4.7 Article

Gut Microbiome in Progressive Multiple Sclerosis

Journal

ANNALS OF NEUROLOGY
Volume 89, Issue 6, Pages 1195-1211

Publisher

WILEY
DOI: 10.1002/ana.26084

Keywords

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Funding

  1. NIH from the National Institute of Neurologic Disorders and Stroke (NINDS) [R01NS087226]
  2. NextGen Collaborative Grant from the Brigham Research Institute
  3. Water Cove Charitable Foundation
  4. Nancy Davis Race to Erase MS Young Investigator Award
  5. National MS Society

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This study investigated gut microbiome in progressive MS and found differences in microbiota beta-diversity between MS patients and controls, with unique bacteria associated with progressive MS. Elevated Akkermansia in MS may have a beneficial role in the disease, as indicated by lower disability and amelioration of EAE.
Objective This study was undertaken to investigate the gut microbiome in progressive multiple sclerosis (MS) and how it relates to clinical disease. Methods We sequenced the microbiota from healthy controls and relapsing-remitting MS (RRMS) and progressive MS patients and correlated the levels of bacteria with clinical features of disease, including Expanded Disability Status Scale (EDSS), quality of life, and brain magnetic resonance imaging lesions/atrophy. We colonized mice with MS-derived Akkermansia and induced experimental autoimmune encephalomyelitis (EAE). Results Microbiota beta-diversity differed between MS patients and controls but did not differ between RRMS and progressive MS or differ based on disease-modifying therapies. Disease status had the greatest effect on the microbiome beta-diversity, followed by body mass index, race, and sex. In both progressive MS and RRMS, we found increased Clostridium bolteae, Ruthenibacterium lactatiformans, and Akkermansia and decreased Blautia wexlerae, Dorea formicigenerans, and Erysipelotrichaceae CCMM. Unique to progressive MS, we found elevated Enterobacteriaceae and Clostridium g24 FCEY and decreased Blautia and Agathobaculum. Several Clostridium species were associated with higher EDSS and fatigue scores. Contrary to the view that elevated Akkermansia in MS has a detrimental role, we found that Akkermansia was linked to lower disability, suggesting a beneficial role. Consistent with this, we found that Akkermansia isolated from MS patients ameliorated EAE, which was linked to a reduction in ROR gamma t+ and IL-17-producing gamma delta T cells. Interpretation Whereas some microbiota alterations are shared in relapsing and progressive MS, we identified unique bacteria associated with progressive MS and clinical measures of disease. Furthermore, elevated Akkermansia in MS may be a compensatory beneficial response in the MS microbiome. ANN NEUROL 2021

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