Complete genome sequence of Helicobacter pylori B128 7.13 and a single‐step method for the generation of unmarked mutations

Research output: Contribution to journalArticle

Authors

  • Emma M. Dawson
  • Karl A. Dunne
  • Judyta Praszkier
  • Dana Alfawaz
  • Simon Woelfel
  • Amanda De Paoli
  • Mohammad Hassan
  • Richard L. Ferrero

Colleges, School and Institutes

External organisations

  • Institute of Microbiology & Infection, College of Medical and Dental Sciences, University of Birmingham, Birmingham B152TT, UK.
  • Hudson Institute for Medical Research, Monash Melbourne Victoria Australia
  • Infection and Immunity Program, Monash Biomedicine Discovery Institute and Department of Microbiology Monash University Melbourne Victoria Australia

Abstract

Background: Helicobacter pylori represents an interesting model of bacterial pathogenesis given that most infections are asymptomatic, while a minority of infections cause severe gastric disease. H pylori strain B128 7.13 is used extensively to understand H pylori pathophysiology. Due to extensive restriction‐modification systems, the fact that only some H pylori strains are naturally transformable, the inability of common plasmid and transposon vectors to replicate in this bacterium, as well as the limited number of antibiotic cassettes that are functional in H pylori, there are relatively few genetic tools for the mutagenesis of this bacterium.

Materials and Methods: Here, we use PacBio and Illumina sequencing to reveal the complete genome sequence of H pylori B128 7.13. Furthermore, we describe a system to generate markerless and scarless mutations on the H pylori chromosome using the counter‐selection marker, galactokinase from Escherichia coli.

Results: We show that this mutagenesis strategy can be used to generate in‐frame insertions, gene deletions, and multiple independent mutations in B128 7.13. Using the closed genome as a reference, we also report the absence of second site chromosomal mutations and/or rearrangements in our mutagenized strains. We compare the genome sequence of H pylori B128 7.13 with a closely related strain, H pylori B8, and reveal one notable region of difference, which is a 1430 bp insertion encoding a H pylori‐specific DUF874 family protein of unknown function.

Conclusions: This article reports the closed genome of the important H pylori B128 7.13 strain and a mutagenesis method that can be adopted by researchers as an alternative strategy to generate isogenic mutants of H pylori in order to further our understanding of this bacterium.

Bibliographic note

© 2019. The Authors. Helicobacter Published by John Wiley & Sons Ltd.

Details

Original languageEnglish
Article numbere12587
Number of pages10
JournalHelicobacter
Volume24
Issue number4
Early online date7 May 2019
Publication statusPublished - Aug 2019

Keywords

  • gene mutation, genetic, Helicobacter pylori