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Functional metagenomics identifies novel genes ABCTPP, TMSRP1 and TLSRP1 among human gut enterotypes

Every niche in the biosphere is touched by the seemingly endless capacity of microbes to transform the world around them by adapting swiftly and flexibly to the environmental changes, likewise the gastrointestinal tract is no exception. The ability to cope with rapid changes in external osmolarity i...

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Autores principales: Verma, Manoj Kumar, Ahmed, Vasim, Gupta, Shashank, Kumar, Jitendra, Pandey, Rajesh, Mandhan, Vibha, Chauhan, Nar Singh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780487/
https://www.ncbi.nlm.nih.gov/pubmed/29362424
http://dx.doi.org/10.1038/s41598-018-19862-5
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author Verma, Manoj Kumar
Ahmed, Vasim
Gupta, Shashank
Kumar, Jitendra
Pandey, Rajesh
Mandhan, Vibha
Chauhan, Nar Singh
author_facet Verma, Manoj Kumar
Ahmed, Vasim
Gupta, Shashank
Kumar, Jitendra
Pandey, Rajesh
Mandhan, Vibha
Chauhan, Nar Singh
author_sort Verma, Manoj Kumar
collection PubMed
description Every niche in the biosphere is touched by the seemingly endless capacity of microbes to transform the world around them by adapting swiftly and flexibly to the environmental changes, likewise the gastrointestinal tract is no exception. The ability to cope with rapid changes in external osmolarity is an important aspect of gut microbes for their survival and colonization. Identification of these survival mechanisms is a pivotal step towards understanding genomic suitability of a symbiont for successful human gut colonization. Here we highlight our recent work applying functional metagenomics to study human gut microbiome to identify candidate genes responsible for the salt stress tolerance. A plasmid borne metagenomic library of Bacteroidetes enriched human fecal metagenomic DNA led to identification of unique salt osmotolerance clones SR6 and SR7. Subsequent gene analysis combined with functional studies revealed that TLSRP1 within pSR7 and TMSRP1 and ABCTPP of pSR6 are the active loci responsible for osmotolerance through an energy dependent mechanism. Our study elucidates the novel genetic machinery involved in bestowing osmotolerance in Prevotella and Bacteroidetes, the predominant microbial groups in a North Indian population. This study unravels an alternative method for imparting ionic stress tolerance, which may be prevalent in the human gut microbiome.
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spelling pubmed-57804872018-02-06 Functional metagenomics identifies novel genes ABCTPP, TMSRP1 and TLSRP1 among human gut enterotypes Verma, Manoj Kumar Ahmed, Vasim Gupta, Shashank Kumar, Jitendra Pandey, Rajesh Mandhan, Vibha Chauhan, Nar Singh Sci Rep Article Every niche in the biosphere is touched by the seemingly endless capacity of microbes to transform the world around them by adapting swiftly and flexibly to the environmental changes, likewise the gastrointestinal tract is no exception. The ability to cope with rapid changes in external osmolarity is an important aspect of gut microbes for their survival and colonization. Identification of these survival mechanisms is a pivotal step towards understanding genomic suitability of a symbiont for successful human gut colonization. Here we highlight our recent work applying functional metagenomics to study human gut microbiome to identify candidate genes responsible for the salt stress tolerance. A plasmid borne metagenomic library of Bacteroidetes enriched human fecal metagenomic DNA led to identification of unique salt osmotolerance clones SR6 and SR7. Subsequent gene analysis combined with functional studies revealed that TLSRP1 within pSR7 and TMSRP1 and ABCTPP of pSR6 are the active loci responsible for osmotolerance through an energy dependent mechanism. Our study elucidates the novel genetic machinery involved in bestowing osmotolerance in Prevotella and Bacteroidetes, the predominant microbial groups in a North Indian population. This study unravels an alternative method for imparting ionic stress tolerance, which may be prevalent in the human gut microbiome. Nature Publishing Group UK 2018-01-23 /pmc/articles/PMC5780487/ /pubmed/29362424 http://dx.doi.org/10.1038/s41598-018-19862-5 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Verma, Manoj Kumar
Ahmed, Vasim
Gupta, Shashank
Kumar, Jitendra
Pandey, Rajesh
Mandhan, Vibha
Chauhan, Nar Singh
Functional metagenomics identifies novel genes ABCTPP, TMSRP1 and TLSRP1 among human gut enterotypes
title Functional metagenomics identifies novel genes ABCTPP, TMSRP1 and TLSRP1 among human gut enterotypes
title_full Functional metagenomics identifies novel genes ABCTPP, TMSRP1 and TLSRP1 among human gut enterotypes
title_fullStr Functional metagenomics identifies novel genes ABCTPP, TMSRP1 and TLSRP1 among human gut enterotypes
title_full_unstemmed Functional metagenomics identifies novel genes ABCTPP, TMSRP1 and TLSRP1 among human gut enterotypes
title_short Functional metagenomics identifies novel genes ABCTPP, TMSRP1 and TLSRP1 among human gut enterotypes
title_sort functional metagenomics identifies novel genes abctpp, tmsrp1 and tlsrp1 among human gut enterotypes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780487/
https://www.ncbi.nlm.nih.gov/pubmed/29362424
http://dx.doi.org/10.1038/s41598-018-19862-5
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