Hamada C, Sato N L, Niimura S, Kato A, Fujisawa N, Maeda Y, Kumanishi T, Lee H W
Jikken Dobutsu. 1986 Jan;35(1):1-9. doi: 10.1538/expanim1978.35.1_1.
An assay method for the infectivity of Hantaan virus, a causative agent of HFRS (hemorrhagic fever with renal syndrome), was developed by the use of IFA (immunofluorescent antibody technique). With the aid of this method, the growth characteristics of Hantaan virus, 76-118 strain, were followed in A549 cells. At a maximal MOI (multiplicity of infection) of 1.6 VAIU (viral antigen-inducing units) per cell, the conventionally available value, plateau level potencies of the viral antigen and virus infectivity were attained at eight and ten days postinfection, respectively, and most of the infective virus produced accumulated in the culture fluids of infected cells. When infections were defined with MOI values in terms of VAIU per cell, development of the viral antigen was highly consistent and followed a given pattern of kinetics. Based on these findings, a protocol for preparation of the viral antigen in IFA was presented, wherein spot culture and FBS treatment were emphasized as effective procedures to minimize non-specific staining.
利用免疫荧光抗体技术(IFA)开发了一种检测肾综合征出血热(HFRS)病原体汉坦病毒感染性的检测方法。借助该方法,在A549细胞中追踪了汉坦病毒76-118株的生长特性。在每个细胞最大感染复数(MOI)为1.6个病毒抗原诱导单位(VAIU)(传统可用值)时,病毒抗原的平台期效价和病毒感染性分别在感染后第8天和第10天达到,并且产生的大多数感染性病毒积聚在受感染细胞的培养液中。当根据每个细胞的VAIU值用MOI值定义感染时,病毒抗原的发育高度一致,并遵循给定的动力学模式。基于这些发现,提出了一种在IFA中制备病毒抗原的方案,其中强调斑点培养和胎牛血清(FBS)处理是将非特异性染色降至最低的有效程序。