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Influence of Cationic meso-Substituted Porphyrins on the Antimicrobial Photodynamic Efficacy and Cell Membrane Interaction in Escherichia coli

Photodynamic inactivation (PDI) is a non-antibiotic option for the treatment of infectious diseases. Although Gram-positive bacteria have been shown to be highly susceptible to PDI, the inactivation of Gram-negative bacteria has been more challenging due to the impermeability properties of the outer...

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Autores principales: Hurst, Alexandra N., Scarbrough, Beth, Saleh, Roa, Hovey, Jessica, Ari, Farideh, Goyal, Shreya, Chi, Richard J., Troutman, Jerry M., Vivero-Escoto, Juan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337135/
https://www.ncbi.nlm.nih.gov/pubmed/30609680
http://dx.doi.org/10.3390/ijms20010134
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author Hurst, Alexandra N.
Scarbrough, Beth
Saleh, Roa
Hovey, Jessica
Ari, Farideh
Goyal, Shreya
Chi, Richard J.
Troutman, Jerry M.
Vivero-Escoto, Juan L.
author_facet Hurst, Alexandra N.
Scarbrough, Beth
Saleh, Roa
Hovey, Jessica
Ari, Farideh
Goyal, Shreya
Chi, Richard J.
Troutman, Jerry M.
Vivero-Escoto, Juan L.
author_sort Hurst, Alexandra N.
collection PubMed
description Photodynamic inactivation (PDI) is a non-antibiotic option for the treatment of infectious diseases. Although Gram-positive bacteria have been shown to be highly susceptible to PDI, the inactivation of Gram-negative bacteria has been more challenging due to the impermeability properties of the outer membrane. In the present study, a series of photosensitizers which contain one to four positive charges (1–4) were used to evaluate the charge influence on the PDI of a Gram-negative bacteria, Escherichia coli (E. coli), and their interaction with the cell membrane. The dose-response PDI results confirm the relevance of the number of positive charges on the porphyrin molecule in the PDI of E. coli. The difference between the Hill coefficients of cationic porphyrins with 1–3 positive charges and the tetra-cationic porphyrin (4) revealed potential variations in their mechanism of inactivation. Fluorescent live-cell microscopy studies showed that cationic porphyrins with 1–3 positive charges bind to the cell membrane of E. coli, but are not internalized. On the contrary, the tetra-cationic porphyrin (4) permeates through the membrane of the cells. The contrast in the interaction of cationic porphyrins with E. coli confirmed that they followed different mechanisms of inactivation. This work helps to have a better understanding of the structure-activity relationship in the efficiency of the PDI process of cationic porphyrins against Gram-negative bacteria.
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spelling pubmed-63371352019-01-22 Influence of Cationic meso-Substituted Porphyrins on the Antimicrobial Photodynamic Efficacy and Cell Membrane Interaction in Escherichia coli Hurst, Alexandra N. Scarbrough, Beth Saleh, Roa Hovey, Jessica Ari, Farideh Goyal, Shreya Chi, Richard J. Troutman, Jerry M. Vivero-Escoto, Juan L. Int J Mol Sci Article Photodynamic inactivation (PDI) is a non-antibiotic option for the treatment of infectious diseases. Although Gram-positive bacteria have been shown to be highly susceptible to PDI, the inactivation of Gram-negative bacteria has been more challenging due to the impermeability properties of the outer membrane. In the present study, a series of photosensitizers which contain one to four positive charges (1–4) were used to evaluate the charge influence on the PDI of a Gram-negative bacteria, Escherichia coli (E. coli), and their interaction with the cell membrane. The dose-response PDI results confirm the relevance of the number of positive charges on the porphyrin molecule in the PDI of E. coli. The difference between the Hill coefficients of cationic porphyrins with 1–3 positive charges and the tetra-cationic porphyrin (4) revealed potential variations in their mechanism of inactivation. Fluorescent live-cell microscopy studies showed that cationic porphyrins with 1–3 positive charges bind to the cell membrane of E. coli, but are not internalized. On the contrary, the tetra-cationic porphyrin (4) permeates through the membrane of the cells. The contrast in the interaction of cationic porphyrins with E. coli confirmed that they followed different mechanisms of inactivation. This work helps to have a better understanding of the structure-activity relationship in the efficiency of the PDI process of cationic porphyrins against Gram-negative bacteria. MDPI 2019-01-01 /pmc/articles/PMC6337135/ /pubmed/30609680 http://dx.doi.org/10.3390/ijms20010134 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hurst, Alexandra N.
Scarbrough, Beth
Saleh, Roa
Hovey, Jessica
Ari, Farideh
Goyal, Shreya
Chi, Richard J.
Troutman, Jerry M.
Vivero-Escoto, Juan L.
Influence of Cationic meso-Substituted Porphyrins on the Antimicrobial Photodynamic Efficacy and Cell Membrane Interaction in Escherichia coli
title Influence of Cationic meso-Substituted Porphyrins on the Antimicrobial Photodynamic Efficacy and Cell Membrane Interaction in Escherichia coli
title_full Influence of Cationic meso-Substituted Porphyrins on the Antimicrobial Photodynamic Efficacy and Cell Membrane Interaction in Escherichia coli
title_fullStr Influence of Cationic meso-Substituted Porphyrins on the Antimicrobial Photodynamic Efficacy and Cell Membrane Interaction in Escherichia coli
title_full_unstemmed Influence of Cationic meso-Substituted Porphyrins on the Antimicrobial Photodynamic Efficacy and Cell Membrane Interaction in Escherichia coli
title_short Influence of Cationic meso-Substituted Porphyrins on the Antimicrobial Photodynamic Efficacy and Cell Membrane Interaction in Escherichia coli
title_sort influence of cationic meso-substituted porphyrins on the antimicrobial photodynamic efficacy and cell membrane interaction in escherichia coli
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337135/
https://www.ncbi.nlm.nih.gov/pubmed/30609680
http://dx.doi.org/10.3390/ijms20010134
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