RssAB-FlhDC-ShlBA as a Major Pathogenesis Pathway in Serratia marcescens
Serratia marcescens has long been recognized as an important opportunistic pathogen, but the underlying pathogenesis mechanism is not completely clear. Here, we report a key pathogenesis pathway in S. marcescens comprising the RssAB two-component system and its downstream elements, FlhDC and the dom...
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Veröffentlicht in: | Infection and Immunity 2010-11, Vol.78 (11), p.4870-4881 |
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creator | Lin, Chuan-Sheng Horng, Jim-Tong Yang, Chun-Hung Tsai, Yu-Huan Su, Lin-Hui Wei, Chia-Fong Chen, Chang-Chieh Hsieh, Shang-Chen Lu, Chia-Chen Lai, Hsin-Chih |
description | Serratia marcescens has long been recognized as an important opportunistic pathogen, but the underlying pathogenesis mechanism is not completely clear. Here, we report a key pathogenesis pathway in S. marcescens comprising the RssAB two-component system and its downstream elements, FlhDC and the dominant virulence factor hemolysin ShlBA. Expression of shlBA is under the positive control of FlhDC, which is repressed by RssAB signaling. At 37°C, functional RssAB inhibits swarming, represses hemolysin production, and promotes S. marcescens biofilm formation. In comparison, when rssBA is deleted, S. marcescens displays aberrant multicellularity favoring motile swarming with unbridled hemolysin production. Cellular and animal infection models further demonstrate that loss of rssBA transforms this opportunistic pathogen into hypervirulent phenotypes, leading to extensive inflammatory responses coupled with destructive and systemic infection. Hemolysin production is essential in this context. Collectively, a major virulence regulatory pathway is identified in S. marcescens. |
doi_str_mv | 10.1128/IAI.00661-10 |
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Here, we report a key pathogenesis pathway in S. marcescens comprising the RssAB two-component system and its downstream elements, FlhDC and the dominant virulence factor hemolysin ShlBA. Expression of shlBA is under the positive control of FlhDC, which is repressed by RssAB signaling. At 37°C, functional RssAB inhibits swarming, represses hemolysin production, and promotes S. marcescens biofilm formation. In comparison, when rssBA is deleted, S. marcescens displays aberrant multicellularity favoring motile swarming with unbridled hemolysin production. Cellular and animal infection models further demonstrate that loss of rssBA transforms this opportunistic pathogen into hypervirulent phenotypes, leading to extensive inflammatory responses coupled with destructive and systemic infection. Hemolysin production is essential in this context. Collectively, a major virulence regulatory pathway is identified in S. marcescens.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/IAI.00661-10</identifier><identifier>PMID: 20713626</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Animals ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Bronchi - cytology ; Bronchi - microbiology ; Cells, Cultured ; Epithelial Cells - microbiology ; Gene Expression Regulation, Bacterial ; Hemolysin Proteins - genetics ; Hemolysin Proteins - metabolism ; Hemolysis ; Humans ; Male ; Molecular Pathogenesis ; Pneumonia, Bacterial - microbiology ; Pneumonia, Bacterial - pathology ; Rats ; Rats, Sprague-Dawley ; Serratia Infections - microbiology ; Serratia Infections - pathology ; Serratia marcescens ; Serratia marcescens - genetics ; Serratia marcescens - metabolism ; Serratia marcescens - pathogenicity ; Signal Transduction ; Virulence</subject><ispartof>Infection and Immunity, 2010-11, Vol.78 (11), p.4870-4881</ispartof><rights>Copyright © 2010, American Society for Microbiology 