Zheng Y Z, Webb R, Greenfield P F, Reid S
Department of Chemical Engineering, University of Queensland, Brisbane, Australia.
J Virol Methods. 1996 Dec;62(2):153-9. doi: 10.1016/s0166-0934(96)02100-3.
An improved method for counting virus and virus like particles by electron microscopy (EM) was developed. The procedure involves the determination of the absolute concentration of pure or semi-pure particles once deposited evenly on EM grids using either centrifugation or antibody capture techniques. The counting of particles was done with a Microfiche unit which enlarged approximately 50 x the image of particles on a developed negative film which had been taken at a relatively low magnification (2500 x) by EM. Initially, latex particles of a known concentration were counted using this approach, to prove the accuracy of the technique. The latex particles were deposited evenly on an EM grid using centrifugation (Modified Beckmen EM-90 Airfuge technique). Subsequently, recombinant Bluetongue virus (BTV) core-like particles (CLPs) captured by a Monoclonal antibody using a novel sample loading method were counted by the Microfiche unit method and by a direct EM method. Comparison of the simplified counting method developed with a conventional method, showed good agreement. The method is simple, accurate, rapid, and reproducible when used with either pure particles or with particles from crude cell culture extracts.
开发了一种通过电子显微镜(EM)计数病毒和病毒样颗粒的改进方法。该程序涉及使用离心或抗体捕获技术,一旦将纯的或半纯的颗粒均匀沉积在EM网格上,就确定其绝对浓度。颗粒计数是使用缩微胶片装置进行的,该装置将在相对低倍率(2500倍)下通过EM拍摄的显影负片上的颗粒图像放大约50倍。最初,使用这种方法对已知浓度的乳胶颗粒进行计数,以证明该技术的准确性。使用离心法(改良的贝克曼EM-90空气离心机技术)将乳胶颗粒均匀沉积在EM网格上。随后,通过缩微胶片装置法和直接EM法对使用新型样品加载方法由单克隆抗体捕获的重组蓝舌病毒(BTV)核心样颗粒(CLP)进行计数。将开发的简化计数方法与传统方法进行比较,结果显示出良好的一致性。该方法与纯颗粒或粗细胞培养提取物中的颗粒一起使用时,简单、准确、快速且可重复。