A truncated lipoglycan from mycobacteria with altered immunological properties.

Helen Birch, Luke Alderwick, BJ Appelmelk, J Maaskant, Apoorva Bhatt, Albel Singh, J Nigou, L Eggeling, J Geurtsen, Gurdyal Besra

Research output: Contribution to journalArticlepeer-review

39 Citations (Scopus)
153 Downloads (Pure)


Maintenance of cell-wall integrity in Mycobacterium tuberculosis is essential and is the target of several antitubercular drugs. For example, ethambutol targets arabinogalactan and lipoarabinomannan (LAM) biosynthesis through the inhibition of several arabinofuranosyltransferases. Apart from their role in cell-wall integrity, mycobacterial LAMs also exhibit important immunomodulatory activities. Here we report the isolation and detailed structural characterization of a unique LAM molecule derived from Mycobacterium smegmatis deficient in the arabinofuranosyltransferase AftC (AftC-LAM). This mutant LAM expresses a severely truncated arabinan domain completely devoid of 3,5-Araf–branching residues, revealing an intrinsic involvement of AftC in the biosynthesis of LAM. Furthermore, we found that ethambutol efficiently inhibits biosynthesis of the AftC-LAM arabinan core, unambiguously demonstrating the involvement of the arabinofuranosyltransferase EmbC in early stages of LAM-arabinan biosynthesis. Finally, we demonstrate that AftC-LAM exhibits an enhanced proinflammatory activity, which is due to its ability to activate Toll-like receptor 2 (TLR2). Overall, our efforts further describe the mechanism of action of an important antitubercular drug, ethambutol, and demonstrate a role for specific arabinofuranosyltransferases in LAM biosynthesis. In addition, the availability of sufficient amounts of chemically defined wild-type and isogenic truncated LAMs paves the way for further investigations of the structure–function relationship of TLR2 activation by mycobacterial lipoglycans.
Original languageEnglish
Pages (from-to)2634-9
Number of pages6
JournalNational Academy of Sciences. Proceedings
Issue number6
Publication statusPublished - 9 Feb 2010


  • lipoarabinomannan
  • cell wall
  • arabinofuranosyltransferase
  • ethambutol
  • Mycobacterium tuberculosis


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