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...
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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 |
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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. 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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. 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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> |
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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 |
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