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Bactericidal mechanisms and effector targets of TiO((2)) and Ag-TiO((2)) against Staphylococcus aureus
PURPOSE: In our previous study, Ag(+)-loaded TiO(2) and Ag(+)-loaded SiO(2) coatings for tracheal intubation were prepared to prevent ventilator-associated pneumonia (VAP), but the antimicrobial targets and the underlying mechanisms of TiO(2) and Ag-TiO(2) (Ag(+)) are still unclear. We attempted to...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817198/ https://www.ncbi.nlm.nih.gov/pubmed/28463658 http://dx.doi.org/10.1099/jmm.0.000457 |
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author | Jiang, Xuhong Lv, Bin Wang, Yuan Shen, Qianhong Wang, Xinmin |
author_facet | Jiang, Xuhong Lv, Bin Wang, Yuan Shen, Qianhong Wang, Xinmin |
author_sort | Jiang, Xuhong |
collection | PubMed |
description | PURPOSE: In our previous study, Ag(+)-loaded TiO(2) and Ag(+)-loaded SiO(2) coatings for tracheal intubation were prepared to prevent ventilator-associated pneumonia (VAP), but the antimicrobial targets and the underlying mechanisms of TiO(2) and Ag-TiO(2) (Ag(+)) are still unclear. We attempted to elucidate the antimicrobial activity and potential mechanisms against Staphylococcus aureus. METHODOLOGY: The study tested the TiO(2) and Ag(+) bacteriostatic activity against S. aureus strains by MIC assays and S. aureus growth curves, lesion in the membranes by surface hydrophobicity tests, conductivity tests and measurements of DNA and RNA contents in S. aureus cultures, and investigated the inhibition of soluble protein and nucleic acid synthesis by measurements of soluble protein content, fluorescent intensity and nucleic acid content of living S. aureus. RESULTS: The MIC values of TiO(2) and Ag(+) were 1.6 mg ml(−1) and 5.781 µg ml(−1). TiO(2) and Ag(+) could inhibit the growth of S. aureus. After treatment with TiO(2) and Ag(+), the surface hydrophobicity was significantly reduced, the conductivity of cultures increased, and DNA and RNA content in cultures showed no obvious changes. The expressions of soluble proteins and nucleic acid contents of living S. aureus were reduced after treatment with TiO(2) and Ag(+). CONCLUSION: TiO(2) and Ag(+) could cause slight lesion in the membrane to affect S. aureus membrane permeability, but not decomposition of membrane. Moreover, TiO(2) and Ag(+) could lead to reduced expression of soluble protein by inhibiting the synthesis of nucleic acids, thereby further inhibiting the growth of S. aureus. |
format | Online Article Text |
id | pubmed-5817198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-58171982018-02-20 Bactericidal mechanisms and effector targets of TiO((2)) and Ag-TiO((2)) against Staphylococcus aureus Jiang, Xuhong Lv, Bin Wang, Yuan Shen, Qianhong Wang, Xinmin J Med Microbiol Research Article PURPOSE: In our previous study, Ag(+)-loaded TiO(2) and Ag(+)-loaded SiO(2) coatings for tracheal intubation were prepared to prevent ventilator-associated pneumonia (VAP), but the antimicrobial targets and the underlying mechanisms of TiO(2) and Ag-TiO(2) (Ag(+)) are still unclear. We attempted to elucidate the antimicrobial activity and potential mechanisms against Staphylococcus aureus. METHODOLOGY: The study tested the TiO(2) and Ag(+) bacteriostatic activity against S. aureus strains by MIC assays and S. aureus growth curves, lesion in the membranes by surface hydrophobicity tests, conductivity tests and measurements of DNA and RNA contents in S. aureus cultures, and investigated the inhibition of soluble protein and nucleic acid synthesis by measurements of soluble protein content, fluorescent intensity and nucleic acid content of living S. aureus. RESULTS: The MIC values of TiO(2) and Ag(+) were 1.6 mg ml(−1) and 5.781 µg ml(−1). TiO(2) and Ag(+) could inhibit the growth of S. aureus. After treatment with TiO(2) and Ag(+), the surface hydrophobicity was significantly reduced, the conductivity of cultures increased, and DNA and RNA content in cultures showed no obvious changes. The expressions of soluble proteins and nucleic acid contents of living S. aureus were reduced after treatment with TiO(2) and Ag(+). CONCLUSION: TiO(2) and Ag(+) could cause slight lesion in the membrane to affect S. aureus membrane permeability, but not decomposition of membrane. Moreover, TiO(2) and Ag(+) could lead to reduced expression of soluble protein by inhibiting the synthesis of nucleic acids, thereby further inhibiting the growth of S. aureus. Microbiology Society 2017-04 2017-04-28 /pmc/articles/PMC5817198/ /pubmed/28463658 http://dx.doi.org/10.1099/jmm.0.000457 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article 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 the original author and source are credited. |
spellingShingle | Research Article Jiang, Xuhong Lv, Bin Wang, Yuan Shen, Qianhong Wang, Xinmin Bactericidal mechanisms and effector targets of TiO((2)) and Ag-TiO((2)) against Staphylococcus aureus |
title | Bactericidal mechanisms and effector targets of TiO((2)) and Ag-TiO((2)) against Staphylococcus aureus |
title_full | Bactericidal mechanisms and effector targets of TiO((2)) and Ag-TiO((2)) against Staphylococcus aureus |
title_fullStr | Bactericidal mechanisms and effector targets of TiO((2)) and Ag-TiO((2)) against Staphylococcus aureus |
title_full_unstemmed | Bactericidal mechanisms and effector targets of TiO((2)) and Ag-TiO((2)) against Staphylococcus aureus |
title_short | Bactericidal mechanisms and effector targets of TiO((2)) and Ag-TiO((2)) against Staphylococcus aureus |
title_sort | bactericidal mechanisms and effector targets of tio((2)) and ag-tio((2)) against staphylococcus aureus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817198/ https://www.ncbi.nlm.nih.gov/pubmed/28463658 http://dx.doi.org/10.1099/jmm.0.000457 |
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