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禽逆转录病毒env基因家族:宿主范围和抗原变异体的分子分析

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

作者信息

Bova C A, Olsen J C, Swanstrom R

机构信息

Department of Biochemistry, University of North Carolina, Chapel Hill 27599.

出版信息

J Virol. 1988 Jan;62(1):75-83. doi: 10.1128/JVI.62.1.75-83.1988.

Abstract

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.

摘要

测定了两种禽肉瘤和白血病逆转录病毒分离株的env gp85编码区的核苷酸序列,以确定宿主范围和抗原决定簇。将Rous肉瘤病毒Schmidt-Ruppin株D亚群病毒分离株的gp85预测氨基酸序列与先前报道的A、B、C和E亚群禽肉瘤和白血病逆转录病毒序列进行了比较。D亚群病毒与B亚群病毒密切相关,但具有扩展的宿主范围,包括穿透某些哺乳动物细胞的能力。D亚群序列与三个B亚群序列共有27个氨基酸差异。在其中16个位点,D亚群序列与一种或多种其他亚群病毒(A、C和E)的序列相同。其余11个位点是D亚群特有的,并且在两个大的可变区域中表现出一些聚集,这两个区域被认为是宿主范围的主要决定因素。对含有显性选择标记的重组病毒的生物学分析证实了gp85编码区在确定D亚群病毒感染哺乳动物细胞时的宿主范围中的作用。我们还比较了两种A亚群病毒Rous相关病毒1型和Rous肉瘤病毒Schmidt-Ruppin株的A亚群病毒的gp85编码区序列。比较揭示了24个非保守氨基酸变化,其中6个导致潜在糖基化位点的变化。10个氨基酸差异的位置与两个B亚群病毒env基因序列之间发现的10个差异的位置一致。这10个位点在序列中确定了七个结构域,可能构成型特异性抗原性的决定因素。使用分子重组体,我们证明了两种A亚群病毒的型特异性中和与病毒的gp85编码区有关。

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