Coordinate Expression of Fimbriae in Uropathogenic Escherichia coli

Uropathogenic Escherichia coli is the most common etiological agent of urinary tract infections. Bacteria can often express multiple adhesins during infection in order to favor attachment to specific niches within the urinary tract. We have recently demonstrated that type 1 fimbria, a phase-variable...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Infection and Immunity 2005-11, Vol.73 (11), p.7588-7596
Hauptverfasser: Snyder, Jennifer A, Haugen, Brian J, Lockatell, C. Virginia, Maroncle, Nathalie, Hagan, Erin C, Johnson, David E, Welch, Rodney A, Mobley, Harry L. T
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 7596
container_issue 11
container_start_page 7588
container_title Infection and Immunity
container_volume 73
creator Snyder, Jennifer A
Haugen, Brian J
Lockatell, C. Virginia
Maroncle, Nathalie
Hagan, Erin C
Johnson, David E
Welch, Rodney A
Mobley, Harry L. T
description Uropathogenic Escherichia coli is the most common etiological agent of urinary tract infections. Bacteria can often express multiple adhesins during infection in order to favor attachment to specific niches within the urinary tract. We have recently demonstrated that type 1 fimbria, a phase-variable virulence factor involved in adherence, was the most highly expressed adhesin during urinary tract infection. Here, we examine whether the expression of type 1 fimbriae can affect the expression of other adhesins. Type 1 fimbrial phase-locked mutants of E. coli strain CFT073, which harbors genes for numerous adhesins, were employed in this study. CFT073-specific DNA microarray analysis of these strains demonstrates that the expression of type 1 fimbriae coordinately affects the expression of P fimbriae in an inverse manner. This represents evidence for direct communication between genes relating to pathogenesis, perhaps to aid the sequential occupation of different urinary tract tissues. While the role of type 1 fimbriae during infection has been clear, the role of P fimbriae must be further defined to assert the relevance of coordinated regulation in vivo. Therefore, we examined the ability of P fimbrial isogenic mutants, constructed in a type 1 fimbrial-negative background, to compete in the murine urinary tract over a period of 168 h. No differences in the colonization of these mutants were observed. However, comparison of these results with previous studies suggests that inversely coordinated expression of adhesin gene clusters does occur in vivo. Interestingly, the mutant that was incapable of expressing either type 1 or P fimbriae compensated by synthesizing F1C fimbriae.
doi_str_mv 10.1128/IAI.73.11.7588-7596.2005
format Article
fullrecord <record><control><sourceid>proquest_pasca</sourceid><recordid>TN_cdi_pascalfrancis_primary_17220106</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20985130</sourcerecordid><originalsourceid>FETCH-LOGICAL-c680t-79a2a3af4733748f4ad9ebde5685a97645b904e7e13f90d5d151c863ecdd13053</originalsourceid><addsrcrecordid>eNqFkUuP0zAUhS0EYsrAX4AICXYpfsSvDdKo6kClkVhA19atc9MYJXGxUx7_HletKKxY-dr-zvH1PYRUjC4Z4-bd5m6z1KLUSy2NqbW0askplY_IglFraik5f0wWlDJbW6n0DXmW89eybZrGPCU3THFRzvmCrFYxpjZMMGO1_nlImHOIUxW76j6MuxQAqzBV2xQPMPdxj1Pw1Tr7HlPwfYDKxyE8J086GDK-uKy3ZHu__rL6WD98-rBZ3T3UXhk619oCBwFdo4XQjekaaC3uWpTKSLBaNXJnaYMamegsbWXLJPNGCfRtywSV4pa8P_sejrsRW4_TnGBwhxRGSL9chOD-vZlC7_bxu2NcC0tNMXh7MUjx2xHz7MaQPQ4DTBiP2SmjGZfy_yAvQ5alpwKaM-hTzDlh96cbRt0pKleiclqU2p2icqeo3CmqIn3592-uwks2BXhzASB7GLoEkw_5ymnOKaOqcK_PXB_2_Y-Q0EEeXSjTuL5boFdnqIPoYJ-K0fZz0YtiISSTVvwGWP2xyQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20985130</pqid></control><display><type>article</type><title>Coordinate Expression of Fimbriae in Uropathogenic Escherichia coli</title><source>MEDLINE</source><source>American Society for Microbiology Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Snyder, Jennifer A ; Haugen, Brian J ; Lockatell, C. Virginia ; Maroncle, Nathalie ; Hagan, Erin C ; Johnson, David E ; Welch, Rodney A ; Mobley, Harry L. T</creator><creatorcontrib>Snyder, Jennifer A ; Haugen, Brian J ; Lockatell, C. Virginia ; Maroncle, Nathalie ; Hagan, Erin C ; Johnson, David E ; Welch, Rodney A ; Mobley, Harry L. T</creatorcontrib><description>Uropathogenic Escherichia coli is the most common etiological agent of urinary tract infections. Bacteria can often express multiple adhesins during infection in order to favor attachment to specific niches within