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Pathogenesis of mucosal disease: a cytopathogenic pestivirus generated by an internal deletion.

机译:粘膜疾病的发病机制:由内部缺失产生的细胞致病性瘟病毒。

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摘要

Cytopathogenic bovine viral diarrhea virus (BVDV) arises by RNA recombination in animals persistently infected with noncytopathogenic BVDV. Such animals develop fatal mucosal disease. In this report, the genome of a cytopathogenic BVDV isolate, termed CP9, is characterized. CP9-infected cells contained not only viral genomic RNA of 12.3 kb but also a BVDV-specific RNA of 8 kb. cDNA cloning and sequencing revealed that the 8-kb RNA is a BVDV genome with an internal deletion of 4.3 kb. The 8-kb RNA represents the genome of a typical defective interfering particle (DI), since its replication was strictly dependent on the presence of a helper virus and strongly interfered with the replication of the helper. Cell culture experiments demonstrated that the CP9 virus stock contains two viruses, namely, a helper virus and DI9. While the helper virus alone was noncytopathogenic, the presence of the DI conferred cytopathogenicity. Expression experiments demonstrated that p80, the marker protein of cytopathogenic BVDV, is translated from the defective genome. The occurrence of this cytopathogenic DI is linked to a fatal disease in cattle.
机译:细胞病原性牛病毒性腹泻病毒(BVDV)是由RNA重组在持续感染非细胞病原性BVDV的动物中引起的。这样的动物发展致命的粘膜疾病。在该报告中,对细胞致病性BVDV分离株(称为CP9)的基因组进行了表征。受CP9感染的细胞不仅包含12.3 kb的病毒基因组RNA,而且还包含8 kb的BVDV特异性RNA。 cDNA克隆和测序表明,该8 kb RNA是BVDV基因组,内部缺失4.3 kb。 8-kb RNA代表典型缺陷干扰颗粒(DI)的基因组,因为其复制严格依赖于辅助病毒的存在并强烈干扰了辅助病毒的复制。细胞培养实验表明,CP9病毒原种包含两种病毒,即辅助病毒和DI9。虽然单独的辅助病毒是非致病性的,但是DI的存在赋予了细胞致病性。表达实验表明,p80是细胞致病性BVDV的标志蛋白,是从有缺陷的基因组中翻译得到的。这种细胞致病性DI的发生与牛的致命疾病有关。

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