Allen P T, Giron D J
Appl Microbiol. 1970 Sep;20(3):317-22. doi: 10.1128/am.20.3.317-322.1970.
A method for assaying mouse interferon based on the inhibition of viral ribonucleic acid (RNA) synthesis was devised. The amount of MM virus and RNA synthesized in interferon-treated L-cell cultures was determined by measuring the amount of (3)H-uridine converted into a trichloroacetic acid-insoluble form after treatment of the infected cultures with 2.5 mug of actinomycin D per ml. The amount of RNA synthesized was inversely related to the concentration of interferon used for treatment. A linear dose-response regression curve was obtained by plotting the log of the amount of RNA made, expressed as a percentage of the control, versus the log of the reciprocal of the interferon dilution. A unit of interferon was defined as that concentration which inhibited nucleic acid synthesis by 50% (INAS(50)). The concentration of mouse interferon could be determined within 24 hr. This assay method, on the average, was approximately half as sensitive as the method which measured the 50% reduction of MM virus plaque number (PDD(50)-MM method), but was, on the average, almost 1.7 times as sensitive as the PDD(50)-VSV method. It averaged approximately 20 times the sensitivity of the methods which used as end points the 70% reduction in yield of MM virus or the complete inhibition of cytopathic effect by MM virus. The reproducibility of the INAS(50) technique was tested in two ways. (i) Four independent assays of an interferon specimen were performed with replicate cultures. The standard deviation was 11.2% of the mean titer. (ii) On different dates, one interferon specimen was assayed seven times and another was assayed four times. The standard deviations were 21.5 and 26.6% of the respective mean titers.
设计了一种基于抑制病毒核糖核酸(RNA)合成来检测小鼠干扰素的方法。通过测量每毫升感染培养物用2.5微克放线菌素D处理后转化为三氯乙酸不溶性形式的(3)H-尿苷的量,来确定在干扰素处理的L细胞培养物中合成的MM病毒和RNA的量。合成的RNA量与用于处理的干扰素浓度呈负相关。通过绘制以对照的百分比表示的RNA合成量的对数与干扰素稀释倍数倒数的对数的关系图,获得了线性剂量反应回归曲线。一个干扰素单位定义为抑制核酸合成50%的浓度(INAS(50))。小鼠干扰素的浓度可在24小时内测定。该检测方法平均灵敏度约为测量MM病毒空斑数减少50%的方法(PDD(50)-MM方法)的一半,但平均灵敏度几乎是PDD(50)-VSV方法的1.7倍。它的平均灵敏度约为以MM病毒产量降低70%或MM病毒完全抑制细胞病变效应为终点的方法的20倍。通过两种方式测试了INAS(50)技术的重现性。(i)对一个干扰素标本进行了四次独立检测,使用重复培养物。标准偏差为平均滴度的11.2%。(ii)在不同日期,对一个干扰素标本进行了七次检测,对另一个进行了四次检测。标准偏差分别为各自平均滴度的21.5%和26.6%。