/AAC.02116-16
PMID:28069653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5328579/
Abstract

The emergence of resistance to artemisinin in Southeast Asia threatens malaria control and elimination activities worldwide. Multiple polymorphisms in the gene found in chromosome 13 () have been associated with artemisinin resistance. Surveillance of potential drug resistance loci within a population that may emerge under increasing drug pressure is an important public health activity. In this context, infections from an observational surveillance study in Senegal were genotyped using targeted amplicon deep sequencing (TADS) for polymorphisms. The results were compared to previously reported polymorphisms from around the world. A total of 22 propeller domain polymorphisms were identified in this study, of which 12 have previously not been reported. Interestingly, of the 10 polymorphisms identified in the present study that were also previously reported, all had a different amino acid substitution at these codon positions. Most of the polymorphisms were present at low frequencies and were confined to single isolates, suggesting they are likely transient polymorphisms that are part of naturally evolving parasite populations. The results of this study underscore the need to identify potential drug resistance loci existing within a population, which may emerge under increasing drug pressure.

摘要

东南亚地区青蒿素耐药性的出现威胁着全球疟疾控制与消除行动。在13号染色体( )上发现的该基因中的多个多态性与青蒿素耐药性相关。监测在不断增加的药物压力下可能出现的人群中潜在的耐药位点是一项重要的公共卫生活动。在此背景下,对塞内加尔一项观察性监测研究中的感染样本使用靶向扩增子深度测序(TADS)对 多态性进行基因分型。将结果与此前全球报道的 多态性进行比较。本研究共鉴定出22个 螺旋桨结构域多态性,其中12个此前未被报道。有趣的是,在本研究中鉴定出的10个此前也有报道的多态性中,所有这些密码子位置都有不同的氨基酸替换。大多数多态性以低频出现且局限于单个分离株,表明它们可能是自然进化的寄生虫群体中一部分的短暂多态性。本研究结果强调了识别群体中存在的潜在耐药位点的必要性,这些位点可能在不断增加的药物压力下出现。