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Does the microbiome and virome contribute to myalgic encephalomyelitis/chronic fatigue syndrome?

Myalgic encephalomyelitis (ME)/chronic fatigue syndrome (CFS) (ME/CFS) is a disabling and debilitating disease of unknown aetiology. It is a heterogeneous disease characterized by various inflammatory, immune, viral, neurological and endocrine symptoms. Several microbiome studies have described alte...

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Autores principales: Newberry, Fiona, Hsieh, Shen-Yuan, Wileman, Tom, Carding, Simon R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843715/
https://www.ncbi.nlm.nih.gov/pubmed/29523751
http://dx.doi.org/10.1042/CS20171330
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author Newberry, Fiona
Hsieh, Shen-Yuan
Wileman, Tom
Carding, Simon R.
author_facet Newberry, Fiona
Hsieh, Shen-Yuan
Wileman, Tom
Carding, Simon R.
author_sort Newberry, Fiona
collection PubMed
description Myalgic encephalomyelitis (ME)/chronic fatigue syndrome (CFS) (ME/CFS) is a disabling and debilitating disease of unknown aetiology. It is a heterogeneous disease characterized by various inflammatory, immune, viral, neurological and endocrine symptoms. Several microbiome studies have described alterations in the bacterial component of the microbiome (dysbiosis) consistent with a possible role in disease development. However, in focusing on the bacterial components of the microbiome, these studies have neglected the viral constituent known as the virome. Viruses, particularly those infecting bacteria (bacteriophages), have the potential to alter the function and structure of the microbiome via gene transfer and host lysis. Viral-induced microbiome changes can directly and indirectly influence host health and disease. The contribution of viruses towards disease pathogenesis is therefore an important area for research in ME/CFS. Recent advancements in sequencing technology and bioinformatics now allow more comprehensive and inclusive investigations of human microbiomes. However, as the number of microbiome studies increases, the need for greater consistency in study design and analysis also increases. Comparisons between different ME/CFS microbiome studies are difficult because of differences in patient selection and diagnosis criteria, sample processing, genome sequencing and downstream bioinformatics analysis. It is therefore important that microbiome studies adopt robust, reproducible and consistent study design to enable more reliable and valid comparisons and conclusions to be made between studies. This article provides a comprehensive review of the current evidence supporting microbiome alterations in ME/CFS patients. Additionally, the pitfalls and challenges associated with microbiome studies are discussed.
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spelling pubmed-58437152018-03-26 Does the microbiome and virome contribute to myalgic encephalomyelitis/chronic fatigue syndrome? Newberry, Fiona Hsieh, Shen-Yuan Wileman, Tom Carding, Simon R. Clin Sci (Lond) Review Articles Myalgic encephalomyelitis (ME)/chronic fatigue syndrome (CFS) (ME/CFS) is a disabling and debilitating disease of unknown aetiology. It is a heterogeneous disease characterized by various inflammatory, immune, viral, neurological and endocrine symptoms. Several microbiome studies have described alterations in the bacterial component of the microbiome (dysbiosis) consistent with a possible role in disease development. However, in focusing on the bacterial components of the microbiome, these studies have neglected the viral constituent known as the virome. Viruses, particularly those infecting bacteria (bacteriophages), have the potential to alter the function and structure of the microbiome via gene transfer and host lysis. Viral-induced microbiome changes can directly and indirectly influence host health and disease. The contribution of viruses towards disease pathogenesis is therefore an important area for research in ME/CFS. Recent advancements in sequencing technology and bioinformatics now allow more comprehensive and inclusive investigations of human microbiomes. However, as the number of microbiome studies increases, the need for greater consistency in study design and analysis also increases. Comparisons between different ME/CFS microbiome studies are difficult because of differences in patient selection and diagnosis criteria, sample processing, genome sequencing and downstream bioinformatics analysis. It is therefore important that microbiome studies adopt robust, reproducible and consistent study design to enable more reliable and valid comparisons and conclusions to be made between studies. This article provides a comprehensive review of the current evidence supporting microbiome alterations in ME/CFS patients. Additionally, the pitfalls and challenges associated with microbiome studies are discussed. Portland Press Ltd. 2018-03-09 /pmc/articles/PMC5843715/ /pubmed/29523751 http://dx.doi.org/10.1042/CS20171330 Text en © 2018 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Articles
Newberry, Fiona
Hsieh, Shen-Yuan
Wileman, Tom
Carding, Simon R.
Does the microbiome and virome contribute to myalgic encephalomyelitis/chronic fatigue syndrome?
title Does the microbiome and virome contribute to myalgic encephalomyelitis/chronic fatigue syndrome?
title_full Does the microbiome and virome contribute to myalgic encephalomyelitis/chronic fatigue syndrome?
title_fullStr Does the microbiome and virome contribute to myalgic encephalomyelitis/chronic fatigue syndrome?
title_full_unstemmed Does the microbiome and virome contribute to myalgic encephalomyelitis/chronic fatigue syndrome?
title_short Does the microbiome and virome contribute to myalgic encephalomyelitis/chronic fatigue syndrome?
title_sort does the microbiome and virome contribute to myalgic encephalomyelitis/chronic fatigue syndrome?
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843715/
https://www.ncbi.nlm.nih.gov/pubmed/29523751
http://dx.doi.org/10.1042/CS20171330
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