| Literature DB >> 27572165 |
Mary Speir1, Kate E Lawlor2,3, Stefan P Glaser2,3, Gilu Abraham1, Seong Chow1, Adam Vogrin1, Keith E Schulze4, Ralf Schuelein5, Lorraine A O'Reilly2,3, Kylie Mason6, Elizabeth L Hartland5, Trevor Lithgow7, Andreas Strasser2,3, Guillaume Lessene2,3, David C S Huang2,3, James E Vince2,3, Thomas Naderer1.
Abstract
Human pathogenic Legionella replicate in alveolar macrophages and cause a potentially lethal form of pneumonia known as Legionnaires' disease(1). Here, we have identified a host-directed therapeutic approach to eliminate intracellular Legionella infections. We demonstrate that the genetic deletion, or pharmacological inhibition, of the host cell pro-survival protein BCL-XL induces intrinsic apoptosis of macrophages infected with virulent Legionella strains, thereby abrogating Legionella replication. BCL-XL is essential for the survival of Legionella-infected macrophages due to bacterial inhibition of host-cell protein synthesis, resulting in reduced levels of the short-lived, related BCL-2 pro-survival family member, MCL-1. Consequently, a single dose of a BCL-XL-targeted BH3-mimetic therapy, or myeloid cell-restricted deletion of BCL-XL, limits Legionella replication and prevents lethal lung infections in mice. These results indicate that repurposing BH3-mimetic compounds, originally developed to induce cancer cell apoptosis, may have efficacy in treating Legionnaires' and other diseases caused by intracellular microbes.Entities:
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Year: 2016 PMID: 27572165 DOI: 10.1038/nmicrobiol.2015.34
Source DB: PubMed Journal: Nat Microbiol ISSN: 2058-5276 Impact factor: 17.745