Kelly R K, Loh P C
Proc Soc Exp Biol Med. 1975 Mar;148(3):688-93. doi: 10.3181/00379727-148-38611.
Although IPN virus failed to multiply at 30 degrees, it replicated at 16 degrees and 22 degrees in SWT cells. At 22 degrees the viral eclipse period lasted nearly 6 hr with maximal virion titers attained by 24 hr, whereas replication at 16 degrees was much slower. The replication of the virion was inhibited by 0.05 mug/ml of AD which did not interfere with the production of reovirus. Biochemical studies revealed that cellular DNA synthesis was markedly reduced (greater than 50%) soon after infection whereas total RNA synthesis was enhanced. The period of rapid increase in RNA synthesis paralleled the exponential production of infectious virus. Viral inclusion bodies, revealed by acridine orange-staining of virus-infected cells (SWT and RGG-2) late in the infectious cycle, were found to contain single-stranded RNA on the basis of their staining characteristics and sensitivity to RNase.
尽管IPN病毒在30摄氏度时无法增殖,但它在SWT细胞中于16摄氏度和22摄氏度时能够复制。在22摄氏度时,病毒隐蔽期持续近6小时,24小时达到最大病毒体滴度,而在16摄氏度时复制则慢得多。0.05微克/毫升的AD可抑制病毒体的复制,但不干扰呼肠孤病毒的产生。生化研究表明,感染后不久细胞DNA合成显著减少(超过50%),而总RNA合成增强。RNA合成快速增加的时期与感染性病毒的指数产生平行。在感染周期后期,通过吖啶橙对病毒感染细胞(SWT和RGG-2)进行染色发现的病毒包涵体,根据其染色特性和对核糖核酸酶的敏感性,发现含有单链RNA。