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By using a high-throughput, signature-tagged mutagenic approach, we created 5,088 mutants of\n            <jats:named-content content-type=\"genus-species\">Y. pestis<\/jats:named-content>\n            strain CO92 and screened them in a mouse model of pneumonic plague at a dose equivalent to 5 50% lethal doses (LD\n            <jats:sub>50<\/jats:sub>\n            ) of wild-type (WT) CO92. From this screen, we obtained 118 clones showing impairment in disseminating to the spleen, based on hybridization of input versus output DNA from mutant pools with 53 unique signature tags. In the subsequent screen, 20\/118 mutants exhibited attenuation at 8 LD\n            <jats:sub>50<\/jats:sub>\n            when tested in a mouse model of bubonic plague, with infection by 10\/20 of the aforementioned mutants resulting in 40% or higher survival rates at an infectious dose of 40 LD\n            <jats:sub>50<\/jats:sub>\n            . Upon sequencing, six of the attenuated mutants were found to carry interruptions in genes encoding hypothetical proteins or proteins with putative functions. Mutants with in-frame deletion mutations of two of the genes identified from the screen, namely,\n            <jats:italic>rbsA<\/jats:italic>\n            , which codes for a putative sugar transport system ATP-binding protein, and\n            <jats:italic>vasK<\/jats:italic>\n            , a component of the type VI secretion system, were also found to exhibit some attenuation at 11 or 12 LD\n            <jats:sub>50<\/jats:sub>\n            in a mouse model of pneumonic plague. Likewise, among the remaining 18 signature-tagged mutants, 9 were also attenuated (40 to 100%) at 12 LD\n            <jats:sub>50<\/jats:sub>\n            in a pneumonic plague mouse model. Previously, we found that deleting genes encoding Braun lipoprotein (Lpp) and acyltransferase (MsbB), the latter of which modifies lipopolysaccharide function, reduced the virulence of\n            <jats:named-content content-type=\"genus-species\">Y. pestis<\/jats:named-content>\n            CO92 in mouse models of bubonic and pneumonic plague. Deletion of\n            <jats:italic>rbsA<\/jats:italic>\n            and\n            <jats:italic>vasK<\/jats:italic>\n            genes from either the \u0394\n            <jats:italic>lpp<\/jats:italic>\n            single or the \u0394\n            <jats:italic>lpp<\/jats:italic>\n            \u0394\n            <jats:italic>msbB<\/jats:italic>\n            double mutant augmented the attenuation to provide 90 to 100% survivability to mice in a pneumonic plague model at 20 to 50 LD\n            <jats:sub>50<\/jats:sub>\n            . The mice infected with the \u0394\n            <jats:italic>lpp<\/jats:italic>\n            \u0394\n            <jats:italic>msbB<\/jats:italic>\n            \u0394\n            <jats:italic>rbsA<\/jats:italic>\n            triple mutant at 50 LD\n            <jats:sub>50<\/jats:sub>\n            were 90% protected upon subsequent challenge with 12 LD\n            <jats:sub>50<\/jats:sub>\n            of WT CO92, suggesting that this mutant or others carrying combinational deletions of genes identified through our screen could potentially be further tested and developed into a live attenuated plague vaccine(s).\n          <\/jats:p>","DOI":"10.1128\/iai.02913-14","type":"journal-article","created":{"date-parts":[[2015,3,10]],"date-time":"2015-03-10T01:52:45Z","timestamp":1425952365000},"page":"2065-2081","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":22,"title":["High-Throughput, Signature-Tagged Mutagenic Approach To Identify Novel Virulence Factors of Yersinia pestis CO92 in a Mouse Model of Infection"],"prefix":"10.1128","volume":"83","author":[{"given":"Duraisamy","family":"Ponnusamy","sequence":"first","affiliation":[{"name":"Department of Microbiology and Immunology, UTMB, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eric C.","family":"Fitts","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, UTMB, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jian","family":"Sha","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, UTMB, Galveston, Texas, USA"},{"name":"Institute for Human Infections and Immunity, UTMB, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tatiana E.","family":"Erova","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, UTMB, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elena V.","family":"Kozlova","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, UTMB, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michelle L.","family":"Kirtley","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, UTMB, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bethany L.","family":"Tiner","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, UTMB, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jourdan A.","family":"Andersson","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, UTMB, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ashok K.","family":"Chopra","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Immunology, UTMB, Galveston, Texas, USA"},{"name":"Institute for Human Infections and Immunity, UTMB, Galveston, Texas, USA"},{"name":"Sealy Center for Vaccine Development, UTMB, Galveston, Texas, USA"},{"name":"Center for Biodefense and Emerging Infectious Diseases, UTMB, Galveston, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"235","reference":[{"key":"e_1_3_2_2_2","doi-asserted-by":"publisher","DOI":"10.1128\/CMR.10.1.35"},{"key":"e_1_3_2_3_2","first-page":"447","article-title":"Plague manual: epidemiology, distribution, surveillance and control","volume":"74","author":"Anonymous","year":"1999","unstructured":"Anonymous. 1999. 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