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首页> 外文期刊>Journal of Virological Methods >Infrared fluorescent immunofocus assay (IR-FIFA) for the quantitation of non-cytopathic and minimally cytopathic viruses.
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Infrared fluorescent immunofocus assay (IR-FIFA) for the quantitation of non-cytopathic and minimally cytopathic viruses.

机译:红外荧光免疫聚焦测定法(IR-FIFA)用于定量非细胞病变和最小程度的细胞病变病毒。

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摘要

A novel method was developed for the precise quantitation of viruses using infrared fluorescent detection of foci of infection in conventional cell culture plates. In this assay, termed the infrared fluorescent immunofocus assay (IR-FIFA), appropriate cell cultures were infected with serial dilutions of hepatitis A virus (HAV) or measles virus (MV) and maintained with a semi-solid overlay for 1-5 days. Cell monolayers were fixed with formaldehyde, and then stained in succession with a primary monoclonal antibody and an Alexa Fluor 680 conjugate. Foci of infection (analogous to plaques) were detected by scanning culture plates using the Odyssey infrared imaging system and counted to determine the virus titre, expressed as focus forming units (FFU) per mL, as is done for conventional plaque assays. HAV and MV were used as models of minimally cytopathic viruses, and showed a linear dose-response between focus formation and virus dilution. Viral titres calculated using this method were comparable to conventionally used methods. The IR-FIFA was also successfully adapted to quantify duck hepatitis B virus (DHBV) as a model for a non-cytopathic virus. This simple and sensitive assay will have wide use for the quantitation of non-cytopathic and minimally cytopathic viruses.
机译:开发了一种新颖的方法,通过红外荧光检测常规细胞培养板中的感染灶来精确定量病毒。在这种称为红外荧光免疫聚焦测定(IR-FIFA)的测定中,将适当的细胞培养物用甲型肝炎病毒(HAV)或麻疹病毒(MV)的系列稀释液感染,并用半固体覆盖物保持1-5天。用甲醛固定细胞单层,然后依次用一抗单克隆抗体和Alexa Fluor 680偶联物染色。通过使用Odyssey红外成像系统扫描培养板来检测感染的病灶(类似于噬菌斑),并进行计数以确定病毒滴度,以每毫升的斑块形成单位(FFU)表示,就像常规噬菌斑测定一样。 HAV和MV用作最小程度的细胞病变病毒的模型,并显示了病灶形成和病毒稀释之间的线性剂量反应。使用该方法计算的病毒滴度与常规使用的方法相当。 IR-FIFA还成功地用于量化鸭乙型肝炎病毒(DHBV),作为非细胞病变病毒的模型。这种简单而灵敏的测定方法将广泛用于定量非细胞病变和最小细胞病变的病毒。

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