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In vitro synergistic activity of colistin and teicoplanin combination against multidrug-resistant Acinetobacter spp

Drug combinations may have a crucial role in treating infections due to multidrug resistant Acinetobacter spp. One suggested combination is colistin with teicoplanin. The effect of colistin on Acinetobacter spp. outer membrane can permit teicoplanin to its target in the cell wall. The aim of this st...

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Autores principales: Rady, Osama Mohamed Samy Mohamed, El-Attar, Laila, Amine, Amira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816723/
https://www.ncbi.nlm.nih.gov/pubmed/35091666
http://dx.doi.org/10.1038/s41429-022-00509-7
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author Rady, Osama Mohamed Samy Mohamed
El-Attar, Laila
Amine, Amira
author_facet Rady, Osama Mohamed Samy Mohamed
El-Attar, Laila
Amine, Amira
author_sort Rady, Osama Mohamed Samy Mohamed
collection PubMed
description Drug combinations may have a crucial role in treating infections due to multidrug resistant Acinetobacter spp. One suggested combination is colistin with teicoplanin. The effect of colistin on Acinetobacter spp. outer membrane can permit teicoplanin to its target in the cell wall. The aim of this study was to evaluate the synergistic activity of colistin and teicoplanin combination against 29 multidrug resistant isolates of Acinetobacter spp. The antimicrobial activity of colistin alone and in combination with teicoplanin was assessed using MIC and time–kill assays. The combination of 1 mg/l colistin and 10 mg/l teicoplanin showed in vitro synergism against all tested Acinetobacter isolates except one (Acinetobacter lowffii). The combination of 1 mg/l colistin and 10 mg/l teicoplanin was bactericidal at 6 h against 100% of Acinetobacter baumannii isolates with no bacterial regrowth at 24 h. The same combination was bactericidal against three out of seven non-baumannii Acinetobacter isolates. The increased concentration of teicoplanin (20 mg/l) was synergistic but still not bactericidal against the four remaining isolates. The combination of colistin and teicoplanin was synergistic against all tested Acinetobacter spp It is therefore recommended that clinical trials are conducted to clarify the therapeutic potential of the combination.
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spelling pubmed-88167232022-02-16 In vitro synergistic activity of colistin and teicoplanin combination against multidrug-resistant Acinetobacter spp Rady, Osama Mohamed Samy Mohamed El-Attar, Laila Amine, Amira J Antibiot (Tokyo) Brief Communication Drug combinations may have a crucial role in treating infections due to multidrug resistant Acinetobacter spp. One suggested combination is colistin with teicoplanin. The effect of colistin on Acinetobacter spp. outer membrane can permit teicoplanin to its target in the cell wall. The aim of this study was to evaluate the synergistic activity of colistin and teicoplanin combination against 29 multidrug resistant isolates of Acinetobacter spp. The antimicrobial activity of colistin alone and in combination with teicoplanin was assessed using MIC and time–kill assays. The combination of 1 mg/l colistin and 10 mg/l teicoplanin showed in vitro synergism against all tested Acinetobacter isolates except one (Acinetobacter lowffii). The combination of 1 mg/l colistin and 10 mg/l teicoplanin was bactericidal at 6 h against 100% of Acinetobacter baumannii isolates with no bacterial regrowth at 24 h. The same combination was bactericidal against three out of seven non-baumannii Acinetobacter isolates. The increased concentration of teicoplanin (20 mg/l) was synergistic but still not bactericidal against the four remaining isolates. The combination of colistin and teicoplanin was synergistic against all tested Acinetobacter spp It is therefore recommended that clinical trials are conducted to clarify the therapeutic potential of the combination. Nature Publishing Group UK 2022-01-28 2022 /pmc/articles/PMC8816723/ /pubmed/35091666 http://dx.doi.org/10.1038/s41429-022-00509-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Brief Communication
Rady, Osama Mohamed Samy Mohamed
El-Attar, Laila
Amine, Amira
In vitro synergistic activity of colistin and teicoplanin combination against multidrug-resistant Acinetobacter spp
title In vitro synergistic activity of colistin and teicoplanin combination against multidrug-resistant Acinetobacter spp
title_full In vitro synergistic activity of colistin and teicoplanin combination against multidrug-resistant Acinetobacter spp
title_fullStr In vitro synergistic activity of colistin and teicoplanin combination against multidrug-resistant Acinetobacter spp
title_full_unstemmed In vitro synergistic activity of colistin and teicoplanin combination against multidrug-resistant Acinetobacter spp
title_short In vitro synergistic activity of colistin and teicoplanin combination against multidrug-resistant Acinetobacter spp
title_sort in vitro synergistic activity of colistin and teicoplanin combination against multidrug-resistant acinetobacter spp
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816723/
https://www.ncbi.nlm.nih.gov/pubmed/35091666
http://dx.doi.org/10.1038/s41429-022-00509-7
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