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Updated: Sep 24, 2025

Mouse Models Of Helicobacter Infection And Gastric Pathologies
Published on: October 18, 2018
Helicobacter cinaedi is a human-adapted lineage in the Helicobacter cinaedi/canicola/'magdeburgensis' complex
Yasuhiro Gotoh1, Yuya Atsuta2, Takako Taniguchi3
1Department of Bacteriology, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.
Insights
Helicobacter cinaedi, a human pathogen, is genetically distinct from animal strains, forming a human-adapted lineage (clade I) with unique antimicrobial resistance and virulence factors. This finding aids in identifying H. cinaedi in human samples.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Helicobacter cinaedi causes human diseases like bacteremia.
- Genetic differences between human H. cinaedi and animal H. canicola strains are poorly understood.
- Enterohepatic Helicobacter species are increasingly recognized pathogens.
Purpose of the Study:
- To investigate the genetic diversity within the Helicobacter cinaedi/canicola/'magderbugensis' (HCCM) complex.
- To identify genomic features distinguishing human-adapted H. cinaedi from animal-associated strains.
- To develop a method for detecting H. cinaedi in metagenomic data.
Main Methods:
- Whole-genome sequencing of 43 human and animal H. cinaedi/canicola-like strains.
- Bioinformatic analysis and comparative genomics of 81 public genome sequences.
- Development and application of a metagenomic search tool for H. cinaedi.
Main Results:
- Four distinct clades (I-IV) were identified within the HCCM complex.
- Clade I represents a human-adapted H. cinaedi sensu stricto lineage.
- Clade I strains possess unique antimicrobial resistance mutations, larger genomes, CRISPR-Cas, and T6SS systems, indicative of horizontal gene transfer and adaptation.
Conclusions:
- H. cinaedi sensu stricto is a distinct human-adapted lineage within the HCCM complex.
- Genomic features of clade I suggest adaptation to the human host and potential roles in pathogenesis.
- The developed metagenomic method successfully identified human-adapted H. cinaedi in fecal samples.
Abstract:
Helicobacter cinaedi is an enterohepatic Helicobacter that causes bacteremia and other diseases in humans. While H. cinaedi-like strains are isolated from animals, including dog isolates belonging to a recently proposed H. canicola, little is known about the genetic differences between H. cinaedi and these animal isolates. Here, we sequenced 43 H. cinaedi- or H. canicola-like strains isolated from humans, hamsters, rats and dogs and collected 81 genome sequences of H. cinaedi, H. canicola and other enterohepatic Helicobacter strains from public databases. Genomic comparison of these strains identified four distinct clades (clades I-IV) in H. cinaedi/canicola/'magderbugensis' (HCCM) complex. Among these, clade I corresponds to H. cinaedi sensu stricto and represents a human-adapted lineage in the complex. We identified several genomic features unique to clade I. They include the accumulation of antimicrobial resistance-related mutations that reflects the human association of clade I and the larger genome size and the presence of a CRISPR-Cas system and multiple toxin-antitoxin and restriction-modification systems, both of which indicate the contribution of horizontal gene transfer to the evolution of clade I. In addition, nearly all clade I strains but only a few strains belonging to one minor clade contained a highly variable genomic region encoding a type VI secretion system (T6SS), which could play important roles in gut colonization by killing competitors or inhibiting their growth. We also developed a method to systematically search for H. cinaedi sequences in large metagenome data sets based on the results of genome comparison. Using this method, we successfully identified multiple HCCM complex-containing human faecal metagenome samples and obtained the sequence information covering almost the entire genome of each strain. Importantly, all were clade I strains, supporting our conclusion that H. cinaedi sensu stricto is a human-adapted lineage in the HCCM complex.
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