伴侣动物肠道微生物组的综合概况,整合基于参考和无参考的方法

Tobyn Branck, Zhiji Hu, William A Nickols, Aaron M Walsh, Amrisha Bhosle, Meghan I Short, Jacob T Nearing, Francesco Asnicar, Lauren J McIver, Sagun Maharjan, Ali Rahnavard, Artemis Louyakis, Dayakar V Badri, Christoph Brockel, Kelsey N Thompson, Curtis Huttenhower
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引用次数: 0

摘要

尽管伴侣动物的肠道微生物组与动物健康、宠物主人健康和基础微生物群落生物学息息相关,但对它们的研究却相对不足。在这里,我们提供了迄今为止最全面的犬科和猫科动物肠道微生物组分析,纳入了 2639 个粪便猎枪元基因组(犬科 2272 个,猫科 367 个),涵盖 14 个公开可用的数据集(n = 730)和 8 个新的研究群体(n = 1909)。这些数据分别与来自人类微生物组计划 1-II 和马达加斯加传统生活人群的 238 个和 112 个基线人类肠道元基因组进行了比较,处理方式与动物元基因组相同。所有微生物组都采用了基于参考的分类和功能分析方法,并进行了从头组装,得到了按物种级基因组分组的元基因组。伴侣动物共有 184 个人类没有的物种级基因组,而所有三个宿主共有 198 个物种级基因组。我们采用了新的方法来区分这些共有生物的菌株,这些菌株要么是宿主物种转移的,要么是宿主物种独有的,其系统发育模式表明微生物菌系的宿主特异性适应。这与这些菌系按宿主的功能分化(如代谢和抗生素耐药性基因的差异)相对应,可能对伴侣动物的健康很重要。这项研究提供了迄今为止最大的伴侣动物肠道元基因组资源,极大地促进了我们对 "同一健康 "概念的理解,即人类和伴侣动物共享微生物环境,从而影响传染病、免疫反应和特定遗传因子。
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Comprehensive profile of the companion animal gut microbiome integrating reference-based and reference-free methods
The gut microbiome of companion animals is relatively underexplored, despite its relevance to animal health, pet owner health, and basic microbial community biology. Here, we provide the most comprehensive analysis of the canine and feline gut microbiomes to date, incorporating 2639 stool shotgun metagenomes (2272 dog and 367 cat) spanning 14 publicly available datasets (n = 730) and 8 new study populations (n = 1909). These are compared with 238 and 112 baseline human gut metagenomes from the Human Microbiome Project 1-II and a traditionally living Malagasy cohort, respectively, processed in a manner identical to the animal metagenomes. All microbiomes were characterized using reference-based taxonomic and functional profiling, as well as de novo assembly yielding metagenomic assembled genomes clustered into species-level genome bins. Companion animals shared 184 species-level genome bins not found in humans, whereas 198 were found in all three hosts. We applied novel methodology to distinguish strains of these shared organisms either transferred or unique to host species, with phylogenetic patterns suggesting host-specific adaptation of microbial lineages. This corresponded with functional divergence of these lineages by host (e.g., differences in metabolic and antibiotic resistance genes) likely important to companion animal health. This study provides the largest resource to date of companion animal gut metagenomes and greatly contributes to our understanding of the “One Health” concept of a shared microbial environment among humans and companion animals, affecting infectious diseases, immune response, and specific genetic elements.
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