Generation and characterization of an attenuated mutant in a response regulator gene of Francisella tularensis live vaccine strain (LVS)
Francisella tularensis is a zoonotic bacterium that must exist in diverse environments ranging from arthropod vectors to mammalian hosts. To better understand how virulence genes are regulated in these different environments, a transcriptional response regulator gene (genome locus FTL0552) was delet...
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Veröffentlicht in: | DNA and cell biology 2008-07, Vol.27 (7), p.387-403 |
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description | Francisella tularensis is a zoonotic bacterium that must exist in diverse environments ranging from arthropod vectors to mammalian hosts. To better understand how virulence genes are regulated in these different environments, a transcriptional response regulator gene (genome locus FTL0552) was deleted in F. tularensis live vaccine strain (LVS). The FTL0552 deletion mutant exhibited slightly reduced rates of extracellular growth but was unable to replicate or survive in mouse macrophages and was avirulent in the mouse model using either BALB/c or C57BL/6 mice. Mice infected with the FTL0552 mutant produced reduced levels of inflammatory cytokines, exhibited reduced histopathology, and cleared the bacteria quicker than mice infected with LVS. Mice that survived infection with the FTL0552 mutant were afforded partial protection when challenged with a lethal dose of the virulent SchuS4 strain (4 of 10 survivors, day 21 postinfection) when compared to naive mice (0 of 10 survivors by day 7 postinfection). Microarray experiments indicate that 148 genes are regulated by FTL0552. Most of the genes are downregulated, indicating that FTL0552 controls transcription of genes in a positive manner. Genes regulated by FTL0552 include genes located within the Francisella pathogenicity island that are essential for intracellular survival and virulence of F. tularensis. Further, a mutant in FTL0552 or the comparable locus in SchuS4 (FTT1557c) may be an alternative candidate vaccine for tularemia. |
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To better understand how virulence genes are regulated in these different environments, a transcriptional response regulator gene (genome locus FTL0552) was deleted in F. tularensis live vaccine strain (LVS). The FTL0552 deletion mutant exhibited slightly reduced rates of extracellular growth but was unable to replicate or survive in mouse macrophages and was avirulent in the mouse model using either BALB/c or C57BL/6 mice. Mice infected with the FTL0552 mutant produced reduced levels of inflammatory cytokines, exhibited reduced histopathology, and cleared the bacteria quicker than mice infected with LVS. Mice that survived infection with the FTL0552 mutant were afforded partial protection when challenged with a lethal dose of the virulent SchuS4 strain (4 of 10 survivors, day 21 postinfection) when compared to naive mice (0 of 10 survivors by day 7 postinfection). Microarray experiments indicate that 148 genes are regulated by FTL0552. Most of the genes are downregulated, indicating that FTL0552 controls transcription of genes in a positive manner. Genes regulated by FTL0552 include genes located within the Francisella pathogenicity island that are essential for intracellular survival and virulence of F. tularensis. Further, a mutant in FTL0552 or the comparable locus in SchuS4 (FTT1557c) may be an alternative candidate vaccine for tularemia.</description><identifier>ISSN: 1044-5498</identifier><identifier>EISSN: 1557-7430</identifier><identifier>DOI: 10.1089/dna.2007.0687</identifier><identifier>PMID: 18613792</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Animals ; Arthropoda ; Bacterial Vaccines - immunology ; Cells, Cultured ; Cytokines - metabolism ; Female ; Francisella tularensis ; Francisella tularensis - genetics ; Francisella tularensis - immunology ; Francisella tularensis - pathogenicity ; Genes, Bacterial ; Inflammation Mediators - metabolism ; Macrophages - immunology ; Macrophages - virology ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mutant Proteins - genetics ; Mutant Proteins - immunology ; Mutation ; Original Papers ; Survival Analysis ; Tularemia - immunology ; Tularemia - metabolism ; Tularemia - mortality ; Tularemia - therapy ; Vaccines, Attenuated ; Virus Replication - genetics</subject><ispartof>DNA and cell biology, 2008-07, Vol.27 (7), p.387-403</ispartof><rights>Copyright 