Abstract
Here, we present the draft genome sequences of four Staphylococcus aureus strains isolated from mastitic milk collected from animals with subclinical manifestations. Three of them were typed as sequence type 126 (ST126), a genotype with no genome sequence available. ST126 is found in several herds of southern Brazil and is described as a bovine pathogen strongly associated with milk around the world.
GENOME ANNOUNCEMENT
Staphylococcus aureus is one of the main pathogens isolated from bovine mastitis infections (1). Intense efforts have been made to understand the molecular mechanisms of bacterial pathogenesis (2, 3) and to link bacterial characteristics with the specific clinical manifestations of bovine mastitis (4). These strain-specific markers could be used to track relevant strains in herds that would positively affect animal health and welfare.
We monitored two herds in the State of Minas Gerais, Brazil, for the presence of subclinical mastitis for 6 months. Bacteria identified as S. aureus were genotyped by multilocus variable-number tandem-repeat analysis (MLVA) and pulsed-field gel electrophoresis (PFGE). Four isolates were selected for genome sequencing. SAU-302 and SAU-1364 were isolated from two cows with a persistent subclinical infection, while SAU-170 and SAU-1269 were isolated from two cows with subclinical infections for a month. The infection was considered persistent if it was detected after three or more consecutive months from the same animal.
Four 200-bp single-end genomic libraries were constructed and sequenced on an Ion Torrent Personal Genome Machine (PGM). Four data sets were generated, containing 1,422,030 reads (SAU-170), 1,250,612 reads (SAU-302), 2,572,399 reads (SAU-1269), and 634,729 reads (SAU-1364). The sequenced reads were trimmed for length (minimum, 100 bp) and quality (minimum score, Q20) and de novo assembled to contigs using CLC Genomics Workbench version 6.5.1 (CLC bio). This assembly produced 194 contigs and overall G+C content of 32.8% for SAU-170, 568 contigs and 32.9% G+C content for SAU-302, 93 contigs and 32.7% G+C content for SAU-1269, and 287 contigs and 32.7% G+C content for SAU-1364. Genes were predicted from the contigs using Prodigal version 2.50 (5), which revealed the coding sequence (CDS) set of SAU-170 (2,599 CDSs), SAU-302 (2,666 CDSs), SAU-1269 (2,545 CDSs), and SAU-1364 (2,547 CDSs). The protein sets were functionally annotated using BLAST searches (http://blast.ncbi.nlm.nih.gov/), and approximately 77% of the proteins of each strain were assigned Clusters of Orthologous Groups (COG) families (6).
In genotyping analysis, SAU-170, SAU-302, and SAU-1269 were classified as sequence type 126 (ST126), and SAU-1364 was classified as ST1 by multilocus sequence type (MLST) analysis (http://saureus.mlst.net/misc/info.asp). ST1 is a type isolated from bovine and human infections (7). ST126 is a prevalent genotype found in several herds in southern Brazil (8, 9) and was described elsewhere as a bovine pathogen strongly associated with milk (7). We also genotyped the strains against the reference genome of S. aureus RF122 (accession no. NC_007622), a strain representative of the major clone involved in severe bovine mastitis worldwide (10). We identified single-nucleotide polymorphisms (SNPs) that resulted in amino acid changes in the coded protein. A total of 6,273 SNPs were detected in SAU-170, 5,481 in SAU-302, 7,420 in SAU-1269, and 2,491 in SAU-1364 (CLC bio; minimum, 20X coverage [11]). These new genomes add information to the repertoire of genes described for strains associated with subclinical mastitis that will be useful in studies to elucidate molecular mechanisms of pathogenesis.
Nucleotide sequence accession numbers.
The draft genome sequences of SAU-170, SAU-302, SAU-1269, and SAU-1364 are available in GenBank under the accession numbers LNOQ00000000, LNOR00000000, LNOO000000000, and LNOP00000000, respectively.
ACKNOWLEDGMENTS
We thank the Núcleo de Análise de Biomoléculas (NuBioMol) for support during sequencing and the Programa de Desenvolvimento da Pecuária Leiteira (PDPL) for providing milk samples for bacterial isolation.
Funding Statement
D.M.S., M.P.S., and A.P.A. received scholarships from FAPEMIG and CAPES.
