麦卢卡蜂蜜对SARS-CoV-2抗病毒活性的评价

Israa Elbashir, Aisha Aisha Nasser J M Al-Saei, P. Thornalley, N. Rabbani
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MG may modify arginine residues in the functional domains of viral spike and nucleocapsid proteins, resulting in loss of charge, protein misfolding and inactivation. The aim of this study was to characterize the antiviral activity of Manuka honey against SARS-CoV-2 in vitro Materials and methods: Wild-type SARS-CoV-2 with titers of multiplicities of infection (MOI) 0.1 and 0.05 were incubated with 2-fold serial dilutions of 250+ Manuka honey (equivalent to 250 to 31 µM) in infection medium (Dulbecco's Modified Eagle Medium + 2% fetal bovine serum + 100 units/ml penicillin + 100 µg/ml streptomycin) for 3 h. Manuka honey treated and untreated control SARS-CoV-2 was incubated with confluent cultures of Vero cells in vitro for 1 h, cultures washed with phosphate-buffered saline and incubated in fresh infection medium at 37°C for 4 - 5 days until 70% of virus control cells displayed cytopathic effect. We also studied the effect of scavenging MG in Manuka Honey with aminoguanidine (AG; 500 µM) on virucidal activity. The antiviral activity of MG was judged by median tissue culture infectious dose (TCID50) assays. Data analysis was by logistic regression. TCID50 (mean ± SD) was deduced by interpolation. Results: Diluted Manuka honey inhibited SARS-CoV-2 replication in Vero cells. SARS-CoV-2 was incubated in diluted Manuka honey in medium at 37°C for 3 h before adding to Vero cells. Manuka honey dilutions down to 125 µM MG equivalents completely inhibited cytopathic effect of SARS-CoV-2 whereas 31.25 µM and 62.5 µM MG equivalents had limited effect. Logistic regression and interpolation of the cytopathic effect indicated that the TCID50 = 72 ± 2 µM MG equivalents for MOI of 0.1. Prior scavenging of MG by addition of AG resulted in virus replication levels equivalent to those seen in the virus control without AG. 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引用次数: 2

