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Novel single-nucleotide variations associated with vancomycin resistance in vancomycin-intermediate Staphylococcus aureus
Prolonged vancomycin usage may cause methicillin-resistant Staphylococcus aureus to become vancomycin-intermediate S. aureus (VISA) and heterogeneous VISA (hVISA). Mechanisms of vancomycin resistance of VISA and hVISA are still unclear. In this study, analyses of nucleotide sequence variations in 30...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783010/ https://www.ncbi.nlm.nih.gov/pubmed/29403293 http://dx.doi.org/10.2147/IDR.S148335 |
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author | Lin, Lee-Chung Chang, Shih-Cheng Ge, Mao-Cheng Liu, Tsui-Ping Lu, Jang-Jih |
author_facet | Lin, Lee-Chung Chang, Shih-Cheng Ge, Mao-Cheng Liu, Tsui-Ping Lu, Jang-Jih |
author_sort | Lin, Lee-Chung |
collection | PubMed |
description | Prolonged vancomycin usage may cause methicillin-resistant Staphylococcus aureus to become vancomycin-intermediate S. aureus (VISA) and heterogeneous VISA (hVISA). Mechanisms of vancomycin resistance of VISA and hVISA are still unclear. In this study, analyses of nucleotide sequence variations in 30 vancomycin-sensitive S. aureus (VSSA), 41 hVISA and 16 VISA isolates revealed 29 single-nucleotide variations in 12 genes (fmtC, graR, graS, htrA, mecA, pbp2, pbp4, srtA, tcaA, upps, vicK and vraR) that are related to cell wall synthesis or the two-component system. Six of these 29 single-nucleotide variations were novel and resulted in the following amino acid changes: Q692E in FmtC; T278I, P306L and I311T in HtrA; and I63V and K101E in Upps. Since P306L and I311T in HtrA and I63V in Upps were present in the majority (76.7%–86.7%) of VSSA isolates, these three amino acid variations may not be associated with vancomycin resistance. The other three amino acid variations (T278I in HtrA, K101E in Upps and Q692E in FmtC) were present in the majority (87.5%–93.8%) of hVISA and VISA isolates, but only in a small number (22.9%–25.7%) of VSSA isolates, suggesting that they are associated with vancomycin resistance. |
format | Online Article Text |
id | pubmed-5783010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57830102018-02-05 Novel single-nucleotide variations associated with vancomycin resistance in vancomycin-intermediate Staphylococcus aureus Lin, Lee-Chung Chang, Shih-Cheng Ge, Mao-Cheng Liu, Tsui-Ping Lu, Jang-Jih Infect Drug Resist Original Research Prolonged vancomycin usage may cause methicillin-resistant Staphylococcus aureus to become vancomycin-intermediate S. aureus (VISA) and heterogeneous VISA (hVISA). Mechanisms of vancomycin resistance of VISA and hVISA are still unclear. In this study, analyses of nucleotide sequence variations in 30 vancomycin-sensitive S. aureus (VSSA), 41 hVISA and 16 VISA isolates revealed 29 single-nucleotide variations in 12 genes (fmtC, graR, graS, htrA, mecA, pbp2, pbp4, srtA, tcaA, upps, vicK and vraR) that are related to cell wall synthesis or the two-component system. Six of these 29 single-nucleotide variations were novel and resulted in the following amino acid changes: Q692E in FmtC; T278I, P306L and I311T in HtrA; and I63V and K101E in Upps. Since P306L and I311T in HtrA and I63V in Upps were present in the majority (76.7%–86.7%) of VSSA isolates, these three amino acid variations may not be associated with vancomycin resistance. The other three amino acid variations (T278I in HtrA, K101E in Upps and Q692E in FmtC) were present in the majority (87.5%–93.8%) of hVISA and VISA isolates, but only in a small number (22.9%–25.7%) of VSSA isolates, suggesting that they are associated with vancomycin resistance. Dove Medical Press 2018-01-18 /pmc/articles/PMC5783010/ /pubmed/29403293 http://dx.doi.org/10.2147/IDR.S148335 Text en © 2018 Lin et al. 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. |
spellingShingle | Original Research Lin, Lee-Chung Chang, Shih-Cheng Ge, Mao-Cheng Liu, Tsui-Ping Lu, Jang-Jih Novel single-nucleotide variations associated with vancomycin resistance in vancomycin-intermediate Staphylococcus aureus |
title | Novel single-nucleotide variations associated with vancomycin resistance in vancomycin-intermediate Staphylococcus aureus |
title_full | Novel single-nucleotide variations associated with vancomycin resistance in vancomycin-intermediate Staphylococcus aureus |
title_fullStr | Novel single-nucleotide variations associated with vancomycin resistance in vancomycin-intermediate Staphylococcus aureus |
title_full_unstemmed | Novel single-nucleotide variations associated with vancomycin resistance in vancomycin-intermediate Staphylococcus aureus |
title_short | Novel single-nucleotide variations associated with vancomycin resistance in vancomycin-intermediate Staphylococcus aureus |
title_sort | novel single-nucleotide variations associated with vancomycin resistance in vancomycin-intermediate staphylococcus aureus |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783010/ https://www.ncbi.nlm.nih.gov/pubmed/29403293 http://dx.doi.org/10.2147/IDR.S148335 |
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