Footnotes
Citation Silva DM, da Silva MP, Vidigal PMP, Barcelos RM, Klein RC, Aguilar AP, Fabres-Klein MH, Oliveira G, Ribon AOB. 2016. Draft genome sequences of Staphylococcus aureus strains isolated from subclinical bovine mastitis in Brazil. Genome Announc 4(1):e01594-15. doi:10.1128/genomeA.01594-15.
REFERENCES
- 1.Castelani L, Santos AFS, Miranda M, dos S, Zafalon LF, Pozzi CR, Arcaro JR. 2013. Molecular typing of mastitis causing Staphylococcus aureus isolated from heifers and cows. Int J Mol Sci 14:4326–4333. doi: 10.3390/ijms14024326. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Zadoks RN, Middleton JR, McDougall S, Katholm J, Schukken YH. 2011. Molecular epidemiology of mastitis pathogens of dairy cattle and comparative relevance to humans. J Mammary Gland Biol Neoplasia 16:357–372. doi: 10.1007/s10911-011-9236-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Ben Zakour NL, Guinane CM, Fitzgerald JR. 2008. Pathogenomics of the staphylococci: insights into niche adaptation and the emergence of new virulent strains. FEMS Microbiol Lett 289:1–12. doi: 10.1111/j.1574-6968.2008.01384.x. [DOI] [PubMed] [Google Scholar]
- 4.Guinane CM, Ben Zakour NL, Tormo-Mas MA, Weinert LA, Lowder BV, Cartwright RA, Smyth DS, Smyth CJ, Lindsay JA, Gould KA, Witney A, Hinds J, Bollback JP, Rambaut A, Penadés JR, Fitzgerald JR. 2010. Evolutionary genomics of Staphylococcus aureus reveals insights into the origin and molecular basis of ruminant host adaptation. Genome Biol Evol 2:454–466. doi: 10.1093/gbe/evq031. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Hyatt D, Chen GL, Locascio PF, Land ML, Larimer FW, Hauser LJ. 2010. Prodigal: prokaryotic gene recognition and translation initiation site identification. BMC Bioinformatics 11:119. doi: 10.1186/1471-2105-11-119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Tatusov RL, Natale DA, Garkavtsev IV, Tatusova TA, Shankavaram UT, Rao BS, Kiryutin B, Galperin MY, Fedorova ND, Koonin EV. 2001. The COG database: new developments in phylogenetic classification of proteins from complete genomes. Nucleic Acids Res 29:22–28. doi: 10.1093/nar/29.1.22. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Smith EM, Green LE, Medley GF, Bird HE, Fox LK, Schukken YH, Bradley AJ, Zadoks RN, Dowson CG. 2005. Multilocus sequence typing of intercontinental bovine Staphylococcus aureus isolates. J Clin Microbiol 43:4737–4743. doi: 10.1128/JCM.43.9.4737-4743.2005. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Aires de Sousa M, Parente CESR, Vieira-da-Motta O, Bonna ICF, Silva DA, Lencastre H. 2007. Characterization of Staphylococcus aureus isolates from buffalo, bovine, ovine, and caprine milk samples collected in Rio de Janeiro State, Brazil. Appl Environ Microbiol 73:3845–3849. doi: 10.1128/AEM.00019-07. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Silva NCC, Guimarães FF, Manzi MP, Budri PE, Gómez-Sanz E, Benito D, Langoni H, Torres C. 2013. Molecular characterization and clonal diversity of methicillin-susceptible Staphylococcus aureus in milk of cows with mastitis in Brazil. J Dairy Sci 96:6856–6862. doi: 10.3168/jds.2013-6719. [DOI] [PubMed] [Google Scholar]
- 10.Peton V, Bouchard DS, Almeida S, Rault L, Falentin H, Jardin J, Jan G, Hernandez D, François P, Schrenzel J, Azevedo V, Miyoshi A, Berkova N, Even S, Le Loir Y. 2014. Fine-tuned characterization of Staphylococcus aureus Newbould 305, a strain associated with mild and chronic mastitis in bovines. Vet Res 45:106. doi: 10.1186/s13567-014-0106-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Greminger MP, Stölting KN, Nater A, Goossens B, Arora N, Bruggmann R, Patrignani A, Nussberger B, Sharma R, Kraus RH, Ambu LN, Singleton I, Chikhi L, Van Schaik CP, Krützen M. 2014. Generation of SNP datasets for orangutan population genomics using improved reduced-representation sequencing and direct comparisons of SNP calling algorithms. BMC Genomics 15:16. doi: 10.1186/1471-2164-15-16. [DOI] [PMC free article] [PubMed] [Google Scholar]