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Effect of N-Acetylcysteine in Combination with Antibiotics on the Biofilms of Three Cystic Fibrosis Pathogens of Emerging Importance

Cystic fibrosis (CF) is a genetic disorder causing dysfunctional ion transport resulting in accumulation of viscous mucus that fosters chronic bacterial biofilm-associated infection in the airways. Achromobacter xylosoxidans and Stenotrophomonas maltophilia are increasingly prevalent CF pathogens an...

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Autores principales: Aiyer, Aditi, Visser, Simone K., Bye, Peter, Britton, Warwick J., Whiteley, Gregory S., Glasbey, Trevor, Kriel, Frederik H., Farrell, Jessica, Das, Theerthankar, Manos, Jim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8532722/
https://www.ncbi.nlm.nih.gov/pubmed/34680757
http://dx.doi.org/10.3390/antibiotics10101176
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author Aiyer, Aditi
Visser, Simone K.
Bye, Peter
Britton, Warwick J.
Whiteley, Gregory S.
Glasbey, Trevor
Kriel, Frederik H.
Farrell, Jessica
Das, Theerthankar
Manos, Jim
author_facet Aiyer, Aditi
Visser, Simone K.
Bye, Peter
Britton, Warwick J.
Whiteley, Gregory S.
Glasbey, Trevor
Kriel, Frederik H.
Farrell, Jessica
Das, Theerthankar
Manos, Jim
author_sort Aiyer, Aditi
collection PubMed
description Cystic fibrosis (CF) is a genetic disorder causing dysfunctional ion transport resulting in accumulation of viscous mucus that fosters chronic bacterial biofilm-associated infection in the airways. Achromobacter xylosoxidans and Stenotrophomonas maltophilia are increasingly prevalent CF pathogens and while Burkholderia cencocepacia is slowly decreasing; all are complicated by multidrug resistance that is enhanced by biofilm formation. This study investigates potential synergy between the antibiotics ciprofloxacin (0.5–128 µg/mL), colistin (0.5–128 µg/mL) and tobramycin (0.5–128 µg/mL) when combined with the neutral pH form of N-Acetylcysteine (NAC(neutral)) (0.5–16.3 mg/mL) against 11 cystic fibrosis strains of Burkholderia, Stenotrophomonas and Achromobacter sp. in planktonic and biofilm cultures. We screened for potential synergism using checkerboard assays from which fraction inhibitory concentration indices (FICI) were calculated. Synergistic (FICI ≤ 0.5) and additive (0.5 > FICI ≥ 1) combinations were tested on irreversibly attached bacteria and 48 h mature biofilms via time-course and colony forming units (CFU/mL) assays. This study suggests that planktonic FICI analysis does not necessarily translate to reduction in bacterial loads in a biofilm model. Future directions include refining synergy testing and determining further mechanisms of action of NAC to understand how it may interact with antibiotics to better predict synergy.
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spelling pubmed-85327222021-10-23 Effect of N-Acetylcysteine in Combination with Antibiotics on the Biofilms of Three Cystic Fibrosis Pathogens of Emerging Importance Aiyer, Aditi Visser, Simone K. Bye, Peter Britton, Warwick J. Whiteley, Gregory S. Glasbey, Trevor Kriel, Frederik H. Farrell, Jessica Das, Theerthankar Manos, Jim Antibiotics (Basel) Article Cystic fibrosis (CF) is a genetic disorder causing dysfunctional ion transport resulting in accumulation of viscous mucus that fosters chronic bacterial biofilm-associated infection in the airways. Achromobacter xylosoxidans and Stenotrophomonas maltophilia are increasingly prevalent CF pathogens and while Burkholderia cencocepacia is slowly decreasing; all are complicated by multidrug resistance that is enhanced by biofilm formation. This study investigates potential synergy between the antibiotics ciprofloxacin (0.5–128 µg/mL), colistin (0.5–128 µg/mL) and tobramycin (0.5–128 µg/mL) when combined with the neutral pH form of N-Acetylcysteine (NAC(neutral)) (0.5–16.3 mg/mL) against 11 cystic fibrosis strains of Burkholderia, Stenotrophomonas and Achromobacter sp. in planktonic and biofilm cultures. We screened for potential synergism using checkerboard assays from which fraction inhibitory concentration indices (FICI) were calculated. Synergistic (FICI ≤ 0.5) and additive (0.5 > FICI ≥ 1) combinations were tested on irreversibly attached bacteria and 48 h mature biofilms via time-course and colony forming units (CFU/mL) assays. This study suggests that planktonic FICI analysis does not necessarily translate to reduction in bacterial loads in a biofilm model. Future directions include refining synergy testing and determining further mechanisms of action of NAC to understand how it may interact with antibiotics to better predict synergy. MDPI 2021-09-27 /pmc/articles/PMC8532722/ /pubmed/34680757 http://dx.doi.org/10.3390/antibiotics10101176 Text en © 2021 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
Aiyer, Aditi
Visser, Simone K.
Bye, Peter
Britton, Warwick J.
Whiteley, Gregory S.
Glasbey, Trevor
Kriel, Frederik H.
Farrell, Jessica
Das, Theerthankar
Manos, Jim
Effect of N-Acetylcysteine in Combination with Antibiotics on the Biofilms of Three Cystic Fibrosis Pathogens of Emerging Importance
title Effect of N-Acetylcysteine in Combination with Antibiotics on the Biofilms of Three Cystic Fibrosis Pathogens of Emerging Importance
title_full Effect of N-Acetylcysteine in Combination with Antibiotics on the Biofilms of Three Cystic Fibrosis Pathogens of Emerging Importance
title_fullStr Effect of N-Acetylcysteine in Combination with Antibiotics on the Biofilms of Three Cystic Fibrosis Pathogens of Emerging Importance
title_full_unstemmed Effect of N-Acetylcysteine in Combination with Antibiotics on the Biofilms of Three Cystic Fibrosis Pathogens of Emerging Importance
title_short Effect of N-Acetylcysteine in Combination with Antibiotics on the Biofilms of Three Cystic Fibrosis Pathogens of Emerging Importance
title_sort effect of n-acetylcysteine in combination with antibiotics on the biofilms of three cystic fibrosis pathogens of emerging importance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8532722/
https://www.ncbi.nlm.nih.gov/pubmed/34680757
http://dx.doi.org/10.3390/antibiotics10101176
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