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      The Yersinia enterocolitica Ysa type III secretion system is expressed during infections both in vitro and in vivo

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          Abstract

          Yersinia enterocolitica biovar 1B maintains two type III secretion systems (T3SS) that are involved in pathogenesis, the plasmid encoded Ysc T3SS and the chromosomally encoded Ysa T3SS. In vitro, the Ysa T3SS has been shown to be expressed only at 26°C in a high-nutrient medium containing an exceptionally high concentration of salt – an artificial condition that provides no clear insight on the nature of signal that Y. enterocolitica responds to in a host. However, previous research has indicated that the Ysa system plays a role in the colonization of gastrointestinal tissues of mice. In this study, a series of Ysa promoter fusions to green fluorescent protein gene ( gfp) were created to analyze the expression of this T3SS during infection. Using reporter strains, infections were carried out in vitro using HeLa cells and in vivo using the mouse model of yersiniosis. Expression of green fluorescent protein (GFP) was measured from the promoters of yspP (encoding a secreted effector protein) and orf6 (encoding a structural component of the T3SS apparatus) in vitro and in vivo. During the infection of HeLa cells GFP intensity was measured by fluorescence microscopy, while during murine infections GFP expression in tissues was measured by flow cytometry. These approaches, combined with quantification of yspP mRNA transcripts by quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR), demonstrate that the Ysa system is expressed in vitro in a contact-dependent manner, and is expressed in vivo during infection of mice.

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          Most cited references34

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          Molecular genetic bases of Salmonella entry into host cells.

          J Galán (1996)
          Salmonella spp. can enter into non-phagocytic cells, a property that is essential for their pathogenicity. Recently, considerable progress has been made in the understanding of the molecular genetic bases of this process. It is now evident that Salmonella entry functions are largely encoded on a 35-40 kb region of the Salmonella chromosome located at centisome 63. The majority of the loci in this region encode components of a type III or contact-dependent secretion system homologous to those described in a variety of animal and plant-pathogenic bacteria as well as a number of proteins that require this system for their export to the extracellular environment. A somewhat unexpected finding has been the remarkable homology between the Salmonella and Shigella proteins that mediate the entry of these organisms into cultured epithelial cells.
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            Yersinia enterocolitica: overview and epidemiologic correlates.

            E Bottone (1999)
            Yersinia enterocolitica comprises both pathogenic and nonpathogenic members. Distinguished by biogrouping, serogrouping, and ecological distribution, commonly occurring pathogenic serobiogroups, e.g., O:3/4; O:5,27/2; O:8/1b; O:9/2, possess both chromosomal and plasmid-mediated virulence traits. Studies have revealed several (oral, blood transfusion) modes of acquisition, elucidated the putative role of chromosomal and plasmid-encoded virulence factors in the pathogenesis of human infection, and have identified major animal reservoirs, e.g., the pig. Diagnosis has been refined though use of selective media, monoclonal antibodies directed against outer membrane proteins, and of purified yersiniae outer membrane proteins for antibody detection. Epidemiological investigations of foodborne outbreaks have been advanced through the use of molecular biology techniques such as ribotyping and pulsed-field gel electrophoresis.
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              In vivo, fliC expression by Salmonella enterica serovar Typhimurium is heterogeneous, regulated by ClpX, and anatomically restricted.

              FliC is a natural antigen recognized by the innate and adaptive immune systems during Salmonella infection in mice and humans; however, the regulatory mechanisms governing its expression in vivo are incompletely understood. Here, we use flow cytometry to quantify fliC gene expression in single bacteria. In vitro, fliC transcription was not uniformly positive; a viable fliC-negative subpopulation was also identified. Intracellular Salmonella repressed transcription of fliC and its positive regulator fliA, but constitutively transcribed the master regulator flhD; fliC repression required ClpXP protease, known to degrade FlhD. In orally infected mice, fliC transcription was anatomically restricted: Salmonella transcribed fliC in the Peyer's Patches (PP) but not in the mesenteric lymph nodes and spleen. The intracellularly transcribed pagC promoter was upregulated by Salmonella in all tissues, defining the infected PP as a unique environment that initiates expression of intracellularly induced genes and yet permits transcription of fliC. Because a single bacterium can escape the GI tract to colonize deeper tissues, heterogeneous gene expression may have important implications for Salmonella pathogenesis: FliC-positive bacteria in the PP could stimulate inflammation and facilitate the priming of FliC-specific immune responses, while FliC-negative bacteria escape host detection in the gut and spread to systemic sites of replication.
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                Author and article information

                Journal
                Microbiologyopen
                Microbiologyopen
                mbo3
                MicrobiologyOpen
                Blackwell Publishing Ltd
                2045-8827
                2045-8827
                December 2013
                24 October 2013
                : 2
                : 6
                : 962-975
                Affiliations
                [1 ]Microbiology Graduate Group, University of California Davis, CA
                [2 ]Systems Biology, Sandia National Laboratories Livermore, CA
                [3 ]Biotechnology and Bioengineering, Sandia National Laboratories Livermore, CA
                [4 ]Department of Food Science and Technology, University of California Davis, CA
                Author notes
                Zachary W. Bent, Systems Biology, Sandia National Laboratories, Livermore, CA., Tel: 1-925-294-4684; Fax: 1-925-294-1489; E-mail: zbent@ 123456sandia.gov

                Funding Information This study was supported by a grant from the National Institutes of Health (NIH), R21 AI156042 to G. M. Y. NIH training grant for graduate research of animal models of human infectious disease T32 AI60555 and the Henry A. Jastro and Peter J. Shields Graduate Research Scholarship Award partially supported Z. W. B. Z. W. B. and S. S. B. were also funded by Sandia National Laboratories' LDRD (Laboratory-Directed Research and Development, grant numbers 165767 and 171001) program.

                Article
                10.1002/mbo3.136
                3892342
                24166928
                bb269670-86a4-4c44-b1e9-add6730dd207
                © 2013 Published by John Wiley & Sons Ltd

                Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

                History
                : 16 July 2013
                : 12 September 2013
                : 12 September 2013
                Categories
                Original Research

                Microbiology & Virology
                t3ss,y. enterocolitica,ysa,in vivo expression,ysp
                Microbiology & Virology
                t3ss, y. enterocolitica, ysa, in vivo expression, ysp

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