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Pilot Screening to Determine Antimicrobial Synergies in a Multidrug-Resistant Bacterial Strain Library

With the rise in multidrug-resistant (MDR) bacterial infections, there has been increasing interest in combinations of ≥2 antimicrobial agents with synergistic effects. We established an MDR bacterial strain library to screen for in vitro antimicrobial synergy by using a broth microdilution checkerb...

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Autores principales: Kim, Si-Hyun, Park, Chulmin, Chun, Hye-Sun, Lee, Dong-Gun, Choi, Jae-Ki, Lee, Hyo-Jin, Cho, Sung-Yeon, Park, Sun Hee, Choi, Su-Mi, Choi, Jung-Hyun, Yoo, Jin-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939386/
https://www.ncbi.nlm.nih.gov/pubmed/26974861
http://dx.doi.org/10.1089/mdr.2015.0251
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author Kim, Si-Hyun
Park, Chulmin
Chun, Hye-Sun
Lee, Dong-Gun
Choi, Jae-Ki
Lee, Hyo-Jin
Cho, Sung-Yeon
Park, Sun Hee
Choi, Su-Mi
Choi, Jung-Hyun
Yoo, Jin-Hong
author_facet Kim, Si-Hyun
Park, Chulmin
Chun, Hye-Sun
Lee, Dong-Gun
Choi, Jae-Ki
Lee, Hyo-Jin
Cho, Sung-Yeon
Park, Sun Hee
Choi, Su-Mi
Choi, Jung-Hyun
Yoo, Jin-Hong
author_sort Kim, Si-Hyun
collection PubMed
description With the rise in multidrug-resistant (MDR) bacterial infections, there has been increasing interest in combinations of ≥2 antimicrobial agents with synergistic effects. We established an MDR bacterial strain library to screen for in vitro antimicrobial synergy by using a broth microdilution checkerboard method and high-throughput luciferase-based bacterial cell viability assay. In total, 39 MDR bacterial strains, including 23 carbapenem-resistant gram-negative bacteria, 9 vancomycin-intermediate Staphylococcus aureus, and 7 vancomycin-resistant Enterococcus faecalis, were used to screen for potential antimicrobial synergies. Synergies were more frequently identified with combinations of imipenem plus trimethoprim–sulfamethoxazole for carbapenem-resistant Acinetobacter baumannii in the library. To verify this finding, we tested 34 A. baumannii clinical isolates resistant to both imipenem and trimethoprim–sulfamethoxazole by the checkerboard method. The imipenem plus trimethoprim–sulfamethoxazole combination showed synergy in the treatment of 21 (62%) of the clinical isolates. The results indicate that pilot screening for antimicrobial synergy in the MDR bacterial strain library could be valuable in the selection of combination therapeutic regimens to treat MDR bacterial infections. Further studies are warranted to determine whether this screening system can be useful to screen for the combined effects of conventional antimicrobials and new-generation antimicrobials or nonantimicrobials.
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spelling pubmed-49393862016-08-05 Pilot Screening to Determine Antimicrobial Synergies in a Multidrug-Resistant Bacterial Strain Library Kim, Si-Hyun Park, Chulmin Chun, Hye-Sun Lee, Dong-Gun Choi, Jae-Ki Lee, Hyo-Jin Cho, Sung-Yeon Park, Sun Hee Choi, Su-Mi Choi, Jung-Hyun Yoo, Jin-Hong Microb Drug Resist Mechanisms With the rise in multidrug-resistant (MDR) bacterial infections, there has been increasing interest in combinations of ≥2 antimicrobial agents with synergistic effects. We established an MDR bacterial strain library to screen for in vitro antimicrobial synergy by using a broth microdilution checkerboard method and high-throughput luciferase-based bacterial cell viability assay. In total, 39 MDR bacterial strains, including 23 carbapenem-resistant gram-negative bacteria, 9 vancomycin-intermediate Staphylococcus aureus, and 7 vancomycin-resistant Enterococcus faecalis, were used to screen for potential antimicrobial synergies. Synergies were more frequently identified with combinations of imipenem plus trimethoprim–sulfamethoxazole for carbapenem-resistant Acinetobacter baumannii in the library. To verify this finding, we tested 34 A. baumannii clinical isolates resistant to both imipenem and trimethoprim–sulfamethoxazole by the checkerboard method. The imipenem plus trimethoprim–sulfamethoxazole combination showed synergy in the treatment of 21 (62%) of the clinical isolates. The results indicate that pilot screening for antimicrobial synergy in the MDR bacterial strain library could be valuable in the selection of combination therapeutic regimens to treat MDR bacterial infections. Further studies are warranted to determine whether this screening system can be useful to screen for the combined effects of conventional antimicrobials and new-generation antimicrobials or nonantimicrobials. Mary Ann Liebert, Inc. 2016-07-01 /pmc/articles/PMC4939386/ /pubmed/26974861 http://dx.doi.org/10.1089/mdr.2015.0251 Text en © Si-Hyun Kim, et al., 2016; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.01/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Mechanisms
Kim, Si-Hyun
Park, Chulmin
Chun, Hye-Sun
Lee, Dong-Gun
Choi, Jae-Ki
Lee, Hyo-Jin
Cho, Sung-Yeon
Park, Sun Hee
Choi, Su-Mi
Choi, Jung-Hyun
Yoo, Jin-Hong
Pilot Screening to Determine Antimicrobial Synergies in a Multidrug-Resistant Bacterial Strain Library
title Pilot Screening to Determine Antimicrobial Synergies in a Multidrug-Resistant Bacterial Strain Library
title_full Pilot Screening to Determine Antimicrobial Synergies in a Multidrug-Resistant Bacterial Strain Library
title_fullStr Pilot Screening to Determine Antimicrobial Synergies in a Multidrug-Resistant Bacterial Strain Library
title_full_unstemmed Pilot Screening to Determine Antimicrobial Synergies in a Multidrug-Resistant Bacterial Strain Library
title_short Pilot Screening to Determine Antimicrobial Synergies in a Multidrug-Resistant Bacterial Strain Library
title_sort pilot screening to determine antimicrobial synergies in a multidrug-resistant bacterial strain library
topic Mechanisms
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939386/
https://www.ncbi.nlm.nih.gov/pubmed/26974861
http://dx.doi.org/10.1089/mdr.2015.0251
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