Literature DB >> 8704991

Extracellular and surface-exposed polysaccharides of non-tuberculous mycobacteria.

Anne Lemassu1, Annick Ortalo-Magné1, Fabienne Bardou1, Gaby Silve1, Marie-Antoinette Lanéelle1, Mamadou Daffé1.   

Abstract

We studied the outermost constituents of the cell envelopes, which are involved in the interaction between the bacilli and the host cells, of five pathogenic and non-pathogenic mycobacterial species for comparison with those we have previously characterized from M. tuberculosis. The extracellular materials (ECMs) were isolated by ethanol precipitation and compared to the surface-exposed materials (SXMs) extracted by mechanical means. The materials from both sources were composed almost exclusively of polysaccharides and proteins. Two groups of mycobacteria were clearly distinguishable. The first group comprised the pathogenic species M. kansasii which produced large amounts of ECM, the glycosyl composition of which was similar to that of the SXM. The second group comprised M. avium and the non-pathogenic strains of M. gastri, M. phlei and M. smegmatis which produced small amounts of ECK This latter group could be subdivided into those which produced carbohydrate-rich ECM (M. avium and M. gastri) and those forming protein-rich ECM (M. phlei and M. smegmatis), a classification that correlated with the difference in the growth rate of the two subgroups. The glycosyl composition of the ECM of a given species was qualitatively similar to that of the SXM, except for M. avium and M. phlei whose SXM were devoid of arabinose. In addition to glucose, mannose and arabinose, xylose was detected in the hydrolysis products of the ECM and SXM of M. smegmatis, the SXM of M. phlei and the ECM of some batches of M. avium. The polysaccharide constituents of the ECM and SXM of the different mycobacteria were purified by anion-exchange and gel-filtration chromatography; all were found to be neutral compounds devoid of acyl substituents. The extracellular polysaccharides consisted of high-molecular-mass glycogen-like glucans, arabinomannans and mannans, structurally similar to the corresponding substances previously characterized from the capsule of M. tuberculosis. The same types of polysaccharides were characterized from the SXM of all the strains, except M. avium and M. phlei which were devoid of arabinomannans. This study questions the unique and universal representation of the mycobacterial cell envelope and the existence of the so-called acidic polysaccharide-rich outer layer.

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Year:  1996        PMID: 8704991     DOI: 10.1099/13500872-142-6-1513

Source DB:  PubMed          Journal:  Microbiology (Reading)        ISSN: 1350-0872            Impact factor:   2.777


  27 in total

1.  Capsular glucan and intracellular glycogen of Mycobacterium tuberculosis: biosynthesis and impact on the persistence in mice.

Authors:  Tounkang Sambou; Premkumar Dinadayala; Gustavo Stadthagen; Nathalie Barilone; Yann Bordat; Patricia Constant; Florence Levillain; Olivier Neyrolles; Brigitte Gicquel; Anne Lemassu; Mamadou Daffé; Mary Jackson
Journal:  Mol Microbiol       Date:  2008-09-18       Impact factor: 3.501

2.  Direct visualization of the outer membrane of mycobacteria and corynebacteria in their native state.

Authors:  Benoît Zuber; Mohamed Chami; Christine Houssin; Jacques Dubochet; Gareth Griffiths; Mamadou Daffé
Journal:  J Bacteriol       Date:  2008-06-20       Impact factor: 3.490

3.  Crystal structure of full-length Mycobacterium tuberculosis H37Rv glycogen branching enzyme: insights of N-terminal beta-sandwich in substrate specificity and enzymatic activity.

Authors:  Kuntal Pal; Shiva Kumar; Shikha Sharma; Saurabh Kumar Garg; Mohammad Suhail Alam; H Eric Xu; Pushpa Agrawal; Kunchithapadam Swaminathan
Journal:  J Biol Chem       Date:  2010-05-05       Impact factor: 5.157

4.  Structural definition of arabinomannans from Mycobacterium bovis BCG.

Authors:  J Nigou; M Gilleron; T Brando; A Vercellone; G Puzo
Journal:  Glycoconj J       Date:  1999-06       Impact factor: 2.916

Review 5.  The Mycobacterium tuberculosis capsule: a cell structure with key implications in pathogenesis.

Authors:  Rainer Kalscheuer; Ainhoa Palacios; Itxaso Anso; Javier Cifuente; Juan Anguita; William R Jacobs; Marcelo E Guerin; Rafael Prados-Rosales
Journal:  Biochem J       Date:  2019-07-18       Impact factor: 3.857

6.  Genetics of Capsular Polysaccharides and Cell Envelope (Glyco)lipids.

Authors:  Mamadou Daffé; Dean C Crick; Mary Jackson
Journal:  Microbiol Spectr       Date:  2014

7.  The glycan-rich outer layer of the cell wall of Mycobacterium tuberculosis acts as an antiphagocytic capsule limiting the association of the bacterium with macrophages.

Authors:  Richard W Stokes; Raymond Norris-Jones; Donald E Brooks; Terry J Beveridge; Dan Doxsee; Lisa M Thorson
Journal:  Infect Immun       Date:  2004-10       Impact factor: 3.441

8.  Direct visualization by cryo-EM of the mycobacterial capsular layer: a labile structure containing ESX-1-secreted proteins.

Authors:  Musa Sani; Edith N G Houben; Jeroen Geurtsen; Jason Pierson; Karin de Punder; Maaike van Zon; Brigitte Wever; Sander R Piersma; Connie R Jiménez; Mamadou Daffé; Ben J Appelmelk; Wilbert Bitter; Nicole van der Wel; Peter J Peters
Journal:  PLoS Pathog       Date:  2010-03-05       Impact factor: 6.823

9.  The cell envelope-associated phospholipid-binding protein LmeA is required for mannan polymerization in mycobacteria.

Authors:  Kathryn C Rahlwes; Stephanie A Ha; Daisuke Motooka; Jacob A Mayfield; Lisa R Baumoel; Justin N Strickland; Ana P Torres-Ocampo; Shota Nakamura; Yasu S Morita
Journal:  J Biol Chem       Date:  2017-08-29       Impact factor: 5.157

10.  Use of gene dosage effects for a whole-genome screen to identify Mycobacterium marinum macrophage infection loci.

Authors:  Bonggoo Park; Selvakumar Subbian; Sahar H El-Etr; Suat L G Cirillo; Jeffrey D Cirillo
Journal:  Infect Immun       Date:  2008-04-28       Impact factor: 3.441

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