Specific microbial ratio in the gut microbiome is associated with multiple sclerosis

S Sudeep Ghimire (Department of Pathology, University of Iowa) P Peter C. Lehman (Department of Pathology, University of Iowa) L Leeann S. Aguilar Meza (Microbiome Core, University of Iowa) S Shailesh K. Shahi (Department of Pathology, University of Iowa) J Jemmie Hoang (College of Nursing, University of Iowa) H Heena Olalde (Department of Neurology, University of Iowa Hospital and Clinics) M Mishelle Paullus (Department of Neurology, University of Iowa Hospital and Clinics) C Catherine Cherwin (College of Nursing, University of Iowa) K Kai Wang C Christine Gill (Department of Neurology, University of Iowa Hospital and Clinics) T Tracey Cho (Department of Neurology, University of Iowa Hospital and Clinics) A Ashutosh K. Mangalam (Department of Pathology, University of Iowa)

Abstract

Gut microbiota dysbiosis is associated with multiple sclerosis (MS), but the causal relationship between specific gut bacteria and MS pathogenesis remains poorly understood. Therefore, we profiled the stool microbiome of people with MS (PwMS) and healthy controls (HC) using shotgun metagenomic sequencing. PwMS showed a distinct microbiome compared to HC, with Prevotella copri ( PC ) and Blautia species as drivers of microbial communities in HC and PwMS, respectively. Administration of MS-driving Blautia species ( Blautia wexlerae; BW ) to mice resulted in increased levels of gut inflammatory markers and altered microbiota with increased capacity to induce proinflammatory cytokines. Utilizing experimental autoimmune encephalomyelitis (EAE), an animal model of MS, we identified a lower gut Bifidobacterium to Akkermansia ratio as a hallmark of the disease. BW -administered mice also showed a lower Bifidobacterium to Akkermansia ratio pre-EAE induction which correlated with increased disease severity post-EAE induction. The importance of the Bifidobacterium to Akkermansia ratio at the species level, lower Bifidobacterium adolescentis to Akkermansia muciniphila ( BA:AM ), was validated in our MS cohort and a large International Multiple Sclerosis Microbiome Study. Thus, our findings highlight the BA:AM ratio as a potential gut microbial marker in PwMS, opening avenues for microbiome-based diagnosis, prognosis, and therapy in MS.

Article Details

Volume / Issue Vol. 122, Issue 10
Published March 11, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (12)

S

Sudeep Ghimire

Department of Pathology, University of Iowa

P

Peter C. Lehman

Department of Pathology, University of Iowa

L

Leeann S. Aguilar Meza

Microbiome Core, University of Iowa

S

Shailesh K. Shahi

Department of Pathology, University of Iowa

J

Jemmie Hoang

College of Nursing, University of Iowa

H

Heena Olalde

Department of Neurology, University of Iowa Hospital and Clinics

M

Mishelle Paullus

Department of Neurology, University of Iowa Hospital and Clinics

C

Catherine Cherwin

College of Nursing, University of Iowa

K

Kai Wang

C

Christine Gill

Department of Neurology, University of Iowa Hospital and Clinics

T

Tracey Cho

Department of Neurology, University of Iowa Hospital and Clinics

A

Ashutosh K. Mangalam

Department of Pathology, University of Iowa