Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Suedufer 10, D-17493 Greifswald-Insel Riems, Germany.
Virology Laboratory, Elizabeth Macarthur Agriculture Institute, New South Wales Department of Primary Industries, Narellan, NSW 2567, Australia.
J Gen Virol. 2014 Oct;95(Pt 10):2216-2222. doi: 10.1099/vir.0.065995-0. Epub 2014 Jun 27.
Bungowannah virus is the most divergent pestivirus, and both origin and reservoir host have not been identified so far. We therefore performed in vitro tropism studies, which showed that Bungowannah virus differs remarkably from other pestiviruses. Interestingly, cell lines of vervet monkey, mouse, human and even of bat origin were susceptible. This broad in vitro tropism was not observed for a chimeric bovine viral diarrhoea virus (BVDV) expressing all structural proteins of Bungowannah virus. The viral envelope was not sufficient to completely transfer the cell tropism of Bungowannah virus to another pestivirus, and viral RNA replication was either markedly reduced or not detectable in a number of different cell lines for the tested BVDV strain and the chimera. We therefore suggest that the replication machinery together with the viral envelope is responsible for the unique broad cell tropism of Bungowannah virus.
邦戈万那病毒是最具差异的瘟病毒,其起源和储存宿主至今尚未确定。因此,我们进行了体外嗜性研究,结果表明邦戈万那病毒与其他瘟病毒有显著差异。有趣的是,猴、鼠、人甚至蝙蝠来源的细胞系均易感。而对于表达邦戈万那病毒所有结构蛋白的嵌合牛病毒性腹泻病毒(BVDV),则未观察到这种广泛的体外嗜性。包膜不足以将邦戈万那病毒的细胞嗜性完全转移到另一种瘟病毒,并且在许多不同的细胞系中,对于所测试的 BVDV 株和嵌合体,病毒 RNA 复制要么明显减少,要么无法检测到。因此,我们认为复制机制和包膜共同负责邦戈万那病毒独特的广泛细胞嗜性。