Pol J M, Broekhuysen-Davies J M, Wagenaar F, La Bonnardière C
Central Veterinary Institute, Virology Department, Lelystad, The Netherlands.
J Gen Virol. 1991 Apr;72 ( Pt 4):933-8. doi: 10.1099/0022-1317-72-4-933.
To determine the effect of interferon (IFN) on the pathogenesis of pseudorabies virus (PRV), porcine nasal mucosal explants were first treated with recombinant porcine methionyl-IFN-alpha 1 and then infected with one of three strains of PRV. The stroma of treated mucosal explants were protected against infection with virulent PRV or PRV of intermediate virulence because the infection was restricted to the epithelial cells. In contrast, untreated mucosal explants were readily infected by virulent PRV or PRV of intermediate virulence; the infection spread from epithelial cells to stromal fibroblasts. Avirulent PRV infection was restricted to the epithelial cells of treated and untreated mucosal explants. IFN treatment limited the extent of all three PRV infections in the epithelial cells. Cultured porcine fibroblasts and porcine kidney cells were also treated with IFN and subsequently infected with PRV; infection was prevented in most porcine fibroblasts and the virus yield from porcine kidney cells was reduced. Budding of virulent PRV nucleocapsids through the inner nuclear membrane was observed more frequently in treated than in untreated mucosal explants were enveloped virus particles accumulated between the inner and outer nuclear membranes, indicating that the membrane-associated events of PRV replication had been affected. We conclude that IFN-alpha protects stromal fibroblasts against PRV infection and reduces virus replication in epithelial cells.
为了确定干扰素(IFN)对伪狂犬病病毒(PRV)发病机制的影响,首先用重组猪甲硫氨酰 - IFN -α1处理猪鼻黏膜外植体,然后用三种PRV毒株之一进行感染。经处理的黏膜外植体的基质受到保护,免受强毒PRV或中等毒力PRV的感染,因为感染仅限于上皮细胞。相比之下,未经处理的黏膜外植体很容易被强毒PRV或中等毒力PRV感染;感染从上皮细胞扩散到基质成纤维细胞。无毒力PRV感染在经处理和未经处理的黏膜外植体中均局限于上皮细胞。IFN处理限制了上皮细胞中所有三种PRV感染的程度。培养的猪成纤维细胞和猪肾细胞也用IFN处理,随后感染PRV;大多数猪成纤维细胞中感染被阻止,猪肾细胞中的病毒产量降低。在经处理的黏膜外植体中,比未经处理的黏膜外植体更频繁地观察到强毒PRV核衣壳通过内核膜出芽,包膜病毒颗粒在内核膜和外核膜之间积累,这表明PRV复制的膜相关事件受到了影响。我们得出结论,IFN -α可保护基质成纤维细胞免受PRV感染,并减少上皮细胞中的病毒复制。