Truyen U, Geissler K, Parrish C R, Hermanns W, Siegl G
Institute for Medical Microbiology, Ludwig Maximillians University, Munich, Germany.
J Gen Virol. 1998 May;79 ( Pt 5):1153-8. doi: 10.1099/0022-1317-79-5-1153.
In this study the early evolution and potential origins of canine parvovirus (CPV) were examined. We cloned and sequenced the VP2 capsid protein genes of three German CPV strains isolated in 1979-1980, as well as two feline panleukopenia virus (FPV) vaccine viruses that were previously shown to have some restriction enzyme cleavage sites in common with CPV. Other partial VP2 gene sequences were obtained by amplifying CPV DNA from paraffin-embedded tissues of dogs which were early parvovirus disease cases in Germany in 1978-1979. Sequences were analysed with respect to their evolutionary relationships to other CPV and FPV isolates. Those analyses did not support the hypothesis that CPV emerged as a variant of an FPV vaccine virus. Neither did they reveal ancestral sequences among the very early CPV isolates examined. Other possible sources for the origin of CPV are examined, including the involvement of viruses from wild carnivores.
在本研究中,对犬细小病毒(CPV)的早期进化和潜在起源进行了研究。我们克隆并测序了1979 - 1980年分离的三株德国CPV毒株的VP2衣壳蛋白基因,以及两种先前显示与CPV有一些共同限制性内切酶切割位点的猫泛白细胞减少症病毒(FPV)疫苗病毒。通过从1978 - 1979年德国早期细小病毒病病例犬的石蜡包埋组织中扩增CPV DNA,获得了其他部分VP2基因序列。分析了这些序列与其他CPV和FPV分离株的进化关系。这些分析不支持CPV作为FPV疫苗病毒变体出现的假说。它们也没有在所检测的早期CPV分离株中揭示出祖先序列。还研究了CPV起源的其他可能来源,包括来自野生食肉动物的病毒的参与情况。