Matsuura Ryosuke, Kawamura Arisa, Matsumoto Yasunobu, Iida Yoshiki, Kanayama Masanori, Kurokawa Masahiko, Aida Yoko
Laboratory of Global Infectious Diseases Control Science, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Laboratory of Global Animal Resource Science, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Microorganisms. 2022 Sep 6;10(9):1796. doi: 10.3390/microorganisms10091796.
Natural products are attractive antiviral agents because they are environment-friendly and mostly harmless. Epigallocatechin gallate (EGCg), a type of catechin, is a well-known natural antiviral agent that can inhibit various viruses. However, EGCg easily oxidizes and loses its physiological activity. Although this problem can be overcome by combining EGCg with cyclodextrin (CD-EGCg), which makes it stable in water at high concentrations, the antiviral effect of this compound remains unclear. Here, we show that in Madin-Darby canine kidney (MDCK) and MRC-5 cells, CD-EGCg is cytotoxic for 50% of cells at 85.61 and 65.34 ppm, respectively. Furthermore, CD-EGCg mainly shows its antiviral effect during the adsorption step for all four influenza virus strains (median effect concentration (EC) was 0.93 to 2.78 ppm). Its antiviral effect post-adsorption is less intense, and no inhibitory effect is observed on influenza viruses pre-adsorption. Moreover, human coronavirus 229E (HCoV-229E) was inhibited at the adsorption step in short contact (EC = 2.5 ppm) and long contact conditions (EC = 0.5 ppm) by mixing CD-EGCg with HCoV-229E. These results suggest that CD-EGCg effectively inhibits various viruses that require an adsorption step, and is an effective tool for preventing infection.
天然产物是具有吸引力的抗病毒剂,因为它们环保且大多无害。表没食子儿茶素没食子酸酯(EGCg)是一种儿茶素,是一种著名的天然抗病毒剂,能够抑制多种病毒。然而,EGCg容易氧化并失去其生理活性。虽然通过将EGCg与环糊精结合(CD - EGCg)可以克服这个问题,使其在高浓度水中稳定,但这种化合物的抗病毒效果仍不清楚。在这里,我们表明,在犬肾传代细胞(MDCK)和人胚肺成纤维细胞(MRC - 5)中,CD - EGCg分别在85.61 ppm和65.34 ppm时对50%的细胞具有细胞毒性。此外,对于所有四种流感病毒株,CD - EGCg主要在吸附步骤中显示其抗病毒作用(半数效应浓度(EC)为0.93至2.78 ppm)。其吸附后抗病毒作用较弱,对预吸附的流感病毒未观察到抑制作用。此外,通过将CD - EGCg与人类冠状病毒229E(HCoV - 229E)混合,在短接触(EC = 2.5 ppm)和长接触条件(EC = 0.5 ppm)下,HCoV - 229E在吸附步骤中受到抑制。这些结果表明,CD - EGCg有效抑制需要吸附步骤的各种病毒,是预防感染的有效工具。