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用于检测蓝舌病病毒群特异性抗体的商用竞争性酶联免疫吸附测定试剂盒的评估

Evaluation of a commercial competitive ELISA test kit for the detection of group-specific antibodies to bluetongue virus.

作者信息

Afshar A, Trotter H C, Dulac G C, Reddington J J

机构信息

Animal Diseases Research Institute, Agriculture Canada, Nepean, Ontario.

出版信息

J Vet Diagn Invest. 1993 Jul;5(3):336-40. doi: 10.1177/104063879300500305.

Abstract

The performance of a competitive (c) enzyme-linked immunosorbent assay (ELISA) test kit, Blueplate Special (BPS), commercially produced by DiagXotics (Wilton, CT) for detection of group-specific antibodies to bluetongue virus (BTV) was compared with that of an internationally endorsed cELISA-I. A total of 1,026 serum samples were tested in this study: 133 samples from 23 calves and 3 sheep experimentally infected with South African isolates of 19 BTV serotypes and US isolates of 5 BTV serotypes and 7 calves infected with US isolates of 2 epizootic haemorrhagic disease of deer virus (EHDV); 102 paired sera from cattle, sheep, and goats experimentally infected with the Australian isolates of BTV, EHDV, and Palyam virus; 229 bovine and ovine samples of Canadian origin (BTV free); and 562 bovine and ovine field samples from the USA and Barbados (BTV endemic). Seroconversion was demonstrable by the BPS cELISA 10 days postinfection in all experimental animals inoculated with BTV, with the exception of 4 calves in which there was a delay of 10-20 days. Similar to the cELISA-I, none of the sera from calves inoculated with US and Australian isolates of EHDV and Palyam viruses cross-reacted with the BTV antigen in the BPS cELISA. The total agreement between the two assays for all the total bovine and ovine field sera was 98.1%. The overall results substantiate the usefulness of the BPS cELISA test kit for monitoring animal sera for group-specific antibodies to BTV.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对DiagXotics公司(位于康涅狄格州威尔顿)商业化生产的用于检测蓝舌病病毒(BTV)群特异性抗体的竞争性(c)酶联免疫吸附测定(ELISA)检测试剂盒Blueplate Special(BPS)的性能,与国际认可的cELISA-I进行了比较。本研究共检测了1026份血清样本:23头犊牛和3只绵羊的133份样本,这些动物经实验感染了19种南非BTV血清型分离株和5种美国BTV血清型分离株,还有7头犊牛感染了2种美国鹿流行性出血病病毒(EHDV)分离株;102对来自经实验感染澳大利亚BTV、EHDV和帕利亚姆病毒分离株的牛、羊和山羊的配对血清;229份加拿大来源的牛和羊样本(无BTV);以及562份来自美国和巴巴多斯的牛和羊现场样本(BTV地方流行)。在接种BTV的所有实验动物中,感染后10天通过BPS cELISA可检测到血清转化,但有4头犊牛延迟了10 - 20天。与cELISA-I类似,接种美国和澳大利亚EHDV及帕利亚姆病毒分离株的犊牛血清在BPS cELISA中均未与BTV抗原发生交叉反应。两种检测方法对所有牛和羊现场血清的总体一致性为98.1%。总体结果证实了BPS cELISA检测试剂盒在监测动物血清中BTV群特异性抗体方面的实用性。(摘要截短至250字)

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