Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1782170958328496128 |
---|---|
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. |
format | Text |
id | pubmed-2731543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kersulytedangeruta helicobacterpylorisplasticityzonesarenoveltransposableelements AT leewookon helicobacterpylorisplasticityzonesarenoveltransposableelements AT subramaniamdharmalingam helicobacterpylorisplasticityzonesarenoveltransposableelements AT anantshrikant helicobacterpylorisplasticityzonesarenoveltransposableelements AT herreraphabiola helicobacterpylorisplasticityzonesarenoveltransposableelements AT cabreralilia helicobacterpylorisplasticityzonesarenoveltransposableelements AT balquijacqueline helicobacterpylorisplasticityzonesarenoveltransposableelements AT barabasorsolya helicobacterpylorisplasticityzonesarenoveltransposableelements AT kaliaawdhesh helicobacterpylorisplasticityzonesarenoveltransposableelements AT gilmanroberth helicobacterpylorisplasticityzonesarenoveltransposableelements AT bergdouglase helicobacterpylorisplasticityzonesarenoveltransposableelements |