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      Bimodal Expression of the Salmonella Typhimurium spv Operon

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      Genetics
      Genetics Society of America

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          Abstract

          <p class="first" id="d723685e169">Passaris <i>et al.</i> show that the well-studied spv virulence operon of <i>Salmonella</i> Typhimurium displays a bimodal expression pattern. Using quantitative single-cell fluorescence microscopy, they demonstrate that this expression pattern originates in the bimodal expression... </p><p class="first" id="d723685e178">The well-studied <i>spv</i> operon of <i>Salmonella</i> <i>typhimurium</i> is important for causing full virulence in mice and both the regulation and function of the Spv proteins have been characterized extensively over the past several decades. Using quantitative single-cell fluorescence microscopy, we demonstrate the <i>spv</i> regulon to display a bimodal expression pattern that originates in the bimodal expression of the SpvR activator. The <i>spv</i> expression pattern is influenced by growth conditions and the specific <i>S</i>. <i>typhimurium</i> strain used, but does not require <i>Salmonella</i>-specific virulence regulators. By monitoring real-time promoter kinetics, we reveal that SpvA has the ability to impart negative feedback on <i>spvABCD</i> expression without affecting <i>spvR</i> expression. Together, our data suggest that the SpvA protein counteracts the positive feedback loop imposed by SpvR, and could thus be responsible for dampening <i>spvABCD</i> expression and coordinating virulence protein production in time. The results presented here yield new insights in the intriguing regulation of the <i>spv</i> operon and adds this operon to the growing list of virulence factors exhibiting marked expression heterogeneity in <i>S</i>. <i>typhimurium</i>. </p>

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          Most cited references63

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          A functional perspective on phenotypic heterogeneity in microorganisms.

          Most microbial communities consist of a genetically diverse assembly of different organisms, and the level of genetic diversity plays an important part in community properties and functions. However, biological diversity also arises at a lower level of biological organization, between genetically identical cells that reside in the same microenvironment. In this Review, I outline the molecular mechanisms responsible for phenotypic heterogeneity and discuss how phenotypic heterogeneity allows genotypes to persist in fluctuating environments. I also describe how it promotes interactions between phenotypic subpopulations in clonal groups, providing microbial groups with new functionality.
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            • Record: found
            • Abstract: found
            • Article: not found

            Self-perpetuating states in signal transduction: positive feedback, double-negative feedback and bistability.

            Cell signaling systems that contain positive-feedback loops or double-negative feedback loops can, in principle, convert graded inputs into switch-like, irreversible responses. Systems of this sort are termed "bistable". Recently, several groups have engineered artificial bistable systems into Escherichia coli and Saccharomyces cerevisiae, and have shown that the systems exhibit interesting and potentially useful properties. In addition, two naturally occurring signaling systems, the p42 mitogen-activated protein kinase and c-Jun amino-terminal kinase pathways in Xenopus oocytes, have been shown to exhibit bistable responses. Here we review the basic properties of bistable circuits, the requirements for construction of a satisfactory bistable switch, and the recent progress towards constructing and analysing bistable signaling systems.
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              • Record: found
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              Salmonella enterica serovar Typhimurium skills to succeed in the host: virulence and regulation.

              Salmonella enterica serovar Typhimurium is a primary enteric pathogen infecting both humans and animals. Infection begins with the ingestion of contaminated food or water so that salmonellae reach the intestinal epithelium and trigger gastrointestinal disease. In some patients the infection spreads upon invasion of the intestinal epithelium, internalization within phagocytes, and subsequent dissemination. In that case, antimicrobial therapy, based on fluoroquinolones and expanded-spectrum cephalosporins as the current drugs of choice, is indicated. To accomplish the pathogenic process, the Salmonella chromosome comprises several virulence mechanisms. The most important virulence genes are those located within the so-called Salmonella pathogenicity islands (SPIs). Thus far, five SPIs have been reported to have a major contribution to pathogenesis. Nonetheless, further virulence traits, such as the pSLT virulence plasmid, adhesins, flagella, and biofilm-related proteins, also contribute to success within the host. Several regulatory mechanisms which synchronize all these elements in order to guarantee bacterial survival have been described. These mechanisms govern the transitions from the different pathogenic stages and drive the pathogen to achieve maximal efficiency inside the host. This review focuses primarily on the virulence armamentarium of this pathogen and the extremely complicated regulatory network controlling its success.
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                Author and article information

                Journal
                Genetics
                Genetics
                Genetics Society of America
                0016-6731
                1943-2631
                October 04 2018
                October 2018
                October 2018
                August 16 2018
                : 210
                : 2
                : 621-635
                Article
                10.1534/genetics.118.300822
                6216589
                30143595
                a212225b-32a8-4521-9e0d-02acba73b129
                © 2018
                History

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