Murrell K D, Zarlenga D S
US Department of Agriculture, Agricultural Research Service, Beltsville, Maryland.
Southeast Asian J Trop Med Public Health. 1991 Dec;22 Suppl:321-5.
A rapid, sensitive and specific serologic test has been developed for the diagnosis of swine trichinellosis. The ELISA based test utilizes L1 stichosome antigens recovered as excretory-secretory (ES) products from in vitro cultivated muscle larvae. Field studies conducted with 20,000 commercial swine using crude ES antigen demonstrated that the test could detect 98% of the medically significant infections. The test had a false-positive rate of less than 3%. Because of difficulties in regulating the quality and quantity of ES antigen and the need to continually maintain infected laboratory animals for producing the diagnostic reagent, efforts have been made to clone and express the gene(s) encoding the immunodominant ES antigens. To date a cDNA sequence, designated TsA-12, which codes in part for a 53-kDa ES antigen, has been identified and expressed in bacteria. Results demonstrate that TsA-12 is recognized by immune sera and further suggest that the immunodominant 45-, 48- and 53-kDa ES proteins which share antigenic epitopes are distinct glycoproteins.
已开发出一种用于诊断猪旋毛虫病的快速、灵敏且特异的血清学检测方法。该基于酶联免疫吸附测定(ELISA)的检测方法利用从体外培养的肌幼虫中作为排泄分泌(ES)产物回收的L1杆状体抗原。使用粗制ES抗原对20,000头商品猪进行的现场研究表明,该检测方法可检测出98%具有医学意义的感染病例。该检测方法的假阳性率低于3%。由于在调节ES抗原的质量和数量方面存在困难,且需要持续饲养感染实验动物以生产诊断试剂,因此已努力克隆和表达编码免疫显性ES抗原的基因。迄今为止,已鉴定出一个名为TsA-12的cDNA序列,其部分编码一种53 kDa的ES抗原,并已在细菌中表达。结果表明,TsA-12可被免疫血清识别,进一步表明共享抗原表位的免疫显性45 kDa、48 kDa和53 kDa ES蛋白是不同的糖蛋白。