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心肌病毒的多聚胞嘧啶序列与病毒致病机制

Cardioviral poly(C) tracts and viral pathogenesis.

作者信息

Palmenberg A C, Osorio J E

机构信息

Department of Animal Health and Biomedical Sciences, University of Wisconsin Madison.

出版信息

Arch Virol Suppl. 1994;9:67-77. doi: 10.1007/978-3-7091-9326-6_8.

Abstract

Mengovirus is a prototypical member of the cardiovirus genus of the family Picornaviridae. The positive-strand RNA genome is 7761 bases in length and encodes a polyprotein of 2293 amino acids. The 5' non-coding region (758 bases) contains an unusual homopolymeric poly(C) tract, which in the wild-type virus, has a sequence of C50UC10. We have discovered through genetic engineering that truncation or deletion of this poly(C) sequence yields infectious virus isolates that grow well in cell culture, but are 10(6) to 10(9) fold less pathogenic to mice than the wild type strain. Animals receiving sublethal doses of the short poly(C) strains characteristically develop high levels of neutralizing antibodies and acquire lifelong protective immunity against challenge with wild type virus. Effectively, the genetically engineered strains are superb vaccines against cardiovirus disease. Moreover, their potential is not limited to murine hosts. Pigs and sub-human primates have also been protectively vaccinated with short poly(C) tract Mengoviruses. The molecular mechanism of poly(C)-mediated pathogenesis is currently under study. Most hypotheses link the activity to induction of the antiviral cytokine, interferon.

摘要

脑心肌炎病毒是微小核糖核酸病毒科心病毒属的典型成员。正链RNA基因组长度为7761个碱基,编码一个由2293个氨基酸组成的多聚蛋白。5'非编码区(758个碱基)包含一个不寻常的同聚多聚(C)序列,在野生型病毒中,其序列为C50UC10。我们通过基因工程发现,截断或删除这个多聚(C)序列会产生在细胞培养中生长良好的感染性病毒分离株,但对小鼠的致病性比野生型毒株低10^6至10^9倍。接受亚致死剂量短多聚(C)毒株的动物通常会产生高水平的中和抗体,并获得针对野生型病毒攻击的终身保护性免疫。实际上,这些基因工程毒株是对抗心病毒疾病的优质疫苗。此外,它们的潜力不仅限于鼠类宿主。猪和非人灵长类动物也已用短多聚(C)序列的脑心肌炎病毒进行了保护性接种。目前正在研究多聚(C)介导的发病机制的分子机制。大多数假说是将这种活性与抗病毒细胞因子干扰素的诱导联系起来。

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