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Inactivation of dried cells and biofilms of Listeria monocytogenes by exposure to blue light at different wavelengths and the influence of surface materials
Antimicrobial blue light (aBL) in the 400–470 nm wavelength range has been reported to kill multiple bacteria. This study assessed its potential for mitigating an important foodborne pathogen, Listeria monocytogenes (Lm), focusing on surface decontamination. Three wavelengths were tested, with galli...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617584/ https://www.ncbi.nlm.nih.gov/pubmed/37846990 http://dx.doi.org/10.1128/aem.01147-23 |
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author | Olszewska, Magdalena A. Dev Kumar, Govindaraj Hur, Minji Diez-Gonzalez, Francisco |
author_facet | Olszewska, Magdalena A. Dev Kumar, Govindaraj Hur, Minji Diez-Gonzalez, Francisco |
author_sort | Olszewska, Magdalena A. |
collection | PubMed |
description | Antimicrobial blue light (aBL) in the 400–470 nm wavelength range has been reported to kill multiple bacteria. This study assessed its potential for mitigating an important foodborne pathogen, Listeria monocytogenes (Lm), focusing on surface decontamination. Three wavelengths were tested, with gallic acid as a photosensitizing agent (Ps), against dried cells obtained from bacterial suspensions, and biofilms on stainless-steel (SS) coupons. Following aBL exposure, standard microbiological analysis of inoculated coupons was conducted to measure viability. Statistical analysis of variance was performed. Confocal laser scanning microscopy was used to observe the biofilm structures. Within 16 h of exposure at 405 nm, viable Lm dried cells and biofilms were reduced by approx. 3 log CFU/cm(2) with doses of 2,672 J/cm(2). Application of Ps resulted in an additional 1 log CFU/cm(2) at 668 J/cm(2), but its effect was not consistent. The highest dose (960 J/cm(2)) at 420 nm reduced viable counts on the biofilms by 1.9 log CFU/cm(2). At 460 nm, after 800 J/cm(2), biofilm counts were reduced by 1.6 log CFU/cm(2). The effect of material composition on Lm viability was also investigated. Irradiation at 405 nm (668 J/cm(2)) of cells dried on polystyrene resulted in one of the largest viability reductions (4.0 log CFU/cm(2)), followed by high-density polyethylene (3.5 log CFU/cm(2)). Increasing the dose to 4,008 J/cm(2) from 405 nm (24 h), improved its efficacy only on SS and polyvinyl chloride. Biofilm micrographs displayed a decrease in biofilm biomass due to the removal of biofilm portions from the surface and a shift from live to dead cells suggesting damage to biofilm cell membranes. These results suggest that aBL is a potential intervention to treat Lm contamination on typical material surfaces used in food production. IMPORTANCE: Current cleaning and sanitation programs are often not capable of controlling pathogen biofilms on equipment surfaces, which transmit the bacteria to ready-to-eat foods. The presence of native plant microbiota and organic matter can protect pathogenic bacteria by reducing the efficacy of sanitizers as well as promoting biofilm formation. Post-operation washing and sanitizing of produce contact surfaces might not be adequate in eliminating the presence of pathogens and commensal bacteria. The use of a dynamic and harmless light technology during downtime and close of operation could serve as a useful tool in preventing biofilm formation and persistence. Antimicrobial blue light (aBL) technology has been explored for hospital disinfection with very promising results, but its application to control foodborne pathogens remains relatively limited. The use of aBL could be a complementary strategy to inactivate surfaces in restaurant or supermarket deli settings. |
format | Online Article Text |
