Cargando…

Benzalkonium chloride antagonises aminoglycoside antibiotics and promotes evolution of resistance

BACKGROUND: Biocide disinfectants are essential tools in infection control, but their use can inadvertently contribute to emergence of antibiotic-resistant bacteria. In this study we systematically examine the effect of the biocide benzalkonium chloride, which is primarily used for surface disinfect...

Descripción completa

Detalles Bibliográficos
Autores principales: Short, Francesca L, Lee, Victor, Mamun, Rafa, Malmberg, Robert, Li, Liping, Espinosa, Monica I, Venkatesan, Koushik, Paulsen, Ian T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577336/
https://www.ncbi.nlm.nih.gov/pubmed/34717227
http://dx.doi.org/10.1016/j.ebiom.2021.103653
_version_ 1784596047467642880
author Short, Francesca L
Lee, Victor
Mamun, Rafa
Malmberg, Robert
Li, Liping
Espinosa, Monica I
Venkatesan, Koushik
Paulsen, Ian T
author_facet Short, Francesca L
Lee, Victor
Mamun, Rafa
Malmberg, Robert
Li, Liping
Espinosa, Monica I
Venkatesan, Koushik
Paulsen, Ian T
author_sort Short, Francesca L
collection PubMed
description BACKGROUND: Biocide disinfectants are essential tools in infection control, but their use can inadvertently contribute to emergence of antibiotic-resistant bacteria. In this study we systematically examine the effect of the biocide benzalkonium chloride, which is primarily used for surface disinfection but is also present as a preservative in many consumer products, on the activity of aminoglycoside antibiotics in Acinetobacter baumannii. METHODS: The effect of subinhibitory BAC on aminoglycoside treatment of A. baumannii ATCC17978 was investigated using time-to-kill assays, MIC determination, directed evolution experiments, fluctuation tests and labelled gentamicin accumulation assays. Further MIC determinations and directed evolution experiments were performed with additional Gram-negative ESKAPE pathogens. FINDINGS: In A. baumannii ATCC17978, BAC prevents gentamicin killing and drastically increases the frequency at which resistant mutants emerge, through reducing intracellular antibiotic accumulation. BAC also increases the MIC of multiple aminoglycoside antibiotics (kanamycin, tobramycin, streptomycin, gentamicin and amikacin). BAC promotes the emergence of mutants with reduced gentamicin susceptibility in other Gram-negative ESKAPE pathogens but does not always alter the MIC. These effects occur at BAC concentrations which are similar to residual levels in high-use environments, and just below the concentration range for BAC when used as a preservative in eye drops and ear drops. INTERPRETATION: Our results suggest that subinhibitory BAC has the potential to antagonise aminoglycoside activity and promote the emergence of bacterial mutants with reduced susceptibility. We suggest that the extremely widespread use of BAC in clinical and home settings and its long half-life mean there is potential for these interactions to occur in the environment, or in patients who use BAC-containing products while taking aminoglycosides to treat skin, eye or ear infections, although such co-exposure is likely to be rare. We suggest that biocide stewardship is needed to prevent the types of exposure that can contribute to antibiotic resistance. FUNDING: This work was funded by the National Health and Medical Research Council of Australia. The funders had no role in study design, interpretation or decision to publish.
format Online
Article
Text
id pubmed-8577336
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-85773362021-11-12 Benzalkonium chloride antagonises aminoglycoside antibiotics and promotes evolution of resistance Short, Francesca L Lee, Victor Mamun, Rafa Malmberg, Robert Li, Liping Espinosa, Monica I Venkatesan, Koushik Paulsen, Ian T EBioMedicine Research Paper BACKGROUND: Biocide disinfectants are essential tools in infection control, but their use can inadvertently contribute to emergence of antibiotic-resistant bacteria. In this study we systematically examine the effect of the biocide benzalkonium chloride, which is primarily used for surface disinfection but is also present as