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Gut virome profiling identifies an association between temperate phages and colorectal cancer promoted by Helicobacter pylori infection

Colorectal cancer (CRC) is one of the most commonly diagnosed cancers worldwide. While a close correlation between chronic Helicobacter pylori infection and CRC has been reported, the role of the virome has been overlooked. Here, we infected Apc-mutant mouse models and C57BL/6 mice with H. pylori an...

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Autores principales: Luo, Shiqi, Ru, Jinlong, Mirzaei, Mohammadali Khan, Xue, Jinling, Peng, Xue, Ralser, Anna, Mejías-Luque, Raquel, Gerhard, Markus, Deng, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578192/
https://www.ncbi.nlm.nih.gov/pubmed/37747149
http://dx.doi.org/10.1080/19490976.2023.2257291
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author Luo, Shiqi
Ru, Jinlong
Mirzaei, Mohammadali Khan
Xue, Jinling
Peng, Xue
Ralser, Anna
Mejías-Luque, Raquel
Gerhard, Markus
Deng, Li
author_facet Luo, Shiqi
Ru, Jinlong
Mirzaei, Mohammadali Khan
Xue, Jinling
Peng, Xue
Ralser, Anna
Mejías-Luque, Raquel
Gerhard, Markus
Deng, Li
author_sort Luo, Shiqi
collection PubMed
description Colorectal cancer (CRC) is one of the most commonly diagnosed cancers worldwide. While a close correlation between chronic Helicobacter pylori infection and CRC has been reported, the role of the virome has been overlooked. Here, we infected Apc-mutant mouse models and C57BL/6 mice with H. pylori and conducted a comprehensive metagenomics analysis of H. pylori-induced changes in lower gastrointestinal tract bacterial and viral communities. We observed an expansion of temperate phages in H. pylori infected Apc(+/1638N) mice at the early stage of carcinogenesis. Some of the temperate phages were predicted to infect bacteria associated with CRC, including Enterococcus faecalis. We also observed a high prevalence of virulent genes, such as flgJ, cwlJ, and sleB, encoded by temperate phages. In addition, we identified phages associated with pre-onset and onset of H. pylori-promoted carcinogenesis. Through co-occurrence network analysis, we found strong associations between the viral and bacterial communities in infected mice before the onset of carcinogenesis. These findings suggest that the expansion of temperate phages, possibly caused by prophage induction triggered by H. pylori infection, may have contributed to the development of CRC in mice by interacting with the bacterial community.
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spelling pubmed-105781922023-10-17 Gut virome profiling identifies an association between temperate phages and colorectal cancer promoted by Helicobacter pylori infection Luo, Shiqi Ru, Jinlong Mirzaei, Mohammadali Khan Xue, Jinling Peng, Xue Ralser, Anna Mejías-Luque, Raquel Gerhard, Markus Deng, Li Gut Microbes Research Paper Colorectal cancer (CRC) is one of the most commonly diagnosed cancers worldwide. While a close correlation between chronic Helicobacter pylori infection and CRC has been reported, the role of the virome has been overlooked. Here, we infected Apc-mutant mouse models and C57BL/6 mice with H. pylori and conducted a comprehensive metagenomics analysis of H. pylori-induced changes in lower gastrointestinal tract bacterial and viral communities. We observed an expansion of temperate phages in H. pylori infected Apc(+/1638N) mice at the early stage of carcinogenesis. Some of the temperate phages were predicted to infect bacteria associated with CRC, including Enterococcus faecalis. We also observed a high prevalence of virulent genes, such as flgJ, cwlJ, and sleB, encoded by temperate phages. In addition, we identified phages associated with pre-onset and onset of H. pylori-promoted carcinogenesis. Through co-occurrence network analysis, we found strong associations between the viral and bacterial communities in infected mice before the onset of carcinogenesis. These findings suggest that the expansion of temperate phages, possibly caused by prophage induction triggered by H. pylori infection, may have contributed to the development of CRC in mice by interacting with the bacterial community. Taylor & Francis 2023-09-25 /pmc/articles/PMC10578192/ /pubmed/37747149 http://dx.doi.org/10.1080/19490976.2023.2257291 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Paper
Luo, Shiqi
Ru, Jinlong
Mirzaei, Mohammadali Khan
Xue, Jinling
Peng, Xue
Ralser, Anna
Mejías-Luque, Raquel
Gerhard, Markus
Deng, Li
Gut virome profiling identifies an association between temperate phages and colorectal cancer promoted by Helicobacter pylori infection
title Gut virome profiling identifies an association between temperate phages and colorectal cancer promoted by Helicobacter pylori infection
title_full Gut virome profiling identifies an association between temperate phages and colorectal cancer promoted by Helicobacter pylori infection
title_fullStr Gut virome profiling identifies an association between temperate phages and colorectal cancer promoted by Helicobacter pylori infection
title_full_unstemmed Gut virome profiling identifies an association between temperate phages and colorectal cancer promoted by Helicobacter pylori infection
title_short Gut virome profiling identifies an association between temperate phages and colorectal cancer promoted by Helicobacter pylori infection
title_sort gut virome profiling identifies an association between temperate phages and colorectal cancer promoted by helicobacter pylori infection
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578192/
https://www.ncbi.nlm.nih.gov/pubmed/37747149
http://dx.doi.org/10.1080/19490976.2023.2257291
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