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Identification and Subcellular Localization of the Legionella pneumophila IcmX Protein: a Factor Essential for Establishment of a Replicative Organelle in Eukaryotic Host Cells

机译:军团菌IcmX蛋白的鉴定和亚细胞定位:在真核宿主细胞中建立复制细胞器必不可少的因素。

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摘要

The gram-negative respiratory pathogen Legionella pneumophila infects and grows within mammalian macrophages and protozoan host cells. Upon uptake into macrophages, L. pneumophila establishes a replicative organelle that avoids fusion with endocytic vesicles. There are 24 dot/icm genes on the L. pneumophila chromosome required for biogenesis of this vacuole. Many of the Dot/Icm proteins are predicted to be components of a membrane-bound secretion apparatus similar to type IV conjugal transfer systems. We have been investigating the function of L. pneumophila dot/icm gene products that do not have obvious orthologs in other type IV transfer systems, since these determinants could govern processes unique to phagosome biogenesis. The icmX gene product falls into this category. To understand the role of the IcmX protein in pathogenesis, we have detailed interactions between an L. pneumophila icmX deletion mutant and murine bone marrow-derived macrophages. These data demonstrate that icmX is required for biogenesis of the L. pneumophila replicative organelle. Immunoblot analysis indicates that the icmX gene product is a polypeptide with an estimated molecular mass of 50 kDa. The IcmX protein was localized to the bacterial periplasm, and periplasmic translocation was mediated by an N-terminal sec-dependent leader peptide. A truncated IcmX product was secreted into culture supernatants by wild-type L. pneumophila growing extracellularly in liquid media; however, transport of the IcmX protein into eukaryotic host cells was not detected. Proteins similar in molecular weight to IcmX were identified in other Legionella species by immunoblot analysis using a monoclonal antibody specific for L. pneumophila IcmX protein. From these data, we conclude that the IcmX protein is an essential component of the dot/icm secretion apparatus, and that a conserved mechanism of host cell parasitism exists for members of the Legionellaceae family.
机译:革兰氏阴性呼吸道病原体肺炎军团菌感染并在哺乳动物巨噬细胞和原生动物宿主细胞内生长。摄入巨噬细胞后,嗜肺乳杆菌会建立复制细胞器,避免与胞吞小泡融合。该液泡的生物发生需要在嗜肺乳杆菌染色体上有24个dot / icm基因。预测许多Dot / Icm蛋白是类似于IV型结合转移系统的膜结合分泌设备的组成部分。我们一直在研究在其他IV型转移系统中没有明显直系同源物的嗜肺乳杆菌L./icm基因产物的功能,因为这些决定因素可以控制吞噬体生物发生所特有的过程。 icmX基因产物属于这一类。为了了解IcmX蛋白在发病机理中的作用,我们详细了解了嗜肺乳杆菌icmX缺失突变体与鼠骨髓来源的巨噬细胞之间的相互作用。这些数据表明icmX是嗜肺乳杆菌复制细胞器的生物发生所必需的。免疫印迹分析表明icmX基因产物是一种多肽,估计分子量为50 kDa。 IcmX蛋白位于细菌周质中,周质易位由N端sec依赖性前导肽介导。截短的IcmX产物通过在液体培养基中在细胞外生长的野生型肺炎支原体分泌到培养上清液中。但是,未检测到IcmX蛋白向真核宿主细胞的转运。使用对肺炎衣原体IcmX蛋白具有特异性的单克隆抗体,通过免疫印迹分析在其他军团菌中鉴定出分子量与IcmX相似的蛋白。从这些数据,我们得出结论,IcmX蛋白是点/ icm分泌设备的重要组成部分,并且军团菌科成员存在宿主细胞寄生的保守机制。

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