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The Role of ZntA in Klebsiella pneumoniae Zinc Homeostasis

Klebsiella pneumoniae is an opportunistic Gram-negative pathogen that is a leading cause of healthcare-associated infections, including pneumonia, urinary tract infections, and sepsis. Essential to the colonization and infection by K. pneumoniae is the acquisition of nutrients, such as the transitio...

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Autores principales: Maunders, Eve A., Ganio, Katherine, Hayes, Andrew J., Neville, Stephanie L., Davies, Mark R., Strugnell, Richard A., McDevitt, Christopher A., Tan, Aimee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8754117/
https://www.ncbi.nlm.nih.gov/pubmed/35019689
http://dx.doi.org/10.1128/spectrum.01773-21
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author Maunders, Eve A.
Ganio, Katherine
Hayes, Andrew J.
Neville, Stephanie L.
Davies, Mark R.
Strugnell, Richard A.
McDevitt, Christopher A.
Tan, Aimee
author_facet Maunders, Eve A.
Ganio, Katherine
Hayes, Andrew J.
Neville, Stephanie L.
Davies, Mark R.
Strugnell, Richard A.
McDevitt, Christopher A.
Tan, Aimee
author_sort Maunders, Eve A.
collection PubMed
description Klebsiella pneumoniae is an opportunistic Gram-negative pathogen that is a leading cause of healthcare-associated infections, including pneumonia, urinary tract infections, and sepsis. Essential to the colonization and infection by K. pneumoniae is the acquisition of nutrients, such as the transition metal ion zinc. Zinc has crucial structural and catalytic roles in the proteome of all organisms. Nevertheless, in excess, it has the potential to mediate significant toxicity by dysregulating the homeostasis of other transition elements, disrupting enzymatic processes, and perturbing metalloprotein cofactor acquisition. Here, we sought to elucidate the zinc detoxification mechanisms of K. pneumoniae, which remain poorly defined. Using the representative K. pneumoniae AJ218 strain, we showed that the P-type ATPase, ZntA, which is upregulated in response to cellular zinc stress, was the primary zinc efflux pathway. Deletion of zntA rendered K. pneumoniae AJ218 highly susceptible to exogenous zinc stress and manifested as an impaired growth phenotype and increased cellular accumulation of the metal. Loss of zntA also increased sensitivity to cadmium stress, indicating a role for this efflux pathway in cadmium resistance. Disruption of zinc homeostasis in the K. pneumoniae AJ218 ΔzntA strain also impacted manganese and iron homeostasis and was associated with increased production of biofilm. Collectively, this work showed the critical role of ZntA in K. pneumoniae zinc tolerance and provided a foundation for further studies on zinc homeostasis and the future development of novel antimicrobials to target this pathway. IMPORTANCE Klebsiella pneumoniae is a leading cause of healthcare-associated infections, including pneumonia, urinary tract infections, and sepsis. Treatment of K. pneumoniae infections is becoming increasingly challenging due to high levels of antibiotic resistance and the rising prevalence of carbapenem-resistant, extended-spectrum β-lactamases producing strains. Zinc is essential to the colonization and infection by many bacterial pathogens but toxic in excess. This work described the first dissection of the pathways associated with resisting extracellular zinc stress in K. pneumoniae. This study revealed that the P-type ATPase ZntA was highly upregulated in response to exogenous zinc stress and played a major role in maintaining bacterial metal homeostasis. Knowledge of how this major bacterial pathogen resists zinc stress provided a foundation for antimicrobial development studies to target and abrogate their essential function.
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spelling pubmed-87541172022-01-24 The Role of ZntA in Klebsiella pneumoniae Zinc Homeostasis Maunders, Eve A. Ganio, Katherine Hayes, Andrew J. Neville, Stephanie L. Davies, Mark R. Strugnell, Richard A. McDevitt, Christopher A. Tan, Aimee Microbiol Spectr Research Article Klebsiella pneumoniae is an opportunistic Gram-negative pathogen that is a leading cause of healthcare-associated infections, including pneumonia, urinary tract infections, and sepsis. Essential to the colonization and infection by K. pneumoniae is the acquisition of nutrients, such as the transition metal ion zinc. Zinc has crucial structural and catalytic roles in the proteome of all organisms. Nevertheless, in excess, it has the potential to mediate significant toxicity by dysregulating the homeostasis of other transition elements, disrupting enzymatic processes, and perturbing metalloprotein cofactor acquisition. Here, we sought to elucidate the zinc detoxification mechanisms of K. pneumoniae, which remain poorly defined. Using the representative K. pneumoniae AJ218 strain, we showed that the P-type ATPase, ZntA, which is upregulated in response to cellular zinc stress, was the primary zinc efflux pathway. Deletion of zntA rendered K. pneumoniae AJ218 highly susceptible to exogenous zinc stress and manifested as an impaired growth phenotype and increased cellular accumulation of the metal. Loss of zntA also increased sensitivity to cadmium stress, indicating a role for this efflux pathway in cadmium resistance. Disruption of zinc homeostasis in the K. pneumoniae AJ218 ΔzntA strain also impacted manganese and iron homeostasis and was associated with increased production of biofilm. Collectively, this work showed the critical role of ZntA in K. pneumoniae zinc tolerance and provided a foundation for further studies on zinc homeostasis and the future development of novel antimicrobials to target this pathway. IMPORTANCE Klebsiella pneumoniae is a leading cause of healthcare-associated infections, including pneumonia, urinary tract infections, and sepsis. Treatment of K. pneumoniae infections is becoming increasingly challenging due to high levels of antibiotic resistance and the rising prevalence of carbapenem-resistant, extended-spectrum β-lactamases producing strains. Zinc is essential to the colonization and infection by many bacterial pathogens but toxic in excess. This work described the first dissection of the pathways associated with resisting extracellular zinc stress in K. pneumoniae. This study revealed that the P-type ATPase ZntA was highly upregulated in response to exogenous zinc stress and played a major role in maintaining bacterial metal homeostasis. Knowledge of how this major bacterial pathogen resists zinc stress provided a foundation for antimicrobial development studies to target and abrogate their essential function. American Society for Microbiology 2022-01-12 /pmc/articles/PMC8754117/ /pubmed/35019689 http://dx.doi.org/10.1128/spectrum.01773-21 Text en Copyright © 2022 Maunders 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
Maunders, Eve A.
Ganio, Katherine
Hayes, Andrew J.
Neville, Stephanie L.
Davies, Mark R.
Strugnell, Richard A.
McDevitt, Christopher A.
Tan, Aimee
The Role of ZntA in Klebsiella pneumoniae Zinc Homeostasis
title The Role of ZntA in Klebsiella pneumoniae Zinc Homeostasis
title_full The Role of ZntA in Klebsiella pneumoniae Zinc Homeostasis
title_fullStr The Role of ZntA in Klebsiella pneumoniae Zinc Homeostasis
title_full_unstemmed The Role of ZntA in Klebsiella pneumoniae Zinc Homeostasis
title_short The Role of ZntA in Klebsiella pneumoniae Zinc Homeostasis
title_sort role of znta in klebsiella pneumoniae zinc homeostasis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8754117/
https://www.ncbi.nlm.nih.gov/pubmed/35019689
http://dx.doi.org/10.1128/spectrum.01773-21
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