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Validating a screening agar for linezolid-resistant enterococci

BACKGROUND: Linezolid is an alternative treatment option for infections with multidrug-resistant Gram-positive bacteria including vancomycin-resistant enterococci. Some countries report an increasing number of isolates with resistance to linezolid. The recent publication of the Commission for Hospit...

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Autores principales: Werner, Guido, Fleige, Carola, Klare, Ingo, Weber, Robert E., Bender, Jennifer K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929501/
https://www.ncbi.nlm.nih.gov/pubmed/31870418
http://dx.doi.org/10.1186/s12879-019-4711-y
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author Werner, Guido
Fleige, Carola
Klare, Ingo
Weber, Robert E.
Bender, Jennifer K.
author_facet Werner, Guido
Fleige, Carola
Klare, Ingo
Weber, Robert E.
Bender, Jennifer K.
author_sort Werner, Guido
collection PubMed
description BACKGROUND: Linezolid is an alternative treatment option for infections with multidrug-resistant Gram-positive bacteria including vancomycin-resistant enterococci. Some countries report an increasing number of isolates with resistance to linezolid. The recent publication of the Commission for Hospital Hygiene in Germany on enterococci/VRE recommends screening for linezolid-resistant enterococci (LRE). However, a suitable selective medium or a genetic test is not available. Our aim was to establish a selective screening agar for LRE detection and validate its application with a comprehensive collection of clinical LRE and linezolid-susceptible enterococci. METHODS: We decided to combine the selective power of an enterococcal screening agar with a supplementation of linezolid. Several rounds of analyses with reference, control and test strains and under varying linezolid concentrations of a wider and a smaller range were investigated and assessed. The collection of linezolid-resistant enterococcal control strains included isolates with different resistance mechanisms (23S rDNA mutations, cfr(B), optrA, poxtA). Finally, we validated our LRE screening agar with 400 samples sent to our National Reference Centre in 2019. RESULTS: Several rounds of pre-tests and confirmatory analyses favored Enterococcosel® Agar supplemented with a concentration of 2 mg/L linezolid. A 48 h incubation period was essential for accurate identification of LRE strains. Performance of the LRE screening agar revealed a sensitivity of 96.6% and a specificity of 94.4%. CONCLUSIONS: Here we describe preparation of a suitable screening agar and a procedure to identify LRE isolates with high accuracy.
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spelling pubmed-69295012019-12-30 Validating a screening agar for linezolid-resistant enterococci Werner, Guido Fleige, Carola Klare, Ingo Weber, Robert E. Bender, Jennifer K. BMC Infect Dis Technical Advance BACKGROUND: Linezolid is an alternative treatment option for infections with multidrug-resistant Gram-positive bacteria including vancomycin-resistant enterococci. Some countries report an increasing number of isolates with resistance to linezolid. The recent publication of the Commission for Hospital Hygiene in Germany on enterococci/VRE recommends screening for linezolid-resistant enterococci (LRE). However, a suitable selective medium or a genetic test is not available. Our aim was to establish a selective screening agar for LRE detection and validate its application with a comprehensive collection of clinical LRE and linezolid-susceptible enterococci. METHODS: We decided to combine the selective power of an enterococcal screening agar with a supplementation of linezolid. Several rounds of analyses with reference, control and test strains and under varying linezolid concentrations of a wider and a smaller range were investigated and assessed. The collection of linezolid-resistant enterococcal control strains included isolates with different resistance mechanisms (23S rDNA mutations, cfr(B), optrA, poxtA). Finally, we validated our LRE screening agar with 400 samples sent to our National Reference Centre in 2019. RESULTS: Several rounds of pre-tests and confirmatory analyses favored Enterococcosel® Agar supplemented with a concentration of 2 mg/L linezolid. A 48 h incubation period was essential for accurate identification of LRE strains. Performance of the LRE screening agar revealed a sensitivity of 96.6% and a specificity of 94.4%. CONCLUSIONS: Here we describe preparation of a suitable screening agar and a procedure to identify LRE isolates with high accuracy. BioMed Central 2019-12-23 /pmc/articles/PMC6929501/ /pubmed/31870418 http://dx.doi.org/10.1186/s12879-019-4711-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Technical Advance
Werner, Guido
Fleige, Carola
Klare, Ingo
Weber, Robert E.
Bender, Jennifer K.
Validating a screening agar for linezolid-resistant enterococci
title Validating a screening agar for linezolid-resistant enterococci
title_full Validating a screening agar for linezolid-resistant enterococci
title_fullStr Validating a screening agar for linezolid-resistant enterococci
title_full_unstemmed Validating a screening agar for linezolid-resistant enterococci
title_short Validating a screening agar for linezolid-resistant enterococci
title_sort validating a screening agar for linezolid-resistant enterococci
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929501/
https://www.ncbi.nlm.nih.gov/pubmed/31870418
http://dx.doi.org/10.1186/s12879-019-4711-y
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