AI Article Synopsis

  • Actinobacillus pleuropneumoniae is a gram-negative bacterium that causes severe pneumonia in pigs, and its gene expression is influenced by the availability of branched-chain amino acids (BCAAs).
  • Researchers hypothesized that A. pleuropneumoniae has a regulatory protein similar to E. coli's Leucine-responsive regulatory protein (Lrp), which likely regulates genes important during infection.
  • The study identified a gene in A. pleuropneumoniae that encodes a protein resembling Lrp and demonstrated that this protein is essential for the expression of specific genes under BCAA limitation.

Article Abstract

Actinobacillus pleuropneumoniae is a gram-negative bacterial pathogen that causes a severe hemorrhagic pneumonia in swine. We have previously shown that the limitation of branched-chain amino acids (BCAAs) is a cue that induces the expression of a subset of A. pleuropneumoniae genes identified as specifically induced during infection of the natural host animal by using an in vivo expression technology screen. Leucine-responsive regulatory protein (Lrp) is a global regulator and has been shown in Escherichia coli to regulate many genes, including genes involved in BCAA biosynthesis. We hypothesized that A. pleuropneumoniae contains a regulator similar to Lrp and that this protein is involved in the regulation of a subset of genes important during infection and recently shown to have increased expression in the absence of BCAAs. We report the identification of an A. pleuropneumoniae serotype 1 gene encoding a protein with similarity to amino acid sequence and functional domains of other reported Lrp proteins. We further show that purified A. pleuropneumoniae His6-Lrp binds in vitro to the A. pleuropneumoniae promoter regions for ilvI, antisense cps1AB, lrp, and nqr. A genetically defined A. pleuropneumoniae lrp mutant was constructed using an allelic replacement and sucrose counterselection method. Analysis of expression from the ilvI and antisense cps1AB promoters in wild-type, lrp mutant, and complemented lrp mutant strains indicated that Lrp is required for induction of expression of ilvI under BCAA limitation.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1828405PMC
http://dx.doi.org/10.1128/IAI.00120-06DOI Listing

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