Campylobacter concisus
is an emerging enteric pathogen that is associated with several gastrointestinal diseases, such as inflammatory bowel disease (IBD), which includes Crohn’s disease (CD) and ulcerative colitis (UC). Currently, only three complete
C. concisus
genomes are available and more complete
C. concisus
genomes are needed in order to better understand the genomic features and pathogenicity of this emerging pathogen. DNA extracted from 22
C
.
concisus
strains were subjected to Oxford Nanopore genome sequencing. Complete genome assembly was performed using Nanopore genome data in combination with previously reported short-read Illumina data. Genome features of complete
C. concisus
genomes were analysed using bioinformatic tools. The enteric disease associations of
C. concisus
plasmids were examined using 239
C
.
concisus
strains and confirmed using PCRs. Proteomic analysis was used to examine T6SS secreted proteins. We successfully obtained 13 complete
C. concisus
genomes in this study. Analysis of 16 complete
C. concisus
genomes (3 from public databases) identified multiple novel plasmids. pSma1 plasmid was found to be associated with severe UC. Sec-SRP, Tat and T6SS were found to be the main secretion systems in
C. concisus
and proteomic data showed a functional T6SS despite the lack of ClpV. T4SS was found in 25% of complete
C. concisus
genomes. This study also found that GS2 strains had larger genomes and higher GC content than GS1 strains and more often had plasmids. In conclusion, this study provides fundamental genomic data for understanding
C. concisus
plasmids, genomospecies features, evolution, secretion systems and pathogenicity.