Antiviral Activity of the Propylamylatin<sup>TM</sup> Formula against the Novel Coronavirus SARS-CoV-2 In Vitro Using Direct Injection and Gas Assays in Virus Suspensions

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of novel coronavirus disease 2019 (COVID-19), has become a severe threat to global public health. There are currently no antiviral therapies approved for the treatment or prevention of mild to moderate COVID-19 as remd...

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Main Authors: Ashley N. Brown, Gary Strobel, Kaley C. Hanrahan, Joe Sears
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/13/3/415
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spelling doaj-97237a2187e9457fa7a2ce57bc4835602021-03-06T00:05:11ZengMDPI AGViruses1999-49152021-03-011341541510.3390/v13030415Antiviral Activity of the Propylamylatin<sup>TM</sup> Formula against the Novel Coronavirus SARS-CoV-2 In Vitro Using Direct Injection and Gas Assays in Virus SuspensionsAshley N. Brown0Gary Strobel1Kaley C. Hanrahan2Joe Sears3Institute for Therapeutic Innovation, Department of Medicine, College of Medicine, University of Florida, Orlando, FL 32827, USADepartment of Plant Sciences, Montana State University, Bozeman, MT 59715, USAInstitute for Therapeutic Innovation, Department of Medicine, College of Medicine, University of Florida, Orlando, FL 32827, USACenter for Lab Services/RJ Lee Group, Pasco, WA 99301, USASevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of novel coronavirus disease 2019 (COVID-19), has become a severe threat to global public health. There are currently no antiviral therapies approved for the treatment or prevention of mild to moderate COVID-19 as remdesivir is only approved for severe COVID-19 cases. Here, we evaluated the antiviral potential of a Propylamylatin formula, which is a mixture of propionic acid and isoamyl hexanoates. The Propylamylatin formula was investigated in gaseous and liquid phases against 1 mL viral suspensions containing 10<sup>5</sup> PFU of SARS-CoV-2. Viral suspensions were sampled at various times post-exposure and infectious virus was quantified by plaque assay on Vero E6 cells. Propylamylatin formula vapors were effective at inactivating infectious SARS-CoV-2 to undetectable levels at room temperature and body temperature, but the decline in virus was substantially faster at the higher temperature (15 min versus 24 h). The direct injection of liquid Propylamylatin formula into viral suspensions also completely inactivated SARS-CoV-2 and the rapidity of inactivation occurred in an exposure dependent manner. The overall volume that resulted in 90% viral inactivation over the course of the direct injection experiment (EC<sub>90</sub>) was 4.28 µls. Further investigation revealed that the majority of the antiviral effect was attributed to the propionic acid which yielded an overall EC<sub>90</sub> value of 11.50 µls whereas the isoamyl hexanoates provided at most a 10-fold reduction in infectious virus. The combination of propionic acid and isoamyl hexanoates was much more potent than the individual components alone, suggesting synergy between these components. These findings illustrate the therapeutic promise of the Propylamylatin formula as a potential treatment strategy for COVID-19 and future studies are warranted.https://www.mdpi.com/1999-4915/13/3/415SARS-CoV-2COVID-19antiviral agent<i>Muscodor albus</i>volatile organic compounds
collection DOAJ
language English
format Article
sources DOAJ
author Ashley N. Brown
Gary Strobel
Kaley C. Hanrahan
Joe Sears
spellingShingle Ashley N. Brown
Gary Strobel
Kaley C. Hanrahan
Joe Sears
Antiviral Activity of the Propylamylatin<sup>TM</sup> Formula against the Novel Coronavirus SARS-CoV-2 In Vitro Using Direct Injection and Gas Assays in Virus Suspensions
Viruses
SARS-CoV-2
COVID-19
antiviral agent
<i>Muscodor albus</i>
volatile organic compounds
author_facet Ashley N. Brown
Gary Strobel
Kaley C. Hanrahan
Joe Sears
author_sort Ashley N. Brown
title Antiviral Activity of the Propylamylatin<sup>TM</sup> Formula against the Novel Coronavirus SARS-CoV-2 In Vitro Using Direct Injection and Gas Assays in Virus Suspensions
title_short Antiviral Activity of the Propylamylatin<sup>TM</sup> Formula against the Novel Coronavirus SARS-CoV-2 In Vitro Using Direct Injection and Gas Assays in Virus Suspensions
title_full Antiviral Activity of the Propylamylatin<sup>TM</sup> Formula against the Novel Coronavirus SARS-CoV-2 In Vitro Using Direct Injection and Gas Assays in Virus Suspensions
title_fullStr Antiviral Activity of the Propylamylatin<sup>TM</sup> Formula against the Novel Coronavirus SARS-CoV-2 In Vitro Using Direct Injection and Gas Assays in Virus Suspensions
title_full_unstemmed Antiviral Activity of the Propylamylatin<sup>TM</sup> Formula against the Novel Coronavirus SARS-CoV-2 In Vitro Using Direct Injection and Gas Assays in Virus Suspensions
title_sort antiviral activity of the propylamylatin<sup>tm</sup> formula against the novel coronavirus sars-cov-2 in vitro using direct injection and gas assays in virus suspensions
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2021-03-01
description Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of novel coronavirus disease 2019 (COVID-19), has become a severe threat to global public health. There are currently no antiviral therapies approved for the treatment or prevention of mild to moderate COVID-19 as remdesivir is only approved for severe COVID-19 cases. Here, we evaluated the antiviral potential of a Propylamylatin formula, which is a mixture of propionic acid and isoamyl hexanoates. The Propylamylatin formula was investigated in gaseous and liquid phases against 1 mL viral suspensions containing 10<sup>5</sup> PFU of SARS-CoV-2. Viral suspensions were sampled at various times post-exposure and infectious virus was quantified by plaque assay on Vero E6 cells. Propylamylatin formula vapors were effective at inactivating infectious SARS-CoV-2 to undetectable levels at room temperature and body temperature, but the decline in virus was substantially faster at the higher temperature (15 min versus 24 h). The direct injection of liquid Propylamylatin formula into viral suspensions also completely inactivated SARS-CoV-2 and the rapidity of inactivation occurred in an exposure dependent manner. The overall volume that resulted in 90% viral inactivation over the course of the direct injection experiment (EC<sub>90</sub>) was 4.28 µls. Further investigation revealed that the majority of the antiviral effect was attributed to the propionic acid which yielded an overall EC<sub>90</sub> value of 11.50 µls whereas the isoamyl hexanoates provided at most a 10-fold reduction in infectious virus. The combination of propionic acid and isoamyl hexanoates was much more potent than the individual components alone, suggesting synergy between these components. These findings illustrate the therapeutic promise of the Propylamylatin formula as a potential treatment strategy for COVID-19 and future studies are warranted.
topic SARS-CoV-2
COVID-19
antiviral agent
<i>Muscodor albus</i>
volatile organic compounds
url https://www.mdpi.com/1999-4915/13/3/415
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