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Identification and regulation of Actinobacillus pleuropneumoniae in vivo induced genes that respond to branched-chain amino acid limitation.

机译:鉴定和调节胸膜肺炎放线杆菌在体内诱导的响应支链氨基酸限制的基因。

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摘要

Actinobacillus pleuropneumoniae is a Gram-negative bacterial pathogen that is the causative agent of a severe hemorrhagic pleuropneumonia in swine. The severe effect of the disease on the swine industry has led to extensive research on development of improved vaccines. To understand the genetic basis of this disease and to identify potential vaccine targets, an in vivo expression technology (IVET) system was developed for use in A. pleuropneumoniae serotype 1. The IVET system was designed to identify A. pleuropneumoniae in vivo induced ( ivi) genes whose expression is specifically induced during infection of the natural swine host, without the need to identify each individual environmental cue necessary for expression of each gene.; However, to analyze the role of ivi genes, it is important to understand the specific cues that regulate expression of each ivi gene. It was hypothesized that a limitation of branched-chain amino acids (BCAAs) acts as a signal to induce expression of ivi genes in a manner similar to iron limitation. A pool of 32 previously isolated ivi promoter clones were analyzed for increased activity of a reporter under BCAA limiting conditions, and 8 ivi promoters were identified as up-regulated in this study. These data suggest that the limitation of BCAAs is an important cue in the regulation of ivi genes and potentially other virulence genes.; One mechanism known to regulate many Escherichia coli genes in response to BCAA limitation is leucine-responsive regulatory protein (Lrp). An A. pleuropneumoniae gene similar to Lrp was identified and cloned. Purified A. pleuropneumoniae His6-Lrp bound in vitro to 2/8 ivi promoters identified to respond to BCAA limitation. A genetically-defined A. pleuropneumoniae lrp mutant was constructed and used to show the requirement for Lrp in the regulation of several A. pleuropneumoniae genes.; To further understand the role of Lrp in virulence, the A. pleuropneumoniae lrp mutant was analyzed in a swine model of respiratory infection. The lrp mutant was able to cause disease under the conditions tested, with progression of disease and pathology similar to that seen with wild-type A. pleuropneumoniae.; The identification of an environmental stimulus, a regulatory mechanism, and genes regulated by these factors is an important step for understanding the virulence of A. pleuropneumoniae. This research offers insight into new avenues of research to further examine the virulence of A. pleuropneumoniae and other respiratory pathogens.
机译:胸膜肺炎放线杆菌是革兰氏阴性细菌病原体,是猪中严重出血性胸膜肺炎的病原体。该病对养猪业的严重影响已导致对开发改良疫苗的广泛研究。为了了解这种疾病的遗传基础并确定潜在的疫苗靶标,开发了一种体内表达技术(IVET)系统用于胸膜肺炎链球菌血清型1。IVET系统旨在识别体内诱导的胸膜肺炎)其表达是在天然猪宿主感染过程中被特异性诱导的基因,而无需确定表达每个基因所必需的每个环境提示。但是,要分析ivi基因的作用,重要的是要了解调节每个ivi基因表达的特定提示。据推测,支链氨基酸(BCAA)的限制以类似于铁限制的方式充当诱导ivi基因表达的信号。分析了32个先前分离的ivi启动子克隆在BCAA限制条件下报道分子活性的增加,并且在本研究中鉴定出8个ivi启动子被上调。这些数据表明,BCAA的局限性是调节ivi基因和潜在的其他毒力基因的重要线索。已知响应于BCAA限制而调节许多大肠杆菌基因的一种机制是亮氨酸响应性调节蛋白(Lrp)。鉴定并克隆了类似于Lrp的肺炎链球菌基因。纯化的胸膜肺炎链球菌His6-Lrp在体外与2/8个ivi启动子结合,该启动子被识别为对BCAA限制有反应。构建了遗传定义的胸膜肺炎链球菌lrp突变体,并用于显示在调节多个胸膜肺炎链球菌基因中对Lrp的需求。为了进一步了解Lrp在毒力中的作用,在猪呼吸道感染模型中分析了胸膜肺炎链球菌lrp突变体。 lrp突变体能够在所测试的条件下引起疾病,其疾病和病理进展与野生型胸膜肺炎放线杆菌相似。识别环境刺激,调节机制和受这些因素调节的基因是了解胸膜肺炎链球菌毒力的重要步骤。该研究为进一步研究胸膜肺炎放线杆菌和其他呼吸道病原体的毒性提供了新的研究途径。

著录项

  • 作者

    Wagner, Trevor Keith.;

  • 作者单位

    Michigan State University.;

  • 授予单位 Michigan State University.;
  • 学科 Biology Genetics.; Biology Microbiology.; Agriculture Animal Pathology.
  • 学位 Ph.D.
  • 年度 2006
  • 页码 211 p.
  • 总页数 211
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 遗传学;微生物学;动物医学(兽医学);
  • 关键词

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