Gérard Emmanuelle, Guyot François, Philippot Pascal, López-García Purificación
Laboratoire de Géosciences Marines, CNRS UMR 7097, Institut de Physique du Globe de Paris, 4 place Jussieu, 75005 Paris, France.
J Microbiol Methods. 2005 Oct;63(1):20-8. doi: 10.1016/j.mimet.2005.02.018.
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 sub-nanometer 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.
我们描述了一种基于荧光原位杂交(FISH)的方法,该方法可通过电子显微镜识别单个细胞。我们将通用和特异性荧光素标记的寡核苷酸探针与异质细胞混合物中原核微生物的核糖体RNA进行杂交。然后,我们使用与亚纳米金颗粒偶联的抗荧光素抗体标记核糖体中的杂交探针。通过银增强使金属颗粒直径增大后,通过光学显微镜、透射电子显微镜(TEM)和扫描电子显微镜(SEM)观察到特异性金银信号。这是首次将SEM应用于检测与细胞内靶标(如核糖体)杂交的金纳米颗粒。将FISH系统发育鉴定与电子显微镜分辨率下的细胞表面和超微结构观察相结合的可能性在微生物生态学中具有广阔的潜在应用前景。