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中国西部采集的多房棘球绦虫分离株线粒体基因的遗传变异

Genetic variation of mitochondrial genes among Echinococcus multilocularis isolates collected in western China.

作者信息

Wu Chuanchuan, Zhang Wenbao, Ran Bo, Fan Haining, Wang Hui, Guo Baoping, Zhou Canlin, Shao Yingmei, Zhang Wei, Giraudoux Patrick, Knapp Jenny, Wen Hao, Kuang Ling, Li Jun

机构信息

Clinic Medicine Research Institute, The First Teaching Hospital of Xinjiang Medical University, Urumqi, China.

Collage of Veterinary Medicine, Xinjiang Agriculture University Urumqi, Xinjiang, 830000, China.

出版信息

Parasit Vectors. 2017 May 30;10(1):265. doi: 10.1186/s13071-017-2172-y.

Abstract

BACKGROUND

Alveolar echinococcosis (AE) is a life-threatening human disease caused by Echinococcus multilocularis transmitted between rodents and dogs/foxes in the Northern Hemisphere. The study aims to identify the genetic variation of the parasite in AE patients from China.

METHODS

E. multilocularis isolates were collected from wild small mammals (n = 6) and AE patients (n = 56) from western China. Genomic DNA was extracted from different tissue samples including paraffin tissue blocks, ethanol fixed tissues and frozen tissues surgically removed. Two mitochondrial gene fragments (526 bp for cob and 474 bp for nad2) of E. multilocularis were amplified and sequenced.

RESULTS

The parasite fragment sequences of cob fragments from AE patients showed two haplotypes, and nad2 gene fragment sequences had four haplotypes. The gene sequences from Microtus sp. were 100% identical to the sequences of some isolates from AE patients. These haplotypes were distributed in both Qinghai and Xinjiang provinces. Alignment analysis with the sequences from the GenBank databases showed five genotypes including three Asian genotypes, one from Europe and one from North America.

CONCLUSIONS

Most AE patients harbored the Asian genotype 1 which may be an indication of its relative frequency in the definitive hosts and the environment or of its pathogenicity to humans, which calls for further research.

摘要

背景

肺泡型包虫病(AE)是一种由多房棘球绦虫引起的危及生命的人类疾病,该绦虫在北半球的啮齿动物与狗/狐狸之间传播。本研究旨在鉴定中国AE患者体内该寄生虫的基因变异情况。

方法

从中国西部的野生小型哺乳动物(n = 6)和AE患者(n = 56)中收集多房棘球绦虫分离株。从包括石蜡组织块、乙醇固定组织和手术切除的冷冻组织等不同组织样本中提取基因组DNA。扩增并测序多房棘球绦虫的两个线粒体基因片段(cob为526 bp,nad2为474 bp)。

结果

AE患者的cob片段的寄生虫片段序列显示出两种单倍型,nad2基因片段序列有四种单倍型。田鼠属的基因序列与部分AE患者分离株的序列100%相同。这些单倍型分布在青海和新疆两省。与GenBank数据库中的序列进行比对分析显示有五种基因型,包括三种亚洲基因型、一种欧洲基因型和一种北美基因型。

结论

大多数AE患者携带亚洲基因型1,这可能表明其在终末宿主和环境中的相对频率或其对人类的致病性,这需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0cc/5450100/08edbfb1b68d/13071_2017_2172_Fig1_HTML.jpg

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