Hejazi A, Keane C T, Falkiner F R
Department of Clinical Microbiology, Trinity College, Dublin, Ireland.
J Med Microbiol. 1997 Nov;46(11):913-9. doi: 10.1099/00222615-46-11-913.
Serratia marcescens has emerged in the last few years as an important nosocomial pathogen. Many methods for typing this organism have been described. In this study the random amplified polymorphic DNA-polymerase chain reaction (RAPD-PCR) was shown to be a convenient typing method for S. marcescens. Different combinations of primers previously used for typing other gram-negative bacilli were assessed. The combination of primer HLWL-74 and 1254 gave distinguishable patterns for different serotypes and proved to be the most satisfactory. By applying this combination to 175 isolates of S. marcescens, which could be classified into 38 groups on the basis of serotyping and phage typing, 73 different RAPD patterns with good reproducibility were obtained. This is, to our knowledge, the first application of the method to a large collection of S. marcescens representing a wide range of serotypes.
粘质沙雷氏菌在过去几年中已成为一种重要的医院病原体。已经描述了许多对这种微生物进行分型的方法。在本研究中,随机扩增多态性DNA - 聚合酶链反应(RAPD - PCR)被证明是一种用于粘质沙雷氏菌的便捷分型方法。评估了先前用于对其他革兰氏阴性杆菌进行分型的引物的不同组合。引物HLWL - 74和1254的组合对不同血清型产生了可区分的图谱,并被证明是最令人满意的。通过将这种组合应用于175株粘质沙雷氏菌分离株(这些分离株基于血清分型和噬菌体分型可分为38组),获得了73种具有良好重复性的不同RAPD图谱。据我们所知,这是该方法首次应用于大量代表广泛血清型的粘质沙雷氏菌。