Deciphering the Chemical Language of the Immunomodulatory Properties of Veillonella parvula Lipopolysaccharide

Author:

Pither Molly Dorothy1,Andretta Emanuela1,Rocca Giuseppe2,Balzarini Fabio3,Matamoros‐Recio Alejandra4,Colicchio Roberta5,Salvatore Paola5,van Kooyk Yvette3,Silipo Alba1,Granucci Francesca2,Martin‐Santamaria Sonsoles4,Chiodo Fabrizio36,Molinaro Antonio1ORCID,Di Lorenzo Flaviana1ORCID

Affiliation:

1. Department of Chemical Sciences University of Naples Federico II via Cinthia, 4 80126 Naples Italy

2. Department of Biotechnology and Biosciences University of Milano-Bicocca Piazza dell'Ateneo Nuovo, 1 20126 Milan Italy

3. Department of Molecular Cell Biology and Immunology Amsterdam UMC Vrije Universiteit Amsterdam 1007 MB Amsterdam The Netherlands

4. Department of Structural and Chemical Biology Centro de Investigaciones Biológicas, CIB-CSIC C/ Ramiro de Maeztu, 9 28040 Madrid Spain

5. Department of Molecular Medicine and Medical Biotechnology University of Naples Federico II Via Pansini, 5 80131 Naples Italy

6. Institute of Biomolecular Chemistry National Research Council (CNR) Via Campi Flegrei, 34 80078 Pozzuoli Naples Italy

Abstract

AbstractVeillonella parvula, prototypical member of the oral and gut microbiota, is at times commensal yet also potentially pathogenic. The definition of the molecular basis tailoring this contrasting behavior is key for broadening our understanding of the microbiota‐driven pathogenic and/or tolerogenic mechanisms that take place within our body. In this study, we focused on the chemistry of the main constituent of the outer membrane of V. parvula, the lipopolysaccharide (LPS). LPS molecules indeed elicit pro‐inflammatory and immunomodulatory responses depending on their chemical structures. Herein we report the structural elucidation of the LPS from two strains of V. parvula and show important and unprecedented differences in both the lipid and carbohydrate moieties, including the identification of a novel galactofuranose and mannitol‐containing O‐antigen repeating unit for one of the two strains. Furthermore, by harnessing computational studies, in vitro human cell models, as well as lectin binding solid‐phase assays, we discovered that the two chemically diverse LPS immunologically behave differently and have attempted to identify the molecular determinant(s) governing this phenomenon. Whereas pro‐inflammatory potential has been evidenced for the lipid A moiety, by contrast a plausible “immune modulating” action has been proposed for the peculiar O‐antigen portion.

Funder

HORIZON EUROPE European Research Council

Ministero degli Affari Esteri e della Cooperazione Internazionale

Ministero dell'Università e della Ricerca

Publisher

Wiley

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