El-Hajj Hiyam H, Marras Salvatore A E, Tyagi Sanjay, Shashkina Elena, Kamboj Mini, Kiehn Timothy E, Glickman Michael S, Kramer Fred Russell, Alland David
Public Health Research Institute, New Jersey Medical School, University of Medicine and Dentistry of New Jersey, Newark, New Jersey 07103, USA.
J Clin Microbiol. 2009 Apr;47(4):1190-8. doi: 10.1128/JCM.02043-08. Epub 2009 Jan 26.
We report here the use of novel "sloppy" molecular beacon probes in homogeneous PCR screening assays in which thermal denaturation of the resulting probe-amplicon hybrids provides a characteristic set of amplicon melting temperature (T(m)) values that identify which species is present in a sample. Sloppy molecular beacons possess relatively long probe sequences, enabling them to form hybrids with amplicons from many different species despite the presence of mismatched base pairs. By using four sloppy molecular beacons, each possessing a different probe sequence and each labeled with a differently colored fluorophore, four different T(m) values can be determined simultaneously. We tested this technique with 27 different species of mycobacteria and found that each species generates a unique, highly reproducible signature that is unaffected by the initial bacterial DNA concentration. Utilizing this general paradigm, screening assays can be designed for the identification of a wide range of species.
我们在此报告新型“宽松”分子信标探针在均相PCR筛选分析中的应用。在该分析中,所得探针 - 扩增子杂交体的热变性提供了一组特征性的扩增子解链温度(T(m))值,可用于识别样品中存在的物种。宽松分子信标具有相对较长的探针序列,这使得它们能够与来自许多不同物种的扩增子形成杂交体,尽管存在错配碱基对。通过使用四个宽松分子信标,每个信标具有不同的探针序列并标记有不同颜色的荧光团,可以同时确定四个不同的T(m)值。我们用27种不同的分枝杆菌对该技术进行了测试,发现每个物种都产生独特的、高度可重复的特征,且不受初始细菌DNA浓度的影响。利用这一通用模式,可以设计筛选分析来鉴定广泛的物种。