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The avian retrovirus env gene family: molecular analysis of host range and antigenic variants.

机译:禽逆转录病毒env基因家族:宿主范围和抗原变异的分子分析。

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摘要

The nucleotide sequence of the env gp85-coding domain from two avian sarcoma and leukosis retrovirus isolates was determined to identify host range and antigenic determinants. The predicted amino acid sequence of gp85 from a subgroup D virus isolate of the Schmidt-Ruppin strain of Rous sarcoma virus was compared with the previously reported sequences of subgroup A, B, C, and E avian sarcoma and leukosis retroviruses. Subgroup D viruses are closely related to the subgroup B viruses but have an extended host range that includes the ability to penetrate certain mammalian cells. There are 27 amino acid differences shared between the subgroup D sequence and three subgroup B sequences. At 16 of these sites, the subgroup D sequence is identical to the sequence of one or more of the other subgroup viruses (A, C, and E). The remaining 11 sites are specific to subgroup D and show some clustering in the two large variable regions that are thought to be major determinants of host range. Biological analysis of recombinant viruses containing a dominant selectable marker confirmed the role of the gp85-coding domain in determining the host range of the subgroup D virus in the infection of mammalian cells. We also compared the sequence of the gp85-coding domain from two subgroup A viruses, Rous-associated virus type 1 and a subgroup A virus of the Schmidt-Ruppin strain of Rous sarcoma virus. The comparison revealed 24 nonconservative amino acid changes, of which 6 result in changes in potential glycosylation sites. The positions of 10 amino acid differences are coincident with the positions of 10 differences found between two subgroup B virus env gene sequences. These 10 sites identify seven domains in the sequence which may constitute determinants of type-specific antigenicity. Using a molecular recombinant, we demonstrated that type-specific neutralization of two subgroup A viruses was associated with the gp85-coding domain of the virus.
机译:确定了来自两个禽肉瘤和白血病逆转录病毒分离株的env gp85编码域的核苷酸序列,以鉴定宿主范围和抗原决定簇。将Rous肉瘤病毒Schmidt-Ruppin株D亚型病毒分离株的gp85预测氨基酸序列与先前报道的A,B,C和E禽肉瘤亚组和白血病逆转录病毒序列进行了比较。 D亚组病毒与B亚组病毒密切相关,但宿主范围扩大,包括能够穿透某些哺乳动物细胞的能力。 D亚组序列和三个B亚序列共有27个氨基酸差异。在这些位点的16个处,D亚组序列与一种或多种其他亚组病毒(A,C和E)的序列相同。其余的11个位点是D组特有的,并且在两个较大的可变区中显示出一些聚类,这两个较大的可变区被认为是宿主范围的主要决定因素。含有显性选择标记的重组病毒的生物学分析证实了gp85编码域在确定D亚型病毒在哺乳动物细胞感染中的宿主范围中的作用。我们还比较了来自两个亚组A病毒,劳斯相关病毒1型和劳斯肉瘤病毒Schmidt-Ruppin株的亚组A病毒的gp85编码域的序列。比较结果显示24个非保守氨基酸变化,其中6个导致潜在的糖基化位点变化。 10个氨基酸差异的位置与在两个B亚组病毒env基因序列之间发现的10个差异的位置一致。这10个位点在序列中鉴定出七个结构域,它们可以构成类型特异性抗原性的决定簇。使用分子重组,我们证明了两种亚组A病毒的类型特异性中和与该病毒的gp85编码域相关。

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