Zwirglmaier Katrin
British Antarctic Survey, Cambridge, UK.
Methods Mol Biol. 2010;659:349-62. doi: 10.1007/978-1-60761-789-1_27.
Fluorescence in situ hybridization with rRNA targeted oligonucleotide probes is nowadays one of the core techniques in microbial ecology, allowing the identification and quantification of microbial cells in environmental samples in situ. Next to the classic FISH protocol, which uses fluorescently monolabelled probes, the more sensitive CARD-FISH (also known as TSA-FISH), which involves an enzyme catalyzed signal amplification step, is becoming increasingly popular. This chapter describes protocols for both methods. While classic FISH has the advantage of being relatively cheap and easy to do on morphologically diverse samples, CARD-FISH offers a significantly higher sensitivity, allowing the detection of slow growing or metabolically inactive cells, which are below the detection limit of classic FISH. The drawback here is the considerably higher price for the probes and advanced cell fixation and permeabilization requirements that have to be optimized for different target cells.
如今,使用靶向rRNA的寡核苷酸探针进行荧光原位杂交是微生物生态学的核心技术之一,可在原位对环境样品中的微生物细胞进行鉴定和定量。除了使用荧光单标记探针的经典荧光原位杂交(FISH)方案外,涉及酶催化信号放大步骤的更灵敏的催化报告沉积荧光原位杂交(CARD-FISH,也称为TSA-FISH)越来越受欢迎。本章介绍了这两种方法的实验方案。虽然经典FISH的优点是相对便宜,并且易于对形态多样的样品进行操作,但CARD-FISH具有显著更高的灵敏度,能够检测生长缓慢或代谢不活跃的细胞,这些细胞低于经典FISH的检测限。这里的缺点是探针价格要高得多,并且需要针对不同靶细胞优化先进的细胞固定和通透处理要求。