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A PCR-Based Technique to Track the Geographic Origin of Plasmodium falciparum With 23-SNP Barcode Analysis

机译:基于PCR的技术,以跟踪疟原虫的地理起源与23-SNP条形码分析

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Increased population movement has increased the risk of reintroducing parasites to elimination areas and also dispersing drug-resistant parasites to new regions. Therefore, reliable and repeatable methods to trace back to the source of imported infections are essential. The recently developed 23-single-nucleotide polymorphism (SNP) barcode from organellar genomes of mitochondrion ( mt ) and apicoplast ( apico ) provides a valuable tool to locate the geographic origin of Plasmodium falciparum . This study aims to explore the feasibility of using the 23-SNP barcode for tracking P. falciparum by polymerase chain reaction and sequencing, while providing geographical haplotypes of isolates that originated from Central Africa. Based on 23-SNP barcode analysis, SNPs were found at seven loci; 27 isolates were confirmed to have originated in West Africa, and this study also showed four isolates from Central Africa (Equatorial Guinea, 3; Republic of Congo, 1) that originated in East Africa. This study provides the sequence data from Central Africa and fills 23-SNP barcode data gaps of sample origins.
机译:增加的人口运动增加了将寄生虫的风险提高到消除区域,并且还将耐药寄生虫分散到新地区。因此,追溯到进口感染源的可靠和可重复的方法是必不可少的。来自线粒体(MT)和Apicoplast(APICO)的细胞细胞基因组的最近开发的23单核苷酸多态性(SNP)条形码提供了有价值的工具,以定位疟原虫的地理来源。本研究旨在探讨使用23-SNP条形码进行聚合酶链反应和测序跟踪P.Malciparum的可行性,同时提供源自中非的分离物的地理单倍型。基于23-SNP条形码分析,在七个位置发现SNP;确认27个分离物起源于西非,本研究还显示出来自中非(赤道几内亚,3;刚果共和国,1)的四个孤立株,该研究起源于东非。本研究提供了来自中非的序列数据,并填充了示例起源的23-SNP条形码数据差距。

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