Entry of Scotophilus Bat Coronavirus-512 and Severe Acute Respiratory Syndrome Coronavirus in Human and Multiple Animal Cells.
Identifieur interne : 000582 ( PubMed/Checkpoint ); précédent : 000581; suivant : 000583Entry of Scotophilus Bat Coronavirus-512 and Severe Acute Respiratory Syndrome Coronavirus in Human and Multiple Animal Cells.
Auteurs : Yi-Ning Chen [Taïwan] ; Hsiao-Chin Hsu [Taïwan] ; Sheng-Wei Wang [Taïwan] ; Hao-Chiang Lien [Taïwan] ; Hsin-Ti Lu [Taïwan] ; Sheng-Kai Peng [Taïwan]Source :
- Pathogens (Basel, Switzerland) [ 2076-0817 ] ; 2019.
Abstract
Bats are natural reservoirs of severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome CoV (MERS-CoV). Scotophilus bat CoV-512 demonstrates potential for cross-species transmission because its viral RNA and specific antibodies have been detected in three bat species of Taiwan. Understanding the cell tropism of Scotophilus bat CoV-512 is the first step for studying the mechanism of cross-species transmission. In this study, a lentivirus-based pseudovirus was produced using the spike (S) protein of Scotophilus bat CoV-512 or SARS-CoV as a surface protein to test the interaction between coronaviral S protein and its cell receptor on 11 different cells. Susceptible cells expressed red fluorescence protein (RFP) after the entry of RFP-bound green fluorescence protein (GFP)-fused S protein of Scotophilus bat CoV-512 (RFP-Sco-S-eGFP) or RFP-SARS-S pseudovirus, and firefly luciferase (FLuc) activity expressed by cells infected with FLuc-Sco-S-eGFP or FLuc-SARS-S pseudovirus was quantified. Scotophilus bat CoV-512 pseudovirus had significantly higher entry efficiencies in Madin Darby dog kidney epithelial cells (MDCK), black flying fox brain cells (Pabr), and rat small intestine epithelial cells (IEC-6). SARS-CoV pseudovirus had significantly higher entry efficiencies in human embryonic kidney epithelial cells (HEK-293T), pig kidney epithelial cells (PK15), and MDCK cells. These findings demonstrated that Scotophilus bat CoV-512 had a broad host range for cross-species transmission like SARS-CoV.
DOI: 10.3390/pathogens8040259
PubMed: 31766704
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<front><div type="abstract" xml:lang="en">Bats are natural reservoirs of severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome CoV (MERS-CoV). <i>Scotophilus</i>
bat CoV-512 demonstrates potential for cross-species transmission because its viral RNA and specific antibodies have been detected in three bat species of Taiwan. Understanding the cell tropism of <i>Scotophilus</i>
bat CoV-512 is the first step for studying the mechanism of cross-species transmission. In this study, a lentivirus-based pseudovirus was produced using the spike (S) protein of <i>Scotophilus</i>
bat CoV-512 or SARS-CoV as a surface protein to test the interaction between coronaviral S protein and its cell receptor on 11 different cells. Susceptible cells expressed red fluorescence protein (RFP) after the entry of RFP-bound green fluorescence protein (GFP)-fused S protein of <i>Scotophilus</i>
bat CoV-512 (RFP-Sco-S-eGFP) or RFP-SARS-S pseudovirus, and firefly luciferase (FLuc) activity expressed by cells infected with FLuc-Sco-S-eGFP or FLuc-SARS-S pseudovirus was quantified. <i>Scotophilus</i>
bat CoV-512 pseudovirus had significantly higher entry efficiencies in Madin Darby dog kidney epithelial cells (MDCK), black flying fox brain cells (Pabr), and rat small intestine epithelial cells (IEC-6). SARS-CoV pseudovirus had significantly higher entry efficiencies in human embryonic kidney epithelial cells (HEK-293T), pig kidney epithelial cells (PK15), and MDCK cells. These findings demonstrated that <i>Scotophilus</i>
bat CoV-512 had a broad host range for cross-species transmission like SARS-CoV.</div>
</front>
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<Title>Pathogens (Basel, Switzerland)</Title>
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<ArticleTitle>Entry of <i>Scotophilus</i>
Bat Coronavirus-512 and Severe Acute Respiratory Syndrome Coronavirus in Human and Multiple Animal Cells.</ArticleTitle>
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<Abstract><AbstractText>Bats are natural reservoirs of severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome CoV (MERS-CoV). <i>Scotophilus</i>
bat CoV-512 demonstrates potential for cross-species transmission because its viral RNA and specific antibodies have been detected in three bat species of Taiwan. Understanding the cell tropism of <i>Scotophilus</i>
bat CoV-512 is the first step for studying the mechanism of cross-species transmission. In this study, a lentivirus-based pseudovirus was produced using the spike (S) protein of <i>Scotophilus</i>
bat CoV-512 or SARS-CoV as a surface protein to test the interaction between coronaviral S protein and its cell receptor on 11 different cells. Susceptible cells expressed red fluorescence protein (RFP) after the entry of RFP-bound green fluorescence protein (GFP)-fused S protein of <i>Scotophilus</i>
bat CoV-512 (RFP-Sco-S-eGFP) or RFP-SARS-S pseudovirus, and firefly luciferase (FLuc) activity expressed by cells infected with FLuc-Sco-S-eGFP or FLuc-SARS-S pseudovirus was quantified. <i>Scotophilus</i>
bat CoV-512 pseudovirus had significantly higher entry efficiencies in Madin Darby dog kidney epithelial cells (MDCK), black flying fox brain cells (Pabr), and rat small intestine epithelial cells (IEC-6). SARS-CoV pseudovirus had significantly higher entry efficiencies in human embryonic kidney epithelial cells (HEK-293T), pig kidney epithelial cells (PK15), and MDCK cells. These findings demonstrated that <i>Scotophilus</i>
bat CoV-512 had a broad host range for cross-species transmission like SARS-CoV.</AbstractText>
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<affiliations><list><country><li>Taïwan</li>
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<tree><country name="Taïwan"><noRegion><name sortKey="Chen, Yi Ning" sort="Chen, Yi Ning" uniqKey="Chen Y" first="Yi-Ning" last="Chen">Yi-Ning Chen</name>
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<name sortKey="Hsu, Hsiao Chin" sort="Hsu, Hsiao Chin" uniqKey="Hsu H" first="Hsiao-Chin" last="Hsu">Hsiao-Chin Hsu</name>
<name sortKey="Lien, Hao Chiang" sort="Lien, Hao Chiang" uniqKey="Lien H" first="Hao-Chiang" last="Lien">Hao-Chiang Lien</name>
<name sortKey="Lu, Hsin Ti" sort="Lu, Hsin Ti" uniqKey="Lu H" first="Hsin-Ti" last="Lu">Hsin-Ti Lu</name>
<name sortKey="Peng, Sheng Kai" sort="Peng, Sheng Kai" uniqKey="Peng S" first="Sheng-Kai" last="Peng">Sheng-Kai Peng</name>
<name sortKey="Wang, Sheng Wei" sort="Wang, Sheng Wei" uniqKey="Wang S" first="Sheng-Wei" last="Wang">Sheng-Wei Wang</name>
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