猫传染性腹膜炎
病毒学
冠状病毒
肽
七肽重复区
生物
肽序列
传染病(医学专业)
医学
2019年冠状病毒病(COVID-19)
生物化学
疾病
病理
基因
作者
I-Jung Liu,Wan-Ting Tsai,Li‐En Hsieh,Ling-Ling Chueh
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2013-12-03
卷期号:8 (12): e82081-e82081
被引量:20
标识
DOI:10.1371/journal.pone.0082081
摘要
Feline infectious peritonitis (FIP) is a lethal immune-mediated disease caused by feline coronavirus (FCoV). Currently, no therapy with proven efficacy is available. In searching for agents that may prove clinically effective against FCoV infection, five analogous overlapping peptides were designed and synthesized based on the putative heptad repeat 2 (HR2) sequence of the spike protein of FCoV, and the antiviral efficacy was evaluated.Plaque reduction assay and MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) cytotoxicity assay were performed in this study. Peptides were selected using a plaque reduction assay to inhibit Feline coronavirus infection.The results demonstrated that peptide (FP5) at concentrations below 20 μM inhibited viral replication by up to 97%. The peptide (FP5) exhibiting the most effective antiviral effect was further combined with a known anti-viral agent, human interferon-α (IFN-α), and a significant synergistic antiviral effect was observed.Our data suggest that the synthetic peptide FP5 could serve as a valuable addition to the current FIP prevention methods.
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