Wagner Trevor K, Mulks Martha H
Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA.
Infect Immun. 2007 Jan;75(1):91-103. doi: 10.1128/IAI.00120-06. Epub 2006 Oct 23.
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.
胸膜肺炎放线杆菌是一种革兰氏阴性细菌病原体,可导致猪严重的出血性肺炎。我们之前已经表明,支链氨基酸(BCAAs)的限制是一种信号,可诱导胸膜肺炎放线杆菌的一部分基因表达,这些基因是通过体内表达技术筛选在天然宿主动物感染期间被特异性诱导的。亮氨酸响应调节蛋白(Lrp)是一种全局调节因子,在大肠杆菌中已显示其可调节许多基因,包括参与BCAA生物合成的基因。我们假设胸膜肺炎放线杆菌含有一种与Lrp相似的调节因子,并且这种蛋白质参与调节感染期间重要的一部分基因,最近显示在没有BCAAs的情况下其表达增加。我们报告了胸膜肺炎放线杆菌1型基因的鉴定,该基因编码一种与其他已报道的Lrp蛋白的氨基酸序列和功能域相似的蛋白质。我们进一步表明,纯化的胸膜肺炎放线杆菌His6-Lrp在体外与ilvI、反义cps1AB、lrp和nqr的胸膜肺炎放线杆菌启动子区域结合。使用等位基因替换和蔗糖反选择方法构建了基因定义的胸膜肺炎放线杆菌lrp突变体。对野生型、lrp突变体和互补的lrp突变体菌株中ilvI和反义cps1AB启动子表达的分析表明,在BCAAs限制下,Lrp是诱导ilvI表达所必需的。