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The gut virome in Irritable Bowel Syndrome differs from that of controls

Irritable Bowel Syndrome (IBS), the most common gastrointestinal disorder, is diagnosed solely on symptoms. Potentially diagnostic alterations in the bacterial component of the gut microbiome (the bacteriome) are associated with IBS, but despite the known role of the virome (particularly bacteriopha...

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Autores principales: Coughlan, S., Das, A., O’Herlihy, E., Shanahan, F., O’Toole, P.W., Jeffery, I.B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7899630/
https://www.ncbi.nlm.nih.gov/pubmed/33602058
http://dx.doi.org/10.1080/19490976.2021.1887719
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author Coughlan, S.
Das, A.
O’Herlihy, E.
Shanahan, F.
O’Toole, P.W.
Jeffery, I.B.
author_facet Coughlan, S.
Das, A.
O’Herlihy, E.
Shanahan, F.
O’Toole, P.W.
Jeffery, I.B.
author_sort Coughlan, S.
collection PubMed
description Irritable Bowel Syndrome (IBS), the most common gastrointestinal disorder, is diagnosed solely on symptoms. Potentially diagnostic alterations in the bacterial component of the gut microbiome (the bacteriome) are associated with IBS, but despite the known role of the virome (particularly bacteriophages), in shaping the gut bacteriome, few studies have investigated the virome in IBS. We performed metagenomic sequencing of fecal Virus-Like Particles (VLPs) from 55 patients with IBS and 51 control individuals. We detected significantly lower alpha diversity of viral clusters comprising both known and novel viruses (viral ‘dark matter’) in IBS and a significant difference in beta diversity compared to controls, but not between IBS symptom subtypes. The three most abundant bacteriophage clusters belonged to the Siphoviridae, Myoviridae, and Podoviridae families (Order Caudovirales). A core virome (defined as a cluster present in at least 50% of samples) of 5 and 12 viral clusters was identified in IBS and control subjects, respectively. We also identified a subset of viral clusters that showed differential abundance between IBS and controls. The virome did not co-vary significantly with the bacteriome, with IBS clinical subtype, or with Bile Acid Malabsorption status. However, differences in the virome could be related back to the bacteriome as analysis of CRISPR spacers indicated that the virome alterations were at least partially related to the alterations in the bacteriome. We found no evidence for a shift from lytic to lysogenic replication of core viral clusters, a phenomenon reported for the gut virome of patients with Inflammatory Bowel Disease. Collectively, our data show alterations in the virome of patients with IBS, regardless of clinical subtype, which may facilitate development of new microbiome-based therapeutics.
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spelling pubmed-78996302021-03-02 The gut virome in Irritable Bowel Syndrome differs from that of controls Coughlan, S. Das, A. O’Herlihy, E. Shanahan, F. O’Toole, P.W. Jeffery, I.B. Gut Microbes Research Paper Irritable Bowel Syndrome (IBS), the most common gastrointestinal disorder, is diagnosed solely on symptoms. Potentially diagnostic alterations in the bacterial component of the gut microbiome (the bacteriome) are associated with IBS, but despite the known role of the virome (particularly bacteriophages), in shaping the gut bacteriome, few studies have investigated the virome in IBS. We performed metagenomic sequencing of fecal Virus-Like Particles (VLPs) from 55 patients with IBS and 51 control individuals. We detected significantly lower alpha diversity of viral clusters comprising both known and novel viruses (viral ‘dark matter’) in IBS and a significant difference in beta diversity compared to controls, but not between IBS symptom subtypes. The three most abundant bacteriophage clusters belonged to the Siphoviridae, Myoviridae, and Podoviridae families (Order Caudovirales). A core virome (defined as a cluster present in at least 50% of samples) of 5 and 12 viral clusters was identified in IBS and control subjects, respectively. We also identified a subset of viral clusters that showed differential abundance between IBS and controls. The virome did not co-vary significantly with the bacteriome, with IBS clinical subtype, or with Bile Acid Malabsorption status. However, differences in the virome could be related back to the bacteriome as analysis of CRISPR spacers indicated that the virome alterations were at least partially related to the alterations in the bacteriome. We found no evidence for a shift from lytic to lysogenic replication of core viral clusters, a phenomenon reported for the gut virome of patients with Inflammatory Bowel Disease. Collectively, our data show alterations in the virome of patients with IBS, regardless of clinical subtype, which may facilitate development of new microbiome-based therapeutics. Taylor & Francis 2021-02-19 /pmc/articles/PMC7899630/ /pubmed/33602058 http://dx.doi.org/10.1080/19490976.2021.1887719 Text en © 2021 Taylor & Francis Group, LLC https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Coughlan, S.
Das, A.
O’Herlihy, E.
Shanahan, F.
O’Toole, P.W.
Jeffery, I.B.
The gut virome in Irritable Bowel Syndrome differs from that of controls
title The gut virome in Irritable Bowel Syndrome differs from that of controls
title_full The gut virome in Irritable Bowel Syndrome differs from that of controls
title_fullStr The gut virome in Irritable Bowel Syndrome differs from that of controls
title_full_unstemmed The gut virome in Irritable Bowel Syndrome differs from that of controls
title_short The gut virome in Irritable Bowel Syndrome differs from that of controls
title_sort gut virome in irritable bowel syndrome differs from that of controls
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7899630/
https://www.ncbi.nlm.nih.gov/pubmed/33602058
http://dx.doi.org/10.1080/19490976.2021.1887719
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