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      The Escherichia coli MarA protein regulates the ycgZymgABC operon to inhibit biofilm formation

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          Summary

          The Escherichia coli marRAB operon is a paradigm for chromosomally encoded antibiotic resistance. The operon exerts its effect via an encoded transcription factor called MarA that modulates efflux pump and porin expression. In this work, we show that MarA is also a regulator of biofilm formation. Control is mediated by binding of MarA to the intergenic region upstream of the ycgZymgABC operon. The operon, known to influence the formation of curli fibres and colanic acid, is usually expressed during periods of starvation. Hence, the ycgZymgABC promoter is recognised by σ 38 (RpoS)‐associated RNA polymerase (RNAP). Surprisingly, MarA does not influence σ 38‐dependent transcription. Instead, MarA drives transcription by the housekeeping σ 70‐associated RNAP. The effects of MarA on ycgZymgABC expression are coupled with biofilm formation by the rcsCDB phosphorelay system, with YcgZ, YmgA and YmgB forming a complex that directly interacts with the histidine kinase domain of RcsC.

          Abstract

          Expression of the multiple antibiotic resistance activator (MarA) protein can give rise to clinically relevant drug resistance in Escherichia coli. Counterintuitively, we showed that MarA production inhibits the formation of biofilms. Inhibition is mediated by the activation of the ycgZymgABC operon. To activate these genes, MarA acts selectively thus enhancing transcription by RNAP associated with the σ 70 but not with the σ 38 factor.

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          Most cited references54

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          Gene disruption in Escherichia coli: TcR and KmR cassettes with the option of Flp-catalyzed excision of the antibiotic-resistance determinant.

          Two cassettes with tetracycline-resistance (TcR) and kanamycin-resistance (KmR) determinants have been developed for the construction of insertion and deletion mutants of cloned genes in Escherichia coli. In both cassettes, the resistance determinants are flanked by the short direct repeats (FRT sites) required for site-specific recombination mediated by the yeast Flp recombinase. In addition, a plasmid with temperature-sensitive replication for temporal production of the Flp enzyme in E. coli has been constructed. After a gene disruption or deletion mutation is constructed in vitro by insertion of one of the cassettes into a given gene, the mutated gene is transferred to the E. coli chromosome by homologous recombination and selection for the antibiotic resistance provided by the cassette. If desired, the resistance determinant can subsequently be removed from the chromosome in vivo by Flp action, leaving behind a short nucleotide sequence with one FRT site and with no polar effect on downstream genes. This system was applied in the construction of an E. coli endA deletion mutation which can be transduced by P1 to the genetic background of interest using TcR as a marker. The transductant can then be freed of the TcR if required.
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            Epitope tagging of chromosomal genes in Salmonella.

            We have developed a simple and efficient procedure for adding an epitope-encoding tail to one or more genes of interest in the bacterial chromosome. The procedure is a modification of the gene replacement method of Datsenko and Wanner [Datsenko, K. A. & Wanner, B. L. (2000) Proc. Natl. Acad. Sci. USA 97, 6640-6645]. A DNA module that begins with the epitope-encoding sequence and includes a selectable marker is amplified by PCR with primers that carry extensions (as short as 36 nt) homologous to the last portion of the targeted gene and to a region downstream from it. Transformation of a strain expressing bacteriophage lambda red functions yields recombinants carrying the targeted gene fused to the epitope-encoding sequence. The resulting C-terminal-tagged protein can be identified by standard immuno-detection techniques. In an initial application of the method, we have added the sequences encoding the FLAG and 3xFLAG and influenza virus hemagglutinin epitopes to various genes of Salmonella enterica serovar Typhimurium, including putative and established pathogenic determinants present in prophage genomes. Epitope fusion proteins were detected in bacteria growing in vitro, tissue culture cells, and infected mouse tissues. This work identified a prophage locus specifically expressed in bacteria growing intracellularly. The procedure described here should be applicable to a wide variety of Gram-negative bacteria and is particularly suited for the study of intracellular pathogens.
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              Transposition and fusion of the lac genes to selected promoters in Escherichia coli using bacteriophage lambda and Mu.

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                Author and article information

                Contributors
                d.grainger@bham.ac.uk
                Journal
                Mol Microbiol
                Mol. Microbiol
                10.1111/(ISSN)1365-2958
                MMI
                Molecular Microbiology
                John Wiley and Sons Inc. (Hoboken )
                0950-382X
                1365-2958
                29 September 2019
                November 2019
                : 112
                : 5 ( doiID: 10.1111/mmi.v112.5 )
                : 1609-1625
                Affiliations
                [ 1 ] School of Biosciences Institute of Microbiology and Infection University of Birmingham Edgbaston Birmingham B15 2TT UK
                [ 2 ] Institut für Biologie/Mikrobiologie Humboldt‐Universität zu Berlin 10115 Berlin Germany
                [ 3 ] Quadram Institute Bioscience Norwich Research Park Norwich NR4 7UQ UK
                Author notes
                [*] [* ] For correspondence. Email d.grainger@ 123456bham.ac.uk ; Tel. +44 (0)121 414 5437.

                Author information
                https://orcid.org/0000-0003-3375-5154
                Article
                MMI14386
                10.1111/mmi.14386
                6900184
                31518447
                0eae9511-46f6-40b9-b7f1-6f6489e9dee2
                © 2019 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                Page count
                Figures: 8, Tables: 1, Pages: 17, Words: 20661
                Funding
                Funded by: Biotechnology and Biological Sciences Research Council , open-funder-registry 10.13039/501100000268;
                Award ID: BB/N014200/1
                Award ID: BB/R012504/1 and its constituent project BBS/E/F/0
                Award ID: MIBTP
                Funded by: Deutsche Forschungsgemeinschaft , open-funder-registry 10.13039/501100001659;
                Award ID: He1556/13‐2
                Funded by: Wellcome Trust , open-funder-registry 10.13039/100004440;
                Award ID: AAMR DTP
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                November 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.2 mode:remove_FC converted:05.12.2019

                Microbiology & Virology
                Microbiology & Virology

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