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一种用于实验室兔多杀性巴氏杆菌感染血清学诊断的斑点免疫结合试验。

A dot-immunobinding assay for the serodiagnosis of Pasteurella multocida infection in laboratory rabbits.

作者信息

Manning P J, Brackee G, Naasz M A, DeLong D, Leary S L

机构信息

Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis 55455.

出版信息

Lab Anim Sci. 1987 Oct;37(5):615-20.

PMID:3695396
Abstract

A dot-immunobinding assay was developed to detect serum IgG specific for lipopolysaccharide of rabbit isolates of P. multocida. The assay detected serum IgG as early as 1 week after experimental subclinical nasal infection, whereas 8 weeks were required to detect antibody by a gel diffusion precipitin test. The assay was more reliable than nasal cultures, in that up to 46% of 16 weekly nasal washings of some infected rabbits failed to yield P. multocida. The bacterial antigen (proteinase k digested cell lysate) used in the assay reacted with IgG that did not cross-react with lipopolysaccharide antigens of B. bronchiseptica, P. pneumotropica or P. hemolytica. The assay is sensitive and specific, easily performed, cost effective, requires no special laboratory instruments and provides a permanent easily stored record.

摘要

开发了一种斑点免疫结合试验来检测针对多杀性巴氏杆菌兔分离株脂多糖的血清IgG。该试验最早在实验性亚临床鼻感染后1周就能检测到血清IgG,而通过凝胶扩散沉淀试验检测抗体则需要8周。该试验比鼻拭子培养更可靠,因为一些感染兔子的16次每周鼻洗液中,高达46%未能培养出多杀性巴氏杆菌。该试验中使用的细菌抗原(蛋白酶K消化的细胞裂解物)与IgG发生反应,而该IgG与支气管败血波氏杆菌、嗜肺巴氏杆菌或溶血巴氏杆菌的脂多糖抗原无交叉反应。该试验灵敏且特异,操作简便,成本效益高,无需特殊实验室仪器,且能提供易于保存的永久记录。

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