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New Insights into the Bacterial Targets of Antimicrobial Blue Light
Antimicrobial blue light (aBL) offers efficacy and safety in treating infections. However, the bacterial targets for aBL are still poorly understood and may be dependent on bacterial species. Here, we investigated the biological targets of bacterial killing by aBL (λ = 410 nm) on three pathogens: St...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101057/ https://www.ncbi.nlm.nih.gov/pubmed/36809152 http://dx.doi.org/10.1128/spectrum.02833-22 |
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author | dos Anjos, Carolina Leanse, Leon G. Ribeiro, Martha S. Sellera, Fábio P. Dropa, Milena Arana-Chavez, Victor E. Lincopan, Nilton Baptista, Maurício S. Pogliani, Fabio C. Dai, Tianhong Sabino, Caetano P. |
author_facet | dos Anjos, Carolina Leanse, Leon G. Ribeiro, Martha S. Sellera, Fábio P. Dropa, Milena Arana-Chavez, Victor E. Lincopan, Nilton Baptista, Maurício S. Pogliani, Fabio C. Dai, Tianhong Sabino, Caetano P. |
author_sort | dos Anjos, Carolina |
collection | PubMed |
description | Antimicrobial blue light (aBL) offers efficacy and safety in treating infections. However, the bacterial targets for aBL are still poorly understood and may be dependent on bacterial species. Here, we investigated the biological targets of bacterial killing by aBL (λ = 410 nm) on three pathogens: Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. Initially, we evaluated the killing kinetics of bacteria exposed to aBL and used this information to calculate the lethal doses (LD) responsible for killing 90 and 99.9% of bacteria. We also quantified endogenous porphyrins and assessed their spatial distribution. We then quantified and suppressed reactive oxygen species (ROS) production in bacteria to investigate their role in bacterial killing by aBL. We also assessed aBL-induced DNA damage, protein carbonylation, lipid peroxidation, and membrane permeability in bacteria. Our data showed that P. aeruginosa was more susceptible to aBL (LD(99.9) = 54.7 J/cm(2)) relative to S. aureus (LD(99.9) = 158.9 J/cm(2)) and E. coli (LD(99.9) = 195 J/cm(2)). P. aeruginosa exhibited the highest concentration of endogenous porphyrins and level of ROS production relative to the other species. However, unlike other species, DNA degradation was not observed in P. aeruginosa. Sublethal doses of blue light (<LD(90)) could damage the cell membrane in Gram-negative species but not in S. aureus. In all bacteria, oxidative damage to bacterial DNA (except P. aeruginosa), proteins, and lipids occurred after high aBL exposures (>LD(99.9)). We conclude that the primary targets of aBL depend on the species, which are probably driven by variable antioxidant and DNA-repair mechanisms. IMPORTANCE Antimicrobial-drug development is facing increased scrutiny following the worldwide antibiotic crisis. Scientists across the world have recognized the urgent need for new antimicrobial therapies. In this sense, antimicrobial blue light (aBL) is a promising option due to its antimicrobial properties. Although aBL can damage different cell structures, the targets responsible for bacterial inactivation have still not been completely established and require further exploration. In our study, we conducted a thorough investigation to identify the possible aBL targets and gain insights into the bactericidal effects of aBL on three relevant pathogens: Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. This research not only adds new content to blue light studies but opens new perspectives to antimicrobial applications. |
format | Online Article Text |
id | pubmed-10101057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-101010572023-04-14 New Insights into the Bacterial Targets of Antimicrobial Blue Light dos Anjos, Carolina Leanse, Leon G. Ribeiro, Martha S. Sellera, Fábio P. Dropa, Milena Arana-Chavez, Victor E. Lincopan, Nilton Baptista, Maurício S. Pogliani, Fabio C. Dai, Tianhong Sabino, Caetano P. Microbiol Spectr Research Article Antimicrobial blue light (aBL) offers efficacy and safety in treating infections. However, the bacterial targets for aBL are still poorly understood and may be dependent on bacterial species. Here, we investigated the biological targets of bacterial killing by aBL (λ = 410 nm) on three pathogens: Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. Initially, we evaluated the killing kinetics of bacteria exposed to aBL and used this information to calculate the lethal doses (LD) responsible for killing 90 and 99.9% of bacteria. We also quantified endogenous porphyrins and assessed their spatial distribution. We then quantified and suppressed reactive oxygen species (ROS) production in bacteria to investigate their role in bacterial killing by aBL. We also assessed aBL-induced DNA damage, protein carbonylation, lipid peroxidation, and membrane permeability in bacteria. Our data showed that P. aeruginosa was more susceptible to aBL (LD(99.9) = 54.7 J/cm(2)) relative to S. aureus (LD(99.9) = 158.9 J/cm(2)) and E. coli (LD(99.9) = 195 J/cm(2)). P. aeruginosa exhibited the highest concentration of endogenous porphyrins and level of ROS production relative to the other species. However, unlike other species, DNA degradation was not observed in P. aeruginosa. Sublethal doses of blue light (<LD(90)) could damage the cell membrane in Gram-negative species but not in S. aureus. In all bacteria, oxidative damage to bacterial DNA (except P. aeruginosa), proteins, and lipids occurred after high aBL exposures (>LD(99.9)). We conclude that the primary targets of aBL depend on the species, which are probably driven by variable antioxidant and DNA-repair mechanisms. IMPORTANCE Antimicrobial-drug development is facing increased scrutiny following the worldwide antibiotic crisis. Scientists across the world have recognized the urgent need for new antimicrobial therapies. In this sense, antimicrobial blue light (aBL) is a promising option due to its antimicrobial properties. Although aBL can damage different cell structures, the targets responsible for bacterial inactivation have still not been completely established and require further exploration. In our study, we conducted a thorough investigation to identify the possible aBL targets and gain insights into the bactericidal effects of aBL on three relevant pathogens: Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. This research not only adds new content to blue light studies but opens new perspectives to antimicrobial applications. American Society for Microbiology 2023-02-21 /pmc/articles/PMC10101057/ /pubmed/36809152 http://dx.doi.org/10.1128/spectrum.02833-22 Text en Copyright © 2023 dos Anjos 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 | Research Article dos Anjos, Carolina Leanse, Leon G. Ribeiro, Martha S. Sellera, Fábio P. Dropa, Milena Arana-Chavez, Victor E. Lincopan, Nilton Baptista, Maurício S. Pogliani, Fabio C. Dai, Tianhong Sabino, Caetano P. New Insights into the Bacterial Targets of Antimicrobial Blue Light |
title | New Insights into the Bacterial Targets of Antimicrobial Blue Light |
title_full | New Insights into the Bacterial Targets of Antimicrobial Blue Light |
title_fullStr | New Insights into the Bacterial Targets of Antimicrobial Blue Light |
title_full_unstemmed | New Insights into the Bacterial Targets of Antimicrobial Blue Light |
title_short | New Insights into the Bacterial Targets of Antimicrobial Blue Light |
title_sort | new insights into the bacterial targets of antimicrobial blue light |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101057/ https://www.ncbi.nlm.nih.gov/pubmed/36809152 http://dx.doi.org/10.1128/spectrum.02833-22 |
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