Please use this identifier to cite or link to this item: https://doi.org/10.3389/fmicb.2018.02656
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dc.titleA new role of OmpR in acid and osmotic stress in salmonella and E. coli
dc.contributor.authorChakraborty, S
dc.contributor.authorKenney, L.J
dc.date.accessioned2020-10-20T04:57:52Z
dc.date.available2020-10-20T04:57:52Z
dc.date.issued2018
dc.identifier.citationChakraborty, S, Kenney, L.J (2018). A new role of OmpR in acid and osmotic stress in salmonella and E. coli. Frontiers in Microbiology 9 (NOV) : 2656. ScholarBank@NUS Repository. https://doi.org/10.3389/fmicb.2018.02656
dc.identifier.issn1664302X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178057
dc.description.abstractBacteria survive and respond to diverse environmental conditions and during infection inside the host by systematic regulation of stress response genes. E. coli and S. Typhimurium can undergo large changes in intracellular osmolality (up to 1.8 Osmol/kg) and can tolerate cytoplasmic acidification to at least pHi 5.6. Recent analyses of single cells challenged a long held view that bacteria respond to extracellular acid stress by rapid acidification followed by a rapid recovery. It is now appreciated that both S. Typhimurium and E. coli maintain an acidic cytoplasm through the actions of the outer membrane protein regulator OmpR via its regulation of distinct signaling pathways. However, a comprehensive comparison of OmpR regulons between S. Typhimurium and E. coli is lacking. In this study, we examined the expression profiles of wild-type and ompR null strains of the intracellular pathogen S. Typhimurium and a commensal E. coli in response to acid and osmotic stress. Herein, we classify distinct OmpR regulons and also identify shared OmpR regulatory pathways between S. Typhimurium and E. coli in response to acid and osmotic stress. Our study establishes OmpR as a key regulator of bacterial virulence, growth and metabolism, in addition to its role in regulating outer membrane proteins. © 2018 Chakraborty and Kenney.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectouter membrane protein regulator
dc.subjectRNA 16S
dc.subjectsigma factor RpoS
dc.subjectacidification
dc.subjectacidity
dc.subjectArticle
dc.subjectatomic force microscopy
dc.subjectbacterial growth
dc.subjectbacterial metabolism
dc.subjectbacterial virulence
dc.subjectcontrolled study
dc.subjectEscherichia coli
dc.subjectgene ontology
dc.subjectgene overexpression
dc.subjectmicroarray analysis
dc.subjectnonhuman
dc.subjectosmolality
dc.subjectosmotic stress
dc.subjectpH
dc.subjectprotein expression
dc.subjectreal time polymerase chain reaction
dc.subjectregulon
dc.subjectreverse transcription polymerase chain reaction
dc.subjectRNA isolation
dc.subjectSalmonella enterica serovar Typhimurium
dc.subjectsignal transduction
dc.subjecttranscription regulation
dc.typeArticle
dc.contributor.departmentMECHANOBIOLOGY INSTITUTE
dc.description.doi10.3389/fmicb.2018.02656
dc.description.sourcetitleFrontiers in Microbiology
dc.description.volume9
dc.description.issueNOV
dc.description.page2656
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