Efficacy of oleandrin and PBI-05204 against bovine viruses of importance to commercial cattle health

Author:

Newman Robert A.12ORCID,Chase Christopher C.L.34,Matos Jose R.56,Abdelsalam Karim4,Buterbaugh Robin4,Van Holland Sonja4,Abdelaal Hadia4,Woolum Amelia5,Jagannadha Sastry K78

Affiliation:

1. Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77054, USA

2. Phoenix Biotechnology, Inc., San Antonio, TX 78217, USA

3. Department of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD 57006, USA

4. RTI, LLC, Brookings SD 57006, USA

5. Department of Pathobiology and Population Medicine, Mississippi State University, Starkville, MS 39762, USA

6. Innovar, LLC, Plano, TX 75025, USA

7. Departments of Thoracic, Head and Neck Medical Oncology and Veterinary Sciences, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

8. MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX, USA

Abstract

Background Bovine viral diarrhea virus (BVDV), bovine respiratory syncytial virus (BRSV). and bovine coronavirus (BCV) threaten the productivity of cattle worldwide. Development of therapeutics that can control the spread of these viruses is an unmet need. The present research was designed to explore the in vitro antiviral activity of the Nerium oleander derived cardiac glycoside oleandrin and a defined N. oleander plant extract (PBI-05204) containing oleandrin. Methods Madin Darby Bovine Kidney (MDBK) cells, Bovine Turbinate (BT) cells, and Human Rectal Tumor-18 (HRT-18) cells were used as in vitro culture systems for BVDV, BRSV and BCV, respectively. Cytotoxicity was established using serial dilutions of oleandrin or PBI-05204. Noncytotoxic concentrations of each drug were used either prior to or at 12 h and 24 h following virus exposure to corresponding viruses. Infectious virus titers were determined following each treatment. Results Both oleandrin as well as PBI-05204 demonstrated strong antiviral activity against BVDV, BRSV, and BCV, in a dose-dependent manner, when added prior to or following infection of host cells. Determination of viral loads by PCR demonstrated a concentration dependent decline in virus replication. Importantly, the relative ability of virus produced from treated cultures to infect new host cells was reduced by as much as 10,000-fold at noncytotoxic concentrations of oleandrin or PBI-05204. Conclusions The research demonstrates the potency of oleandrin and PBI-05204 to inhibit infectivity of three important enveloped bovine viruses in vitro. These data showing non-toxic concentrations of oleandrin inhibiting infectivity of three bovine viruses support further investigation of in vivo antiviral efficacy.

Funder

Phoenix Biotechnology, Inc.

Publisher

SAGE Publications

Subject

General Materials Science

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