Genome Sequencing Reveals a Phage in Helicobacter pylori

Author:

Lehours Philippe12,Vale Filipa F.3,Bjursell Magnus K.4,Melefors Ojar5,Advani Reza5,Glavas Steve5,Guegueniat Julia1,Gontier Etienne6,Lacomme Sabrina6,Alves Matos António78,Menard Armelle1,Mégraud Francis12,Engstrand Lars59,Andersson Anders F.5

Affiliation:

1. INSERM U853, Bordeaux, France

2. Université de Bordeaux, Centre National de Référence des Campylobacters et des Hélicobacters, Bordeaux, France

3. Faculty of Engineering, Catholic University of Portugal, Lisbon, Portugal

4. Science for Life Laboratory and Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden

5. Swedish Institute for Infectious Disease Control, Solna, Sweden

6. Université de Bordeaux, Bordeaux Imaging Center, Bordeaux, France

7. Pathological Anatomy Department, Curry Cabral Hospital, Lisbon, Portugal

8. University of Aveiro, Center for Environmental and Marine Studies, Aveiro, Portugal

9. Karolinska Institute, Department of Microbiology, Tumor and Cell Biology, Stockholm, Sweden

Abstract

ABSTRACT Helicobacter pylori chronically infects the gastric mucosa in more than half of the human population; in a subset of this population, its presence is associated with development of severe disease, such as gastric cancer. Genomic analysis of several strains has revealed an extensive H. pylori pan-genome, likely to grow as more genomes are sampled. Here we describe the draft genome sequence (63 contigs; 26× mean coverage) of H. pylori strain B45, isolated from a patient with gastric mucosa-associated lymphoid tissue (MALT) lymphoma. The major finding was a 24.6-kb prophage integrated in the bacterial genome. The prophage shares most of its genes (22/27) with prophage region II of Helicobacter acinonychis strain Sheeba. After UV treatment of liquid cultures, circular DNA carrying the prophage integrase gene could be detected, and intracellular tailed phage-like particles were observed in H. pylori cells by transmission electron microscopy, indicating that phage production can be induced from the prophage. PCR amplification and sequencing of the integrase gene from 341 H. pylori strains from different geographic regions revealed a high prevalence of the prophage (21.4%). Phylogenetic reconstruction showed four distinct clusters in the integrase gene, three of which tended to be specific for geographic regions. Our study implies that phages may play important roles in the ecology and evolution of H. pylori . IMPORTANCE Helicobacter pylori chronically infects the gastric mucosa in more than half of the human population, and while most of the infected individuals do not develop disease, H. pylori infection doubles the risk of developing gastric cancer. An abundance and diversity of viruses (phages) infect microbial populations in most environments and are important mediators of microbial diversity. Our finding of a 24.6-kb prophage integrated inside an H. pylori genome and the observation of circular integrase gene-containing DNA and phage-like particles inside cells upon UV treatment demonstrate that we have discovered a viable H. pylori phage. The additional finding of integrase genes in a large proportion of screened isolates of diverse geographic origins indicates that the prevalence of prophages may have been underestimated in H. pylori . Since phages are important drivers of microbial evolution, the discovery should be important for understanding and predicting genetic diversity in H. pylori .

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

Reference72 articles.

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