Vir分型:a群链球菌的长pcr分型方法。

D Gardiner, J Hartas, B Currie, J D Mathews, D J Kemp, K S Sriprakash
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引用次数: 88

摘要

我们开发了一种新的程序(Vir分型)来分型化脓性链球菌,通过长PCR扩增整个5- 7kb可变Vir调控子。然后用HaeIII切割扩增的DNA,琼脂糖凝胶电泳后用溴化乙啶荧光观察。同时采用一种简单的程序从96个样品中制备足够高质量的DNA。该DNA也被用于开发随机扩增多态性DNA (RAPD)程序。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。这两种方法都具有高度的歧视性,但Vir分型中限制性内切片段的化学计量学产率允许对结果进行明确的解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vir typing: a long-PCR typing method for group A streptococci.

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.

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