a preservative in many consumer products, on the activity of aminoglycoside antibiotics in Acinetobacter baumannii. METHODS: The effect of subinhibitory BAC on aminoglycoside treatment of A. baumannii ATCC17978 was investigated using time-to-kill assays, MIC determination, directed evolution experiments, fluctuation tests and labelled gentamicin accumulation assays. Further MIC determinations and directed evolution experiments were performed with additional Gram-negative ESKAPE pathogens. FINDINGS: In A. baumannii ATCC17978, BAC prevents gentamicin killing and drastically increases the frequency at which resistant mutants emerge, through reducing intracellular antibiotic accumulation. BAC also increases the MIC of multiple aminoglycoside antibiotics (kanamycin, tobramycin, streptomycin, gentamicin and amikacin). BAC promotes the emergence of mutants with reduced gentamicin susceptibility in other Gram-negative ESKAPE pathogens but does not always alter the MIC. These effects occur at BAC concentrations which are similar to residual levels in high-use environments, and just below the concentration range for BAC when used as a preservative in eye drops and ear drops. INTERPRETATION: Our results suggest that subinhibitory BAC has the potential to antagonise aminoglycoside activity and promote the emergence of bacterial mutants with reduced susceptibility. We suggest that the extremely widespread use of BAC in clinical and home settings and its long half-life mean there is potential for these interactions to occur in the environment, or in patients who use BAC-containing products while taking aminoglycosides to treat skin, eye or ear infections, although such co-exposure is likely to be rare. We suggest that biocide stewardship is needed to prevent the types of exposure that can contribute to antibiotic resistance. FUNDING: This work was funded by the National Health and Medical Research Council of Australia. The funders had no role in study design, interpretation or decision to publish. Elsevier 2021-10-28 /pmc/articles/PMC8577336/ /pubmed/34717227 http://dx.doi.org/10.1016/j.ebiom.2021.103653 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Short, Francesca L
Lee, Victor
Mamun, Rafa
Malmberg, Robert
Li, Liping
Espinosa, Monica I
Venkatesan, Koushik
Paulsen, Ian T
Benzalkonium chloride antagonises aminoglycoside antibiotics and promotes evolution of resistance
title Benzalkonium chloride antagonises aminoglycoside antibiotics and promotes evolution of resistance
title_full Benzalkonium chloride antagonises aminoglycoside antibiotics and promotes evolution of resistance
title_fullStr Benzalkonium chloride antagonises aminoglycoside antibiotics and promotes evolution of resistance
title_full_unstemmed Benzalkonium chloride antagonises aminoglycoside antibiotics and promotes evolution of resistance
title_short Benzalkonium chloride antagonises aminoglycoside antibiotics and promotes evolution of resistance
title_sort benzalkonium chloride antagonises aminoglycoside antibiotics and promotes evolution of resistance
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577336/
https://www.ncbi.nlm.nih.gov/pubmed/34717227
http://dx.doi.org/10.1016/j.ebiom.2021.103653
work_keys_str_mv AT shortfrancescal benzalkoniumchlorideantagonisesaminoglycosideantibioticsandpromotesevolutionofresistance
AT leevictor benzalkoniumchlorideantagonisesaminoglycosideantibioticsandpromotesevolutionofresistance
AT mamunrafa benzalkoniumchlorideantagonisesaminoglycosideantibioticsandpromotesevolutionofresistance
AT malmbergrobert benzalkoniumchlorideantagonisesaminoglycosideantibioticsandpromotesevolutionofresistance
AT liliping benzalkoniumchlorideantagonisesaminoglycosideantibioticsandpromotesevolutionofresistance
AT espinosamonicai benzalkoniumchlorideantagonisesaminoglycosideantibioticsandpromotesevolutionofresistance
AT benzalkoniumchlorideantagonisesaminoglycosideantibioticsandpromotesevolutionofresistance
AT venkatesankoushik benzalkoniumchlorideantagonisesaminoglycosideantibioticsandpromotesevolutionofresistance
AT paulseniant benzalkoniumchlorideantagonisesaminoglycosideantibioticsandpromotesevolutionofresistance