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Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus

Background: Small-colony variants of methicillin-resistant Staphylococcus aureus (SCV-MRSA) recently were described as slow-growing, thymidine-dependent strains; typically, SCV-MRSA were isolated from patients receiving sulfamethoxazole-trimethoprim, but detection of these strains frequently was del...

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Autores principales: Watanabe, Yuji, Oikawa, Nozomi, Hariu, Maya, Seki, Masafumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593740/
https://www.ncbi.nlm.nih.gov/pubmed/31417291
http://dx.doi.org/10.2147/IDR.S207057
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author Watanabe, Yuji
Oikawa, Nozomi
Hariu, Maya
Seki, Masafumi
author_facet Watanabe, Yuji
Oikawa, Nozomi
Hariu, Maya
Seki, Masafumi
author_sort Watanabe, Yuji
collection PubMed
description Background: Small-colony variants of methicillin-resistant Staphylococcus aureus (SCV-MRSA) recently were described as slow-growing, thymidine-dependent strains; typically, SCV-MRSA were isolated from patients receiving sulfamethoxazole-trimethoprim, but detection of these strains frequently was delayed because of their small colony size and slow growth. Bacteremia cases due to SCV-MRSA sometimes become lethal when the initiation of treatment with intravenous anti-methicillin-resistant Staphylococcus aureus (MRSA) drugs starts too late. Methods: Here, we evaluated the use of general MRSA-specific agar plates in Japan, including MS-CFX, X-MRSA, and CHROMagar, for the efficient detection of SCV-MRSA, including the comparative detection efficiencies of these media for stock strains and clinical isolates. Results: Among the three MRSA-specific agar plates that were tested, X-MRSA and CHROMagar showed similar detection efficiencies for both 24 and 48 hrs culturing; in contrast, MS-CFS did not permit the detection of SCV-MRSA in stock strains. For clinical isolates of SCV-MRSA, X-MRSA plates permitted detection of the smallest and slowest-growing colonies of SCV-MRSA at 48 hrs of culturing; in contrast, CHROMagar and MS-CFX sometimes did not identify SCV-MRSA at 24 and 48 hrs. Conclusion: Optimization of media and incubation times will be necessary for efficient identification for SCV-MRSA, which would prevent delays in diagnosis and treatment with anti-MRSA drugs.
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spelling pubmed-65937402019-08-15 Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus Watanabe, Yuji Oikawa, Nozomi Hariu, Maya Seki, Masafumi Infect Drug Resist Original Research Background: Small-colony variants of methicillin-resistant Staphylococcus aureus (SCV-MRSA) recently were described as slow-growing, thymidine-dependent strains; typically, SCV-MRSA were isolated from patients receiving sulfamethoxazole-trimethoprim, but detection of these strains frequently was delayed because of their small colony size and slow growth. Bacteremia cases due to SCV-MRSA sometimes become lethal when the initiation of treatment with intravenous anti-methicillin-resistant Staphylococcus aureus (MRSA) drugs starts too late. Methods: Here, we evaluated the use of general MRSA-specific agar plates in Japan, including MS-CFX, X-MRSA, and CHROMagar, for the efficient detection of SCV-MRSA, including the comparative detection efficiencies of these media for stock strains and clinical isolates. Results: Among the three MRSA-specific agar plates that were tested, X-MRSA and CHROMagar showed similar detection efficiencies for both 24 and 48 hrs culturing; in contrast, MS-CFS did not permit the detection of SCV-MRSA in stock strains. For clinical isolates of SCV-MRSA, X-MRSA plates permitted detection of the smallest and slowest-growing colonies of SCV-MRSA at 48 hrs of culturing; in contrast, CHROMagar and MS-CFX sometimes did not identify SCV-MRSA at 24 and 48 hrs. Conclusion: Optimization of media and incubation times will be necessary for efficient identification for SCV-MRSA, which would prevent delays in diagnosis and treatment with anti-MRSA drugs. Dove 2019-06-21 /pmc/articles/PMC6593740/ /pubmed/31417291 http://dx.doi.org/10.2147/IDR.S207057 Text en © 2019 Watanabe et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Watanabe, Yuji
Oikawa, Nozomi
Hariu, Maya
Seki, Masafumi
Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus
title Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus
title_full Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus
title_fullStr Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus
title_full_unstemmed Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus
title_short Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus
title_sort evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant staphylococcus aureus
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593740/
https://www.ncbi.nlm.nih.gov/pubmed/31417291
http://dx.doi.org/10.2147/IDR.S207057
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