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SGI-4 in Monophasic Salmonella Typhimurium ST34 Is a Novel ICE That Enhances Resistance to Copper

A multi drug resistant Salmonella enterica 4,[5],12:i- of sequence type 34 (monophasic S. Typhimurium ST34) is a current pandemic clone associated with livestock, particularly pigs, and numerous outbreaks in the human population. A large genomic island, termed SGI-4, is present in the monophasic Typ...

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Autores principales: Branchu, Priscilla, Charity, Oliver J., Bawn, Matt, Thilliez, Gaetan, Dallman, Timothy J., Petrovska, Liljana, Kingsley, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543542/
https://www.ncbi.nlm.nih.gov/pubmed/31178839
http://dx.doi.org/10.3389/fmicb.2019.01118
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author Branchu, Priscilla
Charity, Oliver J.
Bawn, Matt
Thilliez, Gaetan
Dallman, Timothy J.
Petrovska, Liljana
Kingsley, Robert A.
author_facet Branchu, Priscilla
Charity, Oliver J.
Bawn, Matt
Thilliez, Gaetan
Dallman, Timothy J.
Petrovska, Liljana
Kingsley, Robert A.
author_sort Branchu, Priscilla
collection PubMed
description A multi drug resistant Salmonella enterica 4,[5],12:i- of sequence type 34 (monophasic S. Typhimurium ST34) is a current pandemic clone associated with livestock, particularly pigs, and numerous outbreaks in the human population. A large genomic island, termed SGI-4, is present in the monophasic Typhimurium ST34 clade and absent from other S. Typhimurium strains. SGI-4 consists of 87 open reading frames including sil and pco genes previously implicated in resistance to copper (Cu) and silver, and multiple genes predicted to be involved in mobilization and transfer by conjugation. SGI-4 was excised from the chromosome, circularized, and transferred to recipient strains of S. Typhimurium at a frequency influenced by stress induced by mitomycin C, and oxygen tension. The presence of SGI-4 was associated with increased resistance to Cu, particularly but not exclusively under anaerobic conditions. The presence of silCBA genes, predicted to encode an RND family efflux pump that transports Cu from the periplasm to the external milieu, was sufficient to impart the observed enhanced resistance to Cu, above that commonly associated with S. Typhimurium isolates. The presence of these genes resulted in the absence of Cu-dependent induction of pco genes encoding multiple proteins linked to Cu resistance, also present on SGI-4, suggesting that the system effectively limits the Cu availability in the periplasm, but did not affect SodCI-dependent macrophage survival.
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spelling pubmed-65435422019-06-07 SGI-4 in Monophasic Salmonella Typhimurium ST34 Is a Novel ICE That Enhances Resistance to Copper Branchu, Priscilla Charity, Oliver J. Bawn, Matt Thilliez, Gaetan Dallman, Timothy J. Petrovska, Liljana Kingsley, Robert A. Front Microbiol Microbiology A multi drug resistant Salmonella enterica 4,[5],12:i- of sequence type 34 (monophasic S. Typhimurium ST34) is a current pandemic clone associated with livestock, particularly pigs, and numerous outbreaks in the human population. A large genomic island, termed SGI-4, is present in the monophasic Typhimurium ST34 clade and absent from other S. Typhimurium strains. SGI-4 consists of 87 open reading frames including sil and pco genes previously implicated in resistance to copper (Cu) and silver, and multiple genes predicted to be involved in mobilization and transfer by conjugation. SGI-4 was excised from the chromosome, circularized, and transferred to recipient strains of S. Typhimurium at a frequency influenced by stress induced by mitomycin C, and oxygen tension. The presence of SGI-4 was associated with increased resistance to Cu, particularly but not exclusively under anaerobic conditions. The presence of silCBA genes, predicted to encode an RND family efflux pump that transports Cu from the periplasm to the external milieu, was sufficient to impart the observed enhanced resistance to Cu, above that commonly associated with S. Typhimurium isolates. The presence of these genes resulted in the absence of Cu-dependent induction of pco genes encoding multiple proteins linked to Cu resistance, also present on SGI-4, suggesting that the system effectively limits the Cu availability in the periplasm, but did not affect SodCI-dependent macrophage survival. Frontiers Media S.A. 2019-05-24 /pmc/articles/PMC6543542/ /pubmed/31178839 http://dx.doi.org/10.3389/fmicb.2019.01118 Text en Copyright © 2019 Branchu, Charity, Bawn, Thilliez, Dallman, Petrovska and Kingsley. 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) and the copyright owner(s) 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
Branchu, Priscilla
Charity, Oliver J.
Bawn, Matt
Thilliez, Gaetan
Dallman, Timothy J.
Petrovska, Liljana
Kingsley, Robert A.
SGI-4 in Monophasic Salmonella Typhimurium ST34 Is a Novel ICE That Enhances Resistance to Copper
title SGI-4 in Monophasic Salmonella Typhimurium ST34 Is a Novel ICE That Enhances Resistance to Copper
title_full SGI-4 in Monophasic Salmonella Typhimurium ST34 Is a Novel ICE That Enhances Resistance to Copper
title_fullStr SGI-4 in Monophasic Salmonella Typhimurium ST34 Is a Novel ICE That Enhances Resistance to Copper
title_full_unstemmed SGI-4 in Monophasic Salmonella Typhimurium ST34 Is a Novel ICE That Enhances Resistance to Copper
title_short SGI-4 in Monophasic Salmonella Typhimurium ST34 Is a Novel ICE That Enhances Resistance to Copper
title_sort sgi-4 in monophasic salmonella typhimurium st34 is a novel ice that enhances resistance to copper
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543542/
https://www.ncbi.nlm.nih.gov/pubmed/31178839
http://dx.doi.org/10.3389/fmicb.2019.01118
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