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通过体外微生物培养和宏基因组测序相结合的方法对克罗恩病黏膜相关微生物群进行新型菌株水平分辨率分析。

Novel strain-level resolution of Crohn's disease mucosa-associated microbiota via an ex vivo combination of microbe culture and metagenomic sequencing.

机构信息

The University of Queensland Diamantina Institute, Faculty of Medicine, University of Queensland, Woolloongabba, QLD, Australia.

Wacker Biotech B.V., Amsterdam, The Netherlands.

出版信息

ISME J. 2021 Nov;15(11):3326-3338. doi: 10.1038/s41396-021-00991-1. Epub 2021 May 25.

Abstract

The mucosa-associated microbiota is widely recognized as a potential trigger for Crohn's disease pathophysiology but remains largely uncharacterised beyond its taxonomic composition. Unlike stool microbiota, the functional characterisation of these communities using current DNA/RNA sequencing approaches remains constrained by the relatively small microbial density on tissue, and the overwhelming amount of human DNA recovered during sample preparation. Here, we have used a novel ex vivo approach that combines microbe culture from anaerobically preserved tissue with metagenome sequencing (MC-MGS) to reveal patient-specific and strain-level differences among these communities in post-operative Crohn's disease patients. The 16 S rRNA gene amplicon profiles showed these cultures provide a representative and holistic representation of the mucosa-associated microbiota, and MC-MGS produced both high quality metagenome-assembled genomes of recovered novel bacterial lineages. The MC-MGS approach also produced a strain-level resolution of key Enterobacteriacea and their associated virulence factors and revealed that urease activity underpins a key and diverse metabolic guild in these communities, which was confirmed by culture-based studies with axenic cultures. Collectively, these findings using MC-MGS show that the Crohn's disease mucosa-associated microbiota possesses taxonomic and functional attributes that are highly individualistic, borne at least in part by novel bacterial lineages not readily isolated or characterised from stool samples using current sequencing approaches.

摘要

黏膜相关微生物群被广泛认为是克罗恩病发病机制的潜在触发因素,但除了其分类组成外,其功能特征在很大程度上仍未得到描述。与粪便微生物群不同,使用当前的 DNA/RNA 测序方法对这些群落进行功能特征描述仍然受到组织上相对较小的微生物密度以及在样品制备过程中回收的大量人 DNA 的限制。在这里,我们使用了一种新颖的离体方法,该方法结合了厌氧保存组织中的微生物培养物和宏基因组测序 (MC-MGS),以揭示术后克罗恩病患者这些群落中的患者特异性和菌株水平差异。16S rRNA 基因扩增子图谱显示,这些培养物提供了黏膜相关微生物群的代表性和整体代表性,并且 MC-MGS 产生了高质量的回收新型细菌谱系的宏基因组组装基因组。MC-MGS 方法还实现了关键肠杆菌科及其相关毒力因子的菌株水平分辨率,并揭示了脲酶活性为这些群落中的一个关键和多样化的代谢群提供了基础,这通过与无菌培养物的基于培养的研究得到了证实。总之,使用 MC-MGS 的这些发现表明,克罗恩病黏膜相关微生物群具有高度个体化的分类和功能属性,至少部分归因于使用当前测序方法从粪便样本中不易分离或表征的新型细菌谱系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3175/8528831/0e5ca82350d0/41396_2021_991_Fig1_HTML.jpg

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