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Association between cell growth and vancomycin resistance in clinical community-associated methicillin-resistant Staphylococcus aureus

OBJECTIVES: We investigated the association between the rate of cell growth and vancomycin (VAN) resistance by comparing the genomic and phenotypic characteristics of different sized colonies isolated from a single origin. METHODS: Vancomycin-intermediate Staphylococcus aureus (VISA) strain TMUS2136...

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Autores principales: Yamaguchi, Tetsuo, Ando, Rina, Matsumoto, Tetsuya, Ishii, Yoshikazu, Tateda, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682180/
https://www.ncbi.nlm.nih.gov/pubmed/31534353
http://dx.doi.org/10.2147/IDR.S209591
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author Yamaguchi, Tetsuo
Ando, Rina
Matsumoto, Tetsuya
Ishii, Yoshikazu
Tateda, Kazuhiro
author_facet Yamaguchi, Tetsuo
Ando, Rina
Matsumoto, Tetsuya
Ishii, Yoshikazu
Tateda, Kazuhiro
author_sort Yamaguchi, Tetsuo
collection PubMed
description OBJECTIVES: We investigated the association between the rate of cell growth and vancomycin (VAN) resistance by comparing the genomic and phenotypic characteristics of different sized colonies isolated from a single origin. METHODS: Vancomycin-intermediate Staphylococcus aureus (VISA) strain TMUS2136 was isolated from the pus of a patient with a brain abscess and a chronic subdural abscess. This strain grew slowly and formed colonies poorly on agar plates within 24 h of incubation. However, variously sized colonies were observed after 48 h of incubation. We isolated five strains from different sized colonies and compared their VAN susceptibility and genomic sequences using next-generation sequencing. RESULTS: The five strains showed different rates of growth and susceptibilities to VAN (range of MIC after 48 h of incubation; 3–5 mg/L), and slower growing strains tended to be more VAN resistant. Deletion of the spdC gene and SNPs in the sarA gene was confirmed in all five strains and six SNPs in other genes (including mreC, hssS, prs, SA2339, sun, and SA1132) were confirmed when comparing the five strains. CONCLUSIONS: Deletion of the spdC gene, a novel virulence factor of S. aureus, and SNPs in the sarA gene may be associated with VAN resistance. It was hypothesized that any of the six genes in which SNPs were detected could affect cell growth rate and VAN resistance in slow-VISA strains.
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spelling pubmed-66821802019-09-18 Association between cell growth and vancomycin resistance in clinical community-associated methicillin-resistant Staphylococcus aureus Yamaguchi, Tetsuo Ando, Rina Matsumoto, Tetsuya Ishii, Yoshikazu Tateda, Kazuhiro Infect Drug Resist Original Research OBJECTIVES: We investigated the association between the rate of cell growth and vancomycin (VAN) resistance by comparing the genomic and phenotypic characteristics of different sized colonies isolated from a single origin. METHODS: Vancomycin-intermediate Staphylococcus aureus (VISA) strain TMUS2136 was isolated from the pus of a patient with a brain abscess and a chronic subdural abscess. This strain grew slowly and formed colonies poorly on agar plates within 24 h of incubation. However, variously sized colonies were observed after 48 h of incubation. We isolated five strains from different sized colonies and compared their VAN susceptibility and genomic sequences using next-generation sequencing. RESULTS: The five strains showed different rates of growth and susceptibilities to VAN (range of MIC after 48 h of incubation; 3–5 mg/L), and slower growing strains tended to be more VAN resistant. Deletion of the spdC gene and SNPs in the sarA gene was confirmed in all five strains and six SNPs in other genes (including mreC, hssS, prs, SA2339, sun, and SA1132) were confirmed when comparing the five strains. CONCLUSIONS: Deletion of the spdC gene, a novel virulence factor of S. aureus, and SNPs in the sarA gene may be associated with VAN resistance. It was hypothesized that any of the six genes in which SNPs were detected could affect cell growth rate and VAN resistance in slow-VISA strains. Dove 2019-08-01 /pmc/articles/PMC6682180/ /pubmed/31534353 http://dx.doi.org/10.2147/IDR.S209591 Text en © 2019 Yamaguchi 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
Yamaguchi, Tetsuo
Ando, Rina
Matsumoto, Tetsuya
Ishii, Yoshikazu
Tateda, Kazuhiro
Association between cell growth and vancomycin resistance in clinical community-associated methicillin-resistant Staphylococcus aureus
title Association between cell growth and vancomycin resistance in clinical community-associated methicillin-resistant Staphylococcus aureus
title_full Association between cell growth and vancomycin resistance in clinical community-associated methicillin-resistant Staphylococcus aureus
title_fullStr Association between cell growth and vancomycin resistance in clinical community-associated methicillin-resistant Staphylococcus aureus
title_full_unstemmed Association between cell growth and vancomycin resistance in clinical community-associated methicillin-resistant Staphylococcus aureus
title_short Association between cell growth and vancomycin resistance in clinical community-associated methicillin-resistant Staphylococcus aureus
title_sort association between cell growth and vancomycin resistance in clinical community-associated methicillin-resistant staphylococcus aureus
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682180/
https://www.ncbi.nlm.nih.gov/pubmed/31534353
http://dx.doi.org/10.2147/IDR.S209591
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