Fasting builds a favorable environment for effective gut microbiota modulation by microbiota-accessible carbohydrates

From BugSigDB
Needs review
study design
Citation
PMID PubMed identifier for scientific articles.
DOI Digital object identifier for electronic documents.
URI Uniform resource identifier for web resources.
Authors
Sato K., Nakashima A., Fukuda S., Inoue J., Kim Y.G.
Journal
BMC microbiology
Year
2025
Keywords:
6ʹ-sialyl lactose, Fasting, Fructo-oligosaccharides, Gut microbiota, Human milk oligosaccharides, IgA, Microbiota-accessible carbohydrates, Paramylon
Dietary nutrients are an important determinant of gut microbial composition (Asnicar et al, Nat Med 27:321-332, 2021; Arifuzzaman. et al, Nature 611:578-584, 2022; Bolte. et al, Gut 70:1287-1298, 2021). Commensal bacteria compete and cross-feed on host-derived nutrients to maintain stable gut microbial communities (Kolodziejczyk. et al, Nat Rev Microbiol. 17:742-753, 2019; Ma. et al, Gut Microbes 12:1785252, 2020). However, the changes to the gut bacteria induced by fasting are not well-defined. Here, we propose a powerful method to selectively and effectively increase specific gut bacteria by combining fasting and administration of microbiota-accessible carbohydrates (MACs). Fasting alters the gut microbial community structure, and the fasting + MAC intervention has profound effects on the gut microbiome with increased specific bacteria and fecal IgA levels than MAC administration alone. The changes in gut microbiota composition are specific to the type of MAC administered. We identified the most effective protocol to combine with fasting + MAC to increase the levels of specific bacteria such as Bifidobacterium. Overall, the integrating fasting with MACs effectively alters the gut microbiome, suggesting that fasting can prepare the environment for gut microbial modulation by MACs.

Experiment 1


incomplete

Curated date: 2025/10/11

Curator: Wendeeeee

Revision editor(s): Wendeeeee

Subjects

Location of subjects
Japan
Host species Species from which microbiome was sampled. Contact us to have more species added.
Mus musculus
Body site Anatomical site where microbial samples were extracted from according to the Uber Anatomy Ontology
Alimentary part of gastrointestinal system GI tract,Alimentary system,Alimentary tract,Gastro-intestinal system,Gastroenterological system,Gastrointestinal (GI) tract,Gastrointestinal system,Gastrointestinal tract,Alimentary part of gastrointestinal system,alimentary part of gastrointestinal system
Condition The experimental condition / phenotype studied according to the Experimental Factor Ontology
Fasting Fast,Fasting,fasting
Group 0 name Corresponds to the control (unexposed) group for case-control studies
Ad libitum
Group 1 name Corresponds to the case (exposed) group for case-control studies
Fasting
Group 1 definition Diagnostic criteria applied to define the specific condition / phenotype represented in the case (exposed) group
C57BL/6J mice subjected to a 36-hour fasting period.
Group 0 sample size Number of subjects in the control (unexposed) group
5
Group 1 sample size Number of subjects in the case (exposed) group
5
Antibiotics exclusion Number of days without antibiotics usage (if applicable) and other antibiotics-related criteria used to exclude participants (if any)
The study does not mention an antibiotic exclusion period.

Lab analysis

Sequencing type
16S
16S variable region One or more hypervariable region(s) of the bacterial 16S gene
V3-V4
Sequencing platform Manufacturer and experimental platform used for quantifying microbial abundance
Illumina

Statistical Analysis

Data transformation Data transformation applied to microbial abundance measurements prior to differential abundance testing (if any).
relative abundances
Statistical test
ANOVA
Dunn's test
PERMANOVA
Welch's T-Test
Significance threshold p-value or FDR threshold used for differential abundance testing (if any)
0.05
MHT correction Have statistical tests be corrected for multiple hypothesis testing (MHT)?
No

Alpha Diversity

Shannon Estimator of species richness and species evenness: more weight on species richness
unchanged
Chao1 Abundance-based estimator of species richness
unchanged
Richness Number of species
unchanged
Faith Phylogenetic diversity, takes into account phylogenetic distance of all taxa identified in a sample
unchanged

Experiment 2


incomplete

Curated date: 2025/10/11

Curator: Wendeeeee

Revision editor(s): Wendeeeee

Differences from previous experiment shown

Subjects

Group 0 name Corresponds to the control (unexposed) group for case-control studies
Ad libitum + FOS (fructo-oligosaccharide)
Group 1 name Corresponds to the case (exposed) group for case-control studies
Fasting + FOS (fructo-oligosaccharide)
Group 1 definition Diagnostic criteria applied to define the specific condition / phenotype represented in the case (exposed) group
BALB/cAJcl mice subjected to a 36-hour fasting period with 10% FOS administration.
Antibiotics exclusion Number of days without antibiotics usage (if applicable) and other antibiotics-related criteria used to exclude participants (if any)
The study does not mention an antibiotics exclusion period.

Lab analysis

Statistical Analysis

Alpha Diversity

Shannon Estimator of species richness and species evenness: more weight on species richness
decreased
Chao1 Abundance-based estimator of species richness
decreased
Richness Number of species
decreased
Faith Phylogenetic diversity, takes into account phylogenetic distance of all taxa identified in a sample
decreased