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Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements

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 a...

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Autores principales: Kersulyte, Dangeruta, Lee, WooKon, Subramaniam, Dharmalingam, Anant, Shrikant, Herrera, Phabiola, Cabrera, Lilia, Balqui, Jacqueline, Barabas, Orsolya, Kalia, Awdhesh, Gilman, Robert H., Berg, Douglas E.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731543/
https://www.ncbi.nlm.nih.gov/pubmed/19727398
http://dx.doi.org/10.1371/journal.pone.0006859
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author Kersulyte, Dangeruta
Lee, WooKon
Subramaniam, Dharmalingam
Anant, Shrikant
Herrera, Phabiola
Cabrera, Lilia
Balqui, Jacqueline
Barabas, Orsolya
Kalia, Awdhesh
Gilman, Robert H.
Berg, Douglas E.
author_facet Kersulyte, Dangeruta
Lee, WooKon
Subramaniam, Dharmalingam
Anant, Shrikant
Herrera, Phabiola
Cabrera, Lilia
Balqui, Jacqueline
Barabas, Orsolya
Kalia, Awdhesh
Gilman, Robert H.
Berg, Douglas E.
author_sort Kersulyte, Dangeruta
collection PubMed
description 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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spelling pubmed-27315432009-09-03 Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements Kersulyte, Dangeruta Lee, WooKon Subramaniam, Dharmalingam Anant, Shrikant Herrera, Phabiola Cabrera, Lilia Balqui, Jacqueline Barabas, Orsolya Kalia, Awdhesh Gilman, Robert H. Berg, Douglas E. PLoS One Research Article 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. Public Library of Science 2009-09-03 /pmc/articles/PMC2731543/ /pubmed/19727398 http://dx.doi.org/10.1371/journal.pone.0006859 Text en Kersulyte et al. http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Kersulyte, Dangeruta
Lee, WooKon
Subramaniam, Dharmalingam
Anant, Shrikant
Herrera, Phabiola
Cabrera, Lilia
Balqui, Jacqueline
Barabas, Orsolya
Kalia, Awdhesh
Gilman, Robert H.
Berg, Douglas E.
Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements
title Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements
title_full Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements
title_fullStr Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements
title_full_unstemmed Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements
title_short Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements
title_sort helicobacter pylori's plasticity zones are novel transposable elements
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731543/
https://www.ncbi.nlm.nih.gov/pubmed/19727398
http://dx.doi.org/10.1371/journal.pone.0006859
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