The whole-genome sequence of Staphylococcus argenteus strain B3-25B, isolated from retail beef liver, comprises a circular chromosome (2,676,222 bp) and a single plasmid (21,570 bp). The chromosome harbors genes encoding the type VII secretion system and several virulence factors.
ABSTRACT
The whole-genome sequence of Staphylococcus argenteus strain B3-25B, isolated from retail beef liver, comprises a circular chromosome (2,676,222 bp) and a single plasmid (21,570 bp). The chromosome harbors genes encoding the type VII secretion system and several virulence factors.
ANNOUNCEMENT
Staphylococcus argenteus belongs to the Staphylococcus aureus-related complex, formerly known as Staphylococcus aureus clonal complex 75 (1). Recent studies revealed the global distribution of S. argenteus isolated from both humans and animals (2–4); however, its prevalence and distribution remain unclear due to the difficulties in differentiating between methicillin-resistant S. aureus (MRSA) and S. argenteus (5). Initially, S. argenteus was thought to be less virulent than S. aureus due to the lack of staphyloxanthin, but subsequent deaths have shown its clinical importance (2, 6, 7). Moreover, genes encoding toxins such as staphylococcal enterotoxin, hemolysin, and Panton-Valentine leukocidin were associated with S. argenteus (4, 7–9). A recent study indicated the ability of S. argenteus to cause staphylococcal food poisoning, which indicates that this bacterium is highly toxigenic and is a potential foodborne pathogen (10).
Herein, we announce the complete genome sequence of S. argenteus strain B3-25B, which comprises a single chromosome and plasmid (pSALNBL21) of 2,676,222 bp and 21,570 bp, respectively. S. argenteus strain B3-25B was previously isolated in our laboratory from retail beef liver (11). S. argenteus cells were grown in tryptic soy agar (TSA) at 37°C for 16 to 24 h and then used for genomic DNA isolation. Genomic DNA was isolated using a DNeasy blood and tissue kit (Qiagen, Valencia, CA). Plasmid DNA was confirmed using S1 nuclease pulsed-field gel electrophoresis (PFGE), as described previously (12). A library was prepared with the Nextera XT kit (Illumina, Inc., San Diego, CA), and next-generation sequencing was conducted using an Illumina V2 reagent kit with 2 × 250 cycles. The sequence reads which passed the initial MiSeq quality standards were assessed using the CLC Genomics Workbench v. 12.0 (Qiagen) and trimmed for adapters, low-quality reads, and short reads. A total of 2,988,566 paired-end reads were submitted to the comprehensive genome analysis service at PATRIC v. 3.5.39 (13) for de novo assembly using the default settings of SPAdes v. 3.13.0 (14). A total of 39 contigs were joined to assemble the circular chromosome by aligning them against the closest reference, Staphylococcus argenteus strain BN75 (NCBI RefSeq accession number NZ_CP015758), using the default parameters of the genome-finishing module plugin v. 1.9 of the CLC Genomics Workbench v. 12.0 (Qiagen). The reads were also submitted to the plasmidSPAdes tool using default settings (15), which resulted in the identification of the plasmid as a single circular contig.
The B3-25B genome was annotated using the RAST toolkit (RASTtk) (16) and the NCBI Prokaryotic Genome Annotation Pipeline. The chromosome has a GC content of 32.3% and contained 2,447 predicted coding DNA sequences (CDSs), including 63 RNAs and 287 subsystems. Chromosomally borne virulence factors included autolysin-, fibronectin-, and fibrinogen-binding proteins, extracellular and intercellular adherence proteins, elastin-binding proteins, and staphylococcal protein A. Genes encoding protease, hyaluronate lyase, lipase, staphylocoagulase, and thermonuclease were identified, along with genes involved in immune system invasion and the type VII secretion system. Of special interest was the presence of genes encoding hemolysin (hly, hld, hlgABC), exfoliative toxin, and exotoxins 2, 7, 9, 10, 11, 12, 13, 15, 16, and 23. Genetic elements that foster survival during food processing were detected, such as those that enhance survival in response to electrophiles, osmotic and oxidative stress, and thermal stress. Genes responsible for heavy metal tolerance (cobalt/zinc/cadmium, arsenate, and mercury), antibiotic resistance (fluoroquinolones and multidrug resistance efflux pumps), and bile resistance were identified. The blaZ gene was detected on the plasmid, which may confer resistance to β-lactam antibiotics.
Data availability.
The whole-genome shotgun data for Staphylococcus argenteus strain B3-25B have been deposited in GenBank under the accession numbers CP042286 for the chromosome and CP042287 for plasmid pSALNBL21. The raw sequence reads have been deposited in the Sequence Read Archive (SRA) under accession number PRJNA555633.
ACKNOWLEDGMENT
We thank Daya Marasini for his technical assistance with the MiSeq run.