the urinary tract. We have recently demonstrated that type 1 fimbria, a phase-variable virulence factor involved in adherence, was the most highly expressed adhesin during urinary tract infection. Here, we examine whether the expression of type 1 fimbriae can affect the expression of other adhesins. Type 1 fimbrial phase-locked mutants of E. coli strain CFT073, which harbors genes for numerous adhesins, were employed in this study. CFT073-specific DNA microarray analysis of these strains demonstrates that the expression of type 1 fimbriae coordinately affects the expression of P fimbriae in an inverse manner. This represents evidence for direct communication between genes relating to pathogenesis, perhaps to aid the sequential occupation of different urinary tract tissues. While the role of type 1 fimbriae during infection has been clear, the role of P fimbriae must be further defined to assert the relevance of coordinated regulation in vivo. Therefore, we examined the ability of P fimbrial isogenic mutants, constructed in a type 1 fimbrial-negative background, to compete in the murine urinary tract over a period of 168 h. No differences in the colonization of these mutants were observed. However, comparison of these results with previous studies suggests that inversely coordinated expression of adhesin gene clusters does occur in vivo. Interestingly, the mutant that was incapable of expressing either type 1 or P fimbriae compensated by synthesizing F1C fimbriae.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/IAI.73.11.7588-7596.2005</identifier><identifier>PMID: 16239562</identifier><identifier>CODEN: INFIBR</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Animals ; Bacteriology ; Biological and medical sciences ; Disease Models, Animal ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Escherichia coli - pathogenicity ; Escherichia coli Infections - microbiology ; Escherichia coli Proteins - biosynthesis ; Escherichia coli Proteins - genetics ; Female ; Fimbria ; Fimbriae Proteins - biosynthesis ; Fimbriae Proteins - genetics ; Fimbriae, Bacterial - metabolism ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation, Bacterial ; Genotype ; Mice ; Mice, Inbred CBA ; Microbiology ; Miscellaneous ; Molecular Pathogenesis ; Mutation ; Oligonucleotide Array Sequence Analysis ; Urinary Tract Infections - microbiology</subject><ispartof>Infection and Immunity, 2005-11, Vol.73 (11), p.7588-7596</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright © 2005, American Society for Microbiology 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c680t-79a2a3af4733748f4ad9ebde5685a97645b904e7e13f90d5d151c863ecdd13053</citedby><cites>FETCH-LOGICAL-c680t-79a2a3af4733748f4ad9ebde5685a97645b904e7e13f90d5d151c863ecdd13053</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/PMC1273908/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1273908/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,3189,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17220106$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16239562$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Snyder, Jennifer A</creatorcontrib><creatorcontrib>Haugen, Brian J</creatorcontrib><creatorcontrib>Lockatell, C. Virginia</creatorcontrib><creatorcontrib>Maroncle, Nathalie</creatorcontrib><creatorcontrib>Hagan, Erin C</creatorcontrib><creatorcontrib>Johnson, David E</creatorcontrib><creatorcontrib>Welch, Rodney A</creatorcontrib><creatorcontrib>Mobley, Harry L. T</creatorcontrib><title>Coordinate Expression of Fimbriae in Uropathogenic Escherichia coli</title><title>Infection and Immunity</title><addtitle>Infect Immun</addtitle><description>Uropathogenic Escherichia coli is the most common etiological agent of urinary tract infections. Bacteria can often express multiple adhesins during infection in order to favor attachment to specific niches within the urinary tract. We have recently demonstrated that type 1 fimbria, a phase-variable virulence factor involved in adherence, was the most highly expressed adhesin during urinary tract infection. Here, we examine whether the expression of type 1 fimbriae can affect the expression of other adhesins. Type 1 fimbrial phase-locked mutants of E. coli strain CFT073, which harbors genes for numerous adhesins, were employed in this study. CFT073-specific DNA microarray analysis of these strains demonstrates that the expression of type 1 fimbriae coordinately affects the expression of P fimbriae in an inverse manner. This represents evidence for direct communication between genes relating to pathogenesis, perhaps to aid the sequential occupation of different urinary tract tissues. While the role of type 1 fimbriae during infection has been clear, the role of P fimbriae must be further defined to assert the relevance of coordinated regulation in vivo. Therefore, we examined the ability of P fimbrial isogenic mutants, constructed in a type 1 fimbrial-negative background, to compete in the murine urinary tract over a period of 168 h. No differences in the colonization of these mutants were observed. However, comparison of these results with previous studies suggests that inversely coordinated expression of adhesin gene clusters does occur in vivo. Interestingly, the mutant that was incapable of expressing either type 1 or P fimbriae compensated by synthesizing F1C fimbriae.</description><subject>Animals</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Disease Models, Animal</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>Escherichia coli - pathogenicity</subject><subject>Escherichia coli Infections - microbiology</subject><subject>Escherichia coli Proteins - biosynthesis</subject><subject>Escherichia coli Proteins - genetics</subject><subject>Female</subject><subject>Fimbria</subject><subject>Fimbriae Proteins - biosynthesis</subject><subject>Fimbriae Proteins - genetics</subject><subject>Fimbriae, Bacterial - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genotype</subject><subject>Mice</subject><subject>Mice, Inbred CBA</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Molecular Pathogenesis</subject><subject>Mutation</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Urinary Tract Infections - microbiology</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuP0zAUhS0EYsrAX4AICXYpfsSvDdKo6kClkVhA19atc9MYJXGxUx7_HletKKxY-dr-zvH1PYRUjC4Z4-bd5m6z1KLUSy2NqbW0askplY_IglFraik5f0wWlDJbW6n0DXmW89eybZrGPCU3THFRzvmCrFYxpjZMMGO1_nlImHOIUxW76j6MuxQAqzBV2xQPMPdxj1Pw1Tr7HlPwfYDKxyE8J086GDK-uKy3ZHu__rL6WD98-rBZ3T3UXhk619oCBwFdo4XQjekaaC3uWpTKSLBaNXJnaYMamegsbWXLJPNGCfRtywSV4pa8P_sejrsRW4_TnGBwhxRGSL9chOD-vZlC7_bxu2NcC0tNMXh7MUjx2xHz7MaQPQ4DTBiP2SmjGZfy_yAvQ5alpwKaM-hTzDlh96cbRt0pKleiclqU2p2icqeo3CmqIn3592-uwks2BXhzASB7GLoEkw_5ymnOKaOqcK_PXB_2_Y-Q0EEeXSjTuL5boFdnqIPoYJ-K0fZz0YtiISSTVvwGWP2xyQ</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Snyder, Jennifer A</creator><creator>Haugen, Brian J</creator><creator>Lockatell, C. Virginia</creator><creator>Maroncle, Nathalie</creator><creator>Hagan, Erin C</creator><creator>Johnson, David E</creator><creator>Welch, Rodney A</creator><creator>Mobley, Harry L. T</creator><general>American Society for Microbiology</general><scope>FBQ</scope><scope>IQODW</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>7QL</scope><scope>7T5</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20051101</creationdate><title>Coordinate Expression of Fimbriae in Uropathogenic Escherichia coli</title><author>Snyder, Jennifer A ; Haugen, Brian J ; Lockatell, C. Virginia ; Maroncle, Nathalie ; Hagan, Erin C ; Johnson, David E ; Welch, Rodney A ; Mobley, Harry L. T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c680t-79a2a3af4733748f4ad9ebde5685a97645b904e7e13f90d5d151c863ecdd13053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Disease Models, Animal</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - metabolism</topic><topic>Escherichia coli - pathogenicity</topic><topic>Escherichia coli Infections - microbiology</topic><topic>Escherichia coli Proteins - biosynthesis</topic><topic>Escherichia coli Proteins - genetics</topic><topic>Female</topic><topic>Fimbria</topic><topic>Fimbriae Proteins - biosynthesis</topic><topic>Fimbriae Proteins - genetics</topic><topic>Fimbriae, Bacterial - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genotype</topic><topic>Mice</topic><topic>Mice, Inbred CBA</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Molecular Pathogenesis</topic><topic>Mutation</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Urinary Tract Infections - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Snyder, Jennifer A</creatorcontrib><creatorcontrib>Haugen, Brian J</creatorcontrib><creatorcontrib>Lockatell, C. Virginia</creatorcontrib><creatorcontrib>Maroncle, Nathalie</creatorcontrib><creatorcontrib>Hagan, Erin C</creatorcontrib><creatorcontrib>Johnson, David E</creatorcontrib><creatorcontrib>Welch, Rodney