2008, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c377t-dc3821d3cd7191920700a8551d6638a8ad89936c5b6767bd5ced7f1ce873d3ba3</citedby><cites>FETCH-LOGICAL-c377t-dc3821d3cd7191920700a8551d6638a8ad89936c5b6767bd5ced7f1ce873d3ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18613792$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sammons-Jackson, Wendy L</creatorcontrib><creatorcontrib>McClelland, Karen</creatorcontrib><creatorcontrib>Manch-Citron, Jean N</creatorcontrib><creatorcontrib>Metzger, Dennis W</creatorcontrib><creatorcontrib>Bakshi, Chandra Shekhar</creatorcontrib><creatorcontrib>Garcia, Emilio</creatorcontrib><creatorcontrib>Rasley, Amy</creatorcontrib><creatorcontrib>Anderson, Burt E</creatorcontrib><title>Generation and characterization of an attenuated mutant in a response regulator gene of Francisella tularensis live vaccine strain (LVS)</title><title>DNA and cell biology</title><addtitle>DNA Cell Biol</addtitle><description>Francisella tularensis is a zoonotic bacterium that must exist in diverse environments ranging from arthropod vectors to mammalian hosts. To better understand how virulence genes are regulated in these different environments, a transcriptional response regulator gene (genome locus FTL0552) was deleted in F. tularensis live vaccine strain (LVS). The FTL0552 deletion mutant exhibited slightly reduced rates of extracellular growth but was unable to replicate or survive in mouse macrophages and was avirulent in the mouse model using either BALB/c or C57BL/6 mice. Mice infected with the FTL0552 mutant produced reduced levels of inflammatory cytokines, exhibited reduced histopathology, and cleared the bacteria quicker than mice infected with LVS. Mice that survived infection with the FTL0552 mutant were afforded partial protection when challenged with a lethal dose of the virulent SchuS4 strain (4 of 10 survivors, day 21 postinfection) when compared to naive mice (0 of 10 survivors by day 7 postinfection). Microarray experiments indicate that 148 genes are regulated by FTL0552. Most of the genes are downregulated, indicating that FTL0552 controls transcription of genes in a positive manner. Genes regulated by FTL0552 include genes located within the Francisella pathogenicity island that are essential for intracellular survival and virulence of F. tularensis. Further, a mutant in FTL0552 or the comparable locus in SchuS4 (FTT1557c) may be an alternative candidate vaccine for tularemia.</description><subject>Animals</subject><subject>Arthropoda</subject><subject>Bacterial Vaccines - immunology</subject><subject>Cells, Cultured</subject><subject>Cytokines - metabolism</subject><subject>Female</subject><subject>Francisella tularensis</subject><subject>Francisella tularensis - genetics</subject><subject>Francisella tularensis - immunology</subject><subject>Francisella tularensis - pathogenicity</subject><subject>Genes, Bacterial</subject><subject>Inflammation Mediators - metabolism</subject><subject>Macrophages - immunology</subject><subject>Macrophages - virology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Mutant Proteins - genetics</subject><subject>Mutant Proteins - immunology</subject><subject>Mutation</subject><subject>Original Papers</subject><subject>Survival Analysis</subject><subject>Tularemia - immunology</subject><subject>Tularemia - metabolism</subject><subject>Tularemia - mortality</subject><subject>Tularemia - therapy</subject><subject>Vaccines, Attenuated</subject><subject>Virus Replication - genetics</subject><issn>1044-5498</issn><issn>1557-7430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1vEzEQhi1ERUvhyBX5hOCwqb2Ovy5IqKIFKVIPBa7WxJ6kRhtvsL2R4Bfws_EqER8nTh698_jVzLyEvOBswZmxVyHBomdML5gy-hG54FLqTi8Fe9xqtlx2cmnNOXlaylfGmOw5e0LOuVFcaNtfkJ-3mDBDjWOikAL1D5DBV8zxx1EcN02nUCumCSoGupsqpEpjE2nGsh9TwVZspwHqmOm2-c2fbjIkHwsOA9DaehlTiYUO8YD0AN7HhpWaofm8Xn25f_OMnG1gKPj89F6SzzfvP11_6FZ3tx-v3606L7SuXfDC9DwIHzS33PZMMwZGSh6UEgYMBGOtUF6ulVZ6HaTHoDfco9EiiDWIS_L26Luf1jsMHlMbYnD7HHeQv7sRovu3k-KD244H11vDtBbN4NXJII_fJizV7WLx854Jx6k4ZQXT7bj_BblVzEg7g90R9HksJePm9zScuTlk10J2c8huDrnxL_9e4Q99SlX8Ara9pkE</recordid><startdate>200807</startdate><enddate>200807</enddate><creator>Sammons-Jackson, Wendy L</creator><creator>McClelland, Karen</creator><creator>Manch-Citron, Jean N</creator><creator>Metzger, Dennis W</creator><creator>Bakshi, Chandra Shekhar</creator><creator>Garcia, Emilio</creator><creator>Rasley, Amy</creator><creator>Anderson, Burt E</creator><general>Mary Ann Liebert, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200807</creationdate><title>Generation and characterization of an attenuated mutant in a response regulator gene of Francisella tularensis live vaccine strain (LVS)</title><author>Sammons-Jackson, Wendy L ; McClelland, Karen ; Manch-Citron, Jean N ; Metzger, Dennis W ; Bakshi, Chandra Shekhar ; Garcia, Emilio ; Rasley, Amy ; Anderson, Burt