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      Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements

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          Abstract

          Background

          Genes present in only certain strains of a bacterial species can strongly affect cellular phenotypes and evolutionary potentials. One segment that seemed particularly rich in strain-specific genes was found by comparing the first two sequenced Helicobacter pylori genomes (strains 26695 and J99) and was named a “plasticity zone”.

          Principal Findings

          We studied the nature and evolution of plasticity zones by sequencing them in five more Helicobacter strains, determining their locations in additional strains, and identifying them in recently released genome sequences. They occurred as discrete units, inserted at numerous chromosomal sites, and were usually flanked by direct repeats of 5′AAGAATG, a sequence generally also present in one copy at unoccupied sites in other strains. This showed that plasticity zones are transposable elements, to be called TnPZs. Each full length TnPZ contained a cluster of type IV protein secretion genes ( tfs3), a tyrosine recombinase family gene (“ xerT”), and a large (≥2800 codon) orf encoding a protein with helicase and DNA methylase domains, plus additional orfs with no homology to genes of known function. Several TnPZ types were found that differed in gene arrangement or DNA sequence. Our analysis also indicated that the first-identified plasticity zones (in strains 26695 and J99) are complex mosaics of TnPZ remnants, formed by multiple TnPZ insertions, and spontaneous and transposable element mediated deletions. Tests using laboratory-generated deletions showed that TnPZs are not essential for viability, but identified one TnPZ that contributed quantitatively to bacterial growth during mouse infection and another that affected synthesis of proinflammatory cytokines in cell culture.

          Conclusions

          We propose that plasticity zone genes are contained in conjugative transposons (TnPZs) or remnants of them, that TnPZ insertion is mediated by XerT recombinase, and that some TnPZ genes affect bacterial phenotypes and fitness.

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          Most cited references48

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          Selfish genes, the phenotype paradigm and genome evolution.

          Natural selection operating within genomes will inevitably result in the appearance of DNAs with no phenotypic expression whose only 'function' is survival within genomes. Prokaryotic transposable elements and eukaryotic middle-repetitive sequences can be seen as such DNA's and thus no phenotypic or evolutionary function need be assigned to them.
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            Nod1 responds to peptidoglycan delivered by the Helicobacter pylori cag pathogenicity island.

            Epithelial cells can respond to conserved bacterial products that are internalized after either bacterial invasion or liposome treatment of cells. We report here that the noninvasive Gram-negative pathogen Helicobacter pylori was recognized by epithelial cells via Nod1, an intracellular pathogen-recognition molecule with specificity for Gram-negative peptidoglycan. Nod1 detection of H. pylori depended on the delivery of peptidoglycan to host cells by a bacterial type IV secretion system, encoded by the H. pylori cag pathogenicity island. Consistent with involvement of Nod1 in host defense, Nod1-deficient mice were more susceptible to infection by cag pathogenicity island-positive H. pylori than were wild-type mice. We propose that sensing of H. pylori by Nod1 represents a model for host recognition of noninvasive pathogens.
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              The late Pleistocene dispersal of modern humans in the Americas.

              When did humans colonize the Americas? From where did they come and what routes did they take? These questions have gripped scientists for decades, but until recently answers have proven difficult to find. Current genetic evidence implies dispersal from a single Siberian population toward the Bering Land Bridge no earlier than about 30,000 years ago (and possibly after 22,000 years ago), then migration from Beringia to the Americas sometime after 16,500 years ago. The archaeological records of Siberia and Beringia generally support these findings, as do archaeological sites in North and South America dating to as early as 15,000 years ago. If this is the time of colonization, geological data from western Canada suggest that humans dispersed along the recently deglaciated Pacific coastline.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2009
                3 September 2009
                : 4
                : 9
                : e6859
                Affiliations
                [1 ]Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, United States of America
                [2 ]Division of Gastroenterology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America
                [3 ]Laboratorios de Investigacion y Desarrollo, Facultad de Ciencias, Universidad Peruana Cayetano Heredia, Lima, Peru
                [4 ]Asociacion Benefica PRISMA, Lima, Peru
                [5 ]Laboratory of Molecular Biology, National Institute of Digestive and Kidney Diseases, National Institute of Health, Bethesda, Maryland, United States of America
                [6 ]Department of Biology, University of Louisville, Louisville, Kentucky, United States of America
                [7 ]Department of International Health, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America
                [8 ]Departments of Genetics and Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America
                Universita di Sassari, Italy
                Author notes

                Conceived and designed the experiments: DK DEB. Performed the experiments: DK WL DS. Analyzed the data: DK WL DS OB AK DEB. Contributed reagents/materials/analysis tools: SA PMH LC JB AK RHG. Wrote the paper: DK DEB.

                [¤a]

                Current address: Department of Microbiology, Gyeongsang National University College of Medicine, Jinju, Gyeongsangnam-do, Republic of Korea

                [¤b]

                Current address: Department of Medicine, University of Oklahoma, Oklahoma City, Oklahoma, United States of America

                Article
                09-PONE-RA-10161R1
                10.1371/journal.pone.0006859
                2731543
                19727398
                42ebeef4-35de-4bd9-b2d6-0487e4861f98
                Kersulyte et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 5 May 2009
                : 7 July 2009
                Page count
                Pages: 15
                Categories
                Research Article
                Evolutionary Biology/Microbial Evolution and Genomics
                Genetics and Genomics/Microbial Evolution and Genomics
                Microbiology/Microbial Evolution and Genomics
                Molecular Biology/Molecular Evolution
                Gastroenterology and Hepatology/Gastrointestinal Infections
                Infectious Diseases/Gastrointestinal Infections

                Uncategorized
                Uncategorized

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