Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77054, USA.
Phoenix Biotechnology, Inc., San Antonio, TX 78217, USA.
Antivir Chem Chemother. 2022 Jan-Dec;30:20402066221103960. doi: 10.1177/20402066221103960.
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 antiviral activity of the derived cardiac glycoside oleandrin and a defined plant extract (PBI-05204) containing oleandrin.
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.
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.
The research demonstrates the potency of oleandrin and PBI-05204 to inhibit infectivity of three important enveloped bovine viruses . These data showing non-toxic concentrations of oleandrin inhibiting infectivity of three bovine viruses support further investigation of antiviral efficacy.
牛病毒性腹泻病毒(BVDV)、牛呼吸道合胞体病毒(BRSV)和牛冠状病毒(BCV)威胁着全球牛的生产力。开发能够控制这些病毒传播的治疗方法是未满足的需求。本研究旨在探索衍生强心苷毛地黄苷和含有毛地黄苷的特定植物提取物(PBI-05204)的抗病毒活性。
MDBK 细胞、牛鼻甲(BT)细胞和人直肠肿瘤-18(HRT-18)细胞分别用作 BVDV、BRSV 和 BCV 的体外培养系统。使用毛地黄苷或 PBI-05204 的系列稀释液确定细胞毒性。在暴露于相应病毒之前或之后的 12 小时和 24 小时,使用每种药物的非细胞毒性浓度。在每种处理后确定感染性病毒滴度。
毛地黄苷和 PBI-05204 在添加到宿主细胞感染之前或之后,均以剂量依赖性方式对 BVDV、BRSV 和 BCV 表现出强烈的抗病毒活性。通过 PCR 测定病毒载量表明病毒复制呈浓度依赖性下降。重要的是,用非细胞毒性浓度的毛地黄苷或 PBI-05204 处理培养物产生的病毒感染新宿主细胞的相对能力降低了多达 10,000 倍。
该研究证明了毛地黄苷和 PBI-05204 抑制三种重要包膜牛病毒感染能力的效力。这些显示非毒性浓度的毛地黄苷抑制三种牛病毒感染性的数据支持进一步研究抗病毒功效。