4.7 Article

Fecal Fungal Dysbiosis in Chinese Patients With Alzheimer's Disease

期刊

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2020.631460

关键词

Alzheimer’ s disease; Candida; fungal microbiota; sequencing; TNF-α

资金

  1. National Natural Science Foundation of China [81771724, 31700800, 81790631]
  2. National S&T Major Project of China [2018YFC2000500]
  3. S&T Major Project of Lishui [2017YSKZ-01, 2017ZDYF04]
  4. Lishui & ZJU Cooperation Project [2018zdhz07]
  5. Foundation of China's State Key Laboratory for Diagnosis and Treatment of Infectious Diseases

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This study found altered taxonomic composition of the fecal fungal microbiota in AD patients, with specific fungi enriched or decreased. Key differential fungi such as Candida tropicalis and Schizophyllum commune were positively correlated with certain immune response markers, while Rhodotorula mucilaginosa showed negative correlation with TNF-alpha level. The analysis revealed potential implications for the etiopathogenesis of AD and improved diagnosis and treatment.
Gut bacterial dysbiosis plays a vital role in the development of Alzheimer's disease (AD). However, our understanding of alterations to the gut fungal microbiota and their correlations with host immunity in AD is still limited. Samples were obtained from 88 Chinese patients with AD, and 65 age- and gender-matched, cognitively normal controls. Using these samples, we investigated the fungal microbiota targeting internal transcribed spacer 2 (ITS2) rRNA genes using MiSeq sequencing, and analyzed their associations with the host immune response. Our data demonstrated unaltered fungal diversity but altered taxonomic composition of the fecal fungal microbiota in the AD patients. The analysis of the fungal microbiota was performed using 6,585,557 high-quality reads (2,932,482 reads from the controls and 3,653,075 from the AD patients), with an average of 43,042 reads per sample. We found that several key differential fungi such as Candida tropicalis and Schizophyllum commune were enriched in the AD patients, while Rhodotorula mucilaginosa decreased significantly. Interestingly, C. tropicalis and S. commune were positively correlated with IP-10 and TNF-alpha levels. In contrast, C. tropicalis was negatively correlated with IL-8 and IFN-gamma levels, and R. mucilaginosa was negatively correlated with TNF-alpha level. PiCRUSt analysis revealed that lipoic acid metabolism, starch and sucrose metabolism were significantly decreased in the AD fungal microbiota. This study is the first to demonstrate fecal fungal dysbiosis in stable AD patients at a deeper level, and to identify the key differential fungi involved in regulating host systemic immunity. The analysis of the fungal microbiota in AD performed here may provide novel insights into the etiopathogenesis of AD and pave the way for improved diagnosis and treatment of AD.

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