Chronic fatigue syndrome patients have alterations in their oral microbiome composition and function.

Host-microbe interactions have been implicated in the pathogenesis of chronic fatigue syndrome (CFS), but whether the oral microbiome is altered in CFS patients is unknown. We explored alterations of the oral microbiome in Chinese Han CFS patients using 16S rRNA gene sequencing and alterations in th...

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Main Authors: Taiwu Wang, Lei Yu, Cong Xu, Keli Pan, Minglu Mo, Mingxiang Duan, Yao Zhang, Hongyan Xiong
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6133361?pdf=render
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spelling doaj-4ad275ff2fdb49c383b242ab4d825aa82020-11-25T01:26:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01139e020350310.1371/journal.pone.0203503Chronic fatigue syndrome patients have alterations in their oral microbiome composition and function.Taiwu WangLei YuCong XuKeli PanMinglu MoMingxiang DuanYao ZhangHongyan XiongHost-microbe interactions have been implicated in the pathogenesis of chronic fatigue syndrome (CFS), but whether the oral microbiome is altered in CFS patients is unknown. We explored alterations of the oral microbiome in Chinese Han CFS patients using 16S rRNA gene sequencing and alterations in the functional potential of the oral microbiome using PICRUSt. We found that Shannon and Simpson diversity indices were not different in CFS patients compared to healthy controls, but the overall oral microbiome composition was different (MANOVA, p < 0.01). CFS patients had a higher relative abundance of Fusobacteria compared with healthy controls. Further, the genera Leptotrichia, Prevotella, and Fusobacterium were enriched and Haemophilus, Veillonella, and Porphyromonas were depleted in CFS patients compared to healthy controls. Functional analysis from inferred metagenomes showed that bacterial genera altered in CFS patients were primarily associated with amino acid and energy metabolism. Our findings demonstrate that the oral microbiome in CFS patients is different from healthy controls, and these differences lead to shifts in functional pathways with implications for CFS pathogenesis. These findings increase our understanding of the relationship between the oral microbiota and CFS, which will advance our understanding of CFS pathogenesis and may contribute to future improvements in treatment and diagnosis.http://europepmc.org/articles/PMC6133361?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Taiwu Wang
Lei Yu
Cong Xu
Keli Pan
Minglu Mo
Mingxiang Duan
Yao Zhang
Hongyan Xiong
spellingShingle Taiwu Wang
Lei Yu
Cong Xu
Keli Pan
Minglu Mo
Mingxiang Duan
Yao Zhang
Hongyan Xiong
Chronic fatigue syndrome patients have alterations in their oral microbiome composition and function.
PLoS ONE
author_facet Taiwu Wang
Lei Yu
Cong Xu
Keli Pan
Minglu Mo
Mingxiang Duan
Yao Zhang
Hongyan Xiong
author_sort Taiwu Wang
title Chronic fatigue syndrome patients have alterations in their oral microbiome composition and function.
title_short Chronic fatigue syndrome patients have alterations in their oral microbiome composition and function.
title_full Chronic fatigue syndrome patients have alterations in their oral microbiome composition and function.
title_fullStr Chronic fatigue syndrome patients have alterations in their oral microbiome composition and function.
title_full_unstemmed Chronic fatigue syndrome patients have alterations in their oral microbiome composition and function.
title_sort chronic fatigue syndrome patients have alterations in their oral microbiome composition and function.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Host-microbe interactions have been implicated in the pathogenesis of chronic fatigue syndrome (CFS), but whether the oral microbiome is altered in CFS patients is unknown. We explored alterations of the oral microbiome in Chinese Han CFS patients using 16S rRNA gene sequencing and alterations in the functional potential of the oral microbiome using PICRUSt. We found that Shannon and Simpson diversity indices were not different in CFS patients compared to healthy controls, but the overall oral microbiome composition was different (MANOVA, p < 0.01). CFS patients had a higher relative abundance of Fusobacteria compared with healthy controls. Further, the genera Leptotrichia, Prevotella, and Fusobacterium were enriched and Haemophilus, Veillonella, and Porphyromonas were depleted in CFS patients compared to healthy controls. Functional analysis from inferred metagenomes showed that bacterial genera altered in CFS patients were primarily associated with amino acid and energy metabolism. Our findings demonstrate that the oral microbiome in CFS patients is different from healthy controls, and these differences lead to shifts in functional pathways with implications for CFS pathogenesis. These findings increase our understanding of the relationship between the oral microbiota and CFS, which will advance our understanding of CFS pathogenesis and may contribute to future improvements in treatment and diagnosis.
url http://europepmc.org/articles/PMC6133361?pdf=render
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