Fluorescence in situ hybridisation coupled to ultra small immunogold detection to identify prokaryotic cells using transmission and scanning electron microscopy

被引:19
作者
Gérard, E
Guyot, F
Philippot, P
López-García, P
机构
[1] Univ Paris 11, CNRS, UMR 8079, Unite Ecol Systemat & Evolut, F-91405 Orsay, France
[2] CNRS, UMR 7079, Inst Phys Globe Paris, Lab Geosci Marines, F-75005 Paris, France
[3] CNRS, UMR 7590, Lab Mineral Cristallog, F-75005 Paris, France
[4] Inst Phys Globe, F-75005 Paris, France
关键词
fluorescence in situ hybridisation; immunogold detection; scanning electron microscopy; transmission electron microscopy;
D O I
10.1016/j.mimet.2005.02.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a method based on fluorescence in situ hybridisation (FISH) that allows the identification of individual cells by electron microscopy. We hybridised universal and specific fluorescein-labelled oligonucleotide probes to the ribosomal RNA of prokaryotic microorganisms in heterogeneous cell mixtures. We then used antibodies against fluorescein coupled to subnanometer gold particles to label the hybridised probes in the ribosome. After increasing the diameter of the metal particles by silver enhancement, the specific gold-silver signal was visualised by optical microscopy, transmission electron microscopy (TEM) and scanning electron microscopy (SEM). It is the first time that SEM is applied to the detection of gold nanoparticles hybridised to an intracellular target, such as the ribosome. The possibility to couple phylogenetic identification by FISH to cell surface and ultrastructure observation at electron microscopy resolution has promising potential applications in microbial ecology. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:20 / 28
页数:9
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