{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T08:01:39Z","timestamp":1790755299588,"version":"4.1.0"},"reference-count":37,"publisher":"American Society for Microbiology","issue":"8","license":[{"start":{"date-parts":[[2018,4,15]],"date-time":"2018-04-15T00:00:00Z","timestamp":1523750400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"DOI":"10.13039\/100000002","name":"HHS | National Institutes of Health","doi-asserted-by":"publisher","award":["R56AI101109"],"award-info":[{"award-number":["R56AI101109"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"HHS | National Institutes of Health","doi-asserted-by":"publisher","award":["P01AI056320"],"award-info":[{"award-number":["P01AI056320"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"HHS | National Institutes of Health","doi-asserted-by":"publisher","award":["R15AI107698"],"award-info":[{"award-number":["R15AI107698"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Bacteriol"],"published-print":{"date-parts":[[2018,4,15]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            <jats:named-content content-type=\"genus-species\">Francisella tularensis<\/jats:named-content>\n            , the causative agent of tularemia, lacks typical bacterial virulence factors and toxins but still exhibits extreme virulence. The bacterial multidrug efflux systems consist of an inner membrane, a transmembrane membrane fusion protein, and an outer membrane (OM) component that form a contiguous channel for the secretion of a multitude of bacterial products.\n            <jats:named-content content-type=\"genus-species\">Francisella<\/jats:named-content>\n            contains three orthologs of the OM proteins; two of these, termed TolC and FtlC, are important for tularemia pathogenesis. The third OM protein, SilC, is homologous to the silver cation efflux protein of other bacterial pathogens. The\n            <jats:italic>silC<\/jats:italic>\n            gene (\n            <jats:italic>FTL_0686<\/jats:italic>\n            ) is located on an operon encoding an Emr-type multidrug efflux pump of\n            <jats:named-content content-type=\"genus-species\">F. tularensis<\/jats:named-content>\n            . The role of SilC in tularemia pathogenesis is not known. In this study, we investigated the role of SilC in secretion and virulence of\n            <jats:named-content content-type=\"genus-species\">F. tularensis<\/jats:named-content>\n            by generating a\n            <jats:italic>silC<\/jats:italic>\n            gene deletion (\u0394\n            <jats:italic>silC<\/jats:italic>\n            ) mutant and its transcomplemented strain. Our results demonstrate that the \u0394\n            <jats:italic>silC<\/jats:italic>\n            mutant exhibits increased sensitivity to antibiotics, oxidants, silver, diminished intramacrophage growth, and attenuated virulence in mice compared to wild-type\n            <jats:named-content content-type=\"genus-species\">F. tularensis<\/jats:named-content>\n            . However, the secretion of antioxidant enzymes of\n            <jats:named-content content-type=\"genus-species\">F. tularensis<\/jats:named-content>\n            is not impaired in the \u0394\n            <jats:italic>silC<\/jats:italic>\n            mutant. The virulence of the \u0394\n            <jats:italic>silC<\/jats:italic>\n            mutant is restored in NADPH oxidase-deficient mice, indicating that SilC resists oxidative stress\n            <jats:italic>in vivo<\/jats:italic>\n            . Collectively, this study demonstrates that the OM component SilC serves a specialized role in virulence of\n            <jats:named-content content-type=\"genus-species\">F. tularensis<\/jats:named-content>\n            by conferring resistance against oxidative stress and silver.\n          <\/jats:p>\n          <jats:p>\n            <jats:bold>IMPORTANCE<\/jats:bold>\n            <jats:named-content content-type=\"genus-species\">Francisella tularensis<\/jats:named-content>\n            , the causative agent of a fatal human disease known as tularemia, is a category A select agent and a potential bioterror agent. The virulence mechanisms of\n            <jats:named-content content-type=\"genus-species\">Francisella<\/jats:named-content>\n            are not completely understood. This study investigated the role of a unique outer membrane protein, SilC, of a multidrug efflux pump in the virulence of\n            <jats:named-content content-type=\"genus-species\">F. tularensis<\/jats:named-content>\n            . This is the first report demonstrating that the OM component SilC plays an important role in efflux of silver and contributes to the virulence of\n            <jats:named-content content-type=\"genus-species\">F. tularensis<\/jats:named-content>\n            primarily by providing resistance against oxidative stress. Characterization of these unique virulence mechanisms will provide an understanding of the pathogenesis of tularemia and identification of potential targets for the development of effective therapeutics and prophylactics for protection from this lethal disease.\n          <\/jats:p>","DOI":"10.1128\/jb.00693-17","type":"journal-article","created":{"date-parts":[[2018,1,30]],"date-time":"2018-01-30T12:28:02Z","timestamp":1517315282000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":20,"title":["Characterization of a Unique Outer Membrane Protein Required for Oxidative Stress Resistance and Virulence of Francisella tularensis"],"prefix":"10.1128","volume":"200","author":[{"given":"Maha","family":"Alqahtani","sequence":"first","affiliation":[{"name":"Department of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhuo","family":"Ma","sequence":"additional","affiliation":[{"name":"Department of Basic and Social Sciences, Albany College of Pharmacy and Health Sciences, Albany, New York, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Harshada","family":"Ketkar","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ragavan Varadharajan","family":"Suresh","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Meenakshi","family":"Malik","sequence":"additional","affiliation":[{"name":"Department of Basic and Social Sciences, Albany College of Pharmacy and Health Sciences, Albany, New York, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chandra Shekhar","family":"Bakshi","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"235","reference":[{"key":"e_1_3_2_2_2","first-page":"1126","article-title":"Tularemia, a potential bioterrorism weapon","volume":"32","author":"Bossi P","year":"2003","unstructured":"Bossi P, Bricaire F. 2003. 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