爬行动物肠道内核心细菌属拟杆菌的非培养种水平分类和功能特征。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Carmen Hoffbeck, Danielle M. R. L. Middleton, Jessica A. Wallbank, Jian S. Boey, Michael W. Taylor
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引用次数: 0

摘要

拟杆菌属是与肠道微生物群相关的广泛而丰富的细菌分类群。拟杆菌属的物种填补了许多生态位,包括作为共生菌、共生菌和寄主的病原体。在许多爬行动物中,拟杆菌是一种占主导地位的“核心”肠道细菌,有时在食物短缺的时候,比如在冬眠期间,它们的数量会增加。在这里,我们采取双管齐下的方法来更好地表征爬行动物肠道中的拟杆菌群。首先,我们利用已发表的16S rRNA基因序列数据集来确定拟杆菌纲成员在爬行动物宿主中的物种水平分布。其次,我们从爬行动物、鸟类、两栖动物和哺乳动物的宏基因组中提取拟杆菌的数据,比较拟杆菌在不同宿主分类群中的功能潜力。16S rRNA基因分析表明,嗜酸b杆菌是爬行动物肠道中最常见的拟杆菌种类,并且不同目爬行动物所含的拟杆菌种类不同。在爬行目之间,在鸟类、两栖动物和哺乳动物之间,从宏基因组组装中恢复的拟杆菌属的分类没有显著差异。拟杆菌种的宏基因组组装基因组与宿主的亲缘关系越密切,它们之间的亲缘关系也越密切,特别是爬行动物宿主与其他宿主相比,拥有明显更多独特的拟杆菌种mag。我们的研究结果表明,在广泛的比较中,宿主具有相似的拟杆菌种类,但在爬行动物群体之间存在一些差异,并且无论宿主的亲缘关系如何,拟杆菌在脊椎动物宿主肠道中似乎发挥了很大程度上相似的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Culture-Independent Species-Level Taxonomic and Functional Characterisation of Bacteroides, the Core Bacterial Genus Within Reptile Guts

Culture-Independent Species-Level Taxonomic and Functional Characterisation of Bacteroides, the Core Bacterial Genus Within Reptile Guts

The genus Bacteroides is a widespread and abundant bacterial taxon associated with gut microbiotas. Species within Bacteroides fill many niches, including as mutualists, commensals and pathogens for their hosts. Within many reptiles, Bacteroides is a dominant, ‘core’ gut bacterium that sometimes exhibits increased abundance in times of food scarcity, such as during hibernation. Here, we take a two-pronged approach to better characterise Bacteroides populations in reptile guts. Firstly, we leverage published 16S rRNA gene sequence datasets to determine the species-level distributions of Bacteroides members in reptile hosts. Secondly, we mine publicly available metagenomes to extract data for Bacteroides from reptiles, birds, amphibians and mammals, to compare the functional potential of Bacteroides in different host taxa. The 16S rRNA gene analyses revealed that B. acidifaciens is the most common Bacteroides species in reptile guts, and that different orders of reptiles differ in which Bacteroides species they harbour. The taxonomy of Bacteroides species recovered from metagenomic assembly did not differ between reptile orders or substantially across birds, amphibians and mammals. Metagenome-assembled genomes for Bacteroides species were marginally more related when their hosts were more closely related, with reptile hosts in particular harbouring markedly more unique Bacteroides MAGs compared to other hosts. Our findings indicate that hosts harbour similar profiles of Bacteroides species across broad comparisons, but with some differences between reptile groups, and that Bacteroides appears to perform largely similar roles in vertebrate host guts regardless of host relatedness.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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