Morash Michael G, Brassinga Ann Karen C, Warthan Michelle, Gourabathini Poornima, Garduño Rafael A, Goodman Steven D, Hoffman Paul S
Department of Microbiology and Immunology, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada B3H 4H7.
Appl Environ Microbiol. 2009 Apr;75(7):1826-37. doi: 10.1128/AEM.02756-08. Epub 2009 Feb 5.
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 (Deltaihf) IHF mutants failed to grow in Acanthamoeba castellanii unless complemented in trans when expressed temporally from the ihfA promoter but not under P(tac) (isopropyl-beta-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-beta-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 Deltaihf 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.
嗜肺军团菌是原生动物的一种细胞内寄生虫,在感染后期分化为代谢休眠的囊肿,具有高度传染性。对这一过程的调控了解甚少。在此,我们报告小DNA结合调节蛋白整合宿主因子(IHF)和HU在发育周期中相互表达,HU在指数生长期表达,而IHF在指数生长期后表达。为了评估这些调节蛋白在发育中的作用,构建了染色体缺失突变体。单缺失(ihfA或ihfB)和双缺失(Deltaihf)的IHF突变体在卡氏棘阿米巴中无法生长,除非从ihfA启动子而非P(tac)(异丙基-β-D-硫代半乳糖苷)进行时间表达时通过反式互补。相比之下,IHF突变体对HeLa细胞具有传染性,尽管电子显微镜检查显示后期囊肿形态发生存在缺陷(细胞壁增厚、胞内膜和聚-β-羟基丁酸包涵体),并且发育标志物MagA表达降低。绿色荧光蛋白启动子融合试验表明,magA的完全指数生长期后表达需要IHF和稳定期σ因子RpoS。最后,与野生型囊肿相比,HeLa细胞中Deltaihf突变体的囊肿形态发生缺陷与去污剂抗性和超感染性的丧失相关。这些研究确立了IHF和HU作为发育阶段的标志物,并表明IHF功能是嗜肺军团菌在天然阿米巴宿主中分化和完全毒力所必需的。