摘要

背景和目的:2020年,宣布由严重急性呼吸综合征冠状病毒(SARS-CoV-2)引起的全球大流行。该大流行病仍在继续,并继续在世界范围内造成相当大的死亡率和发病率,并且正在出现该病毒的新变种。针对SARS-CoV-2的疫苗正在快速开发和推广,以应对大流行,但由于出现了新的SARS-CoV-2变体,其中许多变体表现出疫苗有效性降低,因此受到了影响。到目前为止,还没有批准的针对2019冠状病毒病(COVID-19)的抗病毒治疗方法。几项研究表明麦卢卡蜂蜜具有杀病毒/抗病毒作用。甲基乙二醛(MG)是麦卢卡蜂蜜中的一种生物活性成分,在体外具有抗病毒活性。MG可以修饰病毒突刺蛋白和核衣壳蛋白功能域的精氨酸残基,导致电荷丢失、蛋白质错误折叠和失活。本研究的目的是表征麦卢卡蜂蜜对SARS-CoV-2的体外抗病毒活性感染倍数(MOI)为0.1和0.05的野生型SARS-CoV-2在感染培养基(Dulbecco's Modified Eagle medium + 2%胎牛血清+ 100单位/ml青霉素+ 100µg/ml链霉素)中用2倍连续稀释的250+麦卢卡蜂蜜(相当于250至31µM)孵育3小时。麦卢卡蜂蜜处理和未处理的对照SARS-CoV-2与体外Vero细胞融合培养培养1小时。用磷酸盐缓冲盐水洗涤培养物,在新鲜感染培养基中37°C孵育4 - 5天,直到70%的病毒对照细胞显示细胞病变作用。研究了氨基胍(AG)对麦卢卡蜂蜜中MG的清除作用;500µM)的杀病毒活性。采用组织培养感染中剂量(TCID50)测定MG的抗病毒活性。数据分析采用逻辑回归。通过插值得到TCID50 (mean±SD)。结果:稀释麦卢卡蜂蜜抑制Vero细胞的SARS-CoV-2复制。将SARS-CoV-2与稀释的麦卢卡蜂蜜在37°C培养基中孵育3小时,然后加入Vero细胞。麦卢卡蜂蜜稀释至125µM MG当量完全抑制SARS-CoV-2的细胞病变效应,而31.25µM和62.5µM MG当量的效果有限。Logistic回归和细胞病变效应插值结果表明,MOI为0.1时,TCID50 = 72±2µM MG当量。通过添加AG预先清除MG导致病毒复制水平与不添加AG的病毒对照组相当。结论:麦卢卡蜂蜜与SARS-CoV-2在不大于约40倍250+级的无细胞培养基中孵育时具有抗病毒活性。AG的抗病毒活性受到抑制,与MG介导的抗病毒作用一致。麦卢卡蜂蜜中MG当量的稀释剂具有与正宗MG相似的抗病毒作用,也与麦卢卡蜂蜜中MG含量介导抗病毒作用一致。虽然麦卢卡蜂蜜可以在无细胞培养基中灭活SARS-CoV-2,但由于乙二醛酶系统对MG的快速代谢和口服MG的生物利用度有限,它在体内的抗病毒活性可能受到限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of antiviral activity of Manuka honey against SARS-CoV-2.
Background and aims: In 2020 a global pandemic was declared caused by the severe acute respiratory syndrome coronavirus (SARS-CoV-2). The pandemic is still ongoing and continues to cause considerable mortality and morbidity world-wide and new variants of the virus are emerging. Rapid development and rollout of vaccines for SARS-CoV-2 is in progress to counter the pandemic but has been tempered by the emergence of new SARS-CoV-2 variants, many of which exhibit reduced vaccine effectiveness. To date there is no approved antiviral treatment for coronavirus disease 2019 (COVID-19). Several studies have shown that Manuka honey has virucidal/antiviral effect. Methylglyoxal (MG), a bioactive component in Manuka honey, has antiviral activity in vitro. MG may modify arginine residues in the functional domains of viral spike and nucleocapsid proteins, resulting in loss of charge, protein misfolding and inactivation. The aim of this study was to characterize the antiviral activity of Manuka honey against SARS-CoV-2 in vitro Materials and methods: Wild-type SARS-CoV-2 with titers of multiplicities of infection (MOI) 0.1 and 0.05 were incubated with 2-fold serial dilutions of 250+ Manuka honey (equivalent to 250 to 31 µM) in infection medium (Dulbecco's Modified Eagle Medium + 2% fetal bovine serum + 100 units/ml penicillin + 100 µg/ml streptomycin) for 3 h. Manuka honey treated and untreated control SARS-CoV-2 was incubated with confluent cultures of Vero cells in vitro for 1 h, cultures washed with phosphate-buffered saline and incubated in fresh infection medium at 37°C for 4 - 5 days until 70% of virus control cells displayed cytopathic effect. We also studied the effect of scavenging MG in Manuka Honey with aminoguanidine (AG; 500 µM) on virucidal activity. The antiviral activity of MG was judged by median tissue culture infectious dose (TCID50) assays. Data analysis was by logistic regression. TCID50 (mean ± SD) was deduced by interpolation. Results: Diluted Manuka honey inhibited SARS-CoV-2 replication in Vero cells. SARS-CoV-2 was incubated in diluted Manuka honey in medium at 37°C for 3 h before adding to Vero cells. Manuka honey dilutions down to 125 µM MG equivalents completely inhibited cytopathic effect of SARS-CoV-2 whereas 31.25 µM and 62.5 µM MG equivalents had limited effect. Logistic regression and interpolation of the cytopathic effect indicated that the TCID50 = 72 ± 2 µM MG equivalents for MOI of 0.1. Prior scavenging of MG by addition of AG resulted in virus replication levels equivalent to those seen in the virus control without AG. Conclusion: Manuka honey has antiviral activity against SARS-CoV-2 when incubated with the virus in cell-free media at no greater than ca. 40-fold dilutions of 250+ grade. Anti-viral activity was inhibited by AG, consistent with the anti-viral effect being mediated by MG. Manuka honey dilutions in MG equivalents had similar antiviral effect compared to authentic MG, also consistent with MG content of Manuka honey mediating the antiviral effect. Whilst Manuka honey may inactivate SARS-CoV-2 in cell-free culture medium, its antiviral activity in vivo for other than topical application may be limited because of the rapid metabolism of MG by the glyoxalase system and limited bioavailability of oral MG.
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