Antibacterial activity of a lectin-like Burkholderia cenocepacia protein.

TitleAntibacterial activity of a lectin-like Burkholderia cenocepacia protein.
Publication TypeJournal Article
Year of Publication2013
AuthorsGhequire, M. G. K., E. De Canck, P. Wattiau, I. Van Winge, R. Loris, T. Coenye, and R. De Mot
JournalMicrobiologyopen
Volume2
Issue4
Pagination566-75
Date Published2013 Aug
Type of Articlelectins
ISSN2045-8827
Abstract

Bacteriocins of the LlpA family have previously been characterized in the γ-proteobacteria Pseudomonas and Xanthomonas. These proteins are composed of two MMBL (monocot mannose-binding lectin) domains, a module predominantly and abundantly found in lectins from monocot plants. Genes encoding four different types of LlpA-like proteins were identified in genomes from strains belonging to the Burkholderia cepacia complex (Bcc) and the Burkholderia pseudomallei group. A selected recombinant LlpA-like protein from the human isolate Burkholderia cenocepacia AU1054 displayed narrow-spectrum genus-specific antibacterial activity, thus representing the first functionally characterized bacteriocin within this β-proteobacterial genus. Strain-specific killing was confined to other members of the Bcc, with mostly Burkholderia ambifaria strains being susceptible. In addition to killing planktonic cells, this bacteriocin also acted as an antibiofilm agent.

DOI10.1002/mbo3.95
Alternate JournalMicrobiologyopen
PubMed ID23737242
PubMed Central IDPMC3831624
Grant ListGM098791 / GM / NIGMS NIH HHS / United States