Abstract
Campylobacter jejuni, commonly found in poultry and meat products, causes gastroenteritis in humans. Here, we report the complete genome sequence of a C. jejuni strain, YH001, isolated from retail beef liver. The genome is 1,712,361 bp and has a 30.5% G+C content and two plasmids of 46.5 kb and 4.4 kb.
GENOME ANNOUNCEMENT
Campylobacter jejuni is a Gram-negative microaerophilic bacterium that colonizes the intestines of most warm-blooded hosts, including all food-producing animals and humans. The processing of poultry and other food-producing animals often results in pathogen contamination to consumable food products, leading to human infection. The prevalence of Campylobacter in retail meat products can be as high as 70% (1, 2). Each year, >0.8 million cases of Campylobacter illness are reported in the United States, with approximately 8,463 hospitalizations and 76 deaths (3). Additionally, the misuse of antibiotics in food-producing animals and environments has resulted in an increasing occurrence of antibiotic resistance in Campylobacter, which subsequently affects the efficacy of antibiotic treatment (4). Studies have shown that the colonization, adherence, and invasion of host epithelial cells and the induction of cell apoptosis are important virulence factors in Campylobacter infection, but the mechanism of pathogenesis is still poorly understood (5). The complete genome sequence and annotation of a new C. jejuni isolate from beef liver reported here will help identify the potential genetic determinants of virulence and antibiotic resistance in the pathogen.
C. jejuni YH001 was isolated from a beef liver purchased from a local supermarket, using a passive filtration method (6, 7). The genus and species information of the strain was first confirmed by 16S rRNA gene sequencing and multiplex real-time PCR (8, 9). Genomic DNA was extracted using the DNeasy blood and tissue kit (Qiagen) and subjected to sequencing using an Ion Torrent PGM sequencer and Ion 318 Chip (Life Technologies), following the preparation of a 400-bp fragment library and emulsion PCR amplification. The average read length is >300 nucleotides, with 350,000 to 450,000 reads per genome. The raw sequence reads were trimmed and processed using CLC Genomics Workbench 7.0 (Qiagen) and Sequencher 5.2.2 (Gene Codes) to yield de novo assemblies. The contigs were aligned with other Campylobacter genomes for gap-filling using long PCR and Sanger sequencing. The final assembly and potential misassemblies were validated by Sanger sequencing. All putative frameshifts were manually curated based on the coverage and quality of the given nucleotides via genome mapping. Automated gene and pseudogene prediction and annotation were performed using the PROKKA 1.10 software (10).
C. jejuni YH001 has a circular chromosome of 1,712,361 bp (30.5% G+C content), encoding 1,869 proteins. In addition, the strain carries two plasmids of 46,527 bp and 4,356 bp. Several structurally distinct and highly divergent type III secretory proteins were found in the large plasmid, which may represent environmental adaptation. The main virulence factor encoded by the cytolethal distending toxin gene cluster cdtABC is present in this strain. The Campylobacter multidrug efflux pump (CmeABC) and DNA gyrase, contributing to antibiotic resistance, were also found. A whole-genome comparison revealed that C. jejuni YH001 isolated from beef liver was phylogenetically distinct from most of the other C. jejuni strains in GenBank, particularly in the large plasmid containing C. jejuni integrated elements (CJIEs).
Nucleotide sequence accession number.
The sequence has been deposited in GenBank under the accession no. CP010058.
ACKNOWLEDGMENT
This research was supported by the U.S. Department of Agriculture, Agriculture Research Service.
Footnotes
Citation He Y, Yan X, Reed S, Xie Y, Chen C-Y, Irwin P. 2015. Complete genome sequence of Campylobacter jejuni YH001 from beef liver, which contains a novel plasmid. Genome Announc 3(1):e01492-14. doi:10.1128/genomeA.01492-14.
REFERENCES
- 1.Zhao C, Ge B, De Villena J, Sudler R, Yeh E, Zhao S, White DG, Wagner D, Meng J. 2001. Prevalence of Campylobacter spp., Escherichia coli, and Salmonella serovars in retail chicken, turkey, pork, and beef from the greater Washington, D.C., area. Appl Environ Microbiol 67:5431–5436. doi: 10.1128/AEM.67.12.5431-5436.2001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Williams A, Oyarzabal OA. 2012. Prevalence of Campylobacter spp. in skinless, boneless retail broiler meat from 2005 through 2011 in Alabama, USA. BMC Microbiol 12:184. doi: 10.1186/1471-2180-12-184. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Scallan E, Hoekstra RM, Angulo FJ, Tauxe RV, Widdowson M-A, Roy SL, Jones JL, Griffin PM. 2011. Foodborne illness acquired in the United States—major pathogens. Emerg Infect Dis 17:7–15. http://wwwnc.cdc.gov/eid/article/17/1/P1-1101_article. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Luangtongkum T, Jeon B, Han J, Plummer P, Logue CM, Zhang Q. 2009. Antibiotic resistance in Campylobacter: emergence, transmission and persistence. Future Microbiol 4:189–200. doi: 10.2217/17460913.4.2.189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Dasti JI, Tareen AM, Lugert R, Zautner AE, Gross U. 2010. Campylobacter jejuni: a brief overview on pathogenicity-associated factors and disease-mediating mechanisms. Int J Med Microbiol 300:205–211. doi: 10.1016/j.ijmm.2009.07.002. [DOI] [PubMed] [Google Scholar]
- 6.Jokinen CC, Koot JM, Carrillo CD, Gannon VP, Jardine CM, Mutschall SK, Topp E, Taboada EN. 2012. An enhanced technique combining pre-enrichment and passive filtration increases the isolation efficiency of Campylobacter jejuni and Campylobacter coli from water and animal fecal samples. J Microbiol Methods 91:506–513. doi: 10.1016/j.mimet.2012.09.005. [DOI] [PubMed] [Google Scholar]
- 7.Speegle L, Miller ME, Backert S, Oyarzabal OA. 2009. Use of cellulose filters to isolate Campylobacter spp. from naturally contaminated retail broiler meat. J Food Prot 72:2592–2596. [DOI] [PubMed] [Google Scholar]
- 8.He Y, Yao X, Gunther NW, Xie Y, Tu S, Shi X. 2010. Simultaneous detection and differentiation of Campylobacter jejuni, C. coli, and C. lari in chickens using a multiplex real-time PCR assay. Food Anal Methods 3:321–329. doi: 10.1007/s12161-010-9136-6. [DOI] [Google Scholar]
- 9.Irwin P, Nguyen TL, Chen CY. 2008. Binding of nontarget microorganisms from food washes to anti-Salmonella and anti-E. coli O157 immunomagnetic beads: minimizing the errors of random sampling in extreme dilute systems. Anal Bioanal Chem 391:515–524. doi: 10.1007/s00216-008-1961-8. [DOI] [PubMed] [Google Scholar]
- 10.Seemann T. 2014. Prokka: rapid prokaryotic genome annotation. Bioinformatics 30:2068–2069. doi: 10.1093/bioinformatics/btu153. [DOI] [PubMed] [Google Scholar]