An in vivo inducible gene of Pseudomonas aeruginosa encodes an anti‐ExsA to suppress the type III secretion system

Summary We have previously reported on the isolation of in vivo inducible genes of Pseudomonas aeruginosa using IVET system. One of such genes isolated from burn mouse infection model encodes a short open reading frame with unknown function. In this study, we demonstrate that this gene product speci...

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Veröffentlicht in:Molecular microbiology 2004-10, Vol.54 (2), p.307-320
Hauptverfasser: Ha, Un‐Hwan, Kim, Jaewha, Badrane, Hassan, Jia, Jinghua, Baker, Henry V., Wu, Donghai, Jin, Shouguang
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container_end_page 320
container_issue 2
container_start_page 307
container_title Molecular microbiology
container_volume 54
creator Ha, Un‐Hwan
Kim, Jaewha
Badrane, Hassan
Jia, Jinghua
Baker, Henry V.
Wu, Donghai
Jin, Shouguang
description Summary We have previously reported on the isolation of in vivo inducible genes of Pseudomonas aeruginosa using IVET system. One of such genes isolated from burn mouse infection model encodes a short open reading frame with unknown function. In this study, we demonstrate that this gene product specifically suppresses the expression of type III secretion genes in P. aeruginosa, thus named PtrA (Pseudomonas type III repressor A). A direct interaction between the PtrA and type III transcriptional activator ExsA was demonstrated, suggesting that its repressor function is probably realized through inhibition of the ExsA protein function. Indeed, an elevated expression of the exsA compensates the repressor effect of the PtrA. Interestingly, expression of the ptrA is highly and specifically induced by copper cation. A copper‐ responsive two‐component regulatory system, copR‐copS, has also been identified and shown to be essential for the copper resistance in P. aeruginosa as well as the activation of ptrA in response to the copper signal. Elevated expression of the ptrA during the infection of mouse burn wound suggests that P. aeruginosa has evolved tight regulatory systems to shut down energy‐expensive type III secretion apparatus in response to specific environmental signals, such as copper stress.
doi_str_mv 10.1111/j.1365-2958.2004.04282.x
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One of such genes isolated from burn mouse infection model encodes a short open reading frame with unknown function. In this study, we demonstrate that this gene product specifically suppresses the expression of type III secretion genes in P. aeruginosa, thus named PtrA (Pseudomonas type III repressor A). A direct interaction between the PtrA and type III transcriptional activator ExsA was demonstrated, suggesting that its repressor function is probably realized through inhibition of the ExsA protein function. Indeed, an elevated expression of the exsA compensates the repressor effect of the PtrA. Interestingly, expression of the ptrA is highly and specifically induced by copper cation. A copper‐ responsive two‐component regulatory system, copR‐copS, has also been identified and shown to be essential for the copper resistance in P. aeruginosa as well as the activation of ptrA in response to the copper signal. Elevated expression of the ptrA during the infection of mouse burn wound suggests that P. aeruginosa has evolved tight regulatory systems to shut down energy‐expensive type III secretion apparatus in response to specific environmental signals, such as copper stress.</description><identifier>ISSN: 0950-382X</identifier><identifier>EISSN: 1365-2958</identifier><identifier>DOI: 10.1111/j.1365-2958.2004.04282.x</identifier><identifier>PMID: 15469505</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Animals ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Bacteriology ; Biological and medical sciences ; Copper - metabolism ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; Fundamental and applied biological sciences. Psychology ; Gene Expression Profiling ; Gene Expression Regulation, Bacterial ; Humans ; Mice ; Microbiology ; Miscellaneous ; Oligonucleotide Array Sequence Analysis ; Pseudomonas aeruginosa ; Pseudomonas aeruginosa - genetics ; Pseudomonas aeruginosa - metabolism ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - metabolism ; Repressor Proteins - genetics ; Repressor Proteins - metabolism ; Signal Transduction - physiology ; Trans-Activators - genetics ; Trans-Activators - metabolism ; Two-Hybrid System Techniques</subject><ispartof>Molecular microbiology, 2004-10, Vol.54 (2), p.307-320</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright Blackwell Scientific Publications Ltd. 