Ramage G, Patrick S, Houston S
Department of Microbiology and Immunobiology, School of Clinical Medicine, The Queen's University of Belfast, Northern Ireland, UK.
J Immunol Methods. 1998 Mar 15;212(2):139-47. doi: 10.1016/s0022-1759(98)00005-2.
We have demonstrated that pure cultures of Bacteroides fragilis can be riboprobed with the oligoprobes BAC303 and EUB338, whilst simultaneously immunolabelled with either the mAb QUBF7, or polyclonal antiserum specific for a common antigen of B. fragilis. We were also able to distinguish between pure cultures of B. fragilis and Escherichia coli, by means of combined immunolabelling and riboprobing. The success of the combined technique is critically dependent on the size of the bacterial capsules, bacterial growth phase, antibody diluent and the length of the washing steps. The combined FISH and immunolabelling of bacteria has potential applications in studies of bacteria of medical and veterinary importance, as well as bacteria from other environments, as it yields information about both the identity and antigen expression of individual bacterial cells.
我们已经证明,脆弱拟杆菌的纯培养物可用寡核苷酸探针BAC303和EUB338进行核糖核酸探针检测,同时用单克隆抗体QUBF7或针对脆弱拟杆菌共同抗原的多克隆抗血清进行免疫标记。我们还能够通过联合免疫标记和核糖核酸探针检测来区分脆弱拟杆菌和大肠杆菌的纯培养物。联合技术的成功关键取决于细菌荚膜的大小、细菌生长阶段、抗体稀释剂和洗涤步骤的时长。细菌的荧光原位杂交(FISH)与免疫标记相结合在医学和兽医领域重要细菌以及其他环境细菌的研究中具有潜在应用,因为它能提供有关单个细菌细胞的身份和抗原表达的信息。