Literature DB >> 27508119

Draft genome sequence of Staphylococcus aureus KT/312045, an ST1-MSSA PVL positive isolated from pus sample in East Coast Malaysia.

Zarizal Suhaili1, Soo-Sum Lean1, Noor Muzamil Mohamad1, Abdul R Abdul Rachman2, Mohd Nasir Mohd Desa2, Chew Chieng Yeo3.   

Abstract

Most of the efforts in elucidating the molecular relatedness and epidemiology of Staphylococcus aureus in Malaysia have been largely focused on methicillin-resistant S. aureus (MRSA). Therefore, here we report the draft genome sequence of the methicillin-susceptible Staphylococcus aureus (MSSA) with sequence type 1 (ST1), spa type t127 with Panton-Valentine Leukocidin (pvl) pathogenic determinant isolated from pus sample designated as KT/314250 strain. The size of the draft genome is 2.86 Mbp with 32.7% of G + C content consisting 2673 coding sequences. The draft genome sequence has been deposited in DDBJ/EMBL/GenBank under the accession number AOCP00000000.

Entities:  

Keywords:  Methicillin-susceptible Staphylococcus aureus; Panton-Valentibe Leukocidin; ST1-MSSA PVL positive Malaysia isolates

Year:  2016        PMID: 27508119      PMCID: PMC4961218          DOI: 10.1016/j.gdata.2016.07.002

Source DB:  PubMed          Journal:  Genom Data        ISSN: 2213-5960


Specifications

Direct link to deposited data

http://www.ncbi.nlm.nih.gov/bioproject/?term=AOCP00000000

Experimental design, materials and methods

MRSA evolved over the times from Methicillin susceptible S. aureus via acquisition of mobile genetic elements called staphylococcal cassette chromosome mec (SCCmec) [1], [2]. Thus, this makes MSSA to be a potential reservoir for the MRSA strains. S. aureus strains producing PVL have been associated with a variety of illness ranging from skin and soft tissue infections to necrotizing pneumonia as well as septicaemia that are invariably fatal [3]. The genome sequencing of KT/314,250 strain was performed using the Illumina genome analyzer IIx 100-bp paired-end reads. The paired-end reads were trimmed and assembled de novo using CLC genomics workbench 5.1 (CLC Bio, Denmark). Multi Locus Sequence Typing (MLST) was performed by using Local BLAST identification and manually aligned based on primers used to amplified seven gene fragments (arcC, aroE, glpF, gmk, pta, tpi and yqiL) [4]. Meanwhile the spa typing was assigned using DNAGear freely available Software [5]. Thus, all genotypic analysis revealed this strain as ST1, spa type t127, agr III and dru type dt10ao. The draft genome were annotated by using free accessible bioinformatics tools Blast2GO 2.5.0 [6] and subsequently validated using Rapid Annotation Subsystem Technology (RAST) [7] and Bacterial Annotation System (BASys) [8]. Initial sequence analysis revealed a total of 69 contigs from the de novo assembly with an accumulate length of 2,846,051 bp with G + C content of 32.7%. A total of 2673 coding sequences (CDSs) and 48 RNAs regions were annotated. Of the CDS, 4.12% were associated with cell wall and capsule; 3.07% were associated with virulence, disease and defence mechanism and 2.77% were related with stress response which is contributed in host adaptation and survival (Fig. 1).
Fig. 1

Subsystem distribution of methicillin-susceptible S. aureus KT/314,250 (based on RAST annotation server).

Nucleotide sequence accession number

The Draft genome sequence of Methicillin-susceptible Staphylococcus aureus (MSSA) KT/314,250 strain has been deposited under the accession number AOCP00000000. The version described in this paper was the first version, AOCP00000000.
Organism/cell line/tissueMethicillin-susceptible Staphylococcus aureus
StrainKT/314250
Sequencer or array typeIllumina GA IIx
Data formatAssembled
Experimental factorsBacterial strain
Experimental featuresAssembled and annotated draft genome of a strain of methicillin susceptible Staphylococcus aureus PVL+ from east coast Malaysia
ConsentNot applicable
Sample source locationPus
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