id | pubmed-10617584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-106175842023-11-01 Inactivation of dried cells and biofilms of Listeria monocytogenes by exposure to blue light at different wavelengths and the influence of surface materials Olszewska, Magdalena A. Dev Kumar, Govindaraj Hur, Minji Diez-Gonzalez, Francisco Appl Environ Microbiol Food Microbiology Antimicrobial blue light (aBL) in the 400–470 nm wavelength range has been reported to kill multiple bacteria. This study assessed its potential for mitigating an important foodborne pathogen, Listeria monocytogenes (Lm), focusing on surface decontamination. Three wavelengths were tested, with gallic acid as a photosensitizing agent (Ps), against dried cells obtained from bacterial suspensions, and biofilms on stainless-steel (SS) coupons. Following aBL exposure, standard microbiological analysis of inoculated coupons was conducted to measure viability. Statistical analysis of variance was performed. Confocal laser scanning microscopy was used to observe the biofilm structures. Within 16 h of exposure at 405 nm, viable Lm dried cells and biofilms were reduced by approx. 3 log CFU/cm(2) with doses of 2,672 J/cm(2). Application of Ps resulted in an additional 1 log CFU/cm(2) at 668 J/cm(2), but its effect was not consistent. The highest dose (960 J/cm(2)) at 420 nm reduced viable counts on the biofilms by 1.9 log CFU/cm(2). At 460 nm, after 800 J/cm(2), biofilm counts were reduced by 1.6 log CFU/cm(2). The effect of material composition on Lm viability was also investigated. Irradiation at 405 nm (668 J/cm(2)) of cells dried on polystyrene resulted in one of the largest viability reductions (4.0 log CFU/cm(2)), followed by high-density polyethylene (3.5 log CFU/cm(2)). Increasing the dose to 4,008 J/cm(2) from 405 nm (24 h), improved its efficacy only on SS and polyvinyl chloride. Biofilm micrographs displayed a decrease in biofilm biomass due to the removal of biofilm portions from the surface and a shift from live to dead cells suggesting damage to biofilm cell membranes. These results suggest that aBL is a potential intervention to treat Lm contamination on typical material surfaces used in food production. IMPORTANCE: Current cleaning and sanitation programs are often not capable of controlling pathogen biofilms on equipment surfaces, which transmit the bacteria to ready-to-eat foods. The presence of native plant microbiota and organic matter can protect pathogenic bacteria by reducing the efficacy of sanitizers as well as promoting biofilm formation. Post-operation washing and sanitizing of produce contact surfaces might not be adequate in eliminating the presence of pathogens and commensal bacteria. The use of a dynamic and harmless light technology during downtime and close of operation could serve as a useful tool in preventing biofilm formation and persistence. Antimicrobial blue light (aBL) technology has been explored for hospital disinfection with very promising results, but its application to control foodborne pathogens remains relatively limited. The use of aBL could be a complementary strategy to inactivate surfaces in restaurant or supermarket deli settings. American Society for Microbiology 2023-10-17 /pmc/articles/PMC10617584/ /pubmed/37846990 http://dx.doi.org/10.1128/aem.01147-23 Text en Copyright © 2023 Olszewska et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Food Microbiology Olszewska, Magdalena A. Dev Kumar, Govindaraj Hur, Minji Diez-Gonzalez, Francisco Inactivation of dried cells and biofilms of Listeria monocytogenes by exposure to blue light at different wavelengths and the influence of surface materials |
title | Inactivation of dried cells and biofilms of Listeria monocytogenes by exposure to blue light at different wavelengths and the influence of surface materials |
title_full | Inactivation of dried cells and biofilms of Listeria monocytogenes by exposure to blue light at different wavelengths and the influence of surface materials |
title_fullStr | Inactivation of dried cells and biofilms of Listeria monocytogenes by exposure to blue light at different wavelengths and the influence of surface materials |
title_full_unstemmed | Inactivation of dried cells and biofilms of Listeria monocytogenes by exposure to blue light at different wavelengths and the influence of surface materials |
title_short | Inactivation of dried cells and biofilms of Listeria monocytogenes by exposure to blue light at different wavelengths and the influence of surface materials |
title_sort | inactivation of dried cells and biofilms of listeria monocytogenes by exposure to blue light at different wavelengths and the influence of surface materials |
topic | Food Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617584/ https://www.ncbi.nlm.nih.gov/pubmed/37846990 http://dx.doi.org/10.1128/aem.01147-23 |
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