bioRxivMicrobiologyPreprint
Induction of cross-reactive antibody responses against the RBD domain of the spike protein of SARS-CoV-2 by commensal microbiota
J. Ninnemann, L. Budzinski, M. Bondareva, M. Witkowski, S. Angermair, J. Kreye, P. Durek, M. Reincke, E. Sanchez-Sendin, S. Yilmaz, T. Sempert, G. A. Heinz, C. Tizian, M. Raftery, G. Schoenrich, D. Matyushkina, I. Smirnov, V. Govorun, E. V. Schrezenmeier, T. Doerner, S. Zocche, E. Viviano, K. J. Sehmsdorf, H.-D. Chang, P. Enghard, , A. Kruglov
Abstract
The commensal microflora is a source for multiple antigens that may induce cross-reactive antibodies against host proteins and pathogens. However, whether commensal bacteria can induce cross-reactive antibodies against SARS-CoV-2 remains unknown. Here we report that several commensal bacteria contribute to the generation of cross-reactive IgA antibodies against the receptor-binding domain (RBD) of the SARS-CoV-2 Spike protein. We identified SARS-CoV-2 unexposed individuals with RBD-binding IgA antibodies at their mucosal surfaces. Conversely, neutralising monoclonal anti-RBD antibodies recognised distinct commensal bacterial species. Some of these bacteria, such as Streptococcus salivarius, induced a cross-reactive anti-RBD antibodies upon supplementation in mice. Conversely, severely ill COVID-19 patients showed reduction of Streptococcus and Veillonella in their oropharynx and feces and a reduction of anti-RBD IgA at mucosal surfaces. Altogether, distinct microbial species of the human microbiota can induce secretory IgA antibodies cross-reactive for the RBD of SARS-CoV-2.
- organism: human
- assay: proteomics
- assay: clinical cohort / trial
- research focus: host-pathogen & immune response
- research focus: cell type annotation
- approach: experimental assay
- approach: wet-lab / biochemical assay
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