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Selective Isolation of Bifidobacterium From Human Faeces Using Pangenomics, Metagenomics, and Enzymology

Bifidobacterium, an important genus for human health, is difficult to isolate. We applied metagenomics, pangenomics, and enzymology to determine the dominant glycoside hydrolase (GH) families of Bifidobacterium and designed selective medium for Bifidobacterium isolation. Pangenomics results showed t...

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Autores principales: Yang, Shuanghong, Xie, Xinqiang, Ma, Jun, He, Xingxiang, Li, Ying, Du, Mingzhu, Li, Longyan, Yang, Lingshuang, Wu, Qingping, Chen, Wei, Zhang, Jumei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096985/
https://www.ncbi.nlm.nih.gov/pubmed/33967985
http://dx.doi.org/10.3389/fmicb.2021.649698
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author Yang, Shuanghong
Xie, Xinqiang
Ma, Jun
He, Xingxiang
Li, Ying
Du, Mingzhu
Li, Longyan
Yang, Lingshuang
Wu, Qingping
Chen, Wei
Zhang, Jumei
author_facet Yang, Shuanghong
Xie, Xinqiang
Ma, Jun
He, Xingxiang
Li, Ying
Du, Mingzhu
Li, Longyan
Yang, Lingshuang
Wu, Qingping
Chen, Wei
Zhang, Jumei
author_sort Yang, Shuanghong
collection PubMed
description Bifidobacterium, an important genus for human health, is difficult to isolate. We applied metagenomics, pangenomics, and enzymology to determine the dominant glycoside hydrolase (GH) families of Bifidobacterium and designed selective medium for Bifidobacterium isolation. Pangenomics results showed that the GH13, GH3, GH42, and GH43 families were highly conserved in Bifidobacterium. Metagenomic analysis of GH families in human faecal samples was performed. The results indicated that Bifidobacterium contains core GHs for utilizing raffinose, D-trehalose anhydrous, D(+)-cellobiose, melibiose, lactulose, lactose, D(+)-sucrose, resistant starch, pullulan, xylan, and glucan. These carbohydrates as the main carbon sources were applied for selective media, which were more conducive to the growth of bifidobacteria. In the medium with lactose, raffinose and xylan as the main carbon sources, the ratio of cultivable bifidobacteria to cultivable microorganisms were 89.39% ± 2.50%, 71.45% ± 0.99%, and 53.95% ± 1.22%, respectively, whereas the ratio in the ordinary Gifu anaerobic medium was only 17.90% ± 0.58%. Furthermore, the species significantly (p < 0.05) varied among samples from different individuals. Results suggested that xylan might be a prebiotic that benefits host health, and it is feasible to screen and isolate bifidobacteria using the oligosaccharides corresponding to the specific GHs of bifidobacteria as the carbon sources of the selective media.
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spelling pubmed-80969852021-05-06 Selective Isolation of Bifidobacterium From Human Faeces Using Pangenomics, Metagenomics, and Enzymology Yang, Shuanghong Xie, Xinqiang Ma, Jun He, Xingxiang Li, Ying Du, Mingzhu Li, Longyan Yang, Lingshuang Wu, Qingping Chen, Wei Zhang, Jumei Front Microbiol Microbiology Bifidobacterium, an important genus for human health, is difficult to isolate. We applied metagenomics, pangenomics, and enzymology to determine the dominant glycoside hydrolase (GH) families of Bifidobacterium and designed selective medium for Bifidobacterium isolation. Pangenomics results showed that the GH13, GH3, GH42, and GH43 families were highly conserved in Bifidobacterium. Metagenomic analysis of GH families in human faecal samples was performed. The results indicated that Bifidobacterium contains core GHs for utilizing raffinose, D-trehalose anhydrous, D(+)-cellobiose, melibiose, lactulose, lactose, D(+)-sucrose, resistant starch, pullulan, xylan, and glucan. These carbohydrates as the main carbon sources were applied for selective media, which were more conducive to the growth of bifidobacteria. In the medium with lactose, raffinose and xylan as the main carbon sources, the ratio of cultivable bifidobacteria to cultivable microorganisms were 89.39% ± 2.50%, 71.45% ± 0.99%, and 53.95% ± 1.22%, respectively, whereas the ratio in the ordinary Gifu anaerobic medium was only 17.90% ± 0.58%. Furthermore, the species significantly (p < 0.05) varied among samples from different individuals. Results suggested that xylan might be a prebiotic that benefits host health, and it is feasible to screen and isolate bifidobacteria using the oligosaccharides corresponding to the specific GHs of bifidobacteria as the carbon sources of the selective media. Frontiers Media S.A. 2021-04-21 /pmc/articles/PMC8096985/ /pubmed/33967985 http://dx.doi.org/10.3389/fmicb.2021.649698 Text en Copyright © 2021 Yang, Xie, Ma, He, Li, Du, Li, Yang, Wu, Chen and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Yang, Shuanghong
Xie, Xinqiang
Ma, Jun
He, Xingxiang
Li, Ying
Du, Mingzhu
Li, Longyan
Yang, Lingshuang
Wu, Qingping
Chen, Wei
Zhang, Jumei
Selective Isolation of Bifidobacterium From Human Faeces Using Pangenomics, Metagenomics, and Enzymology
title Selective Isolation of Bifidobacterium From Human Faeces Using Pangenomics, Metagenomics, and Enzymology
title_full Selective Isolation of Bifidobacterium From Human Faeces Using Pangenomics, Metagenomics, and Enzymology
title_fullStr Selective Isolation of Bifidobacterium From Human Faeces Using Pangenomics, Metagenomics, and Enzymology
title_full_unstemmed Selective Isolation of Bifidobacterium From Human Faeces Using Pangenomics, Metagenomics, and Enzymology
title_short Selective Isolation of Bifidobacterium From Human Faeces Using Pangenomics, Metagenomics, and Enzymology
title_sort selective isolation of bifidobacterium from human faeces using pangenomics, metagenomics, and enzymology
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096985/
https://www.ncbi.nlm.nih.gov/pubmed/33967985
http://dx.doi.org/10.3389/fmicb.2021.649698
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