Isolation, Sequence, Infectivity and Replication Kinetics of Severe Acute Respiratory Syndrome Coronavirus 2

被引:91
作者
Banerjee, Arinjay [1 ]
Nasir, Jalees A. [1 ]
Budylowski, Patrick [2 ]
Yip, Lily [3 ]
Aftanas, Patryk [3 ]
Christie, Natasha [2 ]
Ghalami, Ayoob [2 ]
Baid, Kaushal [1 ]
Raphenya, Amogelang R. [1 ]
Hirota, Jeremy A. [1 ]
Miller, Matthew S. [1 ]
McGeer, Allison J. [2 ,4 ]
Ostrowski, Mario [2 ]
Kozak, Robert A. [2 ,3 ]
McArthur, Andrew G. [1 ]
Mossman, Karen [1 ]
Mubareka, Samira [2 ,3 ]
机构
[1] McMaster Univ, 1280 Main St W, Hamilton, ON L8S 4L8, Canada
[2] Univ Toronto, Toronto, ON, Canada
[3] Sunnybrook Res Inst, Toronto, ON, Canada
[4] Mt Sinai Hosp, Toronto, ON, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
CELL; SARS-COV-2; ENTRY; TOOL;
D O I
10.3201/eid2609.201495
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since its emergence in Wuhan, China, in December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has infected approximate to 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.
引用
收藏
页码:2054 / 2063
页数:10
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