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蒙古人体棘球蚴基因型的初步研究。

A first insight into the genotypes of Echinococcus granulosus from humans in Mongolia.

机构信息

Department of Veterinary Science, The University of Melbourne, Victoria 3030, Australia.

出版信息

Mol Cell Probes. 2011 Feb;25(1):49-54. doi: 10.1016/j.mcp.2010.11.001. Epub 2010 Nov 12.

Abstract

Polymerase chain reaction (PCR)-based single-strand conformation polymorphism (SSCP) and targeted sequencing were employed to genetically classify Echinococcus granulosus cysts from humans from 12 provinces in Mongolia using two DNA loci, designated pcox-1 and pnad-1, within the mitochondrial cytochrome c oxidase subunit 1 (cox-1) and NADH dehydrogenase subunit 1 (nad-1) genes, respectively. SSCP analysis of pcox-1 and pnad-1 amplicons produced from genomic DNA samples from individual E. granulosus cysts (n = 50) from individual humans displayed four distinct electrophoretic profiles for each pcox-1 and pnad-1. The direct sequencing of selected amplicons representing each of these profiles defined four distinct sequence types for each locus, present in four different combinations (designated as haplotypes M1-M4) for all 50 cyst isolates. Phylogenetic analysis of concatenated sequence data for these four haplotypes, including well-defined reference sequences, inferred that 68% of the cyst isolates belonged to the G1-G3 complex of E. granulosus (or E. granulosus sensu stricto), whereas the remaining (32%) were linked to the G6-G10 complex (or Echinococcus canadensis). Humans infected with E. granulosus cysts of the G1-G3 complex originated mainly from the eastern regions of Mongolia, whereas those harbouring cysts of the G6-G10 complex were from the western part of this country. The present study provides a first glimpse of the genetic composition of E. granulosus from humans in Mongolia, and forms a foundation for future studies of the epidemiology and ecology of the parasite(s) in animals and humans in this and surrounding countries.

摘要

聚合酶链反应(PCR)-基于单链构象多态性(SSCP)和靶向测序用于通过线粒体细胞色素 c 氧化酶亚基 1(cox-1)和 NADH 脱氢酶亚基 1(nad-1)基因内的两个 DNA 位点,分别命名为 pcox-1 和 pnad-1,对来自蒙古 12 个省份的人类的细粒棘球蚴囊肿进行遗传分类。从单个细粒棘球蚴囊肿(n=50)的个体基因组 DNA 样本中扩增 pcox-1 和 pnad-1 扩增子的 SSCP 分析显示,每个 pcox-1 和 pnad-1 的电泳图谱均显示出四种不同的电泳谱带。代表每个图谱的选定扩增子的直接测序定义了每个基因座的四种不同序列类型,这些序列类型存在于四个不同的组合(命名为 haplotypes M1-M4)中,共 50 个囊肿分离株。对这四个单倍型的串联序列数据进行的系统发育分析,包括明确的参考序列,推断 68%的囊肿分离株属于细粒棘球蚴的 G1-G3 复合物(或细粒棘球蚴),而其余(32%)与 G6-G10 复合物(或加拿大棘球蚴)有关。感染细粒棘球蚴 G1-G3 复合物囊肿的人类主要来自蒙古东部地区,而感染 G6-G10 复合物囊肿的人类则来自该国西部。本研究首次揭示了蒙古人类细粒棘球蚴的遗传组成,并为未来在该地区及周边国家对寄生虫的流行病学和生态学进行研究奠定了基础。

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