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猫传染性腹膜炎的免疫致病机制研究进展 被引量:3
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作者 董佳易 李琛琛 张焓 《湖北畜牧兽医》 2020年第4期13-15,共3页
猫传染性腹膜炎(Feline Infectious Peritonitis,FIP)是一种由病毒引起的严重的全身性疾病,死亡率较高。FIP的研究历史并不长,直到20世纪50年代才出现临床报道,因此对其发病机制的认识仍然停留在非常基础的水平。近些年来,针对FIP的研... 猫传染性腹膜炎(Feline Infectious Peritonitis,FIP)是一种由病毒引起的严重的全身性疾病,死亡率较高。FIP的研究历史并不长,直到20世纪50年代才出现临床报道,因此对其发病机制的认识仍然停留在非常基础的水平。近些年来,针对FIP的研究出现了可喜的进展,总结了FIP的免疫致病机制,为该病的预防、诊断及治疗提供参考。 展开更多
关键词 猫传染性腹膜炎(Feline infectious peritonitis FIP) 致病机制 免疫应答 免疫调节
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Two Inhibitors Against the 3C-Like Proteases of Swine Coronavirus and Feline Coronavirus 被引量:1
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作者 Mengxin Zhou Yutong Han +2 位作者 Mengxia Li Gang Ye Guiqing Peng 《Virologica Sinica》 SCIE CAS CSCD 2021年第6期1421-1430,共10页
Coronaviruses(CoVs)are important human and animal pathogens that cause respiratory and gastrointestinal diseases.Porcine epidemic diarrhoea(PED),characterized by severe diarrhoea and vomiting in pigs,is a highly letha... Coronaviruses(CoVs)are important human and animal pathogens that cause respiratory and gastrointestinal diseases.Porcine epidemic diarrhoea(PED),characterized by severe diarrhoea and vomiting in pigs,is a highly lethal disease caused by porcine epidemic diarrhoea virus(PEDV)and causes substantial losses in the swine industry worldwide.However,currently available commercial drugs have not shown great therapeutic effects.In this study,a fluorescence resonance energy transfer(FRET)-based assay was applied to screen a library containing 1,590 compounds and identified two compounds,3-(aminocarbonyl)-1-phenylpyridinium and 2,3-dichloronaphthoquinone,that target the 3C-like protease(3CL^(pro))of PEDV.These compounds are of low molecular weight(MW)and greatly inhibited the activity of this enzyme(IC_(50) values were obtained in this study).Furthermore,these compounds exhibited antiviral capacity against another member of the CoV family,feline infectious peritonitis virus(FIPV).Here,the inhibitory effects of these compounds against CoVs on Vero cells and feline kidney cells were identified(with EC_(50) values)and cell viability assays were performed.The results of putative molecular docking models indicate that these compounds,labeled compound 1 and compound 2,contact the conserved active sites(Cys144,Glu165,Gln191)of 3CL^(pro) via hydrogen bonds.These findings provide insight into the antiviral activities of compounds 1 and 2 that may facilitate future research on anti-CoV drugs. 展开更多
关键词 Coronavirus(CoVs) Inhibitor 3C-like Protease Porcine epidemic diarrhoea virus(PEDV) Feline infectious peritonitis virus(FIPV)
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