Mardassi H, Athanassious R, Mounir S, Dea S
Centre de Recherche en Virologie, Institut Armand-Frappier, Laval, Quebec.
Can J Vet Res. 1994 Jan;58(1):55-64.
Cytolytic and noncytolytic strains of the porcine reproductive and respiratory syndrome virus (PRRSV) were isolated in primary cultures of porcine alveolar macrophages (PAM) from lung homogenates of stillborn fetuses or blood samples of dyspneic piglets collected from Quebec pig farms having experienced acute or chronic outbreaks of PRRS. Serological identification of the virus was confirmed by indirect immunofluorescence and indirect protein A-gold immunoelectron microscopy using reference antiserum prepared from experimentally-infected specific pathogen free (SPF) piglets and monoclonal antibodies (MoAbs) directed against the p15 nucleocapsid (N) protein of the reference ATCC-VR2332 isolate. Intracytoplasmic enveloped viral particles that tended to accumulate into cytoplasmic vesicles were observed in the infected PAM; no budding was demonstrated at the level of the cytoplasmic membrane. The extracellular virions appeared as pleomorphic but mostly spherical enveloped particles, 50-72 nm in diameter (averaged diameter of 50 particles was 58.3 nm), with an isometric core about 25-30 nm. Buoyant density of the virus in CsCL density gradients was estimated to 1.18-1.20 g/mL. No hemagglutinating activity was demonstrated. Analysis of semipurified virions of isolate IAF-exp91 by radioimmunoprecipitation (RIPA) and Western immunoblotting experiments, using reference rabbit and porcine hyperimmune sera, revealed four major viral proteins, a predominant 15 kD N protein and three other proteins with predicted M(r_ of 19, 26 and 42 kD. Progeny viral particles produced in PRRSV-infected PAM in the presence of tunicamycin lacked the 42 kD protein, thus confirming its N-glycosylated nature. Immunoprecipitation experiments using the anti-ATCC-VR2332 MoAbs confirmed the close antigenic relationships between Quebec and American reference isolates of PRRSV.
从魁北克猪场收集的死胎肺匀浆或呼吸困难仔猪的血液样本中,在猪肺泡巨噬细胞(PAM)原代培养物中分离出猪繁殖与呼吸综合征病毒(PRRSV)的细胞溶解型和非细胞溶解型毒株。这些猪场曾经历过PRRS的急性或慢性暴发。使用从实验感染的无特定病原体(SPF)仔猪制备的参考抗血清以及针对参考ATCC-VR2332分离株的p15核衣壳(N)蛋白的单克隆抗体(MoAb),通过间接免疫荧光和间接蛋白A-金免疫电子显微镜对病毒进行血清学鉴定。在感染的PAM中观察到倾向于聚集在细胞质囊泡中的胞质内包膜病毒颗粒;在细胞质膜水平未显示出出芽现象。细胞外病毒粒子呈现多形性,但大多为球形包膜颗粒,直径为50-72nm(50个颗粒的平均直径为58.3nm),具有约25-30nm的等轴核心。病毒在CsCL密度梯度中的浮力密度估计为1.18-1.20g/mL。未显示出血凝活性。使用参考兔和猪超免疫血清,通过放射免疫沉淀(RIPA)和Western免疫印迹实验对分离株IAF-exp91的半纯化病毒粒子进行分析,揭示了四种主要病毒蛋白,一种主要的15kD N蛋白和另外三种预测分子量分别为19、26和42kD的蛋白。在衣霉素存在下,PRRSV感染的PAM中产生的子代病毒颗粒缺乏42kD蛋白,从而证实了其N-糖基化性质。使用抗ATCC-VR2332 MoAb的免疫沉淀实验证实了魁北克PRRSV分离株与美国参考分离株之间密切的抗原关系。