Dea S, Garzon S, Tijssen P
Centre de Recherche en Médecine Comparée Université du Québec, Institut Armand-Frappier, Laval-des-Rapides, Canada.
Arch Virol. 1989;106(3-4):221-37. doi: 10.1007/BF01313955.
The Minnesota strain of turkey enteric coronavirus (TCV) was grown on a human rectal tumor (HRT-18) cell line in the presence of radiolabeled amino acids and glucosamine to analyse virion structural proteins. In addition to the 52,000 unglycosylated nucleocapsid protein, three major glycoprotein species were found to be associated with the viral envelope. A predominant glycosylated protein with a molecular weight of 22-24,000 represented the transmembrane matrix protein. Larger glycoproteins with apparent molecular weights of 180-200,000 (gp 200), 120-125,000 (gp 120) and 95-100,000 (gp 100) were associated to the characteristic large bulbous projections (peplomers) located at the surface of the virion. The gp 100 and gp 120 species apparently arose from a proteolytic cleavage of gp 200, as suggested by digestion studies with trypsin and chymotrypsin. An additional large glycoprotein with mol. wt. of 140,000 (gp 140), that behaved as a disulfide-linked dimer of a 66,000 molecule, was found to be associated to granular projections located near the base of the large peplomers. Digestion studies with trypsin, bromelain and pronase demonstrated that gp 140 was related to the hemagglutinating activity of the virus. An inner membranous sac or tongue-shaped structure could be visualized in the interior of the viral particles following treatment with pronase. In contrast, trypsin or chymotrypsin treatments resulted in evaginations ("budding") on the virus surface. Progeny viral particles produced in TCV-infected cell cultures in the presence of tunicamycin lacked both types of surface projections, as demonstrated by electron microscopy and electrophoresis. The matrix protein also appeared to be reduced to its unglycosylated form, concomitant with a considerable loss of its antigenicity. Thus, with respect to its morphological and biochemical characteristics, TCV resembles viruses belonging to the group of mammalian hemagglutinating coronaviruses, but differs in that both types of envelope glycoproteins are N-glycosylated as in case of the avian infectious bronchitis virus.
将火鸡肠道冠状病毒(TCV)的明尼苏达毒株在存在放射性标记氨基酸和葡糖胺的情况下,于人类直肠肿瘤(HRT - 18)细胞系中培养,以分析病毒粒子的结构蛋白。除了52,000的未糖基化核衣壳蛋白外,发现三种主要糖蛋白与病毒包膜相关。一种分子量为22 - 24,000的主要糖蛋白代表跨膜基质蛋白。表观分子量为180 - 200,000(gp 200)、120 - 125,000(gp 120)和95 - 100,000(gp 100)的较大糖蛋白与位于病毒粒子表面的特征性大球状突起(纤突)相关。如用胰蛋白酶和糜蛋白酶的消化研究所示,gp 100和gp 120似乎源自gp 200的蛋白水解切割。还发现一种分子量为140,000的额外大糖蛋白(gp 140),它表现为一个66,000分子的二硫键连接二聚体,与位于大纤突基部附近的颗粒状突起相关。用胰蛋白酶、菠萝蛋白酶和链霉蛋白酶的消化研究表明,gp 140与病毒的血凝活性有关。在用链霉蛋白酶处理后,在病毒粒子内部可观察到一个内膜囊或舌状结构。相反,胰蛋白酶或糜蛋白酶处理导致病毒表面出现外翻(“出芽”)。如电子显微镜和电泳所示,在衣霉素存在下,在TCV感染的细胞培养物中产生的子代病毒粒子缺乏这两种类型的表面突起。基质蛋白似乎也还原为其未糖基化形式,同时其抗原性显著丧失。因此,就其形态和生化特征而言,TCV类似于属于哺乳动物血凝冠状病毒组的病毒,但不同之处在于,两种包膜糖蛋白都像禽传染性支气管炎病毒一样进行N - 糖基化。