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Structural Study of Lipomannan and Lipoarabinomannan fromMycobacterium chelonae

Authors :
Yves Leroy
Emmanuel Maes
Gurdyal S. Besra
Elisabeth Elass
Philippe Timmerman
Gérard Strecker
Camille Locht
Yann Guérardel
Laurent Kremer
Source :
Journal of Biological Chemistry. 277:30635-30648
Publication Year :
2002
Publisher :
Elsevier BV, 2002.

Abstract

Lipomannan (LM) and lipoarabinomannan (LAM) are major glycolipids present in the mycobacterial cell wall that are able to modulate the host immune response. In this study, we have undertaken the structural determination of these important modulins inMycobacterium chelonae, a fast growing pathogenic mycobacterial species. One-dimensional and two-dimensional NMR spectra were used to demonstrate that LM and LAM from M. chelonae, designated CheLM and CheLAM, respectively, possess structures that differ from the ones reported earlier in other mycobacterial species. Analysis by gas chromatography/mass spectrometry of the phosphatidyl-myo-inositol anchor, which is thought to play a role in the biological functions of these lipoglycans, pointed to a high degree of heterogeneity based on numerous combinations of acyl groups on the C-1 and C-2 positions of the glycerol moiety. Characterization of the mannan core of CheLM and CheLAM revealed the presence of novel α1,3-mannopyranosyl side chains. This motif, which reacted specifically with the lectin from Galanthus nivalis, was found to be unique among a panel of nine mycobacterial species. Then, CheLM and CheLAM were found to be devoid of both the mannooligosaccharide cap present in Mycobacterium tuberculosis and the inositol phosphate cap present inMycobacterium smegmatis and other fast growing species. Tumor necrosis factor-α and interleukin-8 production were assessed from human macrophages with LAM preparations from different species. Our results suggest that the inositol phosphate capping may represent the major cytokine-inducing component of LAMs. This work not only underlines the diversity of LAM structures among various mycobacterial species but also provides new structures that could be useful to dissect the structure-function relationships of these complex molecules.

Details

ISSN :
00219258
Volume :
277
Database :
OpenAIRE
Journal :
Journal of Biological Chemistry
Accession number :
edsair.doi...........1c89e658a72082ff915edf7fb55c8d3e
Full Text :
https://doi.org/10.1074/jbc.m204398200