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首页> 外文期刊>Microbiology Research >Effect of catanospermine, 1-deoxynojirimycin or 1-deoxymannojirimycin on biological and functional activities of Japanese encephalitis virus in porcine stable kidney cells
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Effect of catanospermine, 1-deoxynojirimycin or 1-deoxymannojirimycin on biological and functional activities of Japanese encephalitis virus in porcine stable kidney cells

机译:卡他精胺,1-脱氧野oji霉素或1-脱氧甘露oji霉素对猪稳定肾细胞中日本脑炎病毒的生物学和功能活性的影响

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摘要

In the present study, effect of catanospermine (CST), 1-deoxynojirimycin (DNJ) or 1-deoxymannojirimycin (DMJ) was studied on porcine stable kidney (PS) cells infected with Japanese encephalitis virus (JEV). As both CST and DNJ are potent inhibitors of ER alpha-glucosidases 1 and II, while DMJ is an inhibitor of Golgi mannosidase which removes alpha (1, 2) Man residues from the N-glycan precursor. Treatment of infected cells with CST (200 uM/mL), DNJ (100 uM/mL) or DMJ (200 uM/mL) did not produce much effect on viral gpE epitope presentation within the cells as well as on the cell surface as detected in the immunofluorescence employing monoclonal (MAbs) and polyclonal (PAbs) antibodies. As well the treated (infected) cells showed only a marginal decrease in infectious virus yield along with a slight decrease in haemagglutination activity of the virus that was recorded in comparison to the untreated infected (control) cells and the cells infected with Dengue virus. Immuno-blotting of the separated proteins from infected lysed cells and probed with anti-gpE MAbs also revealed a band corresponding to JEV gpE (MW 53kDa) both with inhibitor treated and the untreated cells; the reactivity with the former however, was somewhat less intense and prominent in comparison to latter (control untreated) indicating some effect on JEV. The present results indicate that these inhibitors by in large, do not affect maturation and the release of infective JE virions in PS cells.
机译:在本研究中,研究了卡他精胺(CST),1-脱氧野oji霉素(DNJ)或1-脱氧甘露菌霉素(DMJ)对感染日本脑炎病毒(JEV)的猪稳定肾脏(PS)细胞的作用。由于CST和DNJ都是ERα-葡萄糖苷酶1和II的有效抑制剂,而DMJ是高尔基甘露糖苷酶的抑制剂,可从N-聚糖前体中去除α(1、2)Man残基。用CST(200 uM / mL),DNJ(100 uM / mL)或DMJ(200 uM / mL)处理感染的细胞对细胞内以及检测到的细胞表面上的病毒gpE表位呈递没有太大影响单克隆抗体(MAbs)和多克隆抗体(PAbs)在免疫荧光中的应用。同样,与未处理的感染(对照)细胞和感染登革热病毒的细胞相比,处理(感染)的细胞仅显示出感染性病毒产量的少量降低,以及病毒的血凝活性的轻微降低。从感染的裂解细胞中分离的蛋白质进行免疫印迹,并用抗gpE MAb进行探测,还发现了一条条带,该条带对应于经抑制剂处理和未处理的细胞的JEV gpE(MW 53kDa);然而,与前者的反应性比后者(未处理的对照物)要弱一些,且表现突出,表明对JEV有一定作用。目前的结果表明,这些抑制剂基本上不影响PS细胞的成熟和感染性JE病毒粒子的释放。

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