TY - JOUR
T1 - Genomic analysis of a serotype 5 streptococcus pneumoniae outbreak in British Columbia, Canada, 2005-2009
AU - Miller, Ruth R.
AU - Langille, Morgan G.I.
AU - Montoya, Vincent
AU - Crisan, Anamaria
AU - Stefanovic, Aleksandra
AU - Martin, Irene
AU - Hoang, Linda
AU - Patrick, David M.
AU - Romney, Marc
AU - Tyrrell, Gregory
AU - Jones, Steven J.M.
AU - Brinkman, Fiona S.L.
AU - Tang, Patrick
N1 - Publisher Copyright:
© 2016 Ruth R. Miller et al.
PY - 2016
Y1 - 2016
N2 - Background. Streptococcus pneumoniae can cause a wide spectrum of disease, including invasive pneumococcal disease (IPD). From 2005 to 2009 an outbreak of IPD occurred in Western Canada, caused by a S. pneumoniae strain with multilocus sequence type (MLST) 289 and serotype 5. We sought to investigate the incidence of IPD due to this S. pneumoniae strain and to characterize the outbreak in British Columbia using whole-genome sequencing. Methods. IPD was defined according to Public Health Agency of Canada guidelines. Two isolates representing the beginning and end of the outbreak were whole-genome sequenced. The sequences were analyzed for single nucleotide variants (SNVs) and putative genomic islands. Results. The peak of the outbreak in British Columbia was in 2006, when 57% of invasive S. pneumoniae isolates were serotype 5. Comparison of two whole-genome sequenced strains showed only 10 SNVs between them. A 15.5 kb genomic island was identified in outbreak strains, allowing the design of a PCR assay to track the spread of the outbreak strain. Discussion. We show that the serotype 5 MLST 289 strain contains a distinguishing genomic island, which remained genetically consistent over time. Whole-genome sequencing holds great promise for real-time characterization of outbreaks in the future and may allow responses tailored to characteristics identified in the genome.
AB - Background. Streptococcus pneumoniae can cause a wide spectrum of disease, including invasive pneumococcal disease (IPD). From 2005 to 2009 an outbreak of IPD occurred in Western Canada, caused by a S. pneumoniae strain with multilocus sequence type (MLST) 289 and serotype 5. We sought to investigate the incidence of IPD due to this S. pneumoniae strain and to characterize the outbreak in British Columbia using whole-genome sequencing. Methods. IPD was defined according to Public Health Agency of Canada guidelines. Two isolates representing the beginning and end of the outbreak were whole-genome sequenced. The sequences were analyzed for single nucleotide variants (SNVs) and putative genomic islands. Results. The peak of the outbreak in British Columbia was in 2006, when 57% of invasive S. pneumoniae isolates were serotype 5. Comparison of two whole-genome sequenced strains showed only 10 SNVs between them. A 15.5 kb genomic island was identified in outbreak strains, allowing the design of a PCR assay to track the spread of the outbreak strain. Discussion. We show that the serotype 5 MLST 289 strain contains a distinguishing genomic island, which remained genetically consistent over time. Whole-genome sequencing holds great promise for real-time characterization of outbreaks in the future and may allow responses tailored to characteristics identified in the genome.
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U2 - 10.1155/2016/5381871
DO - 10.1155/2016/5381871
M3 - Article
AN - SCOPUS:84966293194
SN - 1712-9532
VL - 2016
JO - Canadian Journal of Infectious Diseases and Medical Microbiology
JF - Canadian Journal of Infectious Diseases and Medical Microbiology
M1 - 5381871
ER -