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Metagenome-mining indicates an association between bacteriocin presence and strain diversity in the infant gut
BACKGROUND: Our knowledge about the ecological role of bacterial antimicrobial peptides (bacteriocins) in the human gut is limited, particularly in relation to their role in the diversification of the gut microbiota during early life. The aim of this paper was therefore to address associations betwe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230729/ https://www.ncbi.nlm.nih.gov/pubmed/37259063 http://dx.doi.org/10.1186/s12864-023-09388-0 |
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author | Ormaasen, Ida Rudi, Knut Diep, Dzung B. Snipen, Lars |
author_facet | Ormaasen, Ida Rudi, Knut Diep, Dzung B. Snipen, Lars |
author_sort | Ormaasen, Ida |
collection | PubMed |
description | BACKGROUND: Our knowledge about the ecological role of bacterial antimicrobial peptides (bacteriocins) in the human gut is limited, particularly in relation to their role in the diversification of the gut microbiota during early life. The aim of this paper was therefore to address associations between bacteriocins and bacterial diversity in the human gut microbiota. To investigate this, we did an extensive screening of 2564 healthy human gut metagenomes for the presence of predicted bacteriocin-encoding genes, comparing bacteriocin gene presence to strain diversity and age. RESULTS: We found that the abundance of bacteriocin genes was significantly higher in infant-like metagenomes (< 2 years) compared to adult-like metagenomes (2–107 years). By comparing infant-like metagenomes with and without a given bacteriocin, we found that bacteriocin presence was associated with increased strain diversities. CONCLUSIONS: Our findings indicate that bacteriocins may play a role in the strain diversification during the infant gut microbiota establishment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09388-0. |
format | Online Article Text |
id | pubmed-10230729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102307292023-06-01 Metagenome-mining indicates an association between bacteriocin presence and strain diversity in the infant gut Ormaasen, Ida Rudi, Knut Diep, Dzung B. Snipen, Lars BMC Genomics Research BACKGROUND: Our knowledge about the ecological role of bacterial antimicrobial peptides (bacteriocins) in the human gut is limited, particularly in relation to their role in the diversification of the gut microbiota during early life. The aim of this paper was therefore to address associations between bacteriocins and bacterial diversity in the human gut microbiota. To investigate this, we did an extensive screening of 2564 healthy human gut metagenomes for the presence of predicted bacteriocin-encoding genes, comparing bacteriocin gene presence to strain diversity and age. RESULTS: We found that the abundance of bacteriocin genes was significantly higher in infant-like metagenomes (< 2 years) compared to adult-like metagenomes (2–107 years). By comparing infant-like metagenomes with and without a given bacteriocin, we found that bacteriocin presence was associated with increased strain diversities. CONCLUSIONS: Our findings indicate that bacteriocins may play a role in the strain diversification during the infant gut microbiota establishment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09388-0. BioMed Central 2023-05-31 /pmc/articles/PMC10230729/ /pubmed/37259063 http://dx.doi.org/10.1186/s12864-023-09388-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ormaasen, Ida Rudi, Knut Diep, Dzung B. Snipen, Lars Metagenome-mining indicates an association between bacteriocin presence and strain diversity in the infant gut |
title | Metagenome-mining indicates an association between bacteriocin presence and strain diversity in the infant gut |
title_full | Metagenome-mining indicates an association between bacteriocin presence and strain diversity in the infant gut |
title_fullStr | Metagenome-mining indicates an association between bacteriocin presence and strain diversity in the infant gut |
title_full_unstemmed | Metagenome-mining indicates an association between bacteriocin presence and strain diversity in the infant gut |
title_short | Metagenome-mining indicates an association between bacteriocin presence and strain diversity in the infant gut |
title_sort | metagenome-mining indicates an association between bacteriocin presence and strain diversity in the infant gut |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230729/ https://www.ncbi.nlm.nih.gov/pubmed/37259063 http://dx.doi.org/10.1186/s12864-023-09388-0 |
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