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Prophylactic and Therapeutic Inhibition of In Vitro SARS-CoV-2 Replication by Oleandrin

Kenneth S. Plante, Jessica A. Plante, Diana Fernandez, Divya Mirchandani, Nathen Bopp, Patricia V. Aguilar, K. Jagannadha Sastry, Robert A. Newman, View ORCID ProfileScott C. Weaver
doi: https://doi.org/10.1101/2020.07.15.203489
Kenneth S. Plante
aWorld Reference Center for Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, Texas USA 77555
bInstitute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, Texas USA 77555
cDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas USA 77555
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  • For correspondence: sweaver@utmb.edu ksplante@utmb.edu
Jessica A. Plante
aWorld Reference Center for Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, Texas USA 77555
bInstitute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, Texas USA 77555
cDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas USA 77555
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Diana Fernandez
aWorld Reference Center for Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, Texas USA 77555
bInstitute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, Texas USA 77555
dCenter for Tropical Diseases, University of Texas Medical Branch, Galveston, Texas USA 77555
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Divya Mirchandani
aWorld Reference Center for Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, Texas USA 77555
bInstitute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, Texas USA 77555
cDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas USA 77555
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Nathen Bopp
aWorld Reference Center for Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, Texas USA 77555
bInstitute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, Texas USA 77555
dCenter for Tropical Diseases, University of Texas Medical Branch, Galveston, Texas USA 77555
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Patricia V. Aguilar
aWorld Reference Center for Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, Texas USA 77555
bInstitute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, Texas USA 77555
dCenter for Tropical Diseases, University of Texas Medical Branch, Galveston, Texas USA 77555
eDepartment of Pathology, University of Texas Medical Branch, Galveston, Texas USA 77555
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K. Jagannadha Sastry
fDepartment of Thoracic/Head and Neck Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas USA 77030
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Robert A. Newman
gDepartment of Experimental Therapeutics, University of Texas MD Anderson Cancer Center, Houston, Texas USA 77030
hPhoenix Biotechnology, Inc., San Antonio, Texas USA 78217
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Scott C. Weaver
aWorld Reference Center for Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, Texas USA 77555
bInstitute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, Texas USA 77555
cDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas USA 77555
eDepartment of Pathology, University of Texas Medical Branch, Galveston, Texas USA 77555
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  • ORCID record for Scott C. Weaver
  • For correspondence: sweaver@utmb.edu ksplante@utmb.edu
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ABSTRACT

With continued expansion of the COVID-19 pandemic, antiviral drugs are desperately needed to treat patients at high risk of life-threatening disease and even to limit spread if administered early during infection. Typically, the fastest route to identifying and licensing a safe and effective antiviral drug is to test those already shown safe in early clinical trials for other infections or diseases. Here, we tested in vitro oleandrin, derived from the Nerium oleander plant and shown previously to have inhibitory activity against several viruses. Using Vero cells, we found that prophylactic oleandrin administration at concentrations down to 0.05 μg/ml exhibited potent antiviral activity against SARS-CoV-2, with an 800-fold reduction in virus production, and a 0.1 μg/ml dose resulted in a greater than 3,000-fold reduction in infectious virus production. The EC50 values were 11.98ng/ml when virus output was measured at 24 hours post-infection, and 7.07ng/ml measured at 48 hours post-infection. Therapeutic (post-infection) treatment up to 24 hours after infection of Vero cells also reduced viral titers, with the 0.1 μg/ml dose causing greater than 100-fold reductions as measured at 48 hours, and the 0.05 μg/ml dose resulting in a 78-fold reduction. The potent prophylactic and therapeutic antiviral activities demonstrated here strongly support the further development of oleandrin to reduce the severity of COVID-19 and potentially also to reduce spread by persons diagnosed early after infection.

IMPORTANCE COVID-19, a pandemic disease caused by infection with SARS-CoV-2, has swept around the world to cause millions of infections and hundreds-of-thousands of deaths due to the lack of vaccines and effective therapeutics. We tested oleandrin, derived from the Nerium oleander plant and shown previously to reduce the replication of several viruses, against SARS-CoV-2 infection of Vero cells. When administered both before and after virus infection, nanogram doses of oleandrin significantly inhibited replication by up to 3,000-fold, indicating the potential to prevent disease and virus spread in persons recently exposed to SARS-CoV-2, as well as to prevent severe disease in persons at high risk. These results indicate that oleandrin should be tested in animal models and in humans exposed to infection to determine its medical usefulness in controlling the pandemic.

Competing Interest Statement

RAN is Chief Science Officer of Phoenix Biotechnology Inc. KJS is a paid consultant with Phoenix Biotechnology Inc.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted July 15, 2020.
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Prophylactic and Therapeutic Inhibition of In Vitro SARS-CoV-2 Replication by Oleandrin
Kenneth S. Plante, Jessica A. Plante, Diana Fernandez, Divya Mirchandani, Nathen Bopp, Patricia V. Aguilar, K. Jagannadha Sastry, Robert A. Newman, Scott C. Weaver
bioRxiv 2020.07.15.203489; doi: https://doi.org/10.1101/2020.07.15.203489
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Prophylactic and Therapeutic Inhibition of In Vitro SARS-CoV-2 Replication by Oleandrin
Kenneth S. Plante, Jessica A. Plante, Diana Fernandez, Divya Mirchandani, Nathen Bopp, Patricia V. Aguilar, K. Jagannadha Sastry, Robert A. Newman, Scott C. Weaver
bioRxiv 2020.07.15.203489; doi: https://doi.org/10.1101/2020.07.15.203489

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