Welch S K, Saif L J
Food Animal Health Research Program, Ohio Agricultural Research and Development Center, Ohio State University, Wooster.
Arch Virol. 1988;101(3-4):221-35. doi: 10.1007/BF01311003.
Twelve hybridomas secreting monoclonal antibodies (MAbs) against Miller virulent strain of transmissible gastroenteritis virus (TGEV) were generated and characterized. In a cell culture immunofluorescence (CCIF) assay, three MAbs directed against peplomer protein (E2) had perinuclear fluorescence and four unclassified MAbs showed cell membrane fluorescence. Six of these seven MAbs neutralized both attenuated and virulent TGEV, and the seventh (an unclassified MAb) neutralized only the latter virus. Two MAbs able to bind the cell membrane of infected cells had low neutralizing antibody titers (8 to 72) but were able to distinguish between virulent and attenuated TGEV (9- to 72-fold differences in neutralizing titers). Two E2-specific MAbs had higher neutralizing antibody titers (782 to 34,117) and showed 4- to 13-fold differences in titers against the attenuated and virulent TGEV strains. Five MAbs which were specific for nucleocapsid (N) protein had cytoplasmic, particulate fluorescence in CCIF, and did not neutralize TGEV. Comparison of CCIF antibody titers of MAbs to the virulent and attenuated strains of TGEV indicated that differences existed in titers of most E2 and all N-specific MAbs, with titers consistently higher against virulent TGEV (homologous strain). Hyperimmune antisera prepared in gnotobiotic pigs against the attenuated, virulent and a recent isolate of TGEV immunoprecipitated the 3 major structural proteins of both the attenuated and virulent TGEV strains. Relative mol. wt. differences in the E1 and E2 proteins between the two virus strains were revealed using either the hyperimmune pig sera or MAbs. In addition to the 48 K N protein, a 44 K protein was coimmunoprecipitated by the hyperimmune sera and MAbs, but mainly from lysates of attenuated TGEV.
制备并鉴定了12株分泌抗传染性胃肠炎病毒(TGEV)米勒强毒株单克隆抗体(MAb)的杂交瘤。在细胞培养免疫荧光(CCIF)试验中,3株针对纤突蛋白(E2)的单克隆抗体呈现核周荧光,4株未分类的单克隆抗体呈现细胞膜荧光。这7株单克隆抗体中的6株能中和弱毒和强毒TGEV,第7株(1株未分类的单克隆抗体)仅能中和后者病毒。2株能够结合感染细胞细胞膜的单克隆抗体中和抗体效价较低(8至72),但能够区分强毒和弱毒TGEV(中和效价相差9至72倍)。2株E2特异性单克隆抗体具有较高的中和抗体效价(782至34117),针对弱毒和强毒TGEV毒株的效价相差4至13倍。5株针对核衣壳(N)蛋白的单克隆抗体在CCIF中呈现细胞质颗粒状荧光,不能中和TGEV。比较单克隆抗体对TGEV强毒株和弱毒株的CCIF抗体效价表明,大多数E2特异性单克隆抗体和所有N特异性单克隆抗体的效价存在差异,对强毒TGEV(同源毒株)的效价始终较高。在无菌猪中制备的针对弱毒、强毒和近期分离的TGEV的超免疫血清沉淀了弱毒和强毒TGEV毒株的3种主要结构蛋白。使用超免疫猪血清或单克隆抗体揭示了两种病毒株之间E1和E2蛋白的相对分子量差异。除了48K的N蛋白外,超免疫血清和单克隆抗体还共同沉淀了一种44K的蛋白,但主要来自弱毒TGEV的裂解物。