Behr T, Koob C, Schedl M, Mehlen A, Meier H, Knopp D, Frahm E, Obst U, Schleifer K, Niessner R, Ludwig W
Lehrstuhl für Mikrobiologie, Technische Universität München, Freising, Germany.
Syst Appl Microbiol. 2000 Dec;23(4):563-72. doi: 10.1016/s0723-2020(00)80031-4.
Complete 23S and almost complete 16S rRNA gene sequences were determined for the type strains of the validly described Enterococcus species, Melissococcus pluton and Tetragenococcus halophilus. A comprehensive set of rRNA targeted specific oligonucleotide hybridization probes was designed according to the multiple probe concept. In silico probe design and evaluation was performed using the respective tools of the ARB program package in combination with the ARB databases comprising the currently available 16S as well as 23S rRNA primary structures. The probes were optimized with respect to their application for reverse hybridization in microplate format. The target comprising 16S and 23S rDNA was amplified and labeled by PCR (polymerase chain reaction) using general primers targeting a wide spectrum of bacteria. Alternatively, amplification of two adjacent rDNA fragments of enterococci was performed by using specific primers. In vitro evaluation of the probe set was done including all Enterococcus type strains, and a selection of other representatives of the gram-positive bacteria with a low genomic DNA G+C content. The optimized probe set was used to analyze enriched drinking water samples as well as original samples from waste water treatment plants.
测定了有效描述的肠球菌属、蜂房蜜蜂球菌和嗜盐四联球菌模式菌株的完整23S和几乎完整的16S rRNA基因序列。根据多重探针概念设计了一套全面的rRNA靶向特异性寡核苷酸杂交探针。使用ARB程序包中的相应工具结合包含当前可用的16S以及23S rRNA一级结构的ARB数据库进行了计算机探针设计和评估。针对其在微孔板形式的反向杂交中的应用对探针进行了优化。使用靶向广泛细菌的通用引物通过PCR(聚合酶链反应)扩增并标记包含16S和23S rDNA的靶标。或者,通过使用特异性引物对肠球菌的两个相邻rDNA片段进行扩增。对探针组进行了体外评估,包括所有肠球菌模式菌株以及一些基因组DNA G+C含量低的革兰氏阳性细菌的其他代表菌株。使用优化后的探针组分析了富集的饮用水样品以及来自废水处理厂的原始样品。