Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements
Open Access
- 3 September 2009
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 4 (9) , e6859
Abstract
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”. 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. 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.Keywords
This publication has 57 references indexed in Scilit:
- Asymmetric DNA requirements in Xer recombination activation by FtsKNucleic Acids Research, 2009
- Probing deeper into first American studiesProceedings of the National Academy of Sciences, 2009
- Role of type IV secretion inHelicobacter pyloripathogenesisCellular Microbiology, 2008
- Roles of the plasticity regions of Helicobacter pylori in gastroduodenal pathogenesisJournal of Medical Microbiology, 2008
- Mechanism of IS200/IS605 Family DNA Transposases: Activation and Transposon-Directed Target Site SelectionCell, 2008
- OipA plays a role in Helicobacter pylori-induced focal adhesion kinase activation and cytoskeletal re-organizationCellular Microbiology, 2007
- Agrobacterium ParA/MinD‐like VirC1 spatially coordinates early conjugative DNA transfer reactionsThe EMBO Journal, 2007
- An African origin for the intimate association between humans and Helicobacter pyloriNature, 2007
- The complete genome sequence of a chronic atrophic gastritis Helicobacter pylori strain: Evolution during disease progressionProceedings of the National Academy of Sciences, 2006
- Selfish genes, the phenotype paradigm and genome evolutionNature, 1980