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. 2016 Mar 17;4(2):e00131-16. doi: 10.1128/genomeA.00131-16

Whole-Genome Sequences of Two Campylobacter coli Isolates from the Antimicrobial Resistance Monitoring Program in Colombia

Johan F Bernal a, Pilar Donado-Godoy a, María Fernanda Valencia a, Maribel León b, Yolanda Gómez a, Fernando Rodríguez a, Richa Agarwala c, David Landsman c, Leonardo Mariño-Ramírez c,
PMCID: PMC4796127  PMID: 26988048

Abstract

Campylobacter coli, along with Campylobacter jejuni, is a major agent of gastroenteritis and acute enterocolitis in humans. We report the whole-genome sequences of two multidrug-resistance C. coli strains, isolated from the Colombian poultry chain. The isolates contain a variety of antimicrobial resistance genes for aminoglycosides, lincosamides, fluoroquinolones, and tetracycline.

GENOME ANNOUNCEMENT

Campylobacter spp. are microaerobic, non-spore-forming, Gram-negative, and oxidase-positive members of the Campylobacteraceae family (1). Campylobacter spp. are zoonotic pathogens (2) and some of the main bacteria associated with human food-borne illness (3, 4). Campylobacteriosis is frequently associated with the consumption of undercooked poultry meat and the mishandling of the raw poultry products (5, 6). Different Campylobacter spp. are recognized as causing human gastroenteritis worldwide (79). Campylobacter coli is commonly isolated from swine and less so from poultry and humans (7, 9). Although C. coli accounts for fewer infections in humans than Campylobacter jejuni, its impact is considerable (10), taking into account the increased capability for antimicrobial resistance (11), where multidrug efflux pumps play an important role as mechanisms of antibiotic resistance (3). A small number of studies in Colombia have focused on understanding the epidemiology of Campylobacter spp. and their associated antimicrobial resistance. To correct this deficiency, the Colombian Integrated Program for Antimicrobial Resistance Surveillance (COIPARS) (12, 13) has been included in the Colombia-wide Campylobacter surveillance program, whose priority is to generate information for different governmental institutions, agricultural enterprises, and food animal production systems. The findings from our studies in Colombia have shown that C. coli and C. jejuni contamination of raw poultry and poultry meat products present risk factors associated with acute illness in consumers of these products.

Here, we present the whole-genome sequences of two multidrug-resistant C. coli strains (M1483 and M1486), isolated from poultry meat collected from two retail stores in Bogotá, Colombia, as part of the COIPARS antimicrobial resistance monitoring program. Genomic DNA was isolated from overnight cultures using the PureLink Genomic DNA minikit (Invitrogen, Grand Island, NY, USA), and DNA libraries were prepared using SureSelect QXT sample preparation kit (Agilent, Santa Clara, CA, USA). The libraries were prepared according to the manufacturer’s instructions and sequenced on an Illumina HiScanSQ instrument with 1 × 151-bp single reads, according to standard Illumina protocols. The C. coli M1483 and M1486 genomes were assembled using the reference-guided assembler ARGO, developed at NCBI, and the de novo assembler SPAdes (14). The genome sequence of strains M1483 and M1486 consisted of 45 and 55 contigs, yielding total sequences of 1,683,490 bp and 1,780,967 bp, respectively. The overall G+C content of the isolates was determined to be 32%. Sequences were annotated using the NCBI Prokaryotic Genome Automatic Annotation Pipeline (PGAAP) and have been deposited in GenBank. The results of the genome annotation presenting the number of genes, coding sequences, pseudogenes, CRISPR arrays, rRNAs, tRNAs, and noncoding RNAs are summarized in Table 1.

TABLE 1 .

Campylobacter coli genome annotation statistics

Strain NCBI BioSample No. of genes No. of CDSsa No. of pseudogenes No. of CRISPR arrays No. of rRNAs No. of tRNAs No. of ncRNAsb GenBank accession no.
M1483 SAMN04358093 1,782 1,739 55 0 3 37 3 LQXL00000000
M1486 SAMN04358091 1,916 1,873 58 1 3 37 3 LQXK00000000
a

CDSs, coding sequences.

b

ncRNAs, noncoding RNAs.

A search for resistance-associated genes present in the isolates was performed using ResFinder version 2.1 (15) and enriched using RAST version 2.0 (16), both with default parameters. We found antimicrobial resistance genes for aminoglycosides (Aph 3′-III), lincosamides (InuC), fluoroquinolones (gyrA and gyrB), and tetracyclines (EF-G and TetO). Additionally, we found efflux pump genes (CmeA, CmeB, TolC, MATE, MFS, MacA, MacB, RND, AcrB, and OM) and CmeABCR operon genes, both associated with increased multidrug resistance.

Nucleotide sequence accession numbers.

This whole-genome shotgun project has been deposited in DDBJ/EMBL/GenBank under the accession numbers listed in Table 1. The versions described in this paper are the second versions.

ACKNOWLEDGMENTS

We are grateful to the Direction of the Laboratories of CORPOICA, Angelica Pichimata (CORPOICA), and Ivan Lesende (AGILENT) for performing the genome sequencing. The results of this research are a product of the Colombian Integrated Program for Antimicrobial Resistance Surveillance (COIPARS).

This research was supported by Corporación Colombiana de Investigación Agropecuaria (CORPOICA) and the Intramural Research Program of the NIH, NLM, NCBI.

