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In Vitro Synergism of Colistin and N-acetylcysteine against Stenotrophomonas maltophilia
Stenotrophomonas maltophilia is an emerging global opportunistic pathogen, responsible for a wide range of human infections, including respiratory tract infections. Intrinsic multidrug resistance and propensity to form biofilms make S. maltophilia infections recalcitrant to treatment. Colistin is am...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784201/ https://www.ncbi.nlm.nih.gov/pubmed/31349560 http://dx.doi.org/10.3390/antibiotics8030101 |
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author | Ciacci, Nagaia Boncompagni, Selene Valzano, Felice Cariani, Lisa Aliberti, Stefano Blasi, Francesco Pollini, Simona Rossolini, Gian Maria Pallecchi, Lucia |
author_facet | Ciacci, Nagaia Boncompagni, Selene Valzano, Felice Cariani, Lisa Aliberti, Stefano Blasi, Francesco Pollini, Simona Rossolini, Gian Maria Pallecchi, Lucia |
author_sort | Ciacci, Nagaia |
collection | PubMed |
description | Stenotrophomonas maltophilia is an emerging global opportunistic pathogen, responsible for a wide range of human infections, including respiratory tract infections. Intrinsic multidrug resistance and propensity to form biofilms make S. maltophilia infections recalcitrant to treatment. Colistin is among the second-line options in case of difficult-to-treat S. maltophilia infections, with the advantage of being also administrable by nebulization. We investigated the potential synergism of colistin in combination with N-acetylcysteine (NAC) (a mucolytic agent with antioxidant and anti-inflammatory properties) against S. maltophilia grown in planktonic phase and biofilm. Eighteen S. maltophilia clinical isolates (comprising three isolates from cystic fibrosis (CF) and two trimethoprim-sulfamethoxazole (SXT)-resistant strains) were included. Checkerboard assays showed a synergism of colistin/NAC combinations against the strains with colistin Minimum Inhibitory Concentration (MIC) >2 µg/mL (n = 13), suggesting that NAC could antagonize the mechanisms involved in colistin resistance. Nonetheless, time–kill assays revealed that NAC might potentiate colistin activity also in case of lower colistin MICs. A dose-dependent potentiation of colistin activity by NAC was also clearly observed against S. maltophilia biofilms, also at sub-MIC concentrations. Colistin/NAC combinations, at concentrations likely achievable by topical administration, might represent a valid option for the treatment of S. maltophilia respiratory infections and should be examined further. |
format | Online Article Text |
id | pubmed-6784201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67842012019-10-16 In Vitro Synergism of Colistin and N-acetylcysteine against Stenotrophomonas maltophilia Ciacci, Nagaia Boncompagni, Selene Valzano, Felice Cariani, Lisa Aliberti, Stefano Blasi, Francesco Pollini, Simona Rossolini, Gian Maria Pallecchi, Lucia Antibiotics (Basel) Article Stenotrophomonas maltophilia is an emerging global opportunistic pathogen, responsible for a wide range of human infections, including respiratory tract infections. Intrinsic multidrug resistance and propensity to form biofilms make S. maltophilia infections recalcitrant to treatment. Colistin is among the second-line options in case of difficult-to-treat S. maltophilia infections, with the advantage of being also administrable by nebulization. We investigated the potential synergism of colistin in combination with N-acetylcysteine (NAC) (a mucolytic agent with antioxidant and anti-inflammatory properties) against S. maltophilia grown in planktonic phase and biofilm. Eighteen S. maltophilia clinical isolates (comprising three isolates from cystic fibrosis (CF) and two trimethoprim-sulfamethoxazole (SXT)-resistant strains) were included. Checkerboard assays showed a synergism of colistin/NAC combinations against the strains with colistin Minimum Inhibitory Concentration (MIC) >2 µg/mL (n = 13), suggesting that NAC could antagonize the mechanisms involved in colistin resistance. Nonetheless, time–kill assays revealed that NAC might potentiate colistin activity also in case of lower colistin MICs. A dose-dependent potentiation of colistin activity by NAC was also clearly observed against S. maltophilia biofilms, also at sub-MIC concentrations. Colistin/NAC combinations, at concentrations likely achievable by topical administration, might represent a valid option for the treatment of S. maltophilia respiratory infections and should be examined further. MDPI 2019-07-25 /pmc/articles/PMC6784201/ /pubmed/31349560 http://dx.doi.org/10.3390/antibiotics8030101 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ciacci, Nagaia Boncompagni, Selene Valzano, Felice Cariani, Lisa Aliberti, Stefano Blasi, Francesco Pollini, Simona Rossolini, Gian Maria Pallecchi, Lucia In Vitro Synergism of Colistin and N-acetylcysteine against Stenotrophomonas maltophilia |
title | In Vitro Synergism of Colistin and N-acetylcysteine against Stenotrophomonas maltophilia |
title_full | In Vitro Synergism of Colistin and N-acetylcysteine against Stenotrophomonas maltophilia |
title_fullStr | In Vitro Synergism of Colistin and N-acetylcysteine against Stenotrophomonas maltophilia |
title_full_unstemmed | In Vitro Synergism of Colistin and N-acetylcysteine against Stenotrophomonas maltophilia |
title_short | In Vitro Synergism of Colistin and N-acetylcysteine against Stenotrophomonas maltophilia |
title_sort | in vitro synergism of colistin and n-acetylcysteine against stenotrophomonas maltophilia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784201/ https://www.ncbi.nlm.nih.gov/pubmed/31349560 http://dx.doi.org/10.3390/antibiotics8030101 |
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