<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Stoop EJ</submitter><funding>Medical Research Council</funding><funding>Wellcome Trust</funding><pagination>2093-108</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3963455</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(12)</volume><pubmed_abstract>The causative agent of tuberculosis (TB), Mycobacterium tuberculosis, remains an important worldwide health threat. Although TB is one of the oldest infectious diseases of man, a detailed understanding of the mycobacterial mechanisms underlying pathogenesis remains elusive. Here, we studied the role of the α(1→2) mannosyltransferase MptC in mycobacterial virulence, using the Mycobacterium marinum zebrafish infection model. Like its M. tuberculosis orthologue, disruption of M. marinum mptC (mmar_3225) results in defective elongation of mannose caps of lipoarabinomannan (LAM) and absence of α(1→2)mannose branches on the lipomannan (LM) and LAM mannan core, as determined by biochemical analysis (NMR and GC-MS) and immunoblotting. We found that the M. marinum mptC mutant is strongly attenuated</pubmed_abstract><journal>Cellular microbiology</journal><pubmed_title>Mannan core branching of lipo(arabino)mannan is required for mycobacterial virulence in the context of innate immunity.</pubmed_title><pmcid>PMC3963455</pmcid><funding_grant_id>081569/Z/06/Z</funding_grant_id><funding_grant_id>MR/K012118/1</funding_grant_id><pubmed_authors>Mishra AK</pubmed_authors><pubmed_authors>van der Sar AM</pubmed_authors><pubmed_authors>Appelmelk BJ</pubmed_authors><pubmed_authors>Bouchier P</pubmed_authors><pubmed_authors>Verboom T</pubmed_authors><pubmed_authors>van Zon M</pubmed_authors><pubmed_authors>Geurtsen J</pubmed_authors><pubmed_authors>Driessen NN</pubmed_authors><pubmed_authors>Bitter W</pubmed_authors><pubmed_authors>Sparrius M</pubmed_authors><pubmed_authors>Raadsen SA</pubmed_authors><pubmed_authors>van der Wel NN</pubmed_authors><pubmed_authors>van Stempvoort G</pubmed_authors><pubmed_authors>Stoop EJ</pubmed_authors><pubmed_authors>van Leeuwen LM</pubmed_authors><pubmed_authors>Besra GS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mannan core branching of lipo(arabino)mannan is required for mycobacterial virulence in the context of innate immunity.</name><description>The causative agent of tuberculosis (TB), Mycobacterium tuberculosis, remains an important worldwide health threat. Although TB is one of the oldest infectious diseases of man, a detailed understanding of the mycobacterial mechanisms underlying pathogenesis remains elusive. Here, we studied the role of the α(1→2) mannosyltransferase MptC in mycobacterial virulence, using the Mycobacterium marinum zebrafish infection model. Like its M. tuberculosis orthologue, disruption of M. marinum mptC (mmar_3225) results in defective elongation of mannose caps of lipoarabinomannan (LAM) and absence of α(1→2)mannose branches on the lipomannan (LM) and LAM mannan core, as determined by biochemical analysis (NMR and GC-MS) and immunoblotting. We found that the M. marinum mptC mutant is strongly attenuated</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Dec</publication><modification>2026-05-07T10:26:14.045Z</modification><creation>2026-04-29T03:07:49.446Z</creation></dates><accession>S-EPMC3963455</accession><cross_references><pubmed>23902464</pubmed><doi>10.1111/cmi.12175</doi></cross_references></HashMap>