疱疹病毒2型:用于猴B病毒诊断试验的替代抗原。

Laboratory animal science Pub Date : 1999-12-01
K Ohsawa, T W Lehenbauer, R Eberle
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引用次数: 0

摘要

背景与目的:由于猴B病毒及其抗原的生物危害性,猕猴血清中猴B病毒抗体的血清学检测存在问题。与人类单纯疱疹病毒1型(HSV1)相比,狒狒的疱疹病毒2型(HVP2)在遗传和抗原性上与BV的关系更为密切。评估了HVP2相对于HSV1作为猕猴血清中抗bv抗体检测的替代试验抗原的潜力。方法:采用BV-、HVP2-和hsv1感染细胞提取物,建立ELISA标准格式。HVP2和HSV1测试的性能相对于BV测试进行评估。结果:采用BV抗原ELISA对7种猕猴349份血清进行检测,结果分为阳性(253份)、阴性(94份)和疑似(2份)。采用HVP2抗原的ELISA对BV阳性血清的检出率为98.0%(248份),而采用hsv1抗原的ELISA对BV阳性血清的检出率仅为96.0%(243份)。所有三种酶联免疫吸附试验均将相同的两个样本确定为可疑样本,HSV1酶联免疫吸附试验将另外三个bv阳性血清确定为可疑样本。结论:基于HVP2抗原的ELISA检测BV阳性猕猴血清的灵敏度和特异性均与基于BV抗原的ELISA检测相同,且优于HSV1抗原ELISA检测。此外,与使用BV抗原进行ELISA检测相比,HVP2 ELISA具有更高的实验室安全性。
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Herpesvirus papio 2: alternative antigen for use in monkey B virus diagnostic assays.

Background and purpose: Serologic testing for antibody to monkey B virus (BV) in macaque sera is problematic due to the biohazardous nature of BV and BV antigens. Herpesvirus papio 2 (HVP2), a herpesvirus of baboons, is more closely related genetically and antigenically to BV than is human herpes simplex virus 1 (HSV1). The potential for use of HVP2 relative to HSV1 as an alternative test antigen for detection of anti-BV antibody in macaque sera was assessed.

Methods: Standard ELISA formats were developed, using BV-, HVP2-, and HSV1-infected cell extracts. Performance of the HVP2 and HSV1 tests was assessed relative to that of the BV test.

Results: Using the BV antigen ELISA, 349 sera from 7 macaque species were tested, and results were classified as positive (253), negative (94), or suspect (2). The ELISA using HVP2 antigen detected 98.0% of BV-positive sera (248 of 253), whereas the HSV1-based ELISA detected only 96.0% (243 of 253). All three ELISAs identified the same two samples as suspect, and the HSV1 ELISA identified three additional BV-positive sera as suspect.

Conclusions: The HVP2 antigen-based ELISA was equal in sensitivity and specificity to the BV antigen-based ELISA and was superior to the HSV1 ELISA for detection of BV-positive macaque sera. In addition, the HVP2 ELISA has greater laboratory safety, compared with BV antigen use for ELISA testing.

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