La Torre J L, Underwood B O, Lebendiker M, Gorman B M, Brown F
Infect Immun. 1982 Apr;36(1):142-7. doi: 10.1128/iai.36.1.142-147.1982.
The analysis of several isolates of foot-and-mouth disease virus by RNase T1 fingerprinting of the 32P-labeled RNA is described. It has been shown that use of the 35S induced RNA instead of the virus particle RNA has two advantages. (i) About 40 times more radioactivity is incorporated into the induced RNA. (ii) The RNA can be prepared much more rapidly, thus increasing the value of the technique in rapid diagnosis. One-dimensional maps, in which the RNase T1 oligonucleotides are separated according to size, have been shown to provide a valuable screening method for distinguishing between viruses. Those viruses giving similar one-dimensional maps also gave similar two-dimensional maps. The value of using the length of the polycytidylic acid tract of foot-and-mouth disease virus as a diagnostic tool is also discussed.
本文描述了通过对32P标记的RNA进行RNase T1指纹图谱分析来研究口蹄疫病毒的几种分离株。结果表明,使用35S诱导的RNA而非病毒颗粒RNA有两个优点。(i)诱导的RNA中掺入的放射性比病毒颗粒RNA多约40倍。(ii)RNA的制备速度要快得多,从而提高了该技术在快速诊断中的价值。一维图谱可根据大小分离RNase T1寡核苷酸,已被证明是区分病毒的一种有价值的筛选方法。那些给出相似一维图谱的病毒也给出相似的二维图谱。还讨论了将口蹄疫病毒多聚胞苷酸序列的长度用作诊断工具的价值。