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Relating Antimicrobial Resistance and Virulence in Surface-Water E. coli

The role of the environment in the emergence and spread of antimicrobial resistance (AMR) is being increasingly recognized, raising questions about the public health risks associated with environmental AMR. Yet, little is known about pathogenicity among resistant bacteria in environmental systems. E...

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Autores principales: LaMontagne, Connor D., Christenson, Elizabeth C., Rogers, Anna T., Jacob, Megan E., Stewart, Jill R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673096/
https://www.ncbi.nlm.nih.gov/pubmed/38004659
http://dx.doi.org/10.3390/microorganisms11112647
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author LaMontagne, Connor D.
Christenson, Elizabeth C.
Rogers, Anna T.
Jacob, Megan E.
Stewart, Jill R.
author_facet LaMontagne, Connor D.
Christenson, Elizabeth C.
Rogers, Anna T.
Jacob, Megan E.
Stewart, Jill R.
author_sort LaMontagne, Connor D.
collection PubMed
description The role of the environment in the emergence and spread of antimicrobial resistance (AMR) is being increasingly recognized, raising questions about the public health risks associated with environmental AMR. Yet, little is known about pathogenicity among resistant bacteria in environmental systems. Existing studies on the association between AMR and virulence are contradictory, as fitness costs and genetic co-occurrence can be opposing influences. Using Escherichia coli isolated from surface waters in eastern North Carolina, we compared virulence gene prevalence between isolates resistant and susceptible to antibiotics. We also compared the prevalence of isolates from sub-watersheds with or without commercial hog operations (CHOs). Isolates that had previously been evaluated for phenotypic AMR were paired by matching isolates resistant to any tested antibiotic with fully susceptible isolates from the same sample date and site, forming 87 pairs. These 174 isolates were evaluated by conventional PCR for seven virulence genes (bfp, fimH, cnf-1, STa (estA), EAST-1 (astA), eae, and hlyA). One gene, fimH, was found in 93.1% of isolates. Excluding fimH, at least one virulence gene was detected in 24.7% of isolates. Significant negative associations were found between resistance to at least one antibiotic and presence of at least one virulence gene, tetracycline resistance and presence of a virulence gene, resistance and STa presence, and tetracycline resistance and STa presence. No significant associations were found between CHO presence and virulence, though some sub-significant associations merit further study. This work builds our understanding of factors controlling AMR dissemination through the environment and potential health risks.
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spelling pubmed-106730962023-10-28 Relating Antimicrobial Resistance and Virulence in Surface-Water E. coli LaMontagne, Connor D. Christenson, Elizabeth C. Rogers, Anna T. Jacob, Megan E. Stewart, Jill R. Microorganisms Article The role of the environment in the emergence and spread of antimicrobial resistance (AMR) is being increasingly recognized, raising questions about the public health risks associated with environmental AMR. Yet, little is known about pathogenicity among resistant bacteria in environmental systems. Existing studies on the association between AMR and virulence are contradictory, as fitness costs and genetic co-occurrence can be opposing influences. Using Escherichia coli isolated from surface waters in eastern North Carolina, we compared virulence gene prevalence between isolates resistant and susceptible to antibiotics. We also compared the prevalence of isolates from sub-watersheds with or without commercial hog operations (CHOs). Isolates that had previously been evaluated for phenotypic AMR were paired by matching isolates resistant to any tested antibiotic with fully susceptible isolates from the same sample date and site, forming 87 pairs. These 174 isolates were evaluated by conventional PCR for seven virulence genes (bfp, fimH, cnf-1, STa (estA), EAST-1 (astA), eae, and hlyA). One gene, fimH, was found in 93.1% of isolates. Excluding fimH, at least one virulence gene was detected in 24.7% of isolates. Significant negative associations were found between resistance to at least one antibiotic and presence of at least one virulence gene, tetracycline resistance and presence of a virulence gene, resistance and STa presence, and tetracycline resistance and STa presence. No significant associations were found between CHO presence and virulence, though some sub-significant associations merit further study. This work builds our understanding of factors controlling AMR dissemination through the environment and potential health risks. MDPI 2023-10-28 /pmc/articles/PMC10673096/ /pubmed/38004659 http://dx.doi.org/10.3390/microorganisms11112647 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
LaMontagne, Connor D.
Christenson, Elizabeth C.
Rogers, Anna T.
Jacob, Megan E.
Stewart, Jill R.
Relating Antimicrobial Resistance and Virulence in Surface-Water E. coli
title Relating Antimicrobial Resistance and Virulence in Surface-Water E. coli
title_full Relating Antimicrobial Resistance and Virulence in Surface-Water E. coli
title_fullStr Relating Antimicrobial Resistance and Virulence in Surface-Water E. coli
title_full_unstemmed Relating Antimicrobial Resistance and Virulence in Surface-Water E. coli
title_short Relating Antimicrobial Resistance and Virulence in Surface-Water E. coli
title_sort relating antimicrobial resistance and virulence in surface-water e. coli
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673096/
https://www.ncbi.nlm.nih.gov/pubmed/38004659
http://dx.doi.org/10.3390/microorganisms11112647
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