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Defining the Roles of the Cation Diffusion Facilitators in Fe(2+)/Zn(2+) Homeostasis and Establishment of Their Participation in Virulence in Pseudomonas aeruginosa

Transporters of the cation diffusion facilitator (CDF) family form dimers that export transition metals from the cytosol. The opportunistic pathogen Pseudomonas aeruginosa encodes three homologous CDF genes, czcD (PA0397), aitP (PA1297), and yiiP (PA3963). The three proteins are required for virulen...

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Autores principales: Salusso, Agostina, Raimunda, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357649/
https://www.ncbi.nlm.nih.gov/pubmed/28373967
http://dx.doi.org/10.3389/fcimb.2017.00084
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author Salusso, Agostina
Raimunda, Daniel
author_facet Salusso, Agostina
Raimunda, Daniel
author_sort Salusso, Agostina
collection PubMed
description Transporters of the cation diffusion facilitator (CDF) family form dimers that export transition metals from the cytosol. The opportunistic pathogen Pseudomonas aeruginosa encodes three homologous CDF genes, czcD (PA0397), aitP (PA1297), and yiiP (PA3963). The three proteins are required for virulence in a plant host model. Disruption of the aitP gene leads to higher Fe(2+) and Co(2+) sensitivity together with an intracellular accumulation of these ions and to a decreased survival in presence of H(2)O(2). Strains lacking czcD and yiiP showed low Zn(2+) sensitivity. However, in iron-rich media and in the presence of Zn(2+) these strains secreted higher levels of the iron chelator pyoverdine. Disruption of czcD and yiiP in a non-pyoverdine producer strain and lacking the Zn(2+)-transporting ATPase, increased the Zn(2+) sensitivity and the accumulation of this ion. Most importantly, independent of the pyoverdine production strains lacking CzcD or YiiP, presented lower resistance to imipenem, ciprofloxacin, chloramphenicol, and gentamicin. These observations correlated with a lower survival rate upon EDTA-lysozyme treatment and overexpression of OprN and OprD porins. We hypothesize that while AitP is an Fe(2+)/Co(2+) efflux transporter required for Fe(2+) homeostasis, and ultimately redox stress handling, CzcD, and YiiP export Zn(2+) to the periplasm for proper Zn(2+)-dependent signaling regulating outer membrane stability and therefore antibiotic tolerance.
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spelling pubmed-53576492017-04-03 Defining the Roles of the Cation Diffusion Facilitators in Fe(2+)/Zn(2+) Homeostasis and Establishment of Their Participation in Virulence in Pseudomonas aeruginosa Salusso, Agostina Raimunda, Daniel Front Cell Infect Microbiol Microbiology Transporters of the cation diffusion facilitator (CDF) family form dimers that export transition metals from the cytosol. The opportunistic pathogen Pseudomonas aeruginosa encodes three homologous CDF genes, czcD (PA0397), aitP (PA1297), and yiiP (PA3963). The three proteins are required for virulence in a plant host model. Disruption of the aitP gene leads to higher Fe(2+) and Co(2+) sensitivity together with an intracellular accumulation of these ions and to a decreased survival in presence of H(2)O(2). Strains lacking czcD and yiiP showed low Zn(2+) sensitivity. However, in iron-rich media and in the presence of Zn(2+) these strains secreted higher levels of the iron chelator pyoverdine. Disruption of czcD and yiiP in a non-pyoverdine producer strain and lacking the Zn(2+)-transporting ATPase, increased the Zn(2+) sensitivity and the accumulation of this ion. Most importantly, independent of the pyoverdine production strains lacking CzcD or YiiP, presented lower resistance to imipenem, ciprofloxacin, chloramphenicol, and gentamicin. These observations correlated with a lower survival rate upon EDTA-lysozyme treatment and overexpression of OprN and OprD porins. We hypothesize that while AitP is an Fe(2+)/Co(2+) efflux transporter required for Fe(2+) homeostasis, and ultimately redox stress handling, CzcD, and YiiP export Zn(2+) to the periplasm for proper Zn(2+)-dependent signaling regulating outer membrane stability and therefore antibiotic tolerance. Frontiers Media S.A. 2017-03-20 /pmc/articles/PMC5357649/ /pubmed/28373967 http://dx.doi.org/10.3389/fcimb.2017.00084 Text en Copyright © 2017 Salusso and Raimunda. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Salusso, Agostina
Raimunda, Daniel
Defining the Roles of the Cation Diffusion Facilitators in Fe(2+)/Zn(2+) Homeostasis and Establishment of Their Participation in Virulence in Pseudomonas aeruginosa
title Defining the Roles of the Cation Diffusion Facilitators in Fe(2+)/Zn(2+) Homeostasis and Establishment of Their Participation in Virulence in Pseudomonas aeruginosa
title_full Defining the Roles of the Cation Diffusion Facilitators in Fe(2+)/Zn(2+) Homeostasis and Establishment of Their Participation in Virulence in Pseudomonas aeruginosa
title_fullStr Defining the Roles of the Cation Diffusion Facilitators in Fe(2+)/Zn(2+) Homeostasis and Establishment of Their Participation in Virulence in Pseudomonas aeruginosa
title_full_unstemmed Defining the Roles of the Cation Diffusion Facilitators in Fe(2+)/Zn(2+) Homeostasis and Establishment of Their Participation in Virulence in Pseudomonas aeruginosa
title_short Defining the Roles of the Cation Diffusion Facilitators in Fe(2+)/Zn(2+) Homeostasis and Establishment of Their Participation in Virulence in Pseudomonas aeruginosa
title_sort defining the roles of the cation diffusion facilitators in fe(2+)/zn(2+) homeostasis and establishment of their participation in virulence in pseudomonas aeruginosa
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357649/
https://www.ncbi.nlm.nih.gov/pubmed/28373967
http://dx.doi.org/10.3389/fcimb.2017.00084
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