E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-dc3821d3cd7191920700a8551d6638a8ad89936c5b6767bd5ced7f1ce873d3ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Arthropoda</topic><topic>Bacterial Vaccines - immunology</topic><topic>Cells, Cultured</topic><topic>Cytokines - metabolism</topic><topic>Female</topic><topic>Francisella tularensis</topic><topic>Francisella tularensis - genetics</topic><topic>Francisella tularensis - immunology</topic><topic>Francisella tularensis - pathogenicity</topic><topic>Genes, Bacterial</topic><topic>Inflammation Mediators - metabolism</topic><topic>Macrophages - immunology</topic><topic>Macrophages - virology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Mutant Proteins - genetics</topic><topic>Mutant Proteins - immunology</topic><topic>Mutation</topic><topic>Original Papers</topic><topic>Survival Analysis</topic><topic>Tularemia - immunology</topic><topic>Tularemia - metabolism</topic><topic>Tularemia - mortality</topic><topic>Tularemia - therapy</topic><topic>Vaccines, Attenuated</topic><topic>Virus Replication - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sammons-Jackson, Wendy L</creatorcontrib><creatorcontrib>McClelland, Karen</creatorcontrib><creatorcontrib>Manch-Citron, Jean N</creatorcontrib><creatorcontrib>Metzger, Dennis W</creatorcontrib><creatorcontrib>Bakshi, Chandra Shekhar</creatorcontrib><creatorcontrib>Garcia, Emilio</creatorcontrib><creatorcontrib>Rasley, Amy</creatorcontrib><creatorcontrib>Anderson, Burt E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>DNA and cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sammons-Jackson, Wendy L</au><au>McClelland, Karen</au><au>Manch-Citron, Jean N</au><au>Metzger, Dennis W</au><au>Bakshi, Chandra Shekhar</au><au>Garcia, Emilio</au><au>Rasley, Amy</au><au>Anderson, Burt E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generation and characterization of an attenuated mutant in a response regulator gene of Francisella tularensis live vaccine strain (LVS)</atitle><jtitle>DNA and cell biology</jtitle><addtitle>DNA Cell Biol</addtitle><date>2008-07</date><risdate>2008</risdate><volume>27</volume><issue>7</issue><spage>387</spage><epage>403</epage><pages>387-403</pages><issn>1044-5498</issn><eissn>1557-7430</eissn><abstract>Francisella tularensis is a zoonotic bacterium that must exist in diverse environments ranging from arthropod vectors to mammalian hosts. To better understand how virulence genes are regulated in these different environments, a transcriptional response regulator gene (genome locus FTL0552) was deleted in F. tularensis live vaccine strain (LVS). The FTL0552 deletion mutant exhibited slightly reduced rates of extracellular growth but was unable to replicate or survive in mouse macrophages and was avirulent in the mouse model using either BALB/c or C57BL/6 mice. Mice infected with the FTL0552 mutant produced reduced levels of inflammatory cytokines, exhibited reduced histopathology, and cleared the bacteria quicker than mice infected with LVS. Mice that survived infection with the FTL0552 mutant were afforded partial protection when challenged with a lethal dose of the virulent SchuS4 strain (4 of 10 survivors, day 21 postinfection) when compared to naive mice (0 of 10 survivors by day 7 postinfection). Microarray experiments indicate that 148 genes are regulated by FTL0552. Most of the genes are downregulated, indicating that FTL0552 controls transcription of genes in a positive manner. Genes regulated by FTL0552 include genes located within the Francisella pathogenicity island that are essential for intracellular survival and virulence of F. tularensis. Further, a mutant in FTL0552 or the comparable locus in SchuS4 (FTT1557c) may be an alternative candidate vaccine for tularemia.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>18613792</pmid><doi>10.1089/dna.2007.0687</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Arthropoda Bacterial Vaccines - immunology Cells, Cultured Cytokines - metabolism Female Francisella tularensis Francisella tularensis - genetics Francisella tularensis - immunology Francisella tularensis - pathogenicity Genes, Bacterial Inflammation Mediators - metabolism Macrophages - immunology Macrophages - virology Male Mice Mice, Inbred BALB C Mice, Inbred C57BL Mutant Proteins - genetics Mutant Proteins - immunology Mutation Original Papers Survival Analysis Tularemia - immunology Tularemia - metabolism Tularemia - mortality Tularemia - therapy Vaccines, Attenuated Virus Replication - genetics |
title | Generation and characterization of an attenuated mutant in a response regulator gene of Francisella tularensis live vaccine strain (LVS) |
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