A</creatorcontrib><creatorcontrib>Mobley, Harry L. T</creatorcontrib><collection>AGRIS</collection><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>Immunology 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>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</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>Snyder, Jennifer A</au><au>Haugen, Brian J</au><au>Lockatell, C. Virginia</au><au>Maroncle, Nathalie</au><au>Hagan, Erin C</au><au>Johnson, David E</au><au>Welch, Rodney A</au><au>Mobley, Harry L. T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coordinate Expression of Fimbriae in Uropathogenic Escherichia coli</atitle><jtitle>Infection and Immunity</jtitle><addtitle>Infect Immun</addtitle><date>2005-11-01</date><risdate>2005</risdate><volume>73</volume><issue>11</issue><spage>7588</spage><epage>7596</epage><pages>7588-7596</pages><issn>0019-9567</issn><eissn>1098-5522</eissn><coden>INFIBR</coden><abstract>Uropathogenic Escherichia coli is the most common etiological agent of urinary tract infections. Bacteria can often express multiple adhesins during infection in order to favor attachment to specific niches within the urinary tract. We have recently demonstrated that type 1 fimbria, a phase-variable virulence factor involved in adherence, was the most highly expressed adhesin during urinary tract infection. Here, we examine whether the expression of type 1 fimbriae can affect the expression of other adhesins. Type 1 fimbrial phase-locked mutants of E. coli strain CFT073, which harbors genes for numerous adhesins, were employed in this study. CFT073-specific DNA microarray analysis of these strains demonstrates that the expression of type 1 fimbriae coordinately affects the expression of P fimbriae in an inverse manner. This represents evidence for direct communication between genes relating to pathogenesis, perhaps to aid the sequential occupation of different urinary tract tissues. While the role of type 1 fimbriae during infection has been clear, the role of P fimbriae must be further defined to assert the relevance of coordinated regulation in vivo. Therefore, we examined the ability of P fimbrial isogenic mutants, constructed in a type 1 fimbrial-negative background, to compete in the murine urinary tract over a period of 168 h. No differences in the colonization of these mutants were observed. However, comparison of these results with previous studies suggests that inversely coordinated expression of adhesin gene clusters does occur in vivo. Interestingly, the mutant that was incapable of expressing either type 1 or P fimbriae compensated by synthesizing F1C fimbriae.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>16239562</pmid><doi>10.1128/IAI.73.11.7588-7596.2005</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0019-9567
ispartof Infection and Immunity, 2005-11, Vol.73 (11), p.7588-7596
issn 0019-9567
1098-5522
language eng
recordid cdi_pascalfrancis_primary_17220106
source MEDLINE; American Society for Microbiology Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Animals
Bacteriology
Biological and medical sciences
Disease Models, Animal
Escherichia coli
Escherichia coli - genetics
Escherichia coli - metabolism
Escherichia coli - pathogenicity
Escherichia coli Infections - microbiology
Escherichia coli Proteins - biosynthesis
Escherichia coli Proteins - genetics
Female
Fimbria
Fimbriae Proteins - biosynthesis
Fimbriae Proteins - genetics
Fimbriae, Bacterial - metabolism
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation, Bacterial
Genotype
Mice
Mice, Inbred CBA
Microbiology
Miscellaneous
Molecular Pathogenesis
Mutation
Oligonucleotide Array Sequence Analysis
Urinary Tract Infections - microbiology
title Coordinate Expression of Fimbriae in Uropathogenic Escherichia coli
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T14%3A53%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pasca&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Coordinate%20Expression%20of%20Fimbriae%20in%20Uropathogenic%20Escherichia%20coli&rft.jtitle=Infection%20and%20Immunity&rft.au=Snyder,%20Jennifer%20A&rft.date=2005-11-01&rft.volume=73&rft.issue=11&rft.spage=7588&rft.epage=7596&rft.pages=7588-7596&rft.issn=0019-9567&rft.eissn=1098-5522&rft.coden=INFIBR&rft_id=info:doi/10.1128/IAI.73.11.7588-7596.2005&rft_dat=%3Cproquest_pasca%3E20985130%3C/proquest_pasca%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=20985130&rft_id=info:pmid/16239562&rfr_iscdi=true