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双抗体夹心酶联免疫吸附测定和免疫印迹分析用于山羊和绵羊干酪性淋巴结炎的控制。

Double-antibody sandwich enzyme-linked immunosorbent assay and immunoblot analysis used for control of caseous lymphadenitis in goats and sheep.

作者信息

ter Laak E A, Bosch J, Bijl G C, Schreuder B E

机构信息

Department of Bacteriology, Central Veterinary Institute, Lelystad, The Netherlands.

出版信息

Am J Vet Res. 1992 Jul;53(7):1125-32.

PMID:1497180
Abstract

A double-antibody sandwich ELISA for detection of antibodies directed against the exotoxin of Corynebacterium pseudotuberculosis, the cause of caseous lymphadenitis (CL) in small ruminants, was developed. A concentrated exotoxin was used. For interpretation of ELISA results, these sera were tested: sequentially obtained sera of C pseudotuberculosis-inoculated goats and sheep that were monitored for 68 weeks; sequentially obtained sera from 80 goats of 3 flocks with CL; sera from 652 goats of 7 flocks without CL; sera from 160 sheep of 4 flocks without CL; and 2,265 caprine and 208 ovine sera submitted for diagnostic testing. Data regarding the infection status and history of 10,454 of the 23,302 animals were collected after testing; most of these were goats that had been part of a CL control program. Specificity and sensitivity of the ELISA were nearly 100%. Subsequently, 31,978 animals from which no data on infection status of flocks had been collected were then tested. It was concluded that the ELISA is a useful diagnostic test for CL eradication programs. Sera with doubtful or inconclusive ELISA results were examined by use of immunoblot analysis. Proteins from C pseudotuberculosis culture supernatant were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and blotted onto nitrocellulose. Six proteins with molecular mass of 68, 65, 39, 38, 31, and 29 kDa reacted with sera from goats and sheep with experimentally induced or naturally acquired infection. Immunoblot analysis was valuable in classifying sera with doubtful or inconclusive results by ELISA.

摘要

开发了一种双抗体夹心ELISA,用于检测针对假结核棒状杆菌外毒素的抗体,假结核棒状杆菌是小反刍动物干酪性淋巴结炎(CL)的病因。使用了浓缩外毒素。为了解释ELISA结果,检测了以下血清:对感染假结核棒状杆菌的山羊和绵羊连续采集68周的血清;来自3个患有CL的羊群的80只山羊的连续采集血清;来自7个无CL的羊群的652只山羊的血清;来自4个无CL的羊群的160只绵羊的血清;以及提交用于诊断检测的2265份山羊血清和208份绵羊血清。在检测后收集了23302只动物中10454只动物的感染状况和病史数据;其中大多数是参与CL控制计划的山羊。ELISA的特异性和敏感性接近100%。随后,对31978只未收集到羊群感染状况数据的动物进行了检测。得出结论,ELISA是CL根除计划中一种有用的诊断检测方法。对ELISA结果可疑或不确定的血清采用免疫印迹分析进行检测。将假结核棒状杆菌培养上清液中的蛋白质通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分离,然后印迹到硝酸纤维素膜上。六种分子量分别为68、65、39、38、31和29 kDa的蛋白质与经实验诱导或自然感染的山羊和绵羊的血清发生反应。免疫印迹分析对于通过ELISA对结果可疑或不确定的血清进行分类很有价值。

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