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Detection of Prokaryotic Cells with Fluorescence In Situ Hybridization

  • Katrin ZwirglmaierEmail author
Protocol
Part of the Methods in Molecular Biology book series (MIMB, volume 659)

Abstract

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.

Key words

Fluorescence in situ hybridization Bacteria Oligonucleotide probes 16S rRNA Cell fixation Tyramide signal amplification Catalyzed reporter deposition 

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Copyright information

© Springer Science+Business Media, LLC 2010

Authors and Affiliations

  1. 1.British Antarctic SurveyCambridgeUK

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