Gut microbial factors predict disease severity in a mouse model of multiple sclerosis

Gut bacteria are linked to neurodegenerative diseases but the risk factors beyond microbiota composition are limited. Here we used a pre-clinical model of multiple sclerosis (MS), experimental autoimmune encephalomyelitis (EAE), to identify microbial risk factors. Mice with different genotypes and c...

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Veröffentlicht in:Nature microbiology 2024-09, Vol.9 (9), p.2244-2261
Hauptverfasser: Steimle, Alex, Neumann, Mareike, Grant, Erica T., Willieme, Stéphanie, De Sciscio, Alessandro, Parrish, Amy, Ollert, Markus, Miyauchi, Eiji, Soga, Tomoyoshi, Fukuda, Shinji, Ohno, Hiroshi, Desai, Mahesh S.
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Sprache:eng
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Zusammenfassung:Gut bacteria are linked to neurodegenerative diseases but the risk factors beyond microbiota composition are limited. Here we used a pre-clinical model of multiple sclerosis (MS), experimental autoimmune encephalomyelitis (EAE), to identify microbial risk factors. Mice with different genotypes and complex microbiotas or six combinations of a synthetic human microbiota were analysed, resulting in varying probabilities of severe neuroinflammation. However, the presence or relative abundances of suspected microbial risk factors failed to predict disease severity. Akkermansia muciniphila , often associated with MS, exhibited variable associations with EAE severity depending on the background microbiota. Significant inter-individual disease course variations were observed among mice harbouring the same microbiota. Evaluation of microbial functional characteristics and host immune responses demonstrated that the immunoglobulin A coating index of certain bacteria before disease onset is a robust individualized predictor of disease development. Our study highlights the need to consider microbial community networks and host-specific bidirectional interactions when aiming to predict severity of neuroinflammation. Gut microbiota factors including IgA coating can predict disease severity in a mouse model of multiple sclerosis.
ISSN:2058-5276
2058-5276
DOI:10.1038/s41564-024-01761-3