Department of Immunology and Microbiology, The Scripps Research Institute, Jupiter, Florida, USA.
Department of Molecular Medicine, The Scripps Research Institute, Jupiter, Florida, USA.
J Virol. 2020 Jul 16;94(15). doi: 10.1128/JVI.00147-20.
Oregano essential oil has long been known for its health-promoting benefits. Here, we report its activity against viral replication. Oregano oil was found to specifically inhibit lentiviruses, such as human and simian immunodeficiency viruses (HIV and SIV), irrespective of virus tropism, but not hepatitis C virus, adenovirus 5 (ADV5), Zika virus, and influenza (H1N1) virus. Oregano oil's most abundant components, carvacrol and its isomer, thymol, were shown to block virus-target cell fusion while not perturbing other stages of the virus life cycle. We detected changes in virus particle density, suggesting that cholesterol depletion from the HIV-1 envelope membrane reduces virus entry. Furthermore, infection was rescued by adding exogenous cholesterol. The evolution of viral resistance to carvacrol supported this mechanism of action with the identification of mutations in the viral gp41 fusion protein that counteracted cholesterol depletion. In addition, resistance to carvacrol emerged later than typically observed for other clinically used drugs, strengthening its antiviral potential. Structure-activity relationship studies revealed key motifs of carvacrol and thymol required for HIV neutralization and identified previously unknown active analogs. Carvacrol was also shown to additively cooperate with antiretroviral therapy. In sum, oregano oil and improved carvacrol and thymol analogs could be considered to supplement current HIV therapeutics. Oregano essential oil has multiple benefits in traditional medicine, cosmetics, and food industries. Carvacrol and its analog, thymol, are well-described components of oregano oil. Here, we show that these compounds inhibit HIV-target cell fusion independently of viral tropism. Our results suggest that carvacrol and thymol alter the cholesterol content of the viral membrane, blocking HIV-1 entry into the target cell. Resistance to carvacrol has selected for viruses with mutations in the viral envelope glycoprotein, gp41. This protein is known for its interaction with cholesterol present in membrane lipid rafts. Together, these results demonstrate the potential of therapies targeting the viral envelope membrane, and oregano oil is a safe supplement to antiretrovirals, potentially delaying disease progression and resistance development.
牛至精油以其促进健康的功效而闻名。在这里,我们报告其对抗病毒复制的活性。研究发现,牛至精油特异性抑制 lentiviruses,如人类和猿免疫缺陷病毒(HIV 和 SIV),而不考虑病毒嗜性,但不抑制丙型肝炎病毒、腺病毒 5(ADV5)、寨卡病毒和流感(H1N1)病毒。牛至精油最丰富的成分,香芹酚及其异构体,百里香酚,被证明可以阻止病毒-靶细胞融合,而不干扰病毒生命周期的其他阶段。我们检测到病毒粒子密度的变化,表明 HIV-1 包膜膜中的胆固醇耗竭降低了病毒进入。此外,通过添加外源性胆固醇可以挽救感染。香芹酚对病毒的抗药性的进化支持了这种作用机制,鉴定出病毒 gp41 融合蛋白中的突变,这些突变拮抗了胆固醇耗竭。此外,对香芹酚的抗药性的出现比通常观察到的其他临床使用的药物要晚,这增强了其抗病毒潜力。构效关系研究揭示了香芹酚和百里香酚中和 HIV 的关键基序,并确定了以前未知的活性类似物。香芹酚还被证明可以与抗逆转录病毒疗法相加合作。总之,牛至精油和改良的香芹酚和百里香酚类似物可被考虑用于补充当前的 HIV 治疗方法。牛至精油在传统医学、化妆品和食品工业中有多种益处。香芹酚和其类似物,百里香酚,是牛至油的良好成分。在这里,我们表明这些化合物独立于病毒嗜性抑制 HIV-1 靶细胞融合。我们的结果表明,香芹酚和百里香酚改变了病毒膜的胆固醇含量,阻止了 HIV-1 进入靶细胞。对香芹酚的抗药性选择了病毒包膜糖蛋白,gp41 中的突变。这种蛋白质以其与膜脂筏中存在的胆固醇的相互作用而闻名。总之,这些结果表明针对病毒包膜膜的治疗方法具有潜力,牛至精油是抗逆转录病毒药物的安全补充,可能会延迟疾病进展和耐药性的发展。