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减毒狂犬病病毒SAD B19的分子克隆及全核苷酸序列

Molecular cloning and complete nucleotide sequence of the attenuated rabies virus SAD B19.

作者信息

Conzelmann K K, Cox J H, Schneider L G, Thiel H J

机构信息

Federal Research Centre for Virus Diseases of Animals, Tübingen, Federal Republic of Germany.

出版信息

Virology. 1990 Apr;175(2):485-99. doi: 10.1016/0042-6822(90)90433-r.

Abstract

Complementary DNA spanning the entire genome of the attenuated rabies virus strain SAD B19 which is used for oral immunization of foxes in Europe was cloned and sequenced. The viral genome comprises 11,928 nucleotides and encodes the five viral proteins N, NS, M, G, and L. Deduced protein sequences are highly similar to those of the pathogenic PV strain, homologies ranging from 90.6% for the M to 98.6% for the L protein. The five cistrons are separated by intergenic regions of 2, 5, 5, and 24 nucleotides, respectively. The G transcription stop/polyadenylation consensus signal in SAD B19 is destroyed by a deletion of three A residues. The strong conservation of both noncoding and coding nucleotide sequences indicates a high selective pressure on the primary structure of rabies virus genomic RNA.

摘要

用于欧洲狐狸口服免疫的减毒狂犬病病毒株SAD B19的全基因组互补DNA被克隆并测序。病毒基因组由11928个核苷酸组成,编码五种病毒蛋白N、NS、M、G和L。推导的蛋白质序列与致病性PV株的序列高度相似,同源性从M蛋白的90.6%到L蛋白的98.6%不等。五个顺反子分别被2、5、5和24个核苷酸的基因间隔区隔开。SAD B19中的G转录终止/多聚腺苷酸化共有信号因三个A残基的缺失而被破坏。非编码和编码核苷酸序列的高度保守表明狂犬病病毒基因组RNA一级结构上存在高度选择压力。

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