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Analysis of the expression, regulation and export of NleA-E in Escherichia coli O157 : H7.

Analysis of the expression, regulation and export of NleA-E in Escherichia coli O157 : H7. Research Abstract Details 

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  • Analysis of the expression, regulation and export of NleA-E in Escherichia coli O157 : H7. Abstract Text:

    andrew j roeAndrew J Roe,luke tysallLuke Tysall,tracy dransfieldTracy Dransfield,dai wangDai Wang,douglas fraser-pittDouglas Fraser-Pitt,arvind mahajanArvind Mahajan,chrystala constandinouChrystala Constandinou,neil inglisNeil Inglis,alison downingAlison Downing,richard talbotRichard Talbot,david g e smithDavid G E Smith,david l gallyDavid L Gally,

    Previous work has shown that locus of enterocyte effacement (LEE)-encoded effector proteins such as Tir and Map can be exported via the type III secretion system (T3SS) of Escherichia coli O157 : H7. Additionally, a family of non-LEE-encoded (Nle) effector proteins has been shown to be secreted from Citrobacter rodentium, homologues of which are located on the E. coli O157 chromosome. While NleA has been shown to be secreted from pathogenic E. coli, the secretion of other Nle effector proteins has only been detected under induced conditions, or using a mutated T3SS. This study aimed to determine: (1) which nle genes are expressed in E. coli O157 : H7 under secretion-permissive conditions; (2) if Nle proteins are secreted from wild-type E. coli O157 : H7 under secretion-permissive conditions; and (3) if nle gene expression is regulated co-ordinately with other LEE-encoded effectors. Using data generated from a combination of transcriptome arrays, reporter fusions and proteomics, it was demonstrated that only nleA is expressed co-ordinately with the LEE. Secretion and expression of NleA were regulated directly or indirectly by ler, a key activator of the LEE. MS confirmed the secretion of NleA into the culture supernatant, while NleB-F were not detected.

    Analysis of the expression, regulation and export of NleA-E in Escherichia coli O157 : H7. Publishing Authors By Initials

    aj roeAJ Roe,l tysallL Tysall,t dransfieldT Dransfield,d wangD Wang,d fraser-pittD Fraser-Pitt,a mahajanA Mahajan,c constandinouC Constandinou,n inglisN Inglis,a downingA Downing,r talbotR Talbot,dg smithDG Smith,dl gallyDL Gally,

    For similar biological factors: toxins, biological: virulence factors research abstracts see: biological factors: toxins, biological: virulence factors research

    PUBMED ID PMID:

    MEDLINE DATE:

    Analysis of the expression, regulation and export of NleA-E in Escherichia coli O157 : H7. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Microbiology (Reading, England)

    VOLUME: 153

    Page Numbers: 1350-60

    Journal Abbreviation:

    ISSN: 1350-0872

    DAY: 28

    MONTH: May

    YEAR: 2007

    Analysis of the expression, regulation and export of NleA-E in Escherichia coli O157 : H7. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9430468

    Analysis of the expression, regulation and export of NleA-E in Escherichia coli O157 : H7. Keywords Mesh Terms:

    KEYWORDS: Virulence Factors

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Analysis of the expression, regulation and export of NleA-E in Escherichia coli O157 : H7. Information

    Substance Name: red fluorescent protein

    Registry Number: 0

    Grant and Affiliation Information for Analysis of the expression, regulation and export of NleA-E in Escherichia coli O157 : H7.

    AFFILIATION: Zoonotic and Animal Pathogens Research Laboratory, Centre for Infectious Disease, The Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Microbiology

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