Microbial GenomicsBioinformaticsPeer-reviewed journal article
GBS-SBG - GBS Serotyping by Genome Sequencing
Suma TiruvayipatiiD, Wen TangiD, Timothy BarkhamiD, Swaine Lin CheniD
Abstract
Group B Streptococcus agalactiae (GBS; Streptococcus agalactiae) is the most common cause of neonatal meningitis and a rising cause of sepsis in adults. Recently, it has also been shown to cause foodborne disease. As with many other bacteria, the polysaccharide capsule of GBS is antigenic, enabling its use for strain serotyping. Recent advances in DNA sequencing have made sequence-based typing attractive (as has been implemented for several other bacteria, including Escherichia coli, Klebsiella pneumoniae species complex, Streptococcus pyogenes, and others). For GBS, existing WGS-based serotyping systems do not provide complete coverage of all known GBS serotypes (specifically including subtypes of serotype III), and none are simultaneously compatible with the two most common data types, raw short reads and assembled sequences. Here, we create a serotyping database (GBS-SBG, GBS Serotyping by Genome Sequencing), with associated scripts and running instructions, that can be used to call all currently described GBS serotypes, including subtypes of serotype III, using both direct short-read- and assembly-based typing. We achieved higher concordance using GBS-SBG on a previously reported data set of 790 strains. We further validated GBS-SBG on a new set of 572 strains, achieving 99.8% concordance with PCR-based molecular serotyping using either short-read- or assembly-based typing. The GBS-SBG package is publicly available and will accelerate and simplify serotyping by sequencing for GBS. DATA SUMMARYO_LIThe GBS-SBG package is open source and available for at Github under the MIT license (URL - https://github.com/swainechen/GBS-SBG) C_LIO_LIAccession numbers of the sequencing reads and reference sequences used in the study from earlier reports have been provided within the article and the supplementary data C_LIO_LIThe WGS data for the 572 isolates used in the study is available at https://www.ncbi.nlm.nih.gov/bioproject/PRJNA293392 C_LI
- organism: human
- assay: whole-genome sequencing
- research focus: variant calling
- research focus: database / resource
- research focus: benchmarking
- approach: statistical model
- Citations
- 30
- FWCI
- 4.11
- Field percentile
- top 5%
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