Gut mycobiome and its interaction with diet, gut bacteria and alzheimer's disease markers in subjects with mild cognitive impairment: A pilot study
Autor: | Sidharth P. Mishra, Shaohua Wang, Ravinder Nagpal, Suzanne Craft, Bryan J. Neth, Hariom Yadav |
---|---|
Rok vydání: | 2020 |
Předmět: |
Male
0301 basic medicine Research paper Mediterranean diet medicine.medical_treatment Apolipoprotein E4 lcsh:Medicine Pilot Projects Disease PCoA: principal coordinate analysis Feces 0302 clinical medicine LDA: linear discrimination analysis Mycobiota LPS: lipopolysaccharide tau CN: cognitively normal amyloid peptides AD: Alzheimer disease lcsh:R5-920 LP: lumbar puncture education.field_of_study biology General Medicine Ketogenic diet LEfSe: linear discrimination analysis effect size Alzheimer's ITS: internal transcribed spacer 030220 oncology & carcinogenesis Female KD: ketogenic diet Alzheimer's disease lcsh:Medicine (General) Diet Ketogenic CSF: cerebrospinal fluid Genotype Population Aß: amyloid beta General Biochemistry Genetics and Molecular Biology SCFAs: short-chain fatty acids Short-chain fatty acids 03 medical and health sciences Alzheimer Disease MCI: mildly cognitive impairment medicine Humans Dementia Cognitive Dysfunction Microbiome education AHAD: American Heart Association Diet Nutrition Bacteria MMKD: modified Mediterranean-ketogenic diet lcsh:R Fungi ApoE ε−4: apolipoprotein-E ε−4 allele Computational Biology biology.organism_classification medicine.disease Diet Gastrointestinal Microbiome OTUs: operational taxonomic units 030104 developmental biology Immunology Metagenome Metagenomics Biomarkers |
Zdroj: | EBioMedicine EBioMedicine, Vol 59, Iss, Pp 102950-(2020) |
ISSN: | 2352-3964 |
Popis: | Background Recently, we reported that patients with mild cognitive impairment (MCI) harbor specific signature of bacteria in their gut and that a modified Mediterranean ketogenic diet (MMKD) improves Alzheimer's disease (AD) markers in cerebrospinal fluid (CSF) and the signatures of gut bacteria. However, other microbial population such as gut fungi (mycobiome) in relation to MCI/AD pathology, gut bacteria and diet remain unknown. Methods We measure gut mycobiome by sequencing of the fungal rRNA ITS1 gene in 17 older adults (11 MCI; 6 cognitively normal [CN]) in a single-center, randomized, double-blind, crossover pilot study, before and after 6 weeks intervention of MMKD and American Heart Association Diet (AHAD), and determine its correlation with AD markers in CSF and gut bacteria. Findings Compared to CN counterparts, patients with MCI have higher proportion of families Sclerotiniaceae, Phaffomyceteceae, Trichocomaceae, Cystofilobasidiaceae, Togniniaceae and genera Botrytis, Kazachstania, Phaeoacremonium and Cladosporium and lower abundance of Meyerozyma. Specific fungal taxa exhibit distinct correlation arrays with AD markers and gut bacteria in subjects with versus without MCI. MMKD induces broader effect on fungal diversity in subjects with MCI and increases Agaricus and Mrakia while decreasing Saccharomyces and Claviceps with differential response in subjects with or without MCI. Interpretation The study reveals MCI-specific mycobiome signatures and demonstrates that distinct diets modulate the mycobiome in association with AD markers and fungal-bacterial co-regulation networks in patients with MCI. The findings corroborate the notion of considering gut mycobiome as a unique factor that can affect cognitive health/AD by interacting with gut bacteria and diet and facilitate better understanding of the AD and related microbiome, using unique diet or microbiome modulators. Graphical abstract Image, graphical abstract |
Databáze: | OpenAIRE |
Externí odkaz: |