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1054. Biofilm Formation Among Escherichia coli Bloodstream Infection Isolates Is Associated With Source of Bacteremia and Bacterial Sequence Type

BACKGROUND: The clinical impact of Escherichia coli biofilm formation is unknown. METHODS: Adults with E. coli bloodstream infections (BSI) were prospectively enrolled from 2002 to 2015. All E. coli isolates were genotyped using Multilocus sequence typing (MLST) and underwent crystal violet biofilm...

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Autores principales: Chang, Carolyn, Ruffin, Felicia, Fowler, Vance G, Thaden, Joshua T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254224/
http://dx.doi.org/10.1093/ofid/ofy210.891
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author Chang, Carolyn
Ruffin, Felicia
Fowler, Vance G
Thaden, Joshua T
author_facet Chang, Carolyn
Ruffin, Felicia
Fowler, Vance G
Thaden, Joshua T
author_sort Chang, Carolyn
collection PubMed
description BACKGROUND: The clinical impact of Escherichia coli biofilm formation is unknown. METHODS: Adults with E. coli bloodstream infections (BSI) were prospectively enrolled from 2002 to 2015. All E. coli isolates were genotyped using Multilocus sequence typing (MLST) and underwent crystal violet biofilm formation assay quantified by absorbance at 540 nm (OD540) in triplicate. Associations between biofilm formation and patient/bacterial characteristics were characterized by t-tests and ANOVA tests. RESULTS: Ninety-eight percent (186) of the 189 isolates formed detectable biofilms. Bacterial sequence type (ST) was associated with biofilm formation (P < 0.001), as ST73 (average OD(540) = 0.017) and ST393 (average OD(540) = 0.016) had higher average biofilm formation while ST69 (average OD(540) = 0.007) and ST405 (average OD(540) = 0.002) had lower biofilm formation. E. coli isolates with non-multidrug-resistant (non-MDR) phenotype were associated with increased biofilm formation (MDR: average OD(540) = 0.006; average non-MDR: OD(540) = 0.01; P = 0.003). BSI isolates arising from pneumonia or urine/pyelonephritis were associated with the highest biofilm production (P = 0.04). No associations were identified between biofilm formation and route of infection, APACHE-II score, mortality, or complications of BSI. CONCLUSION: In this prospective study of E. coli BSI isolates, biofilm formation was associated with ST, non-MDR phenotype, and BSI source. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62542242018-11-28 1054. Biofilm Formation Among Escherichia coli Bloodstream Infection Isolates Is Associated With Source of Bacteremia and Bacterial Sequence Type Chang, Carolyn Ruffin, Felicia Fowler, Vance G Thaden, Joshua T Open Forum Infect Dis Abstracts BACKGROUND: The clinical impact of Escherichia coli biofilm formation is unknown. METHODS: Adults with E. coli bloodstream infections (BSI) were prospectively enrolled from 2002 to 2015. All E. coli isolates were genotyped using Multilocus sequence typing (MLST) and underwent crystal violet biofilm formation assay quantified by absorbance at 540 nm (OD540) in triplicate. Associations between biofilm formation and patient/bacterial characteristics were characterized by t-tests and ANOVA tests. RESULTS: Ninety-eight percent (186) of the 189 isolates formed detectable biofilms. Bacterial sequence type (ST) was associated with biofilm formation (P < 0.001), as ST73 (average OD(540) = 0.017) and ST393 (average OD(540) = 0.016) had higher average biofilm formation while ST69 (average OD(540) = 0.007) and ST405 (average OD(540) = 0.002) had lower biofilm formation. E. coli isolates with non-multidrug-resistant (non-MDR) phenotype were associated with increased biofilm formation (MDR: average OD(540) = 0.006; average non-MDR: OD(540) = 0.01; P = 0.003). BSI isolates arising from pneumonia or urine/pyelonephritis were associated with the highest biofilm production (P = 0.04). No associations were identified between biofilm formation and route of infection, APACHE-II score, mortality, or complications of BSI. CONCLUSION: In this prospective study of E. coli BSI isolates, biofilm formation was associated with ST, non-MDR phenotype, and BSI source. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6254224/ http://dx.doi.org/10.1093/ofid/ofy210.891 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Chang, Carolyn
Ruffin, Felicia
Fowler, Vance G
Thaden, Joshua T
1054. Biofilm Formation Among Escherichia coli Bloodstream Infection Isolates Is Associated With Source of Bacteremia and Bacterial Sequence Type
title 1054. Biofilm Formation Among Escherichia coli Bloodstream Infection Isolates Is Associated With Source of Bacteremia and Bacterial Sequence Type
title_full 1054. Biofilm Formation Among Escherichia coli Bloodstream Infection Isolates Is Associated With Source of Bacteremia and Bacterial Sequence Type
title_fullStr 1054. Biofilm Formation Among Escherichia coli Bloodstream Infection Isolates Is Associated With Source of Bacteremia and Bacterial Sequence Type
title_full_unstemmed 1054. Biofilm Formation Among Escherichia coli Bloodstream Infection Isolates Is Associated With Source of Bacteremia and Bacterial Sequence Type
title_short 1054. Biofilm Formation Among Escherichia coli Bloodstream Infection Isolates Is Associated With Source of Bacteremia and Bacterial Sequence Type
title_sort 1054. biofilm formation among escherichia coli bloodstream infection isolates is associated with source of bacteremia and bacterial sequence type
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254224/
http://dx.doi.org/10.1093/ofid/ofy210.891
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