Assessment of the gut bacterial microbiome and metabolome of girls and women with Rett Syndrome

Autor: Mohammed Naqvi, Jessica K. Runge, Nabeel Khan, Kathleen J. Motil, Daniel G. Glaze, Miriam Balderas, Kathleen Hoch, Anthony Haag, Alamelu Venkatachalam, Santosh Thapa, Ruth Ann Luna
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Gastrointestinal Diseases
Glutamine
Physiology
Biochemistry
Severity of Illness Index
Feces
Aromatic Amino Acids
RNA
Ribosomal
16S

Medicine and Health Sciences
Medicine
Amino Acids
Child
Multidisciplinary
Organic Compounds
Acidic Amino Acids
Neurochemistry
Genomics
Neurotransmitters
Chemistry
Phenotype
Medical Microbiology
Child
Preschool

Cohort
Physical Sciences
Metabolome
Female
Glutamate
Research Article
Adult
congenital
hereditary
and neonatal diseases and abnormalities

Adolescent
Science
Rett syndrome
Microbial Genomics
Microbiology
Gas Chromatography-Mass Spectrometry
Young Adult
Metabolomics
Hydroxyl Amino Acids
Genetics
Rett Syndrome
Humans
Microbiome
Nutrition
Bacteria
business.industry
Gut Bacteria
Organic Chemistry
Organisms
Chemical Compounds
Biology and Life Sciences
Proteins
Sequence Analysis
DNA

medicine.disease
Diet
Gastrointestinal Microbiome
Metabolism
Food
Defecation
Tyrosine
business
Dysbiosis
Neuroscience
Zdroj: PLoS ONE
PLoS ONE, Vol 16, Iss 5, p e0251231 (2021)
ISSN: 1932-6203
Popis: Background Gastrointestinal problems affect the health and quality of life of individuals with Rett syndrome (RTT) and pose a medical hardship for their caregivers. We hypothesized that the variability in the RTT phenotype contributes to the dysbiosis of the gut microbiome and metabolome in RTT, predisposing these individuals to gastrointestinal dysfunction. Objectives We characterized the gut bacterial microbiome and metabolome in girls and young women with RTT (n = 44) and unaffected controls (n = 21), and examined the relation between the composition of the microbiome and variations in the RTT phenotype. Methods Demographics and clinical information, including growth and anthropometric measurements, pubertal status, symptoms, clinical severity score, bowel movement, medication use, and dietary intakes were collected from the participants. Fecal samples were collected for analysis of the gut microbiome using Illumina MiSeq-based next-generation sequencing of the 16S rRNA gene followed by bioinformatics analysis of microbial composition, diversity, and community structure. Selected end-products of microbial protein metabolism were characterized by liquid chromatography-mass spectrometry. Results The gut bacterial microbiome differed within the RTT cohort based on pubertal status (p Conclusions Although variability in the RTT phenotype contributes to the dysbiosis of the gut microbiome, we presently cannot infer causality between gut bacterial dysbiosis and gastrointestinal dysfunction. Nevertheless, alterations in the gut metabolome may provide clues to the pathophysiology of gastrointestinal problems in RTT.
Databáze: OpenAIRE