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Multiple Bactericidal Mechanisms of the Zinc Ionophore PBT2

Globally, more antimicrobials are used in food-producing animals than in humans, and the extensive use of medically important human antimicrobials poses a significant public health threat in the face of rising antimicrobial resistance (AMR). The development of novel ionophores, a class of antimicrob...

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Autores principales: Harbison-Price, Nichaela, Ferguson, Scott A., Heikal, Adam, Taiaroa, George, Hards, Kiel, Nakatani, Yoshio, Rennison, David, Brimble, Margaret A., El-Deeb, Ibrahim M., Bohlmann, Lisa, McDevitt, Christopher A., von Itzstein, Mark, Walker, Mark J., Cook, Gregory M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082140/
https://www.ncbi.nlm.nih.gov/pubmed/32188750
http://dx.doi.org/10.1128/mSphere.00157-20
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author Harbison-Price, Nichaela
Ferguson, Scott A.
Heikal, Adam
Taiaroa, George
Hards, Kiel
Nakatani, Yoshio
Rennison, David
Brimble, Margaret A.
El-Deeb, Ibrahim M.
Bohlmann, Lisa
McDevitt, Christopher A.
von Itzstein, Mark
Walker, Mark J.
Cook, Gregory M.
author_facet Harbison-Price, Nichaela
Ferguson, Scott A.
Heikal, Adam
Taiaroa, George
Hards, Kiel
Nakatani, Yoshio
Rennison, David
Brimble, Margaret A.
El-Deeb, Ibrahim M.
Bohlmann, Lisa
McDevitt, Christopher A.
von Itzstein, Mark
Walker, Mark J.
Cook, Gregory M.
author_sort Harbison-Price, Nichaela
collection PubMed
description Globally, more antimicrobials are used in food-producing animals than in humans, and the extensive use of medically important human antimicrobials poses a significant public health threat in the face of rising antimicrobial resistance (AMR). The development of novel ionophores, a class of antimicrobials used exclusively in animals, holds promise as a strategy to replace or reduce essential human antimicrobials in veterinary practice. PBT2 is a zinc ionophore with recently demonstrated antibacterial activity against several Gram-positive pathogens, although the underlying mechanism of action is unknown. Here, we investigated the bactericidal mechanism of PBT2 in the bovine mastitis-causing pathogen, Streptococcus uberis. In this work, we show that PBT2 functions as a Zn(2+)/H(+) ionophore, exchanging extracellular zinc for intracellular protons in an electroneutral process that leads to cellular zinc accumulation. Zinc accumulation occurs concomitantly with manganese depletion and the production of reactive oxygen species (ROS). PBT2 inhibits the activity of the manganese-dependent superoxide dismutase, SodA, thereby impairing oxidative stress protection. We propose that PBT2-mediated intracellular zinc toxicity in S. uberis leads to lethality through multiple bactericidal mechanisms: the production of toxic ROS and the impairment of manganese-dependent antioxidant functions. Collectively, these data show that PBT2 represents a new class of antibacterial ionophores capable of targeting bacterial metal ion homeostasis and cellular redox balance. We propose that this novel and multitarget mechanism of PBT2 makes the development of cross-resistance to medically important antimicrobials unlikely. IMPORTANCE More antimicrobials are used in food-producing animals than in humans, and the extensive use of medically important human antimicrobials poses a significant public health threat in the face of rising antimicrobial resistance. Therefore, the elimination of antimicrobial crossover between human and veterinary medicine is of great interest. Unfortunately, the development of new antimicrobials is an expensive high-risk process fraught with difficulties. The repurposing of chemical agents provides a solution to this problem, and while many have not been originally developed as antimicrobials, they have been proven safe in clinical trials. PBT2, a zinc ionophore, is an experimental therapeutic that met safety criteria but failed efficacy checkpoints against both Alzheimer’s and Huntington’s diseases. It was recently found that PBT2 possessed potent antimicrobial activity, although the mechanism of bacterial cell death is unresolved. In this body of work, we show that PBT2 has multiple mechanisms of antimicrobial action, making the development of PBT2 resistance unlikely.
