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首页> 外文期刊>European Journal of Histochemistry >Immunogold silver staining associated with epi-fluorescence for cucumber mosaic virus localisation on semi-thin sections of banana tissues
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Immunogold silver staining associated with epi-fluorescence for cucumber mosaic virus localisation on semi-thin sections of banana tissues

机译:免疫金银染色与落射荧光相关联,用于黄瓜花叶病毒在香蕉组织半薄切片上的定位

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摘要

The immunogold-silver staining (IGSS) technique in combination with epi-fluorescence detection was used to localise cucumber mosaic virus (CMV) particles within banana infected tissues. For this purpose, tissue samples (2 mm3) were excised from CMV-infected and highly proliferating meristem cultures of Williams BSJ banana (ITC. 0570, AAA, Cavendish subgroup). These samples were immediately fixed in a 2% paraformaldehyde/0.25% glutaraldehyde mixture, dehydrated in ethanol, and finally embedded in L.R.White resin. Semi-thin sections were cut, mounted on clean treated glass slides and immunostained for CMV particles using gold-labelled secondary antibodies and silver enhancement. Sections were counterstained with basic fuchsin and examined using laser scanning confocal microscopy. Negative controls included immuno-stained samples excised from non-virus infected material as well as infected material on which primary or secondary antibodies were not applied. Images of autofluorescence (in red) and of epi-reflectance of silver-enhanced immunogold particles (in green) were recorded separately and merged, allowing the specific localisation of CMV particles at the cellular level on semi-thin sections of aldehyde-fixed banana tissues. The main advantage of this analytical approach compared to previously published protocols is that it combines a fast staining procedure, stable preparation, a high resolution, and a narrow plane of focus with the flexibility in generation, processing and analysis of images offered by laser scanning confocal microscopy. Finally, the presence of numerous CMV particles within banana meristems constitutes a clear explanation of the very low CMV elimination efficiency when using meristem- tip culture alone.
机译:免疫金银染色(IGSS)技术与落射荧光检测相结合,用于在香蕉感染的组织中定位黄瓜花叶病毒(CMV)颗粒。为此目的,从Williams BSJ香蕉(ITC。0570,AAA,卡文迪许亚组)的CMV感染和高度增殖的分生组织培养物中切除组织样品(2 mm3)。将这些样品立即固定在2%多聚甲醛/0.25%戊二醛混合物中,在乙醇中脱水,最后包埋在L.R. White树脂中。切成半薄的切片,安装在干净的载玻片上,并使用金标记的第二抗体和银增强剂对CMV颗粒进行免疫染色。用碱性品红对切片染色,并用激光扫描共聚焦显微镜检查。阴性对照包括从非病毒感染的材料以及未应用第一抗体或第二抗体的感染材料中切除的免疫染色样品。分别记录并合并了自身荧光(红色)和增强银的免疫金颗粒(绿色)的落射反射率的图像,并将其合并,从而使CMV颗粒在醛固定香蕉组织的半薄切片上在细胞水平上特异性定位。 。与以前发布的方案相比,这种分析方法的主要优势在于,它结合了快速的染色过程,稳定的制备,高分辨率和狭窄的焦平面以及激光扫描共焦提供的图像生成,处理和分析的灵活性显微镜检查。最后,香蕉分生组织中大量CMV颗粒的存在清楚地解释了仅使用分生组织培养时CMV消除效率非常低的问题。

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