Jordan L T, Derbyshire J B
Department of Veterinary Microbiology and Immunology, University of Guelph, Canada.
Vet Microbiol. 1995 Jun;45(1):59-70. doi: 10.1016/0378-1135(94)00118-g.
Swine testis (ST) cell cultures were treated with various doses of recombinant human interferon-alpha 2a (IFN), and assayed for 2',5' oligoadenylate synthetase (2-5 A synthetase) activity. Treatment with 100 or 1000 units/ml of IFN resulted in increased 2-5 A synthetase activity, but there was no significant response to 1 unit/ml of IFN. Titres of porcine transmissible gastroenteritis virus (TGEV) were reduced between 6 and 15 hours post-infection in ST cells treated with 1000 or 2500 units/ml of IFN. Polyacrylamide gel electrophoresis of lysates of TGEV-infected ST cells, and of lysates immunoprecipitated with anti-TGEV antibodies, revealed that the synthesis of the N and S proteins of TGEV was reduced in cells treated with 100 or 1000 units/ml of IFN. Viral RNA production, as determined with a probe which hybridized to the S gene of TGEV, was found to be reduced in ST cells treated with 1000 units/ml of IFN, but not in cells treated with 100 units/ml. It was concluded that, in IFN-treated ST cells, TGEV protein production may be decreased in the absence of reduced viral RNA production, and that 2-5 A synthetase may not be a significant factor in the antiviral activity of IFN against TGEV.
用不同剂量的重组人干扰素α2a(IFN)处理猪睾丸(ST)细胞培养物,并检测其2',5'-寡腺苷酸合成酶(2-5A合成酶)活性。用100或1000单位/毫升的IFN处理可导致2-5A合成酶活性增加,但对1单位/毫升的IFN无明显反应。在用1000或2500单位/毫升的IFN处理的ST细胞中,猪传染性胃肠炎病毒(TGEV)的滴度在感染后6至15小时降低。对感染TGEV的ST细胞裂解物以及用抗TGEV抗体免疫沉淀的裂解物进行聚丙烯酰胺凝胶电泳,结果显示,在用100或1000单位/毫升的IFN处理的细胞中,TGEV的N和S蛋白合成减少。用与TGEV的S基因杂交的探针测定,发现用1000单位/毫升的IFN处理的ST细胞中病毒RNA产生减少,但用100单位/毫升处理的细胞中未减少。得出的结论是,在IFN处理的ST细胞中,TGEV蛋白产生可能在病毒RNA产生未减少的情况下降低,并且2-5A合成酶可能不是IFN对TGEV抗病毒活性的重要因素。