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10.1128/IAI.01891-14 http://scihub22266oqcxt.onion/10.1128/IAI.01891-14 C4187856!4187856 !25092908     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25092908 &cmd=llinks): Failed to open stream: HTTP request failed! 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Alveolar macrophages and neutrophils are the primary reservoirs for Legionella pneumophila and mediate cytosolic surveillance of type IV secretion |pdf=|usr=}}{{25092908 }} gab.com Text Alveolar macrophages and neutrophils are the primary reservoirs for Legionella pneumophila and mediate cytosolic surveillance of type IV secretion JO: Infect Immun http://www.kidney.de/pget.php?&tw=1&pmid=25092908 #FOAvip Legionella pneumophila, an intracellular pathogen responsible for the severe pneumonia Legionnaires' disease, uses its dot/icm-encoded type IV secretion system (T4SS) to translocate effector proteins that promote its survival and replication into the host cell cytosol. However, by introducing bacterial products into the host cytosol, L. pneumophila also activates cytosolic immunosurveillance pathways, thereby triggering robust proinflammatory responses that mediate the control of infection. Thus, the pulmonary cell types that L. pneumophila infects not only may act as an intracellular niche that facilitates its pathogenesis but also may contribute to the immune response against L. pneumophila. The identity of these host cells remains poorly understood. Here, we developed a strain of L. pneumophila producing a fusion protein consisting of ?-lactamase fused to the T4SS-translocated effector RalF, which allowed us to track cells injected by the T4SS. Our data reveal that alveolar macrophages and neutrophils both are the primary recipients of T4SS-translocated effectors and harbor viable L. pneumophila during pulmonary infection of mice. Moreover, both alveolar macrophages and neutrophils from infected mice produced tumor necrosis factor and interleukin-1? in response to T4SS-sufficient, but not T4SS-deficient, L. pneumophila. Collectively, our data suggest that alveolar macrophages and neutrophils are both an intracellular reservoir for L. pneumophila and a source of proinflammatory cytokines that contribute to the host immune response against L. pneumophila during pulmonary infection. Twit Text FOAVip Alveolar macrophages and neutrophils are the primary reservoirs for Legionella pneumophila and mediate cytosolic surveillance of type IV secretion ????Infect Immun http://www.kidney.de/pget.php?&tw=1&pmid=25092908 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25092908 #FOAvip English Wikipedia <ref>{{Cite pmid|25092908 }}</ref> Alveolar macrophages and neutrophils are the primary reservoirs for Legionella pneumophila and mediate cytosolic surveillance of type IV secretion #MMPMID25092908 Copenhaver AM ; Casson CN ; Nguyen HT ; Fung TC ; Duda MM ; Roy CR ; Shin S Infect Immun 2014[Oct]; 82 (10 ): 4325-36 PMID25092908 show ga Legionella pneumophila, an intracellular pathogen responsible for the severe pneumonia Legionnaires' disease, uses its dot/icm-encoded type IV secretion system (T4SS) to translocate effector proteins that promote its survival and replication into the host cell cytosol. However, by introducing bacterial products into the host cytosol, L. pneumophila also activates cytosolic immunosurveillance pathways, thereby triggering robust proinflammatory responses that mediate the control of infection. Thus, the pulmonary cell types that L. pneumophila infects not only may act as an intracellular niche that facilitates its pathogenesis but also may contribute to the immune response against L. pneumophila. The identity of these host cells remains poorly understood. Here, we developed a strain of L. pneumophila producing a fusion protein consisting of ?-lactamase fused to the T4SS-translocated effector RalF, which allowed us to track cells injected by the T4SS. Our data reveal that alveolar macrophages and neutrophils both are the primary recipients of T4SS-translocated effectors and harbor viable L. pneumophila during pulmonary infection of mice. Moreover, both alveolar macrophages and neutrophils from infected mice produced tumor necrosis factor and interleukin-1? in response to T4SS-sufficient, but not T4SS-deficient, L. pneumophila. Collectively, our data suggest that alveolar macrophages and neutrophils are both an intracellular reservoir for L. pneumophila and a source of proinflammatory cytokines that contribute to the host immune response against L. pneumophila during pulmonary infection. |*Bacterial Secretion Systems [MESH] |Animals [MESH] |Cytosol/metabolism/microbiology [MESH] |Disease Models, Animal [MESH] |Female [MESH] |Host-Pathogen Interactions [MESH] |Interleukin-1alpha/metabolism [MESH] |Legionella pneumophila/*immunology/*physiology [MESH] |Legionnaires' Disease/immunology/microbiology [MESH] |Macrophages, Alveolar/*immunology/*microbiology [MESH] |Mice [MESH] |Mice, Inbred C57BL [MESH] |Neutrophils/*immunology/*microbiology [MESH]Alveolar macrophages and neutrophils are the primary reservoirs for Le(epmc).pdf DeepDyve Pubget Overpricing