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 in | Proceedings of the National Academy of Sciences - PNAS Vol. 117; no. 13; pp. 7001 - 7003 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
31.03.2020
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Series | Brief Report |
Subjects | |
Online Access | Get full text |
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Abstract | 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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AbstractList | 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. 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.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. |
Author | Tahara, Maino Kuroda, Makoto Suzuki, Tadaki Sakata, Masafumi Kawase, Miyuki Katoh, Hiroshi Takeda, Makoto Ohmagari, Norio Nagata, Noriyo Kutsuna, Satoshi Nao, Naganori Kageyama, Tsutomu Matsuyama, Shutoku Saito, Shinji Shirato, Kazuya Takayama, Ikuyo Kato, Fumihiro Sekizuka, Tsuyoshi |
Author_xml | – sequence: 1 givenname: Shutoku surname: Matsuyama fullname: Matsuyama, Shutoku – sequence: 2 givenname: Naganori surname: Nao fullname: Nao, Naganori – sequence: 3 givenname: Kazuya surname: Shirato fullname: Shirato, Kazuya – sequence: 4 givenname: Miyuki surname: Kawase fullname: Kawase, Miyuki – sequence: 5 givenname: Shinji surname: Saito fullname: Saito, Shinji – sequence: 6 givenname: Ikuyo surname: Takayama fullname: Takayama, Ikuyo – sequence: 7 givenname: Noriyo surname: Nagata fullname: Nagata, Noriyo – sequence: 8 givenname: Tsuyoshi surname: Sekizuka fullname: Sekizuka, Tsuyoshi – sequence: 9 givenname: Hiroshi surname: Katoh fullname: Katoh, Hiroshi – sequence: 10 givenname: Fumihiro surname: Kato fullname: Kato, Fumihiro – sequence: 11 givenname: Masafumi surname: Sakata fullname: Sakata, Masafumi – sequence: 12 givenname: Maino surname: Tahara fullname: Tahara, Maino – sequence: 13 givenname: Satoshi surname: Kutsuna fullname: Kutsuna, Satoshi – sequence: 14 givenname: Norio surname: Ohmagari fullname: Ohmagari, Norio – sequence: 15 givenname: Makoto surname: Kuroda fullname: Kuroda, Makoto – sequence: 16 givenname: Tadaki surname: Suzuki fullname: Suzuki, Tadaki – sequence: 17 givenname: Tsutomu surname: Kageyama fullname: Kageyama, Tsutomu – sequence: 18 givenname: Makoto surname: Takeda fullname: Takeda, Makoto |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32165541$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 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) |
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References_xml | – volume: 25 start-page: 2000045 year: 2020 ident: e_1_3_4_9_2 article-title: Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR publication-title: Euro. Surveill. doi: 10.2807/1560-7917.ES.2020.25.3.2000045 – volume: 102 start-page: 11876 year: 2005 ident: e_1_3_4_13_2 article-title: Inhibitors of cathepsin L prevent severe acute respiratory syndrome coronavirus entry publication-title: Proc. Natl. Acad. Sci. U.S.A. doi: 10.1073/pnas.0505577102 – volume: 87 start-page: 1691 year: 2006 ident: e_1_3_4_7_2 article-title: Analysis of ACE2 in polarized epithelial cells: Surface expression and function as receptor for severe acute respiratory syndrome-associated coronavirus publication-title: J. Gen. Virol. doi: 10.1099/vir.0.81749-0 – volume: 92 start-page: e00683-18 year: 2018 ident: e_1_3_4_14_2 article-title: Middle East respiratory syndrome coronavirus spike protein is not activated directly by cellular furin during viral entry into target cells publication-title: J. Virol. doi: 10.1128/JVI.00683-18 – volume: 152 start-page: 1019 year: 2007 ident: e_1_3_4_8_2 article-title: Enhancement of cytotoxicity against Vero E6 cells persistently infected with SARS-CoV by Mycoplasma fermentans publication-title: Arch. Virol. doi: 10.1007/s00705-006-0924-7 – volume: 87 start-page: 12552 year: 2013 ident: e_1_3_4_12_2 article-title: Middle East respiratory syndrome coronavirus infection mediated by the transmembrane serine protease TMPRSS2 publication-title: J. Virol. doi: 10.1128/JVI.01890-13 – volume: 93 start-page: e01815-18 year: 2019 ident: e_1_3_4_6_2 article-title: TMPRSS2 contributes to virus spread and immunopathology in the airways of murine models after coronavirus infection publication-title: J. Virol. doi: 10.1128/JVI.01815-18 – ident: e_1_3_4_1_2 doi: 10.1038/s41586-020-2008-3 – ident: e_1_3_4_2_2 doi: 10.1038/s41586-020-2012-7 – volume: 382 start-page: 727 year: 2020 ident: e_1_3_4_4_2 article-title: A novel coronavirus from patients with pneumonia in China, 2019 publication-title: N. Engl. J. Med. doi: 10.1056/NEJMoa2001017 – volume: 84 start-page: 12658 year: 2010 ident: e_1_3_4_5_2 article-title: Efficient activation of the severe acute respiratory syndrome coronavirus spike protein by the transmembrane protease TMPRSS2 publication-title: J. Virol. doi: 10.1128/JVI.01542-10 – volume: 395 start-page: 565 year: 2020 ident: e_1_3_4_3_2 article-title: Genomic characterisation and epidemiology of 2019 novel coronavirus: Implications for virus origins and receptor binding publication-title: Lancet doi: 10.1016/S0140-6736(20)30251-8 – volume: 87 start-page: 5502 year: 2013 ident: e_1_3_4_15_2 article-title: The spike protein of the emerging betacoronavirus EMC uses a novel coronavirus receptor for entry, can be activated by TMPRSS2, and is targeted by neutralizing antibodies publication-title: J. Virol. doi: 10.1128/JVI.00128-13 – volume: 85 start-page: 873 year: 2011 ident: e_1_3_4_11_2 article-title: A transmembrane serine protease is linked to the severe acute respiratory syndrome coronavirus receptor and activates virus entry publication-title: J. Virol. doi: 10.1128/JVI.02062-10 – ident: e_1_3_4_10_2 doi: 10.7883/yoken.JJID.2020.061 – reference: 32360584 - Pharmacol Res. 2020 Jul;157:104853 |
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SubjectTerms | Animals Betacoronavirus - isolation & purification Biological Sciences BRIEF REPORTS Cell Line Chlorocebus aethiops Coronavirus Infections - virology Coronaviruses COVID-19 Disease Outbreaks Humans Pandemics Pneumonia, Viral - virology Respiratory diseases RNA, Viral - metabolism SARS-CoV-2 Serine Endopeptidases - metabolism Severe acute respiratory syndrome coronavirus 2 Vero Cells Viral diseases Virus Cultivation |
Title | Enhanced isolation of SARS-CoV-2 by TMPRSS2- expressing cells |
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