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Analysis of the ArcA regulon in anaerobically grown Salmonella enterica sv. Typhimurium

BACKGROUND: Salmonella enterica serovar Typhimurium (S. Typhimurium) is a Gram-negative pathogen that must successfully adapt to the broad fluctuations in the concentration of dissolved dioxygen encountered in the host. In Escherichia coli, ArcA (Aerobic Respiratory Control) helps the cells to sense...

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Autores principales: Evans, Matthew R, Fink, Ryan C, Vazquez-Torres, Andres, Porwollik, Steffen, Jones-Carson, Jessica, McClelland, Michael, Hassan, Hosni M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3075218/
https://www.ncbi.nlm.nih.gov/pubmed/21418628
http://dx.doi.org/10.1186/1471-2180-11-58
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author Evans, Matthew R
Fink, Ryan C
Vazquez-Torres, Andres
Porwollik, Steffen
Jones-Carson, Jessica
McClelland, Michael
Hassan, Hosni M
author_facet Evans, Matthew R
Fink, Ryan C
Vazquez-Torres, Andres
Porwollik, Steffen
Jones-Carson, Jessica
McClelland, Michael
Hassan, Hosni M
author_sort Evans, Matthew R
collection PubMed
description BACKGROUND: Salmonella enterica serovar Typhimurium (S. Typhimurium) is a Gram-negative pathogen that must successfully adapt to the broad fluctuations in the concentration of dissolved dioxygen encountered in the host. In Escherichia coli, ArcA (Aerobic Respiratory Control) helps the cells to sense and respond to the presence of dioxygen. The global role of ArcA in E. coli is well characterized; however, little is known about its role in anaerobically grown S. Typhimurium. RESULTS: We compared the transcriptional profiles of the virulent wild-type (WT) strain (ATCC 14028s) and its isogenic arcA mutant grown under anaerobic conditions. We found that ArcA directly or indirectly regulates 392 genes (8.5% of the genome); of these, 138 genes are poorly characterized. Regulation by ArcA in S. Typhimurium is similar, but distinct from that in E. coli. Thus, genes/operons involved in core metabolic pathways (e.g., succinyl-CoA, fatty acid degradation, cytochrome oxidase complexes, flagellar biosynthesis, motility, and chemotaxis) were regulated similarly in the two organisms. However, genes/operons present in both organisms, but regulated differently by ArcA in S. Typhimurium included those coding for ethanolamine utilization, lactate transport and metabolism, and succinate dehydrogenases. Salmonella-specific genes/operons regulated by ArcA included those required for propanediol utilization, flagellar genes (mcpAC, cheV), Gifsy-1 prophage genes, and three SPI-3 genes (mgtBC, slsA, STM3784). In agreement with our microarray data, the arcA mutant was non-motile, lacked flagella, and was as virulent in mice as the WT. Additionally, we identified a set of 120 genes whose regulation was shared with the anaerobic redox regulator, Fnr. CONCLUSION(S): We have identified the ArcA regulon in anaerobically grown S. Typhimurium. Our results demonstrated that in S. Typhimurium, ArcA serves as a transcriptional regulator coordinating cellular metabolism, flagella biosynthesis, and motility. Furthermore, ArcA and Fnr share in the regulation of 120 S. Typhimurium genes.
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spelling pubmed-30752182011-04-13 Analysis of the ArcA regulon in anaerobically grown Salmonella enterica sv. Typhimurium Evans, Matthew R Fink, Ryan C Vazquez-Torres, Andres Porwollik, Steffen Jones-Carson, Jessica McClelland, Michael Hassan, Hosni M BMC Microbiol Research Article BACKGROUND: Salmonella enterica serovar Typhimurium (S. Typhimurium) is a Gram-negative pathogen that must successfully adapt to the broad fluctuations in the concentration of dissolved dioxygen encountered in the host. In Escherichia coli, ArcA (Aerobic Respiratory Control) helps the cells to sense and respond to the presence of dioxygen. The global role of ArcA in E. coli is well characterized; however, little is known about its role in anaerobically grown S. Typhimurium. RESULTS: We compared the transcriptional profiles of the virulent wild-type (WT) strain (ATCC 14028s) and its isogenic arcA mutant grown under anaerobic conditions. We found that ArcA directly or indirectly regulates 392 genes (8.5% of the genome); of these, 138 genes are poorly characterized. Regulation by ArcA in S. Typhimurium is similar, but distinct from that in E. coli. Thus, genes/operons involved in core metabolic pathways (e.g., succinyl-CoA, fatty acid degradation, cytochrome oxidase complexes, flagellar biosynthesis, motility, and chemotaxis) were regulated similarly in the two organisms. However, genes/operons present in both organisms, but regulated differently by ArcA in S. Typhimurium included those coding for ethanolamine utilization, lactate transport and metabolism, and succinate dehydrogenases. Salmonella-specific genes/operons regulated by ArcA included those required for propanediol utilization, flagellar genes (mcpAC, cheV), Gifsy-1 prophage genes, and three SPI-3 genes (mgtBC, slsA, STM3784). In agreement with our microarray data, the arcA mutant was non-motile, lacked flagella, and was as virulent in mice as the WT. Additionally, we identified a set of 120 genes whose regulation was shared with the anaerobic redox regulator, Fnr. CONCLUSION(S): We have identified the ArcA regulon in anaerobically grown S. Typhimurium. Our results demonstrated that in S. Typhimurium, ArcA serves as a transcriptional regulator coordinating cellular metabolism, flagella biosynthesis, and motility. Furthermore, ArcA and Fnr share in the regulation of 120 S. Typhimurium genes. BioMed Central 2011-03-21 /pmc/articles/PMC3075218/ /pubmed/21418628 http://dx.doi.org/10.1186/1471-2180-11-58 Text en Copyright ©2011 Evans et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Evans, Matthew R
Fink, Ryan C
Vazquez-Torres, Andres
Porwollik, Steffen
Jones-Carson, Jessica
McClelland, Michael
Hassan, Hosni M
Analysis of the ArcA regulon in anaerobically grown Salmonella enterica sv. Typhimurium
title Analysis of the ArcA regulon in anaerobically grown Salmonella enterica sv. Typhimurium
title_full Analysis of the ArcA regulon in anaerobically grown Salmonella enterica sv. Typhimurium
title_fullStr Analysis of the ArcA regulon in anaerobically grown Salmonella enterica sv. Typhimurium
title_full_unstemmed Analysis of the ArcA regulon in anaerobically grown Salmonella enterica sv. Typhimurium
title_short Analysis of the ArcA regulon in anaerobically grown Salmonella enterica sv. Typhimurium
title_sort analysis of the arca regulon in anaerobically grown salmonella enterica sv. typhimurium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3075218/
https://www.ncbi.nlm.nih.gov/pubmed/21418628
http://dx.doi.org/10.1186/1471-2180-11-58
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