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Analysis of the Actinobacillus pleuropneumoniae HlyX (FNR) regulon and identification of iron-regulated protein B as an essential virulence factor

机译:胸膜肺炎放线杆菌HlyX(FNR)调节子的分析和铁调节蛋白B的鉴定为必需毒力因子

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The Gram-negative rod Actinobacillus pleuropneumonias is a facultative anaerobic pathogen of the porcine respiratory tract, and HlyX, the A. pleuropneumonias homologue of fumarate and nitrate reduction regulator (FNR), has been shown to be important for persistence. An A. pleuro- pneumoniae hlyX deletion mutant has a decreased generation time but highly prolonged survival in comparison to its wild type parent strain when grown anaerobically in glucose-supplemented medium. Applying a combination ofproteomic and transcriptomic approaches as well as in silico analyses, we identified 23 different proteins and 418 genes to be modulated by HlyX (> twofold up- or down-regulated). A putative HlyX-box was identified upstream of 54 of these genes implying direct control by HlyX. Consistent with its role as a strong positive regulator, HlyX induced the expression ofgenes for anaerobic metabolism encoding alternative terminal reduc- tases and hydrogenases. In addition, expression of virulence-associated genes encoding iron uptake systems, a putative DNA adenine modification system, and an autotransporter serine protease were induced by HlyX under anaerobic growth conditions. With respect to virulence- associated genes, we focused on the iron-regulated protein B (FrpB) as it is the outer membrane protein most strongly up-regulated by HlyX. An frpB deletion mutant of A. pleuropneumoniae had the same growth characteristics as wild type grown aerobically and anaerobically. In contrast, A. pleuropneumoniae DfrpB did not cause any disease and could not be re-isolated from experimentally infected pigs, thereby identifying FrpB as a previously unknown virulence factor.
机译:革兰氏阴性菌胸膜肺炎放线杆菌是猪呼吸道的兼性厌氧病原体,富马酸酯和硝酸盐还原调节剂(FNR)的胸膜肺炎放线杆菌HlyX同源物对持久性很重要。与在葡萄糖补充培养基中厌氧生长的野生型亲本菌株相比,胸膜肺炎链球菌hlyX缺失突变体的生成时间缩短,但存活时间大大延长。结合蛋白质组学和转录组学方法以及计算机分析,我们确定了23种不同的蛋白质和418个基因受HlyX调控(上调或下调两倍)。在这些基因的54个基因的上游发现了一个推定的HlyX-box,这暗示着HlyX的直接控制。与它作为强阳性调节剂的作用一致,HlyX诱导了厌氧代谢基因的表达,该基因编码其他末端还原酶和氢化酶。此外,在厌氧生长条件下,HlyX诱导了编码铁吸收系统,推定的DNA腺嘌呤修饰系统和自转运丝氨酸蛋白酶的毒力相关基因的表达。关于毒力相关基因,我们专注于铁调节蛋白B(FrpB),因为它是HlyX最强烈上调的外膜蛋白。胸膜肺炎链球菌的frpB缺失突变体与需氧和厌氧的野生型具有相同的生长特性。相反,胸膜肺炎链球菌DfrpB不会引起任何疾病,也不能从实验感染的猪中重新分离出来,从而确定FrpB是以前未知的毒力因子。

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