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Elevated expression of the ptrA during the infection of mouse burn wound suggests that P. aeruginosa has evolved tight regulatory systems to shut down energy‐expensive type III secretion apparatus in response to specific environmental signals, such as copper stress.</description><subject>Animals</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Copper - metabolism</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Humans</topic><topic>Mice</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Pseudomonas aeruginosa</topic><topic>Pseudomonas aeruginosa - genetics</topic><topic>Pseudomonas aeruginosa - metabolism</topic><topic>Recombinant Fusion Proteins - genetics</topic><topic>Recombinant Fusion Proteins - metabolism</topic><topic>Repressor Proteins - genetics</topic><topic>Repressor Proteins - metabolism</topic><topic>Signal Transduction - physiology</topic><topic>Trans-Activators - genetics</topic><topic>Trans-Activators - metabolism</topic><topic>Two-Hybrid System Techniques</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ha, Un‐Hwan</creatorcontrib><creatorcontrib>Kim, Jaewha</creatorcontrib><creatorcontrib>Badrane, Hassan</creatorcontrib><creatorcontrib>Jia, Jinghua</creatorcontrib><creatorcontrib>Baker, Henry V.</creatorcontrib><creatorcontrib>Wu, Donghai</creatorcontrib><creatorcontrib>Jin, Shouguang</creatorcontrib><collection>Pascal-Francis</collection><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>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ha, Un‐Hwan</au><au>Kim, Jaewha</au><au>Badrane, Hassan</au><au>Jia, Jinghua</au><au>Baker, Henry V.</au><au>Wu, Donghai</au><au>Jin, Shouguang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An in vivo inducible gene of Pseudomonas aeruginosa encodes an anti‐ExsA to suppress the type III secretion system</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>2004-10</date><risdate>2004</risdate><volume>54</volume><issue>2</issue><spage>307</spage><epage>320</epage><pages>307-320</pages><issn>0950-382X</issn><eissn>1365-2958</eissn><abstract>Summary We have previously reported on the isolation of in vivo inducible genes of Pseudomonas aeruginosa using IVET system. One of such genes isolated from burn mouse infection model encodes a short open reading frame with unknown function. In this study, we demonstrate that this gene product specifically suppresses the expression of type III secretion genes in P. aeruginosa, thus named PtrA (Pseudomonas type III repressor A). A direct interaction between the PtrA and type III transcriptional activator ExsA was demonstrated, suggesting that its repressor function is probably realized through inhibition of the ExsA protein function. Indeed, an elevated expression of the exsA compensates the repressor effect of the PtrA. Interestingly, expression of the ptrA is highly and specifically induced by copper cation. A copper‐ responsive two‐component regulatory system, copR‐copS, has also been identified and shown to be essential for the copper resistance in P. aeruginosa as well as the activation of ptrA in response to the copper signal. Elevated expression of the ptrA during the infection of mouse burn wound suggests that P. aeruginosa has evolved tight regulatory systems to shut down energy‐expensive type III secretion apparatus in response to specific environmental signals, such as copper stress.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15469505</pmid><doi>10.1111/j.1365-2958.2004.04282.x</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Bacteriology
Biological and medical sciences
Copper - metabolism
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
Fundamental and applied biological sciences. Psychology
Gene Expression Profiling
Gene Expression Regulation, Bacterial
Humans
Mice
Microbiology
Miscellaneous
Oligonucleotide Array Sequence Analysis
Pseudomonas aeruginosa
Pseudomonas aeruginosa - genetics
Pseudomonas aeruginosa - metabolism
Recombinant Fusion Proteins - genetics
Recombinant Fusion Proteins - metabolism
Repressor Proteins - genetics
Repressor Proteins - metabolism
Signal Transduction - physiology
Trans-Activators - genetics
Trans-Activators - metabolism
Two-Hybrid System Techniques
title An in vivo inducible gene of Pseudomonas aeruginosa encodes an anti‐ExsA to suppress the type III secretion system
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