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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/26506
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dc.contributor.authorBanerjee A-
dc.contributor.authorNasir JA-
dc.contributor.authorBudylowski P-
dc.contributor.authorYip L-
dc.contributor.authorAftanas P-
dc.contributor.authorChristie N-
dc.contributor.authorGhalami A-
dc.contributor.authorBaid K-
dc.contributor.authorRaphenya AR-
dc.contributor.authorHirota JA-
dc.contributor.authorMiller MS-
dc.contributor.authorMcGeer AJ-
dc.contributor.authorOstrowski M-
dc.contributor.authorKozak RA-
dc.contributor.authorMcArthur AG-
dc.contributor.authorMossman K-
dc.contributor.authorMubareka S-
dc.date.accessioned2021-06-07T15:13:49Z-
dc.date.available2021-06-07T15:13:49Z-
dc.date.issued2020-09-
dc.identifier.issn1080-6040-
dc.identifier.issn1080-6059-
dc.identifier.urihttp://hdl.handle.net/11375/26506-
dc.description.abstractSince its emergence in Wuhan, China, in December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has infected ≈6 million persons worldwide. As SARS-CoV-2 spreads across the planet, we explored the range of human cells that can be infected by this virus. We isolated SARS-CoV-2 from 2 infected patients in Toronto, Canada; determined the genomic sequences; and identified single-nucleotide changes in representative populations of our virus stocks. We also tested a wide range of human immune cells for productive infection with SARS-CoV-2. We confirm that human primary peripheral blood mononuclear cells are not permissive for SARS-CoV-2. As SARS-CoV-2 continues to spread globally, it is essential to monitor single-nucleotide polymorphisms in the virus and to continue to isolate circulating viruses to determine viral genotype and phenotype by using in vitro and in vivo infection models.-
dc.publisherCenters for Disease Control and Prevention (CDC)-
dc.rightsAttribution - CC BY This Creative Commons license lets others distribute, remix, tweak, and build upon your work, even commercially, as long as they credit you for the original creation. Recommended for maximum dissemination and use of licensed materials.-
dc.rights.uri2-
dc.subject2019 novel coronavirus disease-
dc.subjectCOVID-19-
dc.subjectSARS-CoV-2-
dc.subjectcoronavirus disease-
dc.subjectimmune cells-
dc.subjectisolation-
dc.subjectphylogenetics-
dc.subjectreplication-
dc.subjectrespiratory infections-
dc.subjectsevere acute respiratory syndrome coronavirus 2-
dc.subjectviruses-
dc.subjectzoonoses-
dc.subjectBetacoronavirus-
dc.subjectCOVID-19-
dc.subjectCoronavirus Infections-
dc.subjectDNA, Viral-
dc.subjectGenotype-
dc.subjectHumans-
dc.subjectKinetics-
dc.subjectLeukocytes, Mononuclear-
dc.subjectPandemics-
dc.subjectPneumonia, Viral-
dc.subjectPolymorphism, Single Nucleotide-
dc.subjectSARS-CoV-2-
dc.subjectVirus Replication-
dc.subjectWhole Genome Sequencing-
dc.titleIsolation, Sequence, Infectivity, and Replication Kinetics of Severe Acute Respiratory Syndrome Coronavirus 2-
dc.typeArticle-
dc.date.updated2021-06-07T15:13:40Z-
dc.rights.licenseAttribution - CC BY-
dc.identifier.doihttps://doi.org/10.3201/eid2609.201495-
Appears in Collections:Faculty Publications (via McMaster Experts)

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