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两种不同人类菌群相关小鼠品系肠道微生物群的比较多样性分析

Comparative diversity analysis of gut microbiota in two different human flora-associated mouse strains.

作者信息

Zhang Xiaojing, Zeng Benhua, Liu Zhiwei, Liao Zhenlin, Li Wenxai, Wei Hong, Fang Xiang

机构信息

College of Food Science, South China Agricultural University, Guangzhou, 510642, China.

出版信息

Curr Microbiol. 2014 Sep;69(3):365-73. doi: 10.1007/s00284-014-0592-x. Epub 2014 May 8.

Abstract

The Kunming (KM) mouse is a closed colony mouse strain widely used in Chinese pharmacology, toxicology, and microbiology research laboratories. However, few studies have examined human flora-associated (HFA) microbial communities in KM mice. In this study, HFA models were built from germ-free KM and C57BL/6J mouse strains, and gut microbial diversity was analyzed by denaturing gradient gel electrophoresis (DGGE) and DNA sequencing. We found that the two strains of HFA mice were significantly different based on the UPGMA dendrogram and the Richness index, but dice similarity coefficients of mouse replicates were not significantly different between HFA-KM and HFA-C57BL/6J. Most of the dominant phyla of human gut microflora could be transferred into the guts of the two mouse strains. However, the predominant genus that formed in HFA-KM was Clostridium sp. and that in HFA-C57BL/6J was Blautia sp. These results imply that genotypes difference between the two mice strains is a critical factor in shaping the intestinal microflora. However, genetic differences of individuals within KM mouse populations failed to lead to individual difference in microflora. Successful generation of HFA-KM mice will facilitate studies examining how diet affects gut microbial structure, and will enable comparative studies for uncovering genetic factors that shape gut microbial communities.

摘要

昆明(KM)小鼠是一种封闭群小鼠品系,在中国药理学、毒理学和微生物学研究实验室中广泛使用。然而,很少有研究检测过KM小鼠的人源菌群相关(HFA)微生物群落。在本研究中,从无菌的KM和C57BL/6J小鼠品系构建了HFA模型,并通过变性梯度凝胶电泳(DGGE)和DNA测序分析肠道微生物多样性。我们发现,基于UPGMA树状图和丰富度指数,两种HFA小鼠品系存在显著差异,但HFA-KM和HFA-C57BL/6J小鼠重复样本的骰子相似系数没有显著差异。大多数人类肠道微生物优势菌门可转移至两种小鼠品系的肠道中。然而,HFA-KM中形成的优势菌属是梭菌属(Clostridium sp.),而HFA-C57BL/6J中是布劳特氏菌属(Blautia sp.)。这些结果表明,两种小鼠品系之间的基因型差异是塑造肠道微生物群的关键因素。然而,KM小鼠群体内个体的遗传差异并未导致微生物群的个体差异。成功培育HFA-KM小鼠将有助于研究饮食如何影响肠道微生物结构,并能够开展比较研究以揭示塑造肠道微生物群落的遗传因素。

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