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spelling pubmed-70821402020-04-02 Multiple Bactericidal Mechanisms of the Zinc Ionophore PBT2 Harbison-Price, Nichaela Ferguson, Scott A. Heikal, Adam Taiaroa, George Hards, Kiel Nakatani, Yoshio Rennison, David Brimble, Margaret A. El-Deeb, Ibrahim M. Bohlmann, Lisa McDevitt, Christopher A. von Itzstein, Mark Walker, Mark J. Cook, Gregory M. mSphere Research Article Globally, more antimicrobials are used in food-producing animals than in humans, and the extensive use of medically important human antimicrobials poses a significant public health threat in the face of rising antimicrobial resistance (AMR). The development of novel ionophores, a class of antimicrobials used exclusively in animals, holds promise as a strategy to replace or reduce essential human antimicrobials in veterinary practice. PBT2 is a zinc ionophore with recently demonstrated antibacterial activity against several Gram-positive pathogens, although the underlying mechanism of action is unknown. Here, we investigated the bactericidal mechanism of PBT2 in the bovine mastitis-causing pathogen, Streptococcus uberis. In this work, we show that PBT2 functions as a Zn(2+)/H(+) ionophore, exchanging extracellular zinc for intracellular protons in an electroneutral process that leads to cellular zinc accumulation. Zinc accumulation occurs concomitantly with manganese depletion and the production of reactive oxygen species (ROS). PBT2 inhibits the activity of the manganese-dependent superoxide dismutase, SodA, thereby impairing oxidative stress protection. We propose that PBT2-mediated intracellular zinc toxicity in S. uberis leads to lethality through multiple bactericidal mechanisms: the production of toxic ROS and the impairment of manganese-dependent antioxidant functions. Collectively, these data show that PBT2 represents a new class of antibacterial ionophores capable of targeting bacterial metal ion homeostasis and cellular redox balance. We propose that this novel and multitarget mechanism of PBT2 makes the development of cross-resistance to medically important antimicrobials unlikely. IMPORTANCE More antimicrobials are used in food-producing animals than in humans, and the extensive use of medically important human antimicrobials poses a significant public health threat in the face of rising antimicrobial resistance. Therefore, the elimination of antimicrobial crossover between human and veterinary medicine is of great interest. Unfortunately, the development of new antimicrobials is an expensive high-risk process fraught with difficulties. The repurposing of chemical agents provides a solution to this problem, and while many have not been originally developed as antimicrobials, they have been proven safe in clinical trials. PBT2, a zinc ionophore, is an experimental therapeutic that met safety criteria but failed efficacy checkpoints against both Alzheimer’s and Huntington’s diseases. It was recently found that PBT2 possessed potent antimicrobial activity, although the mechanism of bacterial cell death is unresolved. In this body of work, we show that PBT2 has multiple mechanisms of antimicrobial action, making the development of PBT2 resistance unlikely. American Society for Microbiology 2020-03-18 /pmc/articles/PMC7082140/ /pubmed/32188750 http://dx.doi.org/10.1128/mSphere.00157-20 Text en Copyright © 2020 Harbison-Price 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
Harbison-Price, Nichaela
Ferguson, Scott A.
Heikal, Adam
Taiaroa, George
Hards, Kiel
Nakatani, Yoshio
Rennison, David
Brimble, Margaret A.
El-Deeb, Ibrahim M.
Bohlmann, Lisa
McDevitt, Christopher A.
von Itzstein, Mark
Walker, Mark J.
Cook, Gregory M.
Multiple Bactericidal Mechanisms of the Zinc Ionophore PBT2
title Multiple Bactericidal Mechanisms of the Zinc Ionophore PBT2
title_full Multiple Bactericidal Mechanisms of the Zinc Ionophore PBT2
title_fullStr Multiple Bactericidal Mechanisms of the Zinc Ionophore PBT2
title_full_unstemmed Multiple Bactericidal Mechanisms of the Zinc Ionophore PBT2
title_short Multiple Bactericidal Mechanisms of the Zinc Ionophore PBT2
title_sort multiple bactericidal mechanisms of the zinc ionophore pbt2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082140/
https://www.ncbi.nlm.nih.gov/pubmed/32188750
http://dx.doi.org/10.1128/mSphere.00157-20
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