首页> 美国卫生研究院文献>Canadian Journal of Comparative Medicine >Comparisons of the F and HN gene sequences of different strains of bovine parainfluenza virus type 3: relationship to phenotype and pathogenicity.
【2h】

Comparisons of the F and HN gene sequences of different strains of bovine parainfluenza virus type 3: relationship to phenotype and pathogenicity.

机译:牛副流感病毒3型不同株F和HN基因序列的比较:与表型和致病性的关系。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The genes for the F and HN glycoprotein of a pathogenic field isolate of bovine parainfluenza virus type 3 (BPIV3) were isolated, converted to cDNA, and sequenced using dideoxynucleotides. The resulting nucleotide sequences were converted to protein sequence and were compared to previously sequenced glycoprotein genes with amino acid differences in the glycoproteins of isolates expressing different phenotypes. The HN glycoprotein, involved in the attachment and release of the virus, and the F glycoprotein, involved in penetration and spread of the virus, have been shown to affect pathogenicity of the virus and are the immunodominant proteins of the virus. Both the F and HN proteins have been shown to be required for syncytium formation. Our results suggest that BPIV3 viruses that exhibit greater syncytium-inducing activity in vitro have greater pathogenicity in vivo. By determining which epitopes are involved in syncytium formation and comparing the sequences and enzymatic activities of different strains of virus, it may be possible to design subunit vaccines that protect against disease.
机译:分离了牛副流感病毒3型(BPIV3)病原体分离株的F和HN糖蛋白基因,将其转化为cDNA,并使用双脱氧核苷酸测序。将得到的核苷酸序列转换为蛋白质序列,并与先前测序的糖蛋白基因进行比较,在表达不同表型的分离物的糖蛋白中具有氨基酸差异。已显示参与病毒附着和释放的HN糖蛋白和参与病毒渗透和传播的F糖蛋白会影响病毒的致病性,并且是病毒的免疫主要蛋白。已显示F和HN蛋白都是合胞体形成所必需的。我们的结果表明,在体外表现出更大合胞体诱导活性的BPIV3病毒在体内具有更大的致病性。通过确定哪些表位参与合胞体的形成并比较不同病毒株的序列和酶活性,可能有可能设计出预防疾病的亚单位疫苗。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号