首页> 美国卫生研究院文献>Journal of Virology >Point mutations in the S protein connect the sialic acid binding activity with the enteropathogenicity of transmissible gastroenteritis coronavirus.
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Point mutations in the S protein connect the sialic acid binding activity with the enteropathogenicity of transmissible gastroenteritis coronavirus.

机译:S蛋白中的点突变将唾液酸结合活性与可传播的胃肠炎冠状病毒的肠致病性联系起来。

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摘要

Enteropathogenic transmissible gastroenteritis virus (TGEV), a porcine coronavirus, is able to agglutinate erythrocytes because of sialic acid binding activity. Competitive inhibitors that may mask the sialic acid binding activity can be inactivated by sialidase treatment of virions. Here, we show that TGEV virions with efficient hemagglutinating activity were also obtained when cells were treated with sialidase prior to infection. This method was used to analyze TGEV mutants for hemagglutinating activity. Recently, mutants with strongly reduced enteropathogenicity that have point mutations or a deletion of four amino acids within residues 145 to 155 of the S protein have been described. Here, we show that in addition to their reduced pathogenicity, these mutants also have lost hemagglutinating activity. These results connect sialic acid binding activity with the enteropathogenicity of TGEV.
机译:由于唾液酸的结合活性,肠致病性传染性胃肠炎病毒(TGEV)是一种猪冠状病毒,能够凝集红细胞。可以掩盖唾液酸结合活性的竞争性抑制剂可以通过病毒体的唾液酸酶处理而失活。在这里,我们显示了在感染前用唾液酸酶处理细胞时也获得了具有有效血凝活性的TGEV病毒体。该方法用于分析TGEV突变体的血凝活性。近来,已经描述了具有大大降低的肠致病性的突变体,其在S蛋白的残基145至155内具有点突变或四个氨基酸的缺失。在这里,我们表明,除了其降低的致病性外,这些突变体还失去了血凝活性。这些结果将唾液酸结合活性与TGEV的肠致病性联系起来。

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