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-a0aa8c1d5fdf671ed87dfa971d16b5b477768c557e8b588c447ccdfb83ee7d863</citedby><cites>FETCH-LOGICAL-c466t-a0aa8c1d5fdf671ed87dfa971d16b5b477768c557e8b588c447ccdfb83ee7d863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2976324/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2976324/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20713626$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Chuan-Sheng</creatorcontrib><creatorcontrib>Horng, Jim-Tong</creatorcontrib><creatorcontrib>Yang, Chun-Hung</creatorcontrib><creatorcontrib>Tsai, Yu-Huan</creatorcontrib><creatorcontrib>Su, Lin-Hui</creatorcontrib><creatorcontrib>Wei, Chia-Fong</creatorcontrib><creatorcontrib>Chen, Chang-Chieh</creatorcontrib><creatorcontrib>Hsieh, Shang-Chen</creatorcontrib><creatorcontrib>Lu, Chia-Chen</creatorcontrib><creatorcontrib>Lai, Hsin-Chih</creatorcontrib><title>RssAB-FlhDC-ShlBA as a Major Pathogenesis Pathway in Serratia marcescens</title><title>Infection and Immunity</title><addtitle>Infect Immun</addtitle><description>Serratia marcescens has long been recognized as an important opportunistic pathogen, but the underlying pathogenesis mechanism is not completely clear. Here, we report a key pathogenesis pathway in S. marcescens comprising the RssAB two-component system and its downstream elements, FlhDC and the dominant virulence factor hemolysin ShlBA. Expression of shlBA is under the positive control of FlhDC, which is repressed by RssAB signaling. At 37°C, functional RssAB inhibits swarming, represses hemolysin production, and promotes S. marcescens biofilm formation. In comparison, when rssBA is deleted, S. marcescens displays aberrant multicellularity favoring motile swarming with unbridled hemolysin production. Cellular and animal infection models further demonstrate that loss of rssBA transforms this opportunistic pathogen into hypervirulent phenotypes, leading to extensive inflammatory responses coupled with destructive and systemic infection. Hemolysin production is essential in this context. Collectively, a major virulence regulatory pathway is identified in S. marcescens.</description><subject>Animals</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bronchi - cytology</subject><subject>Bronchi - microbiology</subject><subject>Cells, Cultured</subject><subject>Epithelial Cells - microbiology</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Hemolysin Proteins - genetics</subject><subject>Hemolysin Proteins - metabolism</subject><subject>Hemolysis</subject><subject>Humans</subject><subject>Male</subject><subject>Molecular Pathogenesis</subject><subject>Pneumonia, Bacterial - microbiology</subject><subject>Pneumonia, Bacterial - pathology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Serratia Infections - microbiology</subject><subject>Serratia Infections - pathology</subject><subject>Serratia marcescens</subject><subject>Serratia marcescens - genetics</subject><subject>Serratia marcescens - metabolism</subject><subject>Serratia marcescens - pathogenicity</subject><subject>Signal Transduction</subject><subject>Virulence</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkb1PwzAQxS0EglLYmCFiYSFgO47tLEilfFUCgSidrYvjNEZpUuwUxH-PSwuC6XTnn969e0bogOAzQqg8Hw1GZxhzTmKCN1CP4EzGaUrpJuphTLI4S7nYQbvev4aWMSa30Q7FgiSc8h66e_Z-cBnf1NXVMB5X9eUgAh9B9ACvrYueoKvaqWmMt_67-YDPyDbR2DgHnYVoBk4br03j99BWCbU3--vaR5Ob65fhXXz_eDsaDu5jzTjvYsAAUpMiLYuSC2IKKYoSMkEKwvM0Z0IILnWaCiPzVErNmNC6KHOZGCMKyZM-uljpzhf5zBRhdeegVnNng5dP1YJV_18aW6lp-65oJnhCWRA4WQu49m1hfKdmNlxQ19CYduGV5DgRFEsayNMVqV3rvTPl7xaC1TJ7FbJX39mHScAP_zr7hX_CDsDxCqjstPqwzijwM2WDYyGDnmJSLFWOVlAJrYKps15NxhSTJPwlJpzR5At_pZO6</recordid><startdate>20101101</startdate><enddate>20101101</enddate><creator>Lin, Chuan-Sheng</creator><creator>Horng, Jim-Tong</creator><creator>Yang, Chun-Hung</creator><creator>Tsai, Yu-Huan</creator><creator>Su, Lin-Hui</creator><creator>Wei, Chia-Fong</creator><creator>Chen, Chang-Chieh</creator><creator>Hsieh, Shang-Chen</creator><creator>Lu, Chia-Chen</creator><creator>Lai, Hsin-Chih</creator><general>American Society for Microbiology</general><general>American Society for Microbiology (ASM)</general><scope>FBQ</scope><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>7T5</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20101101</creationdate><title>RssAB-FlhDC-ShlBA as a Major Pathogenesis Pathway in Serratia marcescens</title><author>Lin, Chuan-Sheng ; Horng, Jim-Tong ; Yang, Chun-Hung ; Tsai, Yu-Huan ; Su, Lin-Hui ; Wei, Chia-Fong ; Chen, Chang-Chieh ; Hsieh, Shang-Chen ; Lu, Chia-Chen ; Lai, Hsin-Chih</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-a0aa8c1d5fdf671ed87dfa971d16b5b477768c557e8b588c447ccdfb83ee7d863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bronchi - cytology</topic><topic>Bronchi - microbiology</topic><topic>Cells, Cultured</topic><topic>Epithelial Cells - microbiology</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Hemolysin Proteins - genetics</topic><topic>Hemolysin Proteins - metabolism</topic><topic>Hemolysis</topic><topic>Humans</topic><topic>Male</topic><topic>Molecular Pathogenesis</topic><topic>Pneumonia, Bacterial - microbiology</topic><topic>Pneumonia, Bacterial - pathology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Serratia Infections - microbiology</topic><topic>Serratia Infections - pathology</topic><topic>Serratia marcescens</topic><topic>Serratia marcescens - genetics</topic><topic>Serratia marcescens - metabolism</topic><topic>Serratia marcescens - pathogenicity</topic><topic>Signal Transduction</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Chuan-Sheng</creatorcontrib><creatorcontrib>Horng, Jim-Tong</creatorcontrib><creatorcontrib>Yang, Chun-Hung</creatorcontrib><creatorcontrib>Tsai, Yu-Huan</creatorcontrib><creatorcontrib>Su, Lin-Hui</creatorcontrib><creatorcontrib>Wei, Chia-Fong</creatorcontrib><creatorcontrib>Chen, Chang-Chieh</creatorcontrib><creatorcontrib>Hsieh, Shang-Chen</creatorcontrib><creatorcontrib>Lu, Chia-Chen</creatorcontrib><creatorcontrib>Lai, Hsin-Chih</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection and Immunity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Chuan-Sheng</au><au>Horng, Jim-Tong</au><au>Yang, Chun-Hung</au><au>Tsai, Yu-Huan</au><au>Su, Lin-Hui</au><au>Wei, Chia-Fong</au><au>Chen, Chang-Chieh</au><au>Hsieh, Shang-Chen</au><au>Lu, Chia-Chen</au><au>Lai, Hsin-Chih</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>RssAB-FlhDC-ShlBA as a Major Pathogenesis Pathway in Serratia marcescens</atitle><jtitle>Infection and Immunity</jtitle><addtitle>Infect Immun</addtitle><date>2010-11-01</date><risdate>2010</risdate><volume>78</volume><issue>11</issue><spage>4870</spage><epage>4881</epage><pages>4870-4881</pages><issn>0019-9567</issn><eissn>1098-5522</eissn><abstract>Serratia marcescens has long been recognized as an important opportunistic pathogen, but the underlying pathogenesis mechanism is not completely clear. Here, we report a key pathogenesis pathway in S. marcescens comprising the RssAB two-component system and its downstream elements, FlhDC and the dominant virulence factor hemolysin ShlBA. Expression of shlBA is under the positive control of FlhDC, which is repressed by RssAB signaling. At 37°C, functional RssAB inhibits swarming, represses hemolysin production, and promotes S. marcescens biofilm formation. In comparison, when rssBA is deleted, S. marcescens displays aberrant multicellularity favoring motile swarming with unbridled hemolysin production. Cellular and animal infection models further demonstrate that loss of rssBA transforms this opportunistic pathogen into hypervirulent phenotypes, leading to extensive inflammatory responses coupled with destructive and systemic infection. Hemolysin production is essential in this context. Collectively, a major virulence regulatory pathway is identified in S. marcescens.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>20713626</pmid><doi>10.1128/IAI.00661-10</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Bacterial Proteins - genetics Bacterial Proteins - metabolism Bronchi - cytology Bronchi - microbiology Cells, Cultured Epithelial Cells - microbiology Gene Expression Regulation, Bacterial Hemolysin Proteins - genetics Hemolysin Proteins - metabolism Hemolysis Humans Male Molecular Pathogenesis Pneumonia, Bacterial - microbiology Pneumonia, Bacterial - pathology Rats Rats, Sprague-Dawley Serratia Infections - microbiology Serratia Infections - pathology Serratia marcescens Serratia marcescens - genetics Serratia marcescens - metabolism Serratia marcescens - pathogenicity Signal Transduction Virulence |
title | RssAB-FlhDC-ShlBA as a Major Pathogenesis Pathway in Serratia marcescens |
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