AI Article Synopsis

  • During infection, Legionella pneumophila injects over 300 proteins into host cells, creating a specialized environment (LCV) for bacterial growth.
  • Researchers used CRISPR-Cas9 screening on human immune cells to pinpoint both established and new host factors involved in the bacteria's ability to evade destruction.
  • The study found that certain proteins like Rab10 are crucial for bacterial replication and are modified by bacterial effectors, revealing new understandings of Legionella's interaction with host cells.

Article Abstract

During infection, Legionella pneumophila translocates over 300 effector proteins into the host cytosol, allowing the pathogen to establish an endoplasmic reticulum (ER)-like Legionella-containing vacuole (LCV) that supports bacterial replication. Here, we perform a genome-wide CRISPR-Cas9 screen and secondary targeted screens in U937 human monocyte/macrophage-like cells to systematically identify host factors that regulate killing by L. pneumophila. The screens reveal known host factors hijacked by L. pneumophila, as well as genes spanning diverse trafficking and signaling pathways previously not linked to L. pneumophila pathogenesis. We further characterize C1orf43 and KIAA1109 as regulators of phagocytosis and show that RAB10 and its chaperone RABIF are required for optimal L. pneumophila replication and ER recruitment to the LCV. Finally, we show that Rab10 protein is recruited to the LCV and ubiquitinated by the effectors SidC/SdcA. Collectively, our results provide a wealth of previously undescribed insights into L. pneumophila pathogenesis and mammalian cell function.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800164PMC
http://dx.doi.org/10.1016/j.chom.2019.08.017DOI Listing

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