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Metabolite profiling of human‐originated Lachnospiraceae at the strain level

Authors :
Rashidin Abdugheni
Wen‐Zhao Wang
Yu‐Jing Wang
Meng‐Xuan Du
Feng‐Lan Liu
Nan Zhou
Cheng‐Ying Jiang
Chang‐Yu Wang
Linhuan Wu
Juncai Ma
Chang Liu
Shuang‐Jiang Liu
Source :
iMeta, Vol 1, Iss 4, Pp n/a-n/a (2022)
Publication Year :
2022
Publisher :
Wiley, 2022.

Abstract

Abstract The human gastrointestinal (GI) tract harbors diverse microbes, and the family Lachnospiraceae is one of the most abundant and widely occurring bacterial groups in the human GI tract. Beneficial and adverse effects of the Lachnospiraceae on host health were reported, but the diversities at species/strain levels as well as their metabolites of Lachnospiraceae have been, so far, not well documented. In the present study, we report on the collection of 77 human‐originated Lachnospiraceae species (please refer hLchsp, https://hgmb.nmdc.cn/subject/lachnospiraceae) and the in vitro metabolite profiles of 110 Lachnospiraceae strains (https://hgmb.nmdc.cn/subject/lachnospiraceae/metabolites). The Lachnospiraceae strains in hLchsp produced 242 metabolites of 17 categories. The larger categories were alcohols (89), ketones (35), pyrazines (29), short (C2–C5), and long (C > 5) chain acids (31), phenols (14), aldehydes (14), and other 30 compounds. Among them, 22 metabolites were aromatic compounds. The well‐known beneficial gut microbial metabolite, butyric acid, was generally produced by many Lachnospiraceae strains, and Agathobacter rectalis strain Lach‐101 and Coprococcus comes strain NSJ‐173 were the top 2 butyric acid producers, as 331.5 and 310.9 mg/L of butyric acids were produced in vitro, respectively. Further analysis of the publicly available cohort‐based volatile‐metabolomic data sets of human feces revealed that over 30% of the prevailing volatile metabolites were covered by Lachnospiraceae metabolites identified in this study. This study provides Lachnospiraceae strain resources together with their metabolic profiles for future studies on host–microbe interactions and developments of novel probiotics or biotherapies.

Details

Language :
English
ISSN :
2770596X
Volume :
1
Issue :
4
Database :
Directory of Open Access Journals
Journal :
iMeta
Publication Type :
Academic Journal
Accession number :
edsdoj.184d4987e1a14d6691322751e310df5f
Document Type :
article
Full Text :
https://doi.org/10.1002/imt2.58