Enhanced isolation of SARS-CoV-2 by TMPRSS2- expressing cells

A novel betacoronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which caused a large respiratory outbreak in Wuhan, China in December 2019, is currently spreading across many countries globally. Here, we show that a TMPRSS2- expressing VeroE6 cell line is highly susceptible to...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 117; no. 13; pp. 7001 - 7003
Main Authors Matsuyama, Shutoku, Nao, Naganori, Shirato, Kazuya, Kawase, Miyuki, Saito, Shinji, Takayama, Ikuyo, Nagata, Noriyo, Sekizuka, Tsuyoshi, Katoh, Hiroshi, Kato, Fumihiro, Sakata, Masafumi, Tahara, Maino, Kutsuna, Satoshi, Ohmagari, Norio, Kuroda, Makoto, Suzuki, Tadaki, Kageyama, Tsutomu, Takeda, Makoto
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 31.03.2020
SeriesBrief Report
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Summary:A novel betacoronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which caused a large respiratory outbreak in Wuhan, China in December 2019, is currently spreading across many countries globally. Here, we show that a TMPRSS2- expressing VeroE6 cell line is highly susceptible to SARS-CoV-2 infection, making it useful for isolating and propagating SARS-CoV-2. Our results reveal that, in common with SARS- and Middle East respiratory syndrome-CoV, SARS-CoV-2 infection is enhanced by TMPRSS2.
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Author contributions: S.M., N. Nao, K.S., and M. Takeda designed research; S.M., N. Nao, K.S., M. Kawase, S.S., I.T., N. Nagata, T. Sekizuka, H.K., F.K., M.S., M. Tahara, M. Kuroda, T. Suzuki, and T.K. performed research; S.K. and N.O. contributed new reagents/analytic tools; S.M., N. Nao, K.S., T. Sekizuka, M. Kuroda, T.K., and M. Takeda analyzed data; and S.M. and M. Takeda wrote the paper.
Edited by Yuan Chang, University of Pittsburgh, Pittsburgh, PA, and approved March 5, 2020 (received for review February 11, 2020)
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.2002589117