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Detrimental Effect of Ozone on Pathogenic Bacteria
(1) Background: Disinfection of medical devices designed for clinical use associated or not with the growing area of tissue engineering is an urgent need. However, traditional disinfection methods are not always suitable for some biomaterials, especially those sensitive to chemical, thermal, or radi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779011/ https://www.ncbi.nlm.nih.gov/pubmed/35056489 http://dx.doi.org/10.3390/microorganisms10010040 |
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author | Rangel, Karyne Cabral, Fellipe O. Lechuga, Guilherme C. Carvalho, João P. R. S. Villas-Bôas, Maria H. S. Midlej, Victor De-Simone, Salvatore G. |
author_facet | Rangel, Karyne Cabral, Fellipe O. Lechuga, Guilherme C. Carvalho, João P. R. S. Villas-Bôas, Maria H. S. Midlej, Victor De-Simone, Salvatore G. |
author_sort | Rangel, Karyne |
collection | PubMed |
description | (1) Background: Disinfection of medical devices designed for clinical use associated or not with the growing area of tissue engineering is an urgent need. However, traditional disinfection methods are not always suitable for some biomaterials, especially those sensitive to chemical, thermal, or radiation. Therefore, the objective of this study was to evaluate the minimal concentration of ozone gas (O(3)) necessary to control and kill a set of sensitive or multi-resistant Gram-positive and Gram-negative bacteria. The cell viability, membrane permeability, and the levels of reactive intracellular oxygen (ROS) species were also investigated; (2) Material and Methods: Four standard strains and a clinical MDR strain were exposed to low doses of ozone at different concentrations and times. Bacterial inactivation (cultivability, membrane damage) was investigated using colony counts, resazurin as a metabolic indicator, and propidium iodide (PI). A fluorescent probe (H(2)DCFDA) was used for the ROS analyses; (3) Results: No reduction in the count colony was detected after O(3) exposure compared to the control group. However, the cell viability of E. coli (30%), P. aeruginosa (25%), and A. baumannii (15%) was reduced considerably. The bacterial membrane of all strains was not affected by O(3) but presented a significant increase of ROS in E. coli (90 ± 14%), P. aeruginosa (62.5 ± 19%), and A. baumanni (52.6 ± 5%); (4) Conclusion: Low doses of ozone were able to interfere in the cell viability of most strains studied, and although it does not cause damage to the bacterial membrane, increased levels of reactive ROS are responsible for causing a detrimental effect in the lipids, proteins, and DNA metabolism. |
format | Online Article Text |
id | pubmed-8779011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87790112022-01-22 Detrimental Effect of Ozone on Pathogenic Bacteria Rangel, Karyne Cabral, Fellipe O. Lechuga, Guilherme C. Carvalho, João P. R. S. Villas-Bôas, Maria H. S. Midlej, Victor De-Simone, Salvatore G. Microorganisms Article (1) Background: Disinfection of medical devices designed for clinical use associated or not with the growing area of tissue engineering is an urgent need. However, traditional disinfection methods are not always suitable for some biomaterials, especially those sensitive to chemical, thermal, or radiation. Therefore, the objective of this study was to evaluate the minimal concentration of ozone gas (O(3)) necessary to control and kill a set of sensitive or multi-resistant Gram-positive and Gram-negative bacteria. The cell viability, membrane permeability, and the levels of reactive intracellular oxygen (ROS) species were also investigated; (2) Material and Methods: Four standard strains and a clinical MDR strain were exposed to low doses of ozone at different concentrations and times. Bacterial inactivation (cultivability, membrane damage) was investigated using colony counts, resazurin as a metabolic indicator, and propidium iodide (PI). A fluorescent probe (H(2)DCFDA) was used for the ROS analyses; (3) Results: No reduction in the count colony was detected after O(3) exposure compared to the control group. However, the cell viability of E. coli (30%), P. aeruginosa (25%), and A. baumannii (15%) was reduced considerably. The bacterial membrane of all strains was not affected by O(3) but presented a significant increase of ROS in E. coli (90 ± 14%), P. aeruginosa (62.5 ± 19%), and A. baumanni (52.6 ± 5%); (4) Conclusion: Low doses of ozone were able to interfere in the cell viability of most strains studied, and although it does not cause damage to the bacterial membrane, increased levels of reactive ROS are responsible for causing a detrimental effect in the lipids, proteins, and DNA metabolism. MDPI 2021-12-26 /pmc/articles/PMC8779011/ /pubmed/35056489 http://dx.doi.org/10.3390/microorganisms10010040 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rangel, Karyne Cabral, Fellipe O. Lechuga, Guilherme C. Carvalho, João P. R. S. Villas-Bôas, Maria H. S. Midlej, Victor De-Simone, Salvatore G. Detrimental Effect of Ozone on Pathogenic Bacteria |
title | Detrimental Effect of Ozone on Pathogenic Bacteria |
title_full | Detrimental Effect of Ozone on Pathogenic Bacteria |
title_fullStr | Detrimental Effect of Ozone on Pathogenic Bacteria |
title_full_unstemmed | Detrimental Effect of Ozone on Pathogenic Bacteria |
title_short | Detrimental Effect of Ozone on Pathogenic Bacteria |
title_sort | detrimental effect of ozone on pathogenic bacteria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779011/ https://www.ncbi.nlm.nih.gov/pubmed/35056489 http://dx.doi.org/10.3390/microorganisms10010040 |
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