基于线粒体16S核糖体RNA基因的细粒棘球蚴遗传变异。

Mitochondrial Dna Pub Date : 2015-06-01 Epub Date: 2013-10-14 DOI:10.3109/19401736.2013.840590
Ning Wang, Jiahai Wang, Dandan Hu, Xiuqin Zhong, Zhongrong Jiang, Aiguo Yang, Shijin Deng, Li Guo, Dawa Tsering, Shuxian Wang, Xiaobin Gu, Xuerong Peng, Guangyou Yang
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引用次数: 21

摘要

细粒棘球蚴是囊性棘球蚴病的病原,囊性棘球蚴病是一种主要的人畜共患疾病。本研究首次利用线粒体16s核糖体RNA基因对西藏高原细粒棘球绦虫的遗传变异和遗传结构进行了分析。对西藏高原3个种群的62株细粒棘球绦虫进行了测序。经BLAST分析,61株分离物属于g1 ~ g3基因型的严格感细粒绦虫,1株属于G6基因型的加拿大细粒绦虫。我们检测到16个单倍型,单倍型网络呈星形扩张,最常见的单倍型占据网络的中心。单倍型多样性和核苷酸多样性较低,Tajima’s D和Fu’s f为负值。AMOVA结果和Fst值显示,3个地理种群没有遗传分化。我们的研究结果表明,过去曾发生过种群瓶颈或种群扩张,这解释了青藏高原颗粒棘球绦虫遗传变异性低的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic variability of Echinococcus granulosus based on the mitochondrial 16S ribosomal RNA gene.

Echinococcus granulosus is the etiological agent of cystic echinococcosis, a major zoonotic disease of both humans and animals. In this study, we assessed genetic variability and genetic structure of E. granulosus in the Tibet plateau, using the complete mitochondrial 16 S ribosomal RNA gene for the first time. We collected and sequenced 62 isolates of E. granulosus from 3 populations in the Tibet plateau. A BLAST analysis indicated that 61 isolates belonged to E. granulosus sensu stricto (genotypes G1-G3), while one isolate belonged to E. canadensis (genotype G6). We detected 16 haplotypes with a haplotype network revealing a star-like expansion, with the most common haplotype occupying the center of the network. Haplotype diversity and nucleotide diversity were low, while negative values were observed for Tajima's D and Fu's Fs. AMOVA results and Fst values revealed that the three geographic populations were not genetically differentiated. Our results suggest that a population bottleneck or population expansion has occurred in the past, and that this explains the low genetic variability of E. granulosus in the Tibet Plateau.

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来源期刊
Mitochondrial Dna
Mitochondrial Dna 生物-遗传学
自引率
0.00%
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0
审稿时长
2.4 months
期刊介绍: Previously published under the title DNA Sequence (Vols 1-19.3), Mitochondrial DNA accepts original high-quality reports based on mapping, sequencing and analysis of mitochondrial DNA and RNA. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, medical genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The editorial board will also consider manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences.
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