Author:
Palčeková Zuzana,Obregón-Henao Andrés,De Kavita,Walz Amanda,Lam Ha,Philp Jamie,Angala Shiva Kumar,Patterson Johnathan,Pearce Camron,Zuberogoitia Sophie,Avanzi Charlotte,Nigou Jérôme,McNeil Michael,Muñoz Gutiérrez Juan F.,Gilleron Martine,Wheat William H.,Gonzalez-Juarrero Mercedes,Jackson Mary
Abstract
The covalent modification of bacterial (lipo)polysaccharides with discrete substituents may impact their biosynthesis, export and/or biological activity. Whether mycobacteria use a similar strategy to control the biogenesis of its cell envelope polysaccharides and modulate their interaction with the host during infection is unknown despite the report of a number of tailoring substituents modifying the structure of these glycans. Here, we show that discrete succinyl substituents strategically positioned on Mycobacterium tuberculosis (Mtb) lipoarabinomannan govern the mannose-capping of this lipoglycan and, thus, much of the biological activity of the entire molecule. We further show that the absence of succinyl substituents on the two main cell envelope glycans of Mtb, arabinogalactan and lipoarabinomannan, leads to a significant increase of pro-inflammatory cytokines and chemokines in infected murine and human macrophages. Collectively, our results validate polysaccharide succinylation as a critical mechanism by which Mtb controls inflammation.
Publisher
Public Library of Science (PLoS)
Subject
Virology,Genetics,Molecular Biology,Immunology,Microbiology,Parasitology
Cited by
2 articles.
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