非洲猪瘟病毒
鸟粪
生物
滴答声
病毒学
乌鳢科
病毒
蛋白酶
载体(分子生物学)
微生物学
基因
硬蜱科
酶
重组DNA
遗传学
生物化学
作者
Jingjing Wang,Mengyao Ji,Bingqian Yuan,Anna Luo,Zhenyuan Jiang,Tengyu Zhu,Yang Liu,Peter Muiruri Kamau,Lin Jin,Ren Lai
标识
DOI:10.3389/fmicb.2021.778309
摘要
African swine fever virus (ASFV) is a large double-stranded DNA virus and causes high mortality in swine. ASFV can be transmitted by biological vectors, including soft ticks in genus Ornithodoros but not hard ticks. However, the underlying mechanisms evolved in the vectorial capacity of soft ticks are not well-understood. Here, we found that a defensin-like peptide toxin OPTX-1 identified from Ornithodoros papillipes inhibits the enzyme activity of the ASFV pS273R protease with a K i =0.821±0.526μM and shows inhibitory activity on the replication of ASFV. The analogs of OPTX-1 from hard ticks show more inhibitory efficient on pS273R protease. Considering that ticks are blood-sucking animals, we tested the effects of OPTX-1 and its analogs on the coagulation system. At last, top 3D structures represented surface analyses of the binding sites of pS273R with different inhibitors that were obtained by molecular docking based on known structural information. In summary, our study provides evidence that different inhibitory efficiencies between soft tick-derived OPTX-1 and hard tick-derived defensin-like peptides may determine the vector and reservoir competence of ticks.
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