Biofilm formation by multidrug resistant Escherichia coli ST131 is dependent on type 1 fimbriae and assay conditions

Escherichia coli sequence type 131 (ST131) has emerged as a pandemic lineage of important multidrug resistant pathogens worldwide. Despite many studies examining the epidemiology of ST131, only a few studies to date have investigated the capacity of ST131 strains to form biofilms. Some of these stud...

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Veröffentlicht in:Pathogens and disease 2016-04, Vol.74 (3), p.ftw013
Hauptverfasser: Sarkar, Sohinee, Vagenas, Dimitrios, Schembri, Mark A., Totsika, Makrina
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Vagenas, Dimitrios
Schembri, Mark A.
Totsika, Makrina
description Escherichia coli sequence type 131 (ST131) has emerged as a pandemic lineage of important multidrug resistant pathogens worldwide. Despite many studies examining the epidemiology of ST131, only a few studies to date have investigated the capacity of ST131 strains to form biofilms. Some of these studies have reported contrasting findings, with no specific ST131 biofilm-promoting factors identified. Here, we examined a diverse collection of ST131 isolates for in vitro biofilm formation in different media and assay conditions, including urine from healthy adult women. We found significant differences among strains and assay conditions, which offers an explanation for the contrasting findings reported by previous studies using a single condition. Importantly, we showed that expression of type 1 fimbriae is a critical determinant for biofilm formation by ST131 strains and that inhibition of the FimH adhesin significantly reduces biofilm formation. We also offer direct genetic evidence for the contribution of type 1 fimbriae in biofilm formation by the reference ST131 strain EC958, a representative of the clinically dominant H30-Rx ST131 subgroup. This is the first study of ST131 biofilm formation in biologically relevant conditions and paves the way for the application of FimH inhibitors in treating drug resistant ST131 biofilm infections. This study investigated biofilm formation by the globally disseminated multidrug resistant Escherichia coli ST131 in biologically relevant conditions and identified the first critical biofilm promoting factor in this lineage. Graphical Abstract Figure. This study investigated biofilm formation by the globally disseminated multidrug resistant Escherichia coli ST131 in biologically relevant conditions and identified the first critical biofilm promoting factor in this lineage.
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Despite many studies examining the epidemiology of ST131, only a few studies to date have investigated the capacity of ST131 strains to form biofilms. Some of these studies have reported contrasting findings, with no specific ST131 biofilm-promoting factors identified. Here, we examined a diverse collection of ST131 isolates for in vitro biofilm formation in different media and assay conditions, including urine from healthy adult women. We found significant differences among strains and assay conditions, which offers an explanation for the contrasting findings reported by previous studies using a single condition. Importantly, we showed that expression of type 1 fimbriae is a critical determinant for biofilm formation by ST131 strains and that inhibition of the FimH adhesin significantly reduces biofilm formation. We also offer direct genetic evidence for the contribution of type 1 fimbriae in biofilm formation by the reference ST131 strain EC958, a representative of the clinically dominant H30-Rx ST131 subgroup. This is the first study of ST131 biofilm formation in biologically relevant conditions and paves the way for the application of FimH inhibitors in treating drug resistant ST131 biofilm infections. This study investigated biofilm formation by the globally disseminated multidrug resistant Escherichia coli ST131 in biologically relevant conditions and identified the first critical biofilm promoting factor in this lineage. Graphical Abstract Figure. This study investigated biofilm formation by the globally disseminated multidrug resistant Escherichia coli ST131 in biologically relevant conditions and identified the first critical biofilm promoting factor in this lineage.</description><identifier>ISSN: 2049-632X</identifier><identifier>EISSN: 2049-632X</identifier><identifier>DOI: 10.1093/femspd/ftw013</identifier><identifier>PMID: 26940589</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adhesins, Escherichia coli - genetics ; Adhesins, Escherichia coli - metabolism ; Adult ; Anti-Bacterial Agents - pharmacology ; Bacteriuria - microbiology ; Biofilms - growth &amp; development ; Drug Resistance, Multiple, Bacterial ; Escherichia coli - classification ; Escherichia coli - drug effects ; Escherichia coli - isolation &amp; purification ; Escherichia coli - pathogenicity ; Escherichia coli Infections - microbiology ; Female ; Fimbriae Proteins - antagonists &amp; inhibitors ; Fimbriae Proteins - genetics ; Fimbriae Proteins - metabolism ; Fimbriae, Bacterial - classification ; Humans ; Urinary Tract Infections - microbiology</subject><ispartof>Pathogens and disease, 2016-04, Vol.74 (3), p.ftw013</ispartof><rights>FEMS 2016. 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subjects Adhesins, Escherichia coli - genetics
Adhesins, Escherichia coli - metabolism
Adult
Anti-Bacterial Agents - pharmacology
Bacteriuria - microbiology
Biofilms - growth & development
Drug Resistance, Multiple, Bacterial
Escherichia coli - classification
Escherichia coli - drug effects
Escherichia coli - isolation & purification
Escherichia coli - pathogenicity
Escherichia coli Infections - microbiology
Female
Fimbriae Proteins - antagonists & inhibitors
Fimbriae Proteins - genetics
Fimbriae Proteins - metabolism
Fimbriae, Bacterial - classification
Humans
Urinary Tract Infections - microbiology
title Biofilm formation by multidrug resistant Escherichia coli ST131 is dependent on type 1 fimbriae and assay conditions
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