Published September 6, 2024
| Version v1
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Microbiota-dependent early-life programming of gastrointestinal motility
- 1. University of Chicago
- 2. Mayo Clinic
Description
Gastrointestinal microbes modulate peristalsis and stimulate the enteric nervous system (ENS), whose development, as in the central nervous system (CNS), continues into the murine postweaning period. Given that adult CNS function depends on stimuli received during critical periods of postnatal development, we hypothesized that adult ENS function, namely motility, depends on microbial stimuli during similar critical periods. We gave fecal microbiota transplantation (FMT) to germ-free mice at weaning or as adults and found that only the mice given FMT at weaning recovered normal transit, while those given FMT as adults showed limited improvements. RNA sequencing (RNA-seq) of colonic muscularis propria revealed enrichments in neuron developmental pathways in mice exposed to gut microbes earlier in life, while mice exposed later—or not at all—showed exaggerated expression of inflammatory pathways. These findings highlight a microbiota-dependent sensitive period in ENS development, pointing to potential roles of the early-life microbiome in later-life dysmotility.
Data availability
RNA-seq data have been deposited at Gene Expression Omnibus. Microbial 16S rRNA gene sequencing data have been deposited at NCBI Sequence Read Archive. Both are publicly available as of the date of publication. Accession numbers are listed in the key resources table.
Additional raw data from Figures 1, 3, 4, S1, and S4 were deposited on Mendeley at https://doi.org/10.17632/snpf8f2tcx.1
This paper does not report original code.
Any additional information required to reanalyze the data reported in this paper is available from the lead contact upon request.
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Additional details
Identifiers
- DOI
- 10.1016/j.isci.2024.110895
- Other
- oai:uchicago.tind.io:13565
Funding
- NIDDK
- P30 DK042086
- National Institutes of Health
- T32 GM007281
- National Institutes of Health
- F30DK126309
- National Institutes of Health
- R01DK129315
- National Institutes of Health
- R01DK114007