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蓝舌病及密切相关血清群中多种病毒的个别同源基因的遗传相关性。

The genetic relatedness of a number of individual cognate genes of viruses in the bluetongue and closely related serogroups.

作者信息

Huismans H, Cloete M, le Roux A

机构信息

Biochemistry Section, Veterinary Research Institute, Onderstepoort, South Africa.

出版信息

Virology. 1987 Dec;161(2):421-8. doi: 10.1016/0042-6822(87)90135-8.

Abstract

Genome segments 2, 4, 6, 7, 8, 9, and 10 of bluetongue virus (BTV) serotype 10 were cloned in pBR322. The 2926-bp S2 gene, which codes for the serotype-specific antigen, was cloned as two overlapping 2.4-kb inserts. The relatedness of cognate S2 genes among different isolates of BTV10 was investigated by hybridization, restriction enzyme mapping, and sequencing of the terminal ends. Hybridization under high stringency conditions indicated a genetic diversity between isolates of BTV10 from South Africa and the United States. This was confirmed by a comparison of the restriction map of the cloned S2 gene of a BTV10 isolate from South Africa to that of the S2 gene of the BTV10 strain of the United States which has been cloned and sequenced by Purdy et al. (1985). The part of the genome that was sequenced indicated, however, that this variation was confined to an approximately 10% sequence divergence in the coding region. Very few of the nucleotide substitutions resulted in an amino acid change. The genetic variation of cognate BTV genes within the BTV serogroup as well as among different members of closely related serogroups was also investigated. DNA probes from cloned BTV10 segments were hybridized to dsRNA from 24 different BTV serotypes. Genome segments S2 and S6 were found to be almost equally serotype specific. The stringency of the wash solutions after hybridization can be manipulated to determine an order of relatedness of different cognate genes. This was illustrated by the hybridization of a sensitive RNA probe of S7 to different BTV serotypes as well as to dsRNA from closely related orbiviruses. The results confirmed a relatedness between BTV and members of the epizootic hemorrhagic disease virus (EHDV) serogroups.

摘要

蓝舌病病毒10型(BTV-10)的基因组片段2、4、6、7、8、9和10被克隆到pBR322中。编码血清型特异性抗原的2926bp S2基因被克隆为两个重叠的2.4kb插入片段。通过杂交、限制性酶切图谱分析和末端测序,研究了不同BTV-10分离株中同源S2基因的相关性。高严格条件下的杂交表明,来自南非和美国的BTV-10分离株之间存在遗传多样性。将一株来自南非的BTV-10分离株的克隆S2基因的限制性图谱与Purdy等人(1985年)克隆并测序的美国BTV-10毒株的S2基因的限制性图谱进行比较,证实了这一点。然而,测序的基因组部分表明,这种变异仅限于编码区约10%的序列差异。很少有核苷酸替换导致氨基酸变化。还研究了BTV血清群内以及密切相关血清群不同成员之间同源BTV基因的遗传变异。来自克隆的BTV-10片段的DNA探针与24种不同BTV血清型的双链RNA杂交。发现基因组片段S2和S6几乎同样具有血清型特异性。杂交后洗涤液的严格度可以进行调整,以确定不同同源基因的相关性顺序。这通过S7敏感RNA探针与不同BTV血清型以及密切相关环状病毒的双链RNA杂交得到了说明。结果证实了BTV与流行性出血病病毒(EHDV)血清群成员之间的相关性。

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