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Metagenomics revealed a correlation of gut phageome with autism spectrum disorder

The human gut bacteriome is believed to have pivotal influences on human health and disease while the particular roles associated with the gut phageome have not been fully characterized yet with few exceptions. It is argued that gut microbiota can have a potential role in autism spectrum disorders (...

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Autores principales: Shahin, Khashayar, Soleimani-Delfan, Abbas, He, Zihan, Sansonetti, Philippe, Collard, Jean-Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403902/
https://www.ncbi.nlm.nih.gov/pubmed/37542330
http://dx.doi.org/10.1186/s13099-023-00561-0
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author Shahin, Khashayar
Soleimani-Delfan, Abbas
He, Zihan
Sansonetti, Philippe
Collard, Jean-Marc
author_facet Shahin, Khashayar
Soleimani-Delfan, Abbas
He, Zihan
Sansonetti, Philippe
Collard, Jean-Marc
author_sort Shahin, Khashayar
collection PubMed
description The human gut bacteriome is believed to have pivotal influences on human health and disease while the particular roles associated with the gut phageome have not been fully characterized yet with few exceptions. It is argued that gut microbiota can have a potential role in autism spectrum disorders (ASD). The public microbiota database of ASD and typically developing (TD) Chinese individuals were analyzed for phage protein-coding units (pPCU) to find any link between the phageome and ASD. The gut phageome of ASD individuals showed a wider diversity and higher abundance compared to TD individuals. The ASD phageome was associated with a significant expansion of Caudoviricetes bacteriophages. Phages infecting Bacteroidaceae and prophages encoded within Faecalibacterium were more frequent in ASD than in TD individuals. The expansion and diversification of ASD phageome can influence the bacterial homeostasis by imposing pressure on the bacterial communities. In conclusion, the differences of phages community in in ASD and TD can be used as potential diagnosis biomarkers of ASD. Further investigations are needed to verify the role of gut phage communities in the pathogenesis of ASD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-023-00561-0.
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spelling pubmed-104039022023-08-06 Metagenomics revealed a correlation of gut phageome with autism spectrum disorder Shahin, Khashayar Soleimani-Delfan, Abbas He, Zihan Sansonetti, Philippe Collard, Jean-Marc Gut Pathog Research The human gut bacteriome is believed to have pivotal influences on human health and disease while the particular roles associated with the gut phageome have not been fully characterized yet with few exceptions. It is argued that gut microbiota can have a potential role in autism spectrum disorders (ASD). The public microbiota database of ASD and typically developing (TD) Chinese individuals were analyzed for phage protein-coding units (pPCU) to find any link between the phageome and ASD. The gut phageome of ASD individuals showed a wider diversity and higher abundance compared to TD individuals. The ASD phageome was associated with a significant expansion of Caudoviricetes bacteriophages. Phages infecting Bacteroidaceae and prophages encoded within Faecalibacterium were more frequent in ASD than in TD individuals. The expansion and diversification of ASD phageome can influence the bacterial homeostasis by imposing pressure on the bacterial communities. In conclusion, the differences of phages community in in ASD and TD can be used as potential diagnosis biomarkers of ASD. Further investigations are needed to verify the role of gut phage communities in the pathogenesis of ASD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-023-00561-0. BioMed Central 2023-08-04 /pmc/articles/PMC10403902/ /pubmed/37542330 http://dx.doi.org/10.1186/s13099-023-00561-0 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
Shahin, Khashayar
Soleimani-Delfan, Abbas
He, Zihan
Sansonetti, Philippe
Collard, Jean-Marc
Metagenomics revealed a correlation of gut phageome with autism spectrum disorder
title Metagenomics revealed a correlation of gut phageome with autism spectrum disorder
title_full Metagenomics revealed a correlation of gut phageome with autism spectrum disorder
title_fullStr Metagenomics revealed a correlation of gut phageome with autism spectrum disorder
title_full_unstemmed Metagenomics revealed a correlation of gut phageome with autism spectrum disorder
title_short Metagenomics revealed a correlation of gut phageome with autism spectrum disorder
title_sort metagenomics revealed a correlation of gut phageome with autism spectrum disorder
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403902/
https://www.ncbi.nlm.nih.gov/pubmed/37542330
http://dx.doi.org/10.1186/s13099-023-00561-0
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