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A Type VI Secretion System Encoding Locus Is Required for Bordetella bronchiseptica Immunomodulation and Persistence In Vivo

机译:a型VI分泌系统编码轨迹需要支气管败血波氏杆菌免疫调节和持久性体内

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摘要

Type VI Secretion Systems (T6SSs) have been identified in numerous Gram-negative pathogens, but the lack of a natural host infection model has limited analysis of T6SS contributions to infection and pathogenesis. Here, we describe disruption of a gene within locus encoding a putative T6SS in Bordetella bronchiseptica strain RB50, a respiratory pathogen that circulates in a broad range of mammals, including humans, domestic animals, and mice. The 26 gene locus encoding the B. bronchiseptica T6SS contains apparent orthologs to all known core genes and possesses thirteen novel genes. By generating an in frame deletion of clpV, which encodes a putative ATPase required for some T6SS-dependent protein secretion, we observe that ClpV contributes to in vitro macrophage cytotoxicity while inducing several eukaryotic proteins associated with apoptosis. Additionally, ClpV is required for induction of IL-1β, IL-6, IL-17, and IL-10 production in J774 macrophages infected with RB50. During infections in wild type mice, we determined that ClpV contributes to altered cytokine production, increased pathology, delayed lower respiratory tract clearance, and long term nasal cavity persistence. Together, these results reveal a natural host infection system in which to interrogate T6SS contributions to immunomodulation and pathogenesis.
机译:已经在许多革兰氏阴性病原体中鉴定出VI型分泌系统(T6SS),但是缺乏天然宿主感染模型限制了对T6SS对感染和发病机制的贡献的分析。在这里,我们描述了支气管败血博德特氏菌RB50(一种在许多哺乳动物,包括人,家畜和小鼠中传播的呼吸道病原体)中编码假定的T6SS的基因座内基因的破坏。编码支气管败血性巴斯德氏菌T6SS的26个基因位点包含与所有已知核心基因的直系同源基因,并拥有13个新基因。通过产生一个框内的clpV缺失,该缺失编码一些T6SS依赖性蛋白分泌所需的假定的ATPase,我们观察到ClpV有助于体外巨噬细胞的细胞毒性,同时诱导了几种与凋亡相关的真核蛋白。另外,在被RB50感染的J774巨噬细胞中诱导IL-1β,IL-6,IL-17和IL-10产生需要ClpV。在野生型小鼠感染期间,我们确定ClpV有助于改变细胞因子的产生,增加病理学,延迟下呼吸道清除和长期鼻腔持久性。总之,这些结果揭示了一种天然宿主感染系统,在其中可以询问T6SS对免疫调节和发病机制的贡献。

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