Gut bacteria-derived sphingolipids alter innate immune responses to oral cholera vaccine antigens
D. Chac, F. J. Heller, H. A. Banna, M. H. Kaisar, F. Chowdhury, T. R. Bhuiyan, A. Akter, A. I. Khan, M. G. Dumayas, S. M. Markiewicz, A. Rice, P. C. Karmakar, P. Dash, R. C. LaRocque, E. T. Ryan, S. S. Minot, J. B. Harris, F. Qadri, A. A. Weil
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. We used metagenomic sequencing of the microbiota at the time of vaccination, and then related microbial features to immune responses after OCV using a reference-independent gene-level analysis. We found that the presence of sphingolipid-producing bacteria was associated with the development of protective immune responses after OCV. We experimentally tested these results by stimulating human macrophages with Bacteroides xylanisolvens metabolites and found that sphingolipid-containing extracts increased 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 identified that microbe-derived sphingolipids impact in vitro immune responses to OCV antigens.
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