Alsahafi Tasneem, Bouback Thamer, Albeshri Abdulaziz, Alnhhas Sara, Ali Mohamed, Moatasim Yassmin, Kutkat Omnia, Gaballah Mohamed, Alfasi Fahad, Mater Ehab H, Al-Sarraj Faisal, Badierah Raied, Alotibi Ibrahim A, Almulaiky Yaaser Q
Department of Biological Sciences, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Princess Dr. Najla Bint Saud Al-Saud Center for Excellence Research in Biotechnology, King Abdul-Aziz University, Jeddah, 21589, Saudi Arabia.
Sci Rep. 2025 Apr 9;15(1):12118. doi: 10.1038/s41598-025-96417-5.
Melissa officinalis is a perennial medicinal plant traditionally used for its diverse biological activities, including antiviral properties. This study investigates the antiviral efficacy of various extracts, including water, acetone, alkaloid, non-alkaloid, ethanol, and methanol extracts, against influenza A (H1N1), SARS-CoV-2, and MERS-CoV. The water extract demonstrated significant inhibitory effects on SARS-CoV-2 (IC = 421.9 µg/mL) and MERS-CoV (IC = 222.1 µg/mL) in Vero E6 cells (an African green monkey kidney cell line), with a CC of 4221 µg/mL, indicating a favorable selectivity index. Additionally, it exhibited strong activity against H1N1 in Madin-Darby canine kidney cell line (MDCK cells) (IC = 57.30 µg/mL, CC = 3073 µg/mL). Among all the extracts, the methanol extract showed the highest antiviral activity. It has IC = 2.549 µg/ml and selectivity index (SI) = 230 against H1N1.While it showed IC = 10.83 µg/ml against SARS-CoV-2 and 9.82 µg/ml against MERS-CoV with SI values of 54.2 and 59.77, respectively. Molecular docking studies revealed that 5-Methyl-5 H-naphtho[2,3-c]carbazole,7 H-Dibenzo[b, g]carbazole, 7-methyl, hesperidin, luteolin-7-glucoside-3'-glucuronide, Melitric acid A, and other compounds exhibited high binding affinities to the receptor-binding domains (RBDs) of SARS-CoV-2 and MERS-CoV spike glycoproteins, suggesting their potential to interfere with viral entry. Furthermore, GC-MS-identified bioactive compounds, including docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), paromomycin, and phenolic acids, demonstrated additional antiviral potential. These results underscore the potential of M. officinalis extracts as natural antiviral agents, offering a foundation for further in vitro and in vivo validation and potential therapeutic applications against respiratory viral infections, including coronaviruses and influenza viruses.
蜜蜂花是一种多年生药用植物,传统上因其多种生物活性而被使用,包括抗病毒特性。本研究调查了水、丙酮、生物碱、非生物碱、乙醇和甲醇提取物对甲型流感病毒(H1N1)、严重急性呼吸综合征冠状病毒2(SARS-CoV-2)和中东呼吸综合征冠状病毒(MERS-CoV)的抗病毒效果。水提取物在非洲绿猴肾细胞系Vero E6细胞中对SARS-CoV-2(半数抑制浓度[IC]=421.9微克/毫升)和MERS-CoV(IC=222.1微克/毫升)表现出显著抑制作用,细胞毒性浓度(CC)为4221微克/毫升,表明具有良好的选择性指数。此外,它在麦迪逊-达比犬肾细胞系(MDCK细胞)中对H1N1表现出较强活性(IC=57.30微克/毫升,CC=3073微克/毫升)。在所有提取物中,甲醇提取物显示出最高的抗病毒活性。它对H1N1的IC=2.549微克/毫升,选择性指数(SI)=230。而它对SARS-CoV-2的IC=10.83微克/毫升,对MERS-CoV的IC=9.82微克/毫升,SI值分别为54.2和59.77。分子对接研究表明,5-甲基-5H-萘并[2,3-c]咔唑(即蜜茱萸卡唑)、7H-二苯并[b,g]咔唑、7-甲基、橙皮苷、木犀草素-7-葡萄糖苷-3'-葡萄糖醛酸、蜜茱萸酸A等化合物对SARS-CoV-2和MERS-CoV刺突糖蛋白的受体结合域(RBD)表现出高结合亲和力,表明它们具有干扰病毒进入的潜力。此外,气相色谱-质谱联用鉴定的生物活性化合物,包括二十二碳六烯酸(DHA)、二十碳五烯酸(EPA)、巴龙霉素和酚酸,显示出额外的抗病毒潜力。这些结果强调了蜜蜂花提取物作为天然抗病毒剂的潜力,为进一步的体外和体内验证以及针对包括冠状病毒和流感病毒在内的呼吸道病毒感染的潜在治疗应用奠定了基础。