Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2015 Jun 25;3(3):e00684-15. doi: 10.1128/genomeA.00684-15

Whole-Genome Sequences of 15 Strains of Staphylococcus aureus subsp. aureus Isolated from Foodstuff and Human Clinical Samples

Julien Crovadore a, Gautier Calmin b, Jenna Tonacini c, Romain Chablais a, Andreas Baumgartner d, Bruno Schnyder c, Elisabeth Hodille e,f, François Lefort a,
PMCID: PMC4481287  PMID: 26112789

Abstract

The whole-genome sequences of 15 strains of Staphylococcus aureus (10 strains isolated from foodstuff samples in Switzerland and five from human clinical samples) were obtained by Illumina sequencing. Most strains fit within the known diversity for the species, but one (SA-120) possessed a higher G+C content and a higher number of genes than usual.

GENOME ANNOUNCEMENT

Staphylococcus aureus subsp. aureus, a pathogenic bacterium, is the cause of a broad spectrum of human diseases ranging from mild skin infections to endocarditis, sepsis, and pneumonia (1), and its pathogenic potential is enhanced by various antibiotic resistances (2). It also causes infections in farm animals, which may be passed to farmers (3), and the contamination of primary food products represents a risk of major concern for public health (4). We report here the sequencing of 10 strains collected from various ready-to-eat food by the Federal Food Safety and Veterinary Office (Switzerland), along with 5 reference strains provided by the French National Reference Center for Staphylococcus (France).

Genomic DNA of the 15 S. aureus strains was extracted from pure cultures grown to stationary phase, according to an adapted protocol (5). Libraries were constructed using the Nextera XT kit (Illumina, USA). All genomes were sequenced within one Illumina MiSeq run at 2 × 250-bp read length, using a MiSeq reagent kit version 2 (Illumina). Trimming and quality control of the raw reads were performed with FastQC (6). Genome assemblies were computed with the SPAdes genome assembler 3.1 (7). The resulting contigs were arranged with BioEdit (8) and analyzed with QUAST (9). The genomes were screened in silico with PlasmidFinder (10) to identify all circular or integrated plasmid genomes. Automated gene annotation was carried out by the NCBI Prokaryotic Genome Automatic Annotation Pipeline (PGAAP) (11) and reviewed with RAST version 2.0 (12).

Mass parallel sequencing produced between 775,000 and 1,785,000 reads of 250 bp for a genome coverage ranging between 69-fold and 140-fold. The total genome lengths ranged between 2,740,099 bp (FRI151m) and 3,012,213 bp (SA-120), which is congruent with the known diversity within this species. Genomes varied between 27 and 174 contigs >500 bp. The G+C content was in the known range for the 38 genome groups of S. aureus, except for 3 strains with G+C contents of 33.15% (SA-067 and SA-083) and 35.85% (SA-120). Eight strains (A900624, DSM 799, FRI1151m, SA-022, SA-038, SA-047, SA-067, and SA-260) harbored a single plasmid, while one contained two plasmids (CCM5757). The plasmid lengths varied between 4,566 bp and 37,692 bp (both plasmids from CCM5757). Fourteen genomes contained between 2,823 (FRI1151m) and 3,113 (CCM5757) genes, corresponding to 2,673 (SA-006) to 2,996 (CCM5757) proteins, fitting in the known range for S. aureus, while strain SA-120 displayed 3,351 genes for 3,161 proteins, which is outside the common range. None of the strains was methicillin or vancomycin resistant, six strains were resistant to penicillin, and all contained resistance genes for trimethoprim, sulfonamide, quinolone, rifamycin, kirromycin, teicoplanin, and a multiple peptide resistance factor gene. All strains harbored a variety of enterotoxin, exotoxin, and other virulence factor genes, while 2 strains (SA-006 and SA-260) owned a gene for a toxic shock syndrome toxin.

Nucleotide sequence accession numbers.

The nucleotide sequence accession numbers are shown in Table 1.

Table 1.

Accession numbers for the strains in this study

ACKNOWLEDGMENTS

This work was supported by the Research Call Healthfood of the HES-SO University of Applied Sciences and Arts Western Switzerland under project 39244 (SE-Quicktest).

We acknowledge the cantonal laboratories of food control in Basel-Stadt, Bern, Sankt Gallen, Zürich, Vaud, and Wallis for collecting field isolates of coagulase-positive staphylococci.

Footnotes

Citation Crovadore J, Calmin G, Tonacini J, Chablais R, Baumgartner A, Schnyder B, Hodille E, Lefort F. 2015. Whole-genome sequences of 15 strains of Staphylococcus aureus subsp. aureus isolated from foodstuff and human clinical samples. Genome Announc 3(3):e00684-15. doi:10.1128/genomeA.00684-15.

REFERENCES

  • 1.Tenover FC, Gayne RP. 2000. The epidemiology of Staphylococcus infections, p 414–421. In Fischetti VA, Novick RP, Ferretti JJ, Portnoy DA, Rood JI (ed), Gram-positive pathogens. ASM Press, Washington, DC. [Google Scholar]
  • 2.Lindsay JA, Holden MT. 2004. Staphylococcus aureus: superbug, super genome? Trends Microbiol 12:378–385. doi: 10.1016/j.tim.2004.06.004. [DOI] [PubMed] [Google Scholar]
  • 3.Fluit AC. 2012. Livestock-associated Staphylococcus aureus. Clin Microbiol Infect 18:735–744. doi: 10.1111/j.1469-0691.2012.03846.x. [DOI] [PubMed] [Google Scholar]
  • 4.Kadariya J, Smith TC, Thapaliya D. 2014. Staphylococcus aureus and staphylococcal food-borne disease: an ongoing challenge in public health. Biomed Res Int 2014:827965. doi: 10.1155/2014/827965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Lefort F, Douglas GC. 1999. An efficient micro-method of DNA isolation from mature leaves of four hardwood tree species Acer, Fraxinus, Prunus and Quercus. Ann For Sci 56:259–263. doi: 10.1051/forest:19990308. [DOI] [Google Scholar]
  • 6.Andrews S. 2010. FastQC: a quality control tool for high throughput sequence data. http://www.bioinformatics.babraham.ac.uk/projects/fastqc.
  • 7.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]
  • 8.Hall TA. 1999. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser 41:95–98. [Google Scholar]
  • 9.Gurevich A, Saveliev V, Vyahhi N, Tesler G. 2013. QUAST: quality assessment tool for genome assemblies. Bioinformatics 29:1072–1075. doi: 10.1093/bioinformatics/btt086. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Carattoli A, Zankari E, García-Fernández A, Voldby Larsen M, Lund O, Villa L, Møller Aarestrup F, Hasman H. 2014. In silico detection and typing of plasmids using PlasmidFinder and plasmid multilocus sequence typing. Antimicrob Agents Chemother 58:3895–3903. doi: 10.1128/AAC.02412-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Tatusova T, DiCuccio M, Badretdin A, Chetvernin V, Ciufo S, Li W. 2013. Prokaryotic genome annotation pipeline. In The NCBI handbook, 2nd ed., National Center for Biotechnology Information, Bethesda, MD: http://www.ncbi.nlm.nih.gov/books/NBK174280/. [Google Scholar]
  • 12.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]

Articles from Genome Announcements are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES