Summers M D, Volkman L E, Hsieh C
J Gen Virol. 1978 Sep;40(3):545-57. doi: 10.1099/0022-1317-40-3-545.
The sequence of events in the infection of TN-368-10 and TN-368-13 cells by Autographa californica nuclear polyhedrosis virus (AcMNPV) was investigated by using the indirect immunoperoxidase technique. Antisera raised against enveloped nucleocapsids detected homologous antigens at 6 to 8 h post infection which was about 2 h before the appearance of both intracellular and extracellular infectious virus. Similar tests using polyhedrin antiserum showed that polyhedrin is first synthesized at 12 h post infection, 2 to 4 h after the appearance of infectious nonoccluded virus. The immunoperoxidase technique was also applied to four other invertebrate cell lines after inoculation with AcMNPV. The most significant result was that 90% of AcMNPV-inoculated Bombyx mori 5 cells produced enveloped nucleocapsid antigens and infectious virus but only 1% or less of the cells produced polyhedrin. This disparity emphasizes the need for assays for NPV infection that are independent of polyhedron production.
采用间接免疫过氧化物酶技术研究了苜蓿银纹夜蛾核型多角体病毒(AcMNPV)感染TN - 368 - 10和TN - 368 - 13细胞的事件顺序。针对包膜核衣壳产生的抗血清在感染后6至8小时检测到同源抗原,这比细胞内和细胞外感染性病毒出现的时间早约2小时。使用多角体蛋白抗血清进行的类似试验表明,多角体蛋白在感染后12小时首次合成,在感染性非包涵体病毒出现后2至4小时。在用AcMNPV接种后,免疫过氧化物酶技术也应用于其他四种无脊椎动物细胞系。最显著的结果是,90%接种AcMNPV的家蚕5细胞产生包膜核衣壳抗原和感染性病毒,但只有1%或更少的细胞产生多角体蛋白。这种差异强调了需要独立于多角体产生的NPV感染检测方法。