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      Modulation of host cell function by Legionella pneumophila type IV effectors.

      Annual review of cell and developmental biology
      Animals, Bacterial Proteins, metabolism, Humans, Legionella pneumophila, pathogenicity, Lysosomes, Macrophages, cytology, Microbial Viability, Phagocytosis, Phagosomes, Virulence

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          Abstract

          Macrophages and protozoa ingest bacteria by phagocytosis and destroy these microbes using a conserved pathway that mediates fusion of the phagosome with lysosomes. To survive within phagocytic host cells, bacterial pathogens have evolved a variety of strategies to avoid fusion with lysosomes. A virulence strategy used by the intracellular pathogen Legionella pneumophila is to manipulate host cellular processes using bacterial proteins that are delivered into the cytosolic compartment of the host cell by a specialized secretion system called Dot/Icm. The proteins delivered by the Dot/Icm system target host factors that play evolutionarily conserved roles in controlling membrane transport in eukaryotic cells, which enables L. pneumophila to create an endoplasmic reticulum-like vacuole that supports intracellular replication in both protozoan and mammalian host cells. This review focuses on intracellular trafficking of L. pneumophila and describes how bacterial proteins contribute to modulation of host processes required for survival within host cells.

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          Author and article information

          Journal
          20929312
          10.1146/annurev-cellbio-100109-104034

          Chemistry
          Animals,Bacterial Proteins,metabolism,Humans,Legionella pneumophila,pathogenicity,Lysosomes,Macrophages,cytology,Microbial Viability,Phagocytosis,Phagosomes,Virulence

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