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Characterization of a locus encoding four paralogous outer membrane lipoproteins of Brachyspira hyodysenteriae

机译:编码猪痢疾短螺旋体四种旁源外膜脂蛋白的基因座的表征

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The identification of Brachyspira hyodysenteriae outer membrane proteins (OMPs) that may stimulate immunity to swine dysentery is important for vaccine development. We report here the analysis of a novel locus, blpGFEA, encoding four tandem paralogous proteins of ~30 kDa from B. hyodysenteriae. The four proteins share 31-39% sequence identity with lipoproteins from several species of bacterial pathogens, but the locus possesses a unique genetic organization. Using antisera raised to recombinant versions of each of these proteins, only BlpA and BlpE were found to be immunologically cross-reactive with the other proteins encoded by the locus. Northern hybridization indicated that only blpA was expressed under in vitro growth conditions. In addition, convalescent swine serum recognized recombinant BlpA in immunoblotting experiments, demonstrating that it is also expressed during infection. Analysis of the translated sequences of each of the genes revealed atypical spirochetal signal peptidase II recognition sites, and BlpA was shown to be a lipoprotein by incorporation of tritiated palmitic acid. Native BlpA was completely extracted by Triton X-114 (TX-114) and partitioned exclusively into the detergent phase during extraction of whole B. hyodysenteriae cells, implicating it as a component of the brachyspiral outer membrane. Consistent with the transcriptional and immunological data, analysis of the brachyspiral outer membrane proteome also revealed expression of only BlpA. Notably, inactivation of blpA homologs in Haemophilus influenzae and Salmonella enteritidis resulted in attenuation of virulence.
机译:鉴定可能刺激猪痢疾免疫力的猪痢疾短螺旋体外膜蛋白(OMPs)对于疫苗开发很重要。我们在这里报告了一个新的基因座blpGFEA的分析,该基因编码猪痢疾短螺旋体中〜30 kDa的四个串联旁源蛋白。这四种蛋白质与几种细菌病原体的脂蛋白具有31-39%的序列同一性,但该基因座具有独特的遗传组织。使用针对每种蛋白质的重组形式产生的抗血清,仅发现BlpA和BlpE与该基因座编码的其他蛋白质发生免疫交叉反应。 Northern杂交表明在体外生长条件下仅blpA表达。另外,恢复期的猪血清在免疫印迹实验中识别重组BlpA,表明它在感染过程中也表达。对每个基因翻译序列的分析揭示了非典型的螺旋信号肽酶II识别位点,并且通过掺入tri化的棕榈酸显示出BlpA是脂蛋白。天然BlpA被Triton X-114(TX-114)完全提取,在整个猪痢疾短螺旋体细胞的提取过程中仅分配到去污剂相中,暗示其是短螺旋体外膜的组成部分。与转录和免疫学数据一致,对短螺旋体外膜蛋白质组的分析还显示仅BlpA的表达。值得注意的是,流感嗜血杆菌和肠炎沙门氏菌中blpA同源物的失活导致毒力减弱。

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