Glover D J, Harris W J
National Collections of Industrial and Marine Bacteria Ltd, Aberdeen, UK.
Lett Appl Microbiol. 1998 Aug;27(2):116-20. doi: 10.1046/j.1472-765x.1998.00409.x.
A range of rRNA-targeted alkaline phosphatase labelled oligonucleotide probes was tested for use as culture confirmation reagents for the rapid identification of micro-organisms. The probes were specific to clinically important bacteria (Helicobacter pylori and Mycobacterium tuberculosis), fish and shellfish pathogens (Renibacterium salmoninarum and Vibrio vulnificus), food spoilage bacteria (Listeria spp. and L. monocytogenes), for bacteria of biotechnological importance (Streptomyces spp.) and for bacteria associated with the oil industry (Sulphate-reducing bacteria, SRB). A universal bacterial probe and a eukaryotic probe were included in the study as positive and negative controls, respectively. A total of 93 bacterial strains was screened. With the exception of a large number of cross-reactions of the SRB probe (specificity value of 29.4%) and a single cross-reaction of the R. salmoninarum probe (specificity value of 97.7%), dot blot analysis indicated that each probe hybridized 100% specifically to the organisms tested. A simple culture confirmation method was then developed using these probes to enable the identification of bacterial colonies using a simple hybridization procedure.
测试了一系列靶向rRNA的碱性磷酸酶标记寡核苷酸探针,用作快速鉴定微生物的培养确认试剂。这些探针分别针对临床上重要的细菌(幽门螺杆菌和结核分枝杆菌)、鱼类和贝类病原体(鲑鱼肾杆菌和创伤弧菌)、食品腐败细菌(李斯特菌属和单核细胞增生李斯特菌)、具有生物技术重要性的细菌(链霉菌属)以及与石油工业相关的细菌(硫酸盐还原菌,SRB)。研究中分别纳入了通用细菌探针和真核探针作为阳性和阴性对照。共筛选了93株细菌菌株。除了SRB探针出现大量交叉反应(特异性值为29.4%)和鲑鱼肾杆菌探针出现一次交叉反应(特异性值为97.7%)外,斑点印迹分析表明每个探针与所测试的生物体100%特异性杂交。然后利用这些探针开发了一种简单的培养确认方法,通过简单的杂交程序来鉴定细菌菌落。