Literature DB >> 9563837

A stable shuttle vector system for efficient genetic complementation of Helicobacter pylori strains by transformation and conjugation.

D Heuermann1, R Haas.   

Abstract

A versatile plasmid shuttle vector system was constructed, which is useful for genetic complementation of Helicobacter pylori strains or mutants with cloned genes of homologous or heterologous origin. The individual plasmid vectors consist of the minimal essential genetic elements, including an origin of replication for Escherichia coli, a H. pylori-specific replicon originally identified on a small cryptic H. pylori plasmid, an oriT sequence and a multiple cloning site. Shuttle plasmid pHel2 carries a chloramphenicol resistance cassette (catGC) and pHel3 contains a kanamycin resistance gene (aphA-3) as the selectable marker; both are functional in E. coli and H. pylori. The shuttle plasmids were introduced into the H. pylori strain P1 by natural transformation. A efficiency of 7.0 x 10(-7) and 4.7 x 10(-7) transformants per viable recipient was achieved with pHel2 and pHel3, respectively, and both vectors showed stable, autonomous replication in H. pylori. An approximately 100-fold higher H. pylori transformation rate was obtained when the shuttle vectors for transformation were isolated from the homologous H. pylori strain, rather than E. coli, indicating that DNA restriction and modification mechanisms play a crucial role in plasmid transformation. Interestingly, both shuttle vectors could also be mobilized efficiently from E. coli into different H. pylori recipients, with pHel2 showing an efficiency of 2.0 x 10(-5) transconjugants per viable H. pylori P1 recipient. Thus, DNA restriction seems to be strongly reduced or absent during conjugal transfer. The functional complementation of a recA-deficient H. pylori mutant by the cloned H. pylori recA+ gene, and the expression of the heterologous green fluorescent protein (GFP) in H. pylori demonstrate the general usefulness of this system, which will significantly facilitate the molecular analysis of H. pylori virulence factors in the future.

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Year:  1998        PMID: 9563837     DOI: 10.1007/s004380050677

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  82 in total

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4.  Draft genome sequences of Helicobacter pylori strains 17874 and P79.

Authors:  Ceara D Clancy; Brian M Forde; Stanley A Moore; Paul W O'Toole
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5.  CagA-dependent downregulation of B7-H2 expression on gastric mucosa and inhibition of Th17 responses during Helicobacter pylori infection.

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7.  Loss of a Cardiolipin Synthase in Helicobacter pylori G27 Blocks Flagellum Assembly.

Authors:  Joshua K Chu; Shiwei Zhu; Carmen M Herrera; Jeremy C Henderson; Jun Liu; M Stephen Trent; Timothy R Hoover
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8.  The Helicobacter pylori adhesin protein HopQ exploits the dimer interface of human CEACAMs to facilitate translocation of the oncoprotein CagA.

Authors:  Daniel A Bonsor; Qing Zhao; Barbara Schmidinger; Evelyn Weiss; Jingheng Wang; Daniel Deredge; Robert Beadenkopf; Blaine Dow; Wolfgang Fischer; Dorothy Beckett; Patrick L Wintrode; Rainer Haas; Eric J Sundberg
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9.  The Helicobacter pylori UreI protein is not involved in urease activity but is essential for bacterial survival in vivo.

Authors:  S Skouloubris; J M Thiberge; A Labigne; H De Reuse
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10.  Helicobacter pylori flagellar hook-filament transition is controlled by a FliK functional homolog encoded by the gene HP0906.

Authors:  Kieran A Ryan; Najma Karim; Mulugeta Worku; Charles W Penn; Paul W O'Toole
Journal:  J Bacteriol       Date:  2005-08       Impact factor: 3.490

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