Natural fucoidans inhibit coronaviruses by targeting viral spike protein and host cell furin

褐藻糖胶 毛皮 生物 维罗细胞 病毒进入 病毒学 微生物学 病毒 分子生物学 生物化学 多糖 病毒复制
作者
Cheng‐Wei Yang,Hsing‐Yu Hsu,Yue‐Zhi Lee,Jia‐Tsrong Jan,Sui‐Yuan Chang,Yi‐Ling Lin,Ruey‐Bing Yang,Tai‐Ling Chao,Jian‐Jong Liang,Shujing Lin,Chun‐Che Liao,Chih-Shin Chang,Huey‐Kang Sytwu,Ming‐Shiu Hung,Chiung‐Tong Chen,Shiow‐Ju Lee
出处
期刊:Biochemical Pharmacology [Elsevier]
卷期号:215: 115688-115688 被引量:11
标识
DOI:10.1016/j.bcp.2023.115688
摘要

Fucoidans are a class of long chain sulfated polysaccharides and have multiple biological functions. Herein, four natural fucoidans extracted from Fucus vesiculosus, F. serratus, Laminaria japonica and Undaria pinnatifida, were tested for their HCoV-OC43 inhibition and found to demonstrate EC50 values ranging from 0.15 to 0.61 µg/mL. That from U. pinnatifida exhibited the most potent anti-HCoV-OC43 activity with an EC50 value of 0.15 ± 0.02 µg/mL, a potency largely independent of its sulfate content. Comparison of the gene expression profiles of fucoidan-treated and untreated cells infected with HCoV-OC43 revealed that fucoidan treatment effectively diminished HCoV-OC43 gene expressions associated with induced chemokines, cytokines and viral activities. Further studies using a highly fucoidan-resistant HCoV-OC43 determined that fucoidan inhibited HCoV-OC43 infection via interfering with viral entry and led to the identification of the specific site on the N-terminal region of spike protein, that located adjacent to the host cell receptor binding domain, targeted by the virus. Furthermore, in a SARS-CoV-2 pseudovirus neutralization assay, fucoidan also blocked SARS-CoV-2 entry. In vitro and in vivo, fucoidan decreased SARS-CoV-2 viral loads and inhibited viral infection in Calu-3 or Vero E6 cells and SARS-CoV-2 infected hamsters, respectively. Fucoidan was also found to inhibit furin activity, and reported furin inhibitors were found to inhibit viral infection by wild type HCoV-OC43 or SARS-CoV-2. Accordingly, we conclude that fucoidans inhibit coronaviral infection by targeting viral spike protein and host cell furin to interfere with viral entry.
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