Shiloh
Editor, Senior Moderator
Source: https://www.cell.com/cell-host-microbe/fulltext/S1931-3128(20)30362-0
Neutralizing antibody and soluble ACE2 inhibition of a replication-competent VSV-SARS-CoV-2 and a clinical isolate of SARS-CoV-2.
James Brett Case
Paul W. Rothlauf ∗
Rita E. Chen
Daved H. Fremont
Michael S. Diamond
Sean P.J. Whelan #
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Published:July 01, 2020DOI:https://doi.org/10.1016/j.chom.2020.06.021
Highlights
•
Vesicular stomatitis virus encoding the SARS-CoV-2 spike replicates to high titers
•
Virus propagation is enhanced by a truncation in the cytoplasmic tail of the spike
•
Neutralization can be assessed by BSL2 and BSL3 high-throughput assays
•
SARS-CoV-2 and VSV-SARS-CoV-2-based neutralization assays correlate
Abstract
Antibody-based interventions against SARS-CoV-2 could limit morbidity, mortality, and possibly transmission. An anticipated correlate of such countermeasures is the level of neutralizing antibodies against the SARS-CoV-2 spike protein, which engages with host ACE2 receptor for entry. Using an infectious molecular clone of vesicular stomatitis virus (VSV) expressing eGFP as a marker of infection, we replaced the glycoprotein gene (G) with the spike protein of SARS-CoV-2 (VSV-eGFP-SARS-CoV-2) and developed a high-throughput imaging-based neutralization assay at biosafety level 2. We also developed a focus-reduction neutralization test with a clinical isolate of SARS-CoV-2 at biosafety level 3. Comparing the neutralizing activities of various antibodies and ACE2-Fc soluble decoy protein in both assays revealed a high degree of concordance. These assays will help define correlates of protection for antibody-based countermeasures and vaccines against SARS-CoV-2. Additionally, replication-competent VSV-eGFP-SARS-CoV-2 provides a tool for testing inhibitors of SARS-CoV-2 mediated entry under reduced biosafety containment.
Neutralizing antibody and soluble ACE2 inhibition of a replication-competent VSV-SARS-CoV-2 and a clinical isolate of SARS-CoV-2.
James Brett Case
Paul W. Rothlauf ∗
Rita E. Chen
Daved H. Fremont
Michael S. Diamond
Sean P.J. Whelan #
Show all authors
Show footnotes
Published:July 01, 2020DOI:https://doi.org/10.1016/j.chom.2020.06.021
Highlights
•
Vesicular stomatitis virus encoding the SARS-CoV-2 spike replicates to high titers
•
Virus propagation is enhanced by a truncation in the cytoplasmic tail of the spike
•
Neutralization can be assessed by BSL2 and BSL3 high-throughput assays
•
SARS-CoV-2 and VSV-SARS-CoV-2-based neutralization assays correlate
Abstract
Antibody-based interventions against SARS-CoV-2 could limit morbidity, mortality, and possibly transmission. An anticipated correlate of such countermeasures is the level of neutralizing antibodies against the SARS-CoV-2 spike protein, which engages with host ACE2 receptor for entry. Using an infectious molecular clone of vesicular stomatitis virus (VSV) expressing eGFP as a marker of infection, we replaced the glycoprotein gene (G) with the spike protein of SARS-CoV-2 (VSV-eGFP-SARS-CoV-2) and developed a high-throughput imaging-based neutralization assay at biosafety level 2. We also developed a focus-reduction neutralization test with a clinical isolate of SARS-CoV-2 at biosafety level 3. Comparing the neutralizing activities of various antibodies and ACE2-Fc soluble decoy protein in both assays revealed a high degree of concordance. These assays will help define correlates of protection for antibody-based countermeasures and vaccines against SARS-CoV-2. Additionally, replication-competent VSV-eGFP-SARS-CoV-2 provides a tool for testing inhibitors of SARS-CoV-2 mediated entry under reduced biosafety containment.