GENOME ANNOUNCEMENT
As of this writing, there has been one complete genome of S. uberis assembled, which originated from the United Kingdom (2). Here, we report a second complete genome, that of New Zealand strain NZ01, which was isolated from a cow with a clinical case of bovine mastitis in Palmerston North, New Zealand. This complete genome will support efforts to manage bovine mastitis and further our understanding of the evolutionary responses of
DNA extraction and next-generation sequencing were performed at the Microbiological Diagnostic Unit Public Health Laboratory of the University of Melbourne. Genomic DNA was prepared from a culture grown from a single colony using a JANUS Chemagic workstation and Chemagic DNA/RNA kit (PerkinElmer, USA). DNA libraries were created using the Nextera XT DNA preparation kit (Illumina, USA). Next-generation sequencing was performed using the Illumina NextSeq platform.
The assembly involved a preliminary assembly in Geneious version 10.1.3 (9), followed by repeat spanning and gap closure with Sanger sequencing of PCR products. The complete genome was compared to that of
The complete NZ01 genome comprises a single chromosome of 1,863,842 bp, with 1,808 CDSs and 1,886 predicted genes. Approximately 146 CDSs found in the NZ01 genome are novel, compared to those of strain 1040J from the United Kingdom. Conversely, approximately 163 CDSs found in the UK strain do not appear in NZ01, further illustrating the genomic flexibility of this species (12). Estimates of the
An identified prophage in NZ01 (1,520,084 to 1,560,140 bp) has been shown as active, with a subset of next-generation sequencing reads highlighting the presence of a circular phage particle. This could be of interest for the control of bovine mastitis, as the phage encodes multiple holin and lysin genes and may be able to actively lyse
As further efforts to control
Accession number(s).
This complete genome sequence has been deposited at GenBank under the accession number CP022435.
b Department of Biochemistry, University of Otago, Dunedin, New Zealand
c Doherty Applied Microbial Genomics, Department of Microbiology and Immunology, The University of Melbourne at The Doherty Institute for Infection and Immunity, Melbourne, Australia
d Microbiological Diagnostic Unit Public Health Laboratory, Department of Microbiology and Immunology, The University of Melbourne at The Doherty Institute for Infection and Immunity, Melbourne, Australia
e Centre for Integrative Microbial Evolution (CIME), Faculty of Mathematics and Natural Sciences, University of Oslo, Oslo, Norway
f Laboratory for Microbial Dynamics (LaMDa), Section for Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway
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Abstract
ABSTRACT
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