Nishio M, Tsurudome M, Bando H, Komada H, Ito Y
Department of Microbiology, Mie University School of Medicine, Mie-Prefecture, Japan.
J Gen Virol. 1990 Jan;71 ( Pt 1):61-7. doi: 10.1099/0022-1317-71-1-61.
The antiviral effects of 6-diazo-5-oxo-L-norleucine (L-DON) on the replication of human parainfluenza virus type 2 (HPIV-2), mumps and vesicular stomatitis viruses were studied. L-DON suppressed growth of these viruses and, in particular, HPIV-2 in four cell types. L-DON was not toxic to the cells at the active dose and did not significantly inhibit cellular macromolecular synthesis. The L-DON-sensitive step of HPIV-2 replication was considered to be relatively early. The NP, P and M proteins were, although at a low level, clearly detectable in HPIV-2-infected Vero cells treated with L-DON, whereas the HN and F proteins were scarcely detected by either immunostaining or immunoprecipitation, indicating that L-DON mainly decreased the amounts of viral glycoproteins. Furthermore, Northern blot hybridization showed that secondary transcription of virus RNA was also inhibited.
研究了6-重氮-5-氧代-L-正亮氨酸(L-DON)对人副流感病毒2型(HPIV-2)、腮腺炎病毒和水疱性口炎病毒复制的抗病毒作用。L-DON抑制了这些病毒的生长,尤其是在四种细胞类型中对HPIV-2的抑制作用。L-DON在有效剂量下对细胞无毒,且未显著抑制细胞大分子合成。HPIV-2复制中对L-DON敏感的步骤被认为相对较早。在用L-DON处理的HPIV-2感染的Vero细胞中,虽然NP、P和M蛋白水平较低,但仍可清晰检测到,而通过免疫染色或免疫沉淀几乎检测不到HN和F蛋白,这表明L-DON主要降低了病毒糖蛋白的含量。此外,Northern印迹杂交显示病毒RNA的二级转录也受到抑制。