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牛腺病毒2型的亚型在E3区域表现出主要差异。

Subtypes of bovine adenovirus type 2 exhibit major differences in region E3.

作者信息

Belák S, Virtanen A, Zabielski J, Rusvai M, Berencsi G, Pettersson U

出版信息

Virology. 1986 Sep;153(2):262-71. doi: 10.1016/0042-6822(86)90029-2.

Abstract

The genomes of two adenovirus type 2 strains which were isolated from different hosts have been investigated. One of these strains designated ORT-111 was originally isolated from a lamb in Hungary during an outbreak of pneumoenteritis. This isolate was typed as bovine adenovirus type 2 (Ad bos 2) in a neutralization assay. The genome of ORT-111 was compared to that of the prototype strain of Ad bos 2, a virus which exclusively has been isolated from cattle. Electron microscopic heteroduplex analysis showed that 95% of the genomes were well matched, forming stable duplexes at Tm -6 degrees. Two distinct substitution loops were, however, seen which were approximately 0.5 and 1.0 kbp long. The centers of the two loops were located 5.3 and 7.7 kbp from one end of the Ad bos 2 genome. In order to map these regions relative to the gene map of human adenovirus type 2 (Ad2), restriction enzyme cleavage fragments of the two bovine viruses were cloned and hybridized to different sets of restriction fragments of human Ad2. From these results it was apparent that the centers of the two substitution loops were located at coordinates 76 and 83, respectively; thus at positions which fall within region E3 and the adjacent gene for polypeptide VIII of human Ad2. The observed differences between the genomes of the two Ad bos 2 strains are in sharp contrast to those previously observed when the genomes of different human adenovirus serotypes were compared. In the latter case the hexon and the fiber genes showed the most pronounced variation.

摘要

对从不同宿主分离出的两株2型腺病毒的基因组进行了研究。其中一株命名为ORT - 111的菌株最初是在匈牙利一次肺炎肠炎疫情期间从一只羔羊身上分离出来的。在中和试验中,该分离株被鉴定为牛2型腺病毒(Ad bos 2)。将ORT - 111的基因组与Ad bos 2的原型菌株的基因组进行了比较,Ad bos 2原型菌株是一种仅从牛身上分离出的病毒。电子显微镜异源双链分析表明,95%的基因组匹配良好,在比熔解温度(Tm)低6摄氏度时形成稳定的双链。然而,观察到两个明显的替代环,长度约为0.5和1.0千碱基对。这两个环的中心距离Ad bos 2基因组一端5.3和7.7千碱基对。为了将这些区域相对于人2型腺病毒(Ad2)的基因图谱进行定位,克隆了两种牛病毒的限制性内切酶切割片段,并与不同组的人Ad2限制性片段进行杂交。从这些结果可以明显看出,两个替代环的中心分别位于坐标76和83处;因此位于人Ad2的E3区域和相邻的多肽VIII基因内的位置。观察到的两种Ad bos 2菌株基因组之间的差异与先前比较不同人腺病毒血清型基因组时观察到的差异形成鲜明对比。在后一种情况下,六邻体和纤维基因显示出最明显的变异。

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