{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T22:54:41Z","timestamp":1791327281888,"version":"4.3.1"},"reference-count":42,"publisher":"American Society for Microbiology","issue":"4","license":[{"start":{"date-parts":[[2010,4,1]],"date-time":"2010-04-01T00:00:00Z","timestamp":1270080000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Infect Immun"],"published-print":{"date-parts":[[2010,4]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    ExoU, a cytotoxin translocated into host cells via the type III secretion system of\n                    <jats:italic>Pseudomonas aeruginosa<\/jats:italic>\n                    , is associated with increased mortality and disease severity. We previously showed that impairment of recruited phagocytic cells allowed survival of ExoU-secreting\n                    <jats:italic>P. aeruginosa<\/jats:italic>\n                    in the lung. Here we analyzed types of cells injected with ExoU\n                    <jats:italic>in vivo<\/jats:italic>\n                    using translational fusions of ExoU with a \u03b2-lactamase reporter (ExoU-Bla). Cells injected with ExoU-Bla were detectable\n                    <jats:italic>in vitro<\/jats:italic>\n                    but not\n                    <jats:italic>in vivo<\/jats:italic>\n                    , presumably due to the rapid cytotoxicity induced by the toxin. Therefore, we used a noncytotoxic ExoU variant, designated ExoU(S142A)-Bla, to analyze injection\n                    <jats:italic>in vivo<\/jats:italic>\n                    . We determined that phagocytic cells in the lung were frequently injected with ExoU(S142A). Early during infection, resident macrophages constituted the majority of cells into which ExoU was injected, but neutrophils and monocytes became the predominant types of cells into which ExoU was injected upon recruitment into the lung. We observed a modest preference for injection into neutrophils over injection into other cell types, but in general the repertoire of injected immune cells reflected the relative abundance of these cells in the lung. Our results indicate that phagocytic cells in the lung are injected with ExoU and support the hypothesis that ExoU-mediated impairment of phagocytes has a role in the pathogenesis of pneumonia caused by\n                    <jats:italic>P. aeruginosa<\/jats:italic>\n                    .\n                  <\/jats:p>","DOI":"10.1128\/iai.01134-09","type":"journal-article","created":{"date-parts":[[2010,1,25]],"date-time":"2010-01-25T21:11:16Z","timestamp":1264453876000},"page":"1447-1456","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":110,"title":["<i>Pseudomonas aeruginosa<\/i>\n                    Cytotoxin ExoU Is Injected into Phagocytic Cells during Acute Pneumonia"],"prefix":"10.1128","volume":"78","author":[{"given":"Maureen H.","family":"Diaz","sequence":"first","affiliation":[{"name":"Department of Microbiology-Immunology"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alan 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