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Reciprocal Expression of Integration Host Factor and HU in the Developmental Cycle and Infectivity of Legionella pneumophila▿ †

机译:整合宿主因子和HU在肺炎军团菌发展周期和感染性中的相互表达Expression

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摘要

Legionella pneumophila is an intracellular parasite of protozoa that differentiates late in infection into metabolically dormant cysts that are highly infectious. Regulation of this process is poorly understood. Here we report that the small DNA binding regulatory proteins integration host factor (IHF) and HU are reciprocally expressed over the developmental cycle, with HU expressed during exponential phase and IHF expressed postexponentially. To assess the role of these regulatory proteins in development, chromosomal deletions were constructed. Single (ihfA or ihfB) and double deletion (Δihf) IHF mutants failed to grow in Acanthamoeba castellanii unless complemented in trans when expressed temporally from the ihfA promoter but not under Ptac (isopropyl-β-d-thiogalactopyranoside). In contrast, IHF mutants were infectious for HeLa cells, though electron microscopic examination revealed defects in late-stage cyst morphogenesis (thickened cell wall, intracytoplasmic membranes, and inclusions of poly-β-hydroxybutyrate), and were depressed for the developmental marker MagA. Green fluorescent protein promoter fusion assays indicated that IHF and the stationary-phase sigma factor RpoS were required for full postexponential expression of magA. Finally, defects in cyst morphogenesis noted for Δihf mutants in HeLa cells correlated with a loss of both detergent resistance and hyperinfectivity compared with results for wild-type cysts. These studies establish IHF and HU as markers of developmental stages and show that IHF function is required for both differentiation and full virulence of L. pneumophila in natural amoebic hosts.
机译:肺炎军团菌是原生动物的一种细胞内寄生虫,在感染后期可分化为高度传染性的代谢性休眠囊肿。对该过程的法规了解甚少。在这里我们报告小DNA结合调节蛋白整合宿主因子(IHF)和HU在发展周期中相互表达,HU在指数期表达,而IHF在指数后表达。为了评估这些调节蛋白在发育中的作用,构建了染色体缺失。单发(ihfA或ihfB)和双缺失(Δihf)IHF突变体不能在castantanie castellanii中生长,除非从ihfA启动子暂时表达但在Ptac(异丙基-β-d-硫代半乳糖吡喃糖苷)下不能以反式互补。相比之下,尽管电子显微镜检查显示晚期囊肿形态发生缺陷(细胞壁变厚,胞质内膜和聚-β-羟基丁酸酯的内含物),但IHF突变体对HeLa细胞具有感染性,并因发育标记MagA而受到抑制。绿色荧光蛋白启动子融合试验表明,magA的完整指数后表达需要IHF和固定相sigma因子RpoS。最后,与野生型囊肿的结果相比,HeLa细胞中Δihf突变体的囊肿形态发生缺陷与去污剂抗性和过度感染性的丧失相关。这些研究建立了IHF和HU作为发育阶段的标志物,并表明IHF功能是天然厌氧宿主中嗜肺乳杆菌的分化和完全毒力所必需的。

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