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Genome-wide characterization of Salmonella Typhimurium genes required for the fitness under iron restriction

BACKGROUND: Iron is a crucial element for bacterial survival and virulence. During Salmonella infection, the host utilizes a variety of mechanisms to starve the pathogen from iron. However, Salmonella activates distinctive defense mechanisms to acquire iron and survive in iron-restricted host enviro...

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Autores principales: Karash, Sardar, Jiang, Tieshan, Kwon, Young Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308263/
https://www.ncbi.nlm.nih.gov/pubmed/35869435
http://dx.doi.org/10.1186/s12863-022-01069-3
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author Karash, Sardar
Jiang, Tieshan
Kwon, Young Min
author_facet Karash, Sardar
Jiang, Tieshan
Kwon, Young Min
author_sort Karash, Sardar
collection PubMed
description BACKGROUND: Iron is a crucial element for bacterial survival and virulence. During Salmonella infection, the host utilizes a variety of mechanisms to starve the pathogen from iron. However, Salmonella activates distinctive defense mechanisms to acquire iron and survive in iron-restricted host environments. Yet, the comprehensive set of the conditionally essential genes that underpin Salmonella survival under iron-restricted niches has not been fully explored. RESULTS: Here, we employed transposon sequencing (Tn-seq) method for high-resolution elucidation of the genes in Salmonella Typhimurium (S. Typhimurium) 14028S strain required for the growth under the in vitro conditions with four different levels of iron restriction achieved by iron chelator 2,2′-dipyridyl (Dip): mild (100 and 150 μM), moderate (250 μM) and severe iron restriction (400 μM). We found that the fitness of the mutants reduced significantly for 28 genes, suggesting the importance of these genes for the growth under iron restriction. These genes include sufABCDSE, iron transport fepD, siderophore tonB, sigma factor E ropE, phosphate transport pstAB, and zinc exporter zntA. The siderophore gene tonB was required in mild and moderate iron-restricted conditions, but it became dispensable in severe iron-restricted conditions. Remarkably, rpoE was required in moderate and severe iron restrictions, leading to complete attenuation of the mutant under these conditions. We also identified 30 genes for which the deletion of the genes resulted in increased fitness under iron-restricted conditions. CONCLUSIONS: The findings broaden our knowledge of how S. Typhimurium survives in iron-deficient environments, which could be utilized for the development of new therapeutic strategies targeting the pathways vital for iron metabolism, trafficking, and scavenging. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12863-022-01069-3.
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spelling pubmed-93082632022-07-24 Genome-wide characterization of Salmonella Typhimurium genes required for the fitness under iron restriction Karash, Sardar Jiang, Tieshan Kwon, Young Min BMC Genom Data Research BACKGROUND: Iron is a crucial element for bacterial survival and virulence. During Salmonella infection, the host utilizes a variety of mechanisms to starve the pathogen from iron. However, Salmonella activates distinctive defense mechanisms to acquire iron and survive in iron-restricted host environments. Yet, the comprehensive set of the conditionally essential genes that underpin Salmonella survival under iron-restricted niches has not been fully explored. RESULTS: Here, we employed transposon sequencing (Tn-seq) method for high-resolution elucidation of the genes in Salmonella Typhimurium (S. Typhimurium) 14028S strain required for the growth under the in vitro conditions with four different levels of iron restriction achieved by iron chelator 2,2′-dipyridyl (Dip): mild (100 and 150 μM), moderate (250 μM) and severe iron restriction (400 μM). We found that the fitness of the mutants reduced significantly for 28 genes, suggesting the importance of these genes for the growth under iron restriction. These genes include sufABCDSE, iron transport fepD, siderophore tonB, sigma factor E ropE, phosphate transport pstAB, and zinc exporter zntA. The siderophore gene tonB was required in mild and moderate iron-restricted conditions, but it became dispensable in severe iron-restricted conditions. Remarkably, rpoE was required in moderate and severe iron restrictions, leading to complete attenuation of the mutant under these conditions. We also identified 30 genes for which the deletion of the genes resulted in increased fitness under iron-restricted conditions. CONCLUSIONS: The findings broaden our knowledge of how S. Typhimurium survives in iron-deficient environments, which could be utilized for the development of new therapeutic strategies targeting the pathways vital for iron metabolism, trafficking, and scavenging. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12863-022-01069-3. BioMed Central 2022-07-22 /pmc/articles/PMC9308263/ /pubmed/35869435 http://dx.doi.org/10.1186/s12863-022-01069-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Karash, Sardar
Jiang, Tieshan
Kwon, Young Min
Genome-wide characterization of Salmonella Typhimurium genes required for the fitness under iron restriction
title Genome-wide characterization of Salmonella Typhimurium genes required for the fitness under iron restriction
title_full Genome-wide characterization of Salmonella Typhimurium genes required for the fitness under iron restriction
title_fullStr Genome-wide characterization of Salmonella Typhimurium genes required for the fitness under iron restriction
title_full_unstemmed Genome-wide characterization of Salmonella Typhimurium genes required for the fitness under iron restriction
title_short Genome-wide characterization of Salmonella Typhimurium genes required for the fitness under iron restriction
title_sort genome-wide characterization of salmonella typhimurium genes required for the fitness under iron restriction
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308263/
https://www.ncbi.nlm.nih.gov/pubmed/35869435
http://dx.doi.org/10.1186/s12863-022-01069-3
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