Gardiner D, Hartas J, Currie B, Mathews J D, Kemp D J, Sriprakash K S
Menzies School of Health Research, Darwin, NT, Australia.
PCR Methods Appl. 1995 Apr;4(5):288-93. doi: 10.1101/gr.4.5.288.
We have developed a new procedure (Vir typing) for typing Streptococcus pyogenes, by amplifying the entire 5- to 7-kb variable vir regulon by long PCR. The amplified DNA is then cleaved with HaeIII and visualized by ethidium bromide fluorescence after agarose gel electrophoresis. A simple procedure for preparing DNA of sufficiently high quality from 96 samples was employed simultaneously. This DNA was also used to develop a random amplified polymorphic DNA (RAPD) procedure. The discriminatory power of the two DNA-based procedures was compared with previous methods, M typing, and multilocus enzyme electrophoresis. Both procedures were highly discriminatory, but the stoichiometric yield of restriction fragments in Vir typing allows unambiguous interpretation of results.
我们开发了一种用于化脓性链球菌分型的新方法(Vir分型),通过长PCR扩增整个5至7 kb的可变毒力调节子。然后用HaeIII切割扩增的DNA,并在琼脂糖凝胶电泳后通过溴化乙锭荧光进行可视化。同时采用了一种从96个样本中制备足够高质量DNA的简单方法。该DNA还用于开发随机扩增多态性DNA(RAPD)方法。将这两种基于DNA的方法的鉴别能力与先前的方法、M分型和多位点酶电泳进行了比较。两种方法都具有高度的鉴别力,但Vir分型中限制性片段的化学计量产量允许对结果进行明确的解释。