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[改进狂犬病的实验室诊断及狂犬病病毒滴定]

[Improving the laboratory diagnosis of rabies and titration of rabies viruses].

作者信息

Závadová J, Svrcek S

机构信息

Ustav experimentálnej veterinárnej medicíny, Kosice, Slovak Republic.

出版信息

Vet Med (Praha). 1994;39(11):663-76.

PMID:7817499
Abstract

For primary isolation and titration of street strains of the rabies virus from brains of suspected animals, an assay prepared on the cell culture BHK-21/C 13 (rabies infection test - RTCIT) was used. The above assay proved to be reliable and its sensitivity proved to be comparable to the standard mouse inoculation test. Through this test, the results were obtained within 24 to 48 hrs on Lab-Tek tissue culture chamber/slides. It was found out that DEAE-dextran added to the cell culture only slightly increased the invasiveness of the virus in the samples tested. The method described herein is able to substitute the mouse inoculation test (MIT). In our laboratory, 20 vaccination strains of the rabies virus Vnukovo-32/107 and 25 street strains of the rabies virus (delivered from the field) - original fox brain suspensions. And 10 brain suspensions were negative when tested in laboratory conditions (by PMIF, RTCIT as well as by MIT methods).

摘要

为从疑似动物的脑组织中对狂犬病病毒街毒株进行初次分离和滴定,采用了在细胞培养物BHK - 21/C 13上制备的一种检测方法(狂犬病感染试验 - RTCIT)。上述检测方法被证明是可靠的,其灵敏度与标准小鼠接种试验相当。通过该试验,在Lab - Tek组织培养室/载玻片上24至48小时内即可获得结果。发现添加到细胞培养物中的二乙氨基乙基葡聚糖仅略微增加了所测试样品中病毒的侵袭性。本文所述方法能够替代小鼠接种试验(MIT)。在我们实验室,有20株狂犬病病毒Vnukovo - 32/107疫苗株以及25株狂犬病病毒街毒株(从野外送来)——原始狐脑悬液。并且有10份脑悬液在实验室条件下(通过PMIF、RTCIT以及MIT方法检测)呈阴性。

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