Helicobacter Pylori's Plasticity Zones Are Novel Transposable Elements

被引:75
作者
Kersulyte, Dangeruta
Lee, WooKon
Subramaniam, Dharmalingam
Anant, Shrikant
Herrera, Phabiola
Cabrera, Lilia
Balqui, Jacqueline
Barabas, Orsolya
Kalia, Awdhesh
Gilman, Robert H.
Berg, Douglas E.
机构
[1] Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO
[2] Division of Gastroenterology, Department of Medicine, Washington University School of Medicine, St. Louis, MO
[3] Laboratorios de Investigacion y Desarrollo, Facultad de Ciencias, Universidad Peruana Cayetano Heredia, Lima
[4] Asociacion Benefica PRISMA, Lima
[5] Laboratory of Molecular Biology, National Institute of Digestive and Kidney Diseases, National Institute of Health, Bethesda, MD
[6] Department of Biology, University of Louisville, Louisville, KY
[7] Department of International Health, The Johns Hopkins Bloomberg School of Public Health, Baltimore, MD
[8] Department of Genetics, Washington University School of Medicine, St. Louis, MO
[9] Department of Microbiology, Gyeongsang National University College of Medicine, Jinju, Gyeongsangnam-do
[10] Department of Medicine, University of Oklahoma, Oklahoma City, OK
关键词
D O I
10.1371/journal.pone.0006859
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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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