Cargando…
Altered gut bacterial–fungal interkingdom networks in patients with current depressive episode
INTRODUCTION: Bacterial dysbiosis has been described in patients with current depressive episode (CDE); however, the fungal composition in the gut has not been investigated in these patients. METHODS: Here, we characterized the fungal gut mycobiota in patients with CDE. We systematically characteriz...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428472/ https://www.ncbi.nlm.nih.gov/pubmed/32533650 http://dx.doi.org/10.1002/brb3.1677 |
_version_ | 1783571080267431936 |
---|---|
author | Jiang, Hai‐yin Pan, Li‐ya Zhang, Xue Zhang, Zhe Zhou, Yuan‐yue Ruan, Bing |
author_facet | Jiang, Hai‐yin Pan, Li‐ya Zhang, Xue Zhang, Zhe Zhou, Yuan‐yue Ruan, Bing |
author_sort | Jiang, Hai‐yin |
collection | PubMed |
description | INTRODUCTION: Bacterial dysbiosis has been described in patients with current depressive episode (CDE); however, the fungal composition in the gut has not been investigated in these patients. METHODS: Here, we characterized the fungal gut mycobiota in patients with CDE. We systematically characterized the microbiota and mycobiota in fecal samples obtained from 24 patients with CDE and 16 healthy controls (HC) using 16S rRNA gene‐ and ITS1‐based DNA sequencing, respectively. RESULTS: In patients with CDE, bacterial dysbiosis was characterized by an altered composition and reduced correlation network density, and the gut mycobiota was characterized by a relative reduction in alpha diversity and altered composition. Most notably, the CDE group had higher levels of Candida and lower level of Penicillium than the HC group. Compared with the HC group, the gut microbiota in patients with CDE displayed a significant disruption in the bacteria–fungi correlation network suggestive of altered interkingdom interactions. Furthermore, a gut microbial index based on the combination of eight genera (four bacterial and four fungal CDE‐associated genera) distinguished CDE patients from controls with an area under the curve of approximately 0.84, suggesting that the gut microbiome signature is a promising tool for disease classification. CONCLUSIONS: Our findings suggest that both bacteria and fungi contribute to gut dysbiosis in patients with CDE. Future studies involving larger cohorts and metagenomic or metabolomic analyses may clarify the structure and potential roles and functions of the gut mycobiome and its impact on the development of CDE. |
format | Online Article Text |
id | pubmed-7428472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74284722020-08-17 Altered gut bacterial–fungal interkingdom networks in patients with current depressive episode Jiang, Hai‐yin Pan, Li‐ya Zhang, Xue Zhang, Zhe Zhou, Yuan‐yue Ruan, Bing Brain Behav Original Research INTRODUCTION: Bacterial dysbiosis has been described in patients with current depressive episode (CDE); however, the fungal composition in the gut has not been investigated in these patients. METHODS: Here, we characterized the fungal gut mycobiota in patients with CDE. We systematically characterized the microbiota and mycobiota in fecal samples obtained from 24 patients with CDE and 16 healthy controls (HC) using 16S rRNA gene‐ and ITS1‐based DNA sequencing, respectively. RESULTS: In patients with CDE, bacterial dysbiosis was characterized by an altered composition and reduced correlation network density, and the gut mycobiota was characterized by a relative reduction in alpha diversity and altered composition. Most notably, the CDE group had higher levels of Candida and lower level of Penicillium than the HC group. Compared with the HC group, the gut microbiota in patients with CDE displayed a significant disruption in the bacteria–fungi correlation network suggestive of altered interkingdom interactions. Furthermore, a gut microbial index based on the combination of eight genera (four bacterial and four fungal CDE‐associated genera) distinguished CDE patients from controls with an area under the curve of approximately 0.84, suggesting that the gut microbiome signature is a promising tool for disease classification. CONCLUSIONS: Our findings suggest that both bacteria and fungi contribute to gut dysbiosis in patients with CDE. Future studies involving larger cohorts and metagenomic or metabolomic analyses may clarify the structure and potential roles and functions of the gut mycobiome and its impact on the development of CDE. John Wiley and Sons Inc. 2020-06-12 /pmc/articles/PMC7428472/ /pubmed/32533650 http://dx.doi.org/10.1002/brb3.1677 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Jiang, Hai‐yin Pan, Li‐ya Zhang, Xue Zhang, Zhe Zhou, Yuan‐yue Ruan, Bing Altered gut bacterial–fungal interkingdom networks in patients with current depressive episode |
title | Altered gut bacterial–fungal interkingdom networks in patients with current depressive episode |
title_full | Altered gut bacterial–fungal interkingdom networks in patients with current depressive episode |
title_fullStr | Altered gut bacterial–fungal interkingdom networks in patients with current depressive episode |
title_full_unstemmed | Altered gut bacterial–fungal interkingdom networks in patients with current depressive episode |
title_short | Altered gut bacterial–fungal interkingdom networks in patients with current depressive episode |
title_sort | altered gut bacterial–fungal interkingdom networks in patients with current depressive episode |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428472/ https://www.ncbi.nlm.nih.gov/pubmed/32533650 http://dx.doi.org/10.1002/brb3.1677 |
work_keys_str_mv | AT jianghaiyin alteredgutbacterialfungalinterkingdomnetworksinpatientswithcurrentdepressiveepisode AT panliya alteredgutbacterialfungalinterkingdomnetworksinpatientswithcurrentdepressiveepisode AT zhangxue alteredgutbacterialfungalinterkingdomnetworksinpatientswithcurrentdepressiveepisode AT zhangzhe alteredgutbacterialfungalinterkingdomnetworksinpatientswithcurrentdepressiveepisode AT zhouyuanyue alteredgutbacterialfungalinterkingdomnetworksinpatientswithcurrentdepressiveepisode AT ruanbing alteredgutbacterialfungalinterkingdomnetworksinpatientswithcurrentdepressiveepisode |