Footnotes

Citation Bernal JF, Donado-Godoy P, Valencia MF, León M, Gómez Y, Rodríguez F, Agarwala R, Landsman D, Mariño-Ramírez L. 2016. Whole-genome sequences of two Campylobacter coli isolates from the antimicrobial resistance monitoring program in Colombia. Genome Announc 4(2):e00131-16. doi:10.1128/genomeA.00131-16.

REFERENCES

  • 1.Allos BM. 2001. Campylobacter jejuni infections: update on emerging issues and trends. Clin Infect Dis 32:1201–1206. doi: 10.1086/319760. [DOI] [PubMed] [Google Scholar]
  • 2.Wieczorek K, Osek J. 2013. Antimicrobial resistance mechanisms among Campylobacter. BioMed Res Int 2013:340605. doi: 10.1155/2013/340605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Mavri A, Smole Možina S. 2013. Effects of efflux-pump inducers and genetic variation of the multidrug transporter cmeB in biocide resistance of Campylobacter jejuni and Campylobacter coli. J Med Microbiol 62:400–411. doi: 10.1099/jmm.0.052316-0. [DOI] [PubMed] [Google Scholar]
  • 4.Read DS, Woodcock DJ, Strachan NJ, Forbes KJ, Colles FM, Maiden MC, Clifton-Hadley F, Ridley A, Vidal A, Rodgers J, Whiteley AS, Sheppard SK. 2013. Evidence for phenotypic plasticity among multihost Campylobacter jejuni and C. coli lineages, obtained using ribosomal multilocus sequence typing and Raman spectroscopy. Appl Environ Microbiol 79:965–973. doi: 10.1128/AEM.02521-12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Ma L, Wang Y, Shen J, Zhang Q, Wu C. 2014. Tracking Campylobacter contamination along a broiler chicken production chain from the farm level to retail in China. Int J Food Microbiol 181:77–84. doi: 10.1016/j.ijfoodmicro.2014.04.023. [DOI] [PubMed] [Google Scholar]
  • 6.Marotta F, Garofolo G, Di Donato G, Aprea G, Platone I, Cianciavicchia S, Alessiani A, Di Giannatale E. 2015. Population diversity of Campylobacter jejuni in poultry and its dynamic of contamination in chicken meat. BioMed Res Int 2015:859845. doi: 10.1155/2015/859845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Sheppard SK, Didelot X, Jolley KA, Darling AE, Pascoe B, Meric G, Kelly DJ, Cody A, Colles FM, Strachan NJ, Ogden ID, Forbes K, French NP, Carter P, Miller WG, McCarthy ND, Owen R, Litrup E, Egholm M, Affourtit JP, Bentley SD, Parkhill J, Maiden MC, Falush D. 2013. Progressive genome-wide introgression in agricultural Campylobacter coli. Mol Ecol 22:1051–1064. doi: 10.1111/mec.12162. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Skarp CPA, Hänninen ML, Rautelin HIK. 2015. Campylobacteriosis: the role of poultry meat. Clin Microbiol Infect [Epub ahead of print.] doi: 10.1016/j.cmi.2015.11.019. [DOI] [PubMed] [Google Scholar]
  • 9.Zautner AE, Goldschmidt AM, Thürmer A, Schuldes J, Bader O, Lugert R, Groß U, Stingl K, Salinas G, Lingner T. 2015. SMRT sequencing of the Campylobacter coli BfR-CA-9557 genome sequence reveals unique methylation motifs. BMC Genomics 16:1088. doi: 10.1186/s12864-015-2317-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Richards VP, Lefébure T, Pavinski Bitar PD, Stanhope MJ. 2013. Comparative characterization of the virulence gene clusters (lipooligosaccharide [LOS] and capsular polysaccharide [CPS]) for Campylobacter coli, Campylobacter jejuni subsp. jejuni and related Campylobacter species. Infect Genet Evol 14:200–213. doi: 10.1016/j.meegid.2012.12.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Bakhshi B, Naseri A, Alebouyeh M. 2016. Comparison of antimicrobial susceptibility of Campylobacter strains isolated from food samples and patients with diarrhea. Iran Biomed J 20:91–96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Donado-Godoy P, Bernal JF, Rodríguez F, Gomez Y, Agarwala R, Landsman D, Mariño-Ramírez L. 2015. Genome sequences of multidrug-resistant Salmonella enterica serovar paratyphi B (dT+) and Heidelberg Strains from the Colombian poultry chain. Genome Announc 3(5):e01265-15. doi: 10.1128/genomeA.01265-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Donado-Godoy P, Castellanos R, León M, Arevalo A, Clavijo V, Bernal J, León D, Tafur MA, Byrne BA, Smith WA, Perez-Gutierrez E. 2015. The Establishment of the Colombian Integrated Program for Antimicrobial Resistance Surveillance (COIPARS): A Pilot Project on Poultry Farms, Slaughterhouses and Retail market. Zoonoses Public Health 62(suppl 1):58–69. doi: 10.1111/zph.12192. [DOI] [PubMed] [Google Scholar]
  • 14.Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD, Pyshkin AV, Sirotkin AV, Vyahhi N, Tesler G, Alekseyev MA, Pevzner PA. 2012. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 19:455–477. doi: 10.1089/cmb.2012.0021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Zankari E, Hasman H, Cosentino S, Vestergaard M, Rasmussen S, Lund O, Aarestrup FM, Larsen MV. 2012. Identification of acquired antimicrobial resistance genes. J Antimicrob Chemother 67:2640–2644. doi: 10.1093/jac/dks261. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O. 2008. The RAST server: Rapid Annotations using Subsystems Technology. BMC Genomics 9:75. doi: 10.1186/1471-2164-9-75. [DOI] [PMC free article] [PubMed] [Google Scholar]

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