REFERENCES
- 1.Tong SYC, Sharma-Kuinkel BK, Thaden JT, Whitney AR, Yang S-J, Mishra NN, Rude T, Lilliebridge RA, Selim MA, Ahn SH, Holt DC, Giffard PM, Bayer AS, DeLeo FR, Fowler VG. 2013. Virulence of endemic nonpigmented northern Australian Staphylococcus aureus clone (clonal complex 75, S. argenteus) is not augmented by staphyloxanthin. J Infect Dis 208:520–527. doi: 10.1093/infdis/jit173. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Thaipadungpanit J, Amornchai P, Nickerson EK, Wongsuvan G, Wuthiekanun V, Limmathurotsakul D, Peacock SJ. 2015. Clinical and molecular epidemiology of Staphylococcus argenteus infections in Thailand. J Clin Microbiol 53:1005–1008. doi: 10.1128/JCM.03049-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Schuster D, Rickmeyer J, Gajdiss M, Thye T, Lorenzen S, Reif M, Josten M, Szekat C, Melo LDR, Schmithausen RM, Liégeois F, Sahl H-G, Gonzalez J-PJ, Nagel M, Bierbaum G. 2017. Differentiation of Staphylococcus argenteus (formerly: Staphylococcus aureus clonal complex 75) by mass spectrometry from S. aureus using the first strain isolated from a wild African great ape. Int J Med Microbiol 307:57–63. doi: 10.1016/j.ijmm.2016.11.003. [DOI] [PubMed] [Google Scholar]
- 4.Indrawattana N, Pumipuntu N, Suriyakhun N, Jangsangthong A, Kulpeanprasit S, Chantratita N, Sookrung N, Chaicumpa W, Buranasinsup S. 2019. Staphylococcus argenteus from rabbits in Thailand. Microbiologyopen 8:e00665. doi: 10.1002/mbo3.665. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Tunsjø HS, Kalyanasundaram S, Charnock C, Leegaard TM, Moen AEF. 2018. Challenges in the identification of methicillin‐resistant Staphylococcus argenteus by routine diagnostics. APMIS 126:533–537. doi: 10.1111/apm.12843. [DOI] [PubMed] [Google Scholar]
- 6.Chantratita N, Wikraiphat C, Tandhavanant S, Wongsuvan G, Ariyaprasert P, Suntornsut P, Thaipadungpanit J, Teerawattanasook N, Jutrakul Y, Srisurat N, Chaimanee P, Anukunananchai J, Phiphitaporn S, Srisamang P, Chetchotisakd P, West TE, Peacock SJ. 2016. Comparison of community-onset Staphylococcus argenteus and Staphylococcus aureus sepsis in Thailand: a prospective multicentre observational study. Clin Microbiol Infect 22:458.e11–458.e19. doi: 10.1016/j.cmi.2016.01.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Chen S-Y, Lee H, Wang X-M, Lee T-F, Liao C-H, Teng L-J, Hsueh P-R. 2018. High mortality impact of Staphylococcus argenteus on patients with community-onset staphylococcal bacteraemia. Int J Antimicrob Agents 52:747–753. doi: 10.1016/j.ijantimicag.2018.08.017. [DOI] [PubMed] [Google Scholar]
- 8.Schaumburg F, Alabi AS, Köck R, Mellmann A, Kremsner PG, Boesch C, Becker K, Leendertz FH, Peters G. 2012. Highly divergent Staphylococcus aureus isolates from African non-human primates. Environ Microbiol Rep 4:141–146. doi: 10.1111/j.1758-2229.2011.00316.x. [DOI] [PubMed] [Google Scholar]
- 9.Zhang D-F, Zhi X-Y, Zhang J, Paoli GC, Cui Y, Shi C, Shi X. 2017. Preliminary comparative genomics revealed pathogenic potential and international spread of Staphylococcus argenteus. BMC Genomics 18:808. doi: 10.1186/s12864-017-4149-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Wakabayashi Y, Umeda K, Yonogi S, Nakamura H, Yamamoto K, Kumeda Y, Kawatsu K. 2018. Staphylococcal food poisoning caused by Staphylococcus argenteus harboring staphylococcal enterotoxin genes. Int J Food Microbiol 265:23–29. doi: 10.1016/j.ijfoodmicro.2017.10.022. [DOI] [PubMed] [Google Scholar]
- 11.Abdalrahman LS, Wells H, Fakhr MK. 2015. Staphylococcus aureus is more prevalent in retail beef livers than in pork and other beef cuts. Pathogens 4:182–198. doi: 10.3390/pathogens4020182. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Marasini D, Fakhr MK. 2014. Exploring PFGE for detecting large plasmids in Campylobacter jejuni and Campylobacter coli isolated from various retail meats. Pathogens 3:833–844. doi: 10.3390/pathogens3040833. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Wattam AR, Davis JJ, Assaf R, Boisvert S, Brettin T, Bun C, Conrad N, Dietrich EM, Disz T, Gabbard JL, Gerdes S, Henry CS, Kenyon RW, Machi D, Mao C, Nordberg EK, Olsen GJ, Murphy-Olson DE, Olson R, Overbeek R, Parrello B, Pusch GD, Shukla M, Vonstein V, Warren A, Xia F, Yoo H, Stevens RL. 2017. Improvements to PATRIC, the all-bacterial Bioinformatics Database and Analysis Resource Center. Nucleic Acids Res 45:D535–D542. doi: 10.1093/nar/gkw1017. [DOI] [PMC free article] [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.Antipov D, Hartwick N, Shen M, Raiko M, Lapidus A, Pevzner PA. 2016. plasmidSPAdes: assembling plasmids from whole genome sequencing data. Bioinformatics 32:3380–3387. doi: 10.1093/bioinformatics/btw493. [DOI] [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]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The whole-genome shotgun data for Staphylococcus argenteus strain B3-25B have been deposited in GenBank under the accession numbers CP042286 for the chromosome and CP042287 for plasmid pSALNBL21. The raw sequence reads have been deposited in the Sequence Read Archive (SRA) under accession number PRJNA555633.