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用于常规分离街毒株狂犬病病毒的组织培养技术。

Tissue culture technique for routine isolation of street strain rabies virus.

作者信息

Rudd R J, Trimarchi C V, Abelseth M K

出版信息

J Clin Microbiol. 1980 Oct;12(4):590-3. doi: 10.1128/jcm.12.4.590-593.1980.

Abstract

A tissue culture test for the primary isolation of street strain rabies virus from the brains of suspect animals was evaluated. It was found to be reliable and comparable in sensitivity to the standard mouse inoculation technique. The test, which yields final results in 48 h, was performed in BHK-21 cells on tissue culture chamber slides. The addition of diethylaminoethyl dextran to the cell suspension before seeding the slide promoted the subsequent viral invasiveness of positive test specimens. The method described may be considered as a substitute for the mouse inoculation test which is currently used as a backup to the fluorescent antibody test in the diagnosis of rabies.

摘要

对一种用于从疑似动物大脑中初次分离狂犬病街毒株的组织培养试验进行了评估。结果发现该试验可靠,并且在敏感性方面与标准小鼠接种技术相当。该试验在组织培养室载玻片上的BHK - 21细胞中进行,48小时可得出最终结果。在将细胞悬液接种到载玻片之前向其中添加二乙氨基乙基葡聚糖,可提高阳性试验标本随后的病毒侵袭性。所描述的方法可被视为小鼠接种试验的替代方法,目前小鼠接种试验在狂犬病诊断中作为荧光抗体试验的备用方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4fe/273643/f8a78ee937b3/jcm00171-0137-a.jpg

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