Complementation system for Helicobacter pylori

Jinmoon Kim, Sung Whan Kim, Sungil Jang, Scott S. Merrell, JeongHeon Cha

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Previously Langford et al. (2006) developed the pIR203C04 complementation system for Helicobacter pylori, which can be used to complement and restore phenotypic effects in H. pylori mutant, and furthermore they used the complementation system in vivo experiments to animals without altering the ability of strain SSI to colonize mice. In their previous study, the pIR203C04 was able to transform 26695, SSI, J99, and 43504 H. pylori strains by an electroporation method. However, in the present study using a natural transformation the pIR203C04 transformed only 26695 H. pylori but not SSI, J99, 7.13, and G27 H. pylori strains. Since the useful complementation system has a limitation of narrow selection among H. pylori strains, we redesigned the complementation system for the improvement. The same intergenic chromosomal site between hp0203 and hp0204 was utilized for the new complementation system because the insertion at the intergenic site didn't show any polar effects and disruption of other H. pylori genes. The genome sequence analysis showed that the intergenic regions among H. pylori strains may have too low homology to each others to do a homologous recombination. Thus, in addition to the short intergenic region, the fragments of the new complementation system included 3′ conserved parts of hp0203 and hp0204 coding regions. Between the fragments there are a chloramphenicol acetyltransferase cassette and multicloning sites, resulting in pKJMSH. DNA fragment of the interest can be cloned into the multicloning sites of pKJMSH and the fragment can be integrated at the intergenic region of H. pylori chromosome by the homologous recombination. Indeed, by the natural transformation, pKJMSH was able to transform all five H. pylori strains of 26695, SSI, J99, 7.13, and G27, which are common for the investigation of molecular pathogenesis. Thus, the new pKJMSH complementation system is applicable to most H. pylori wild-type stains.

Original languageEnglish
Pages (from-to)481-486
Number of pages6
JournalJournal of Microbiology
Volume49
Issue number3
DOIs
Publication statusPublished - 2011 Jun 1

Fingerprint

Helicobacter pylori
Intergenic DNA
Homologous Recombination
Chloramphenicol O-Acetyltransferase
Electroporation
Sequence Analysis
Coloring Agents
Chromosomes
Genome
DNA

All Science Journal Classification (ASJC) codes

  • Microbiology
  • Applied Microbiology and Biotechnology

Cite this

Kim, Jinmoon ; Kim, Sung Whan ; Jang, Sungil ; Merrell, Scott S. ; Cha, JeongHeon. / Complementation system for Helicobacter pylori. In: Journal of Microbiology. 2011 ; Vol. 49, No. 3. pp. 481-486.
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Complementation system for Helicobacter pylori. / Kim, Jinmoon; Kim, Sung Whan; Jang, Sungil; Merrell, Scott S.; Cha, JeongHeon.

In: Journal of Microbiology, Vol. 49, No. 3, 01.06.2011, p. 481-486.

Research output: Contribution to journalArticle

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