Gut bacteria-derived sphingolipids alter innate immune responses to oral cholera vaccine antigens

D Denise Chac F Frederick J. Heller H Hasan Al Banna M M. Hasanul Kaisar (Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine) S Susan M. Markiewicz E Emily L. Pruitt F Fahima Chowdhury (Mucosal Immunology and Vaccinology Unit, Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Bangladesh) T Taufiqur R. Bhuiyan A Afroza Akter A Ashraful I. Khan M Mia G. Dumayas A Amelia Rice P Polash Chandra Karmakar P Pinki Dash R Regina C. LaRocque E Edward T. Ryan L Libin Xu S Samuel S. Minot J Jason B. Harris F Firdausi Qadri A Ana A. Weil

Abstract

Abstract The degree of protection conferred after receiving an oral cholera vaccine (OCV) varies based on age, prior exposure to Vibrio cholerae , and unknown factors. Recent evidence suggests that the microbiota may mediate some of the unexplained differences in oral vaccine responses. Here, we use metagenomic sequencing of the fecal microbiota at the time of vaccination and relate microbial features to immune responses after OCV using a reference-independent gene-level method. We find that the presence of sphingolipid-producing bacteria is associated with the development of protective immune responses after OCV. We test these associations by stimulating human macrophages with Bacteroides xylanisolvens metabolites and find that sphingolipid-containing extracts increase innate immune responses to OCV antigens. Our findings demonstrate a new analytic method for translating metagenomic sequencing data into strain-specific results associated with a biological outcome, and in validating this tool, we identify that microbe-derived sphingolipids impact immune responses to OCV antigens.

Article Details

Volume / Issue Vol. 17, Issue 1
Published December 12, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (21)

D

Denise Chac

F

Frederick J. Heller

H

Hasan Al Banna

M

M. Hasanul Kaisar

Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine

S

Susan M. Markiewicz

E

Emily L. Pruitt

F

Fahima Chowdhury

Mucosal Immunology and Vaccinology Unit, Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Bangladesh

T

Taufiqur R. Bhuiyan

A

Afroza Akter

A

Ashraful I. Khan

M

Mia G. Dumayas

A

Amelia Rice

P

Polash Chandra Karmakar

P

Pinki Dash

R

Regina C. LaRocque

E

Edward T. Ryan

L

Libin Xu

S

Samuel S. Minot

J

Jason B. Harris

F

Firdausi Qadri

A

Ana A. Weil