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首页> 外文期刊>Veterinary Parasitology >Performance of commercial ELISA and agglutination test kits for the detection of anti-Toxoplasma gondii antibodies in serum and muscle fluid of swine infected with 100, 300, 500 or 1000 oocysts
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Performance of commercial ELISA and agglutination test kits for the detection of anti-Toxoplasma gondii antibodies in serum and muscle fluid of swine infected with 100, 300, 500 or 1000 oocysts

机译:用于检测感染了100、300、500或1000个卵囊的猪血清和肌肉液中的弓形虫抗体的商业ELISA和凝集测试试剂盒的性能

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摘要

Serum and tissue fluid samples from experimentally infected swine were tested for antibodies to Toxoplasma gondii using both an indirect ELISA and a modified agglutination test (MAT) available commercially in kit form. Ten 8-9week-old swine were fed meatballs containing 100, 300, 500 or 1000 T. gondii oocysts and three control animals were fed meatballs with no oocysts. Post-inoculation blood samples were collected weekly until euthanasia at 35-63 days post inoculation (DPI). Tissue fluid was obtained from diaphragm, heart and sternomastoideus muscles post-mortem. By 16 DPI, nine of 10 inoculated pigs were detected serologically using ELISA at a pre-test serum dilution of 1:50 and all ten pigs were detected by the MAT at a serum dilution of 1:25. The last pig became positive on ELISA by 21 DPI and the 10 pigs maintained their serological status for the duration of the experiment. Heart muscle was the best overall source of tissue fluid for ELISA and all six pigs inoculated with either 500 or 1000 oocysts were positive using either diaphragm or heart tissue fluid samples. However, 10 of 18 fluid samples from pigs receiving <=300 oocysts were not detected using ELISA, including 5 of 6 from sternomastoideus muscle. The MAT used at a 1:10 pre-test dilution of tissue fluid correctly identified all 10 inoculated pigs regardless of the source muscle. Based on these data, we conclude that either assay would be useful for herd evaluation or surveillance testing using sera, and the MAT would be a good candidate assay for testing tissue fluid for the same purposes.Digital Object Identifier http://dx.doi.org/10.1016/j.vetpar.2012.06.040
机译:使用间接ELISA和改良的凝集试验(MAT),以试剂盒形式购得来自实验感染猪的血清和组织液样品的弓形虫抗体。给十只8-9周大的猪喂食包含100、300、500或1000个弓形虫卵囊的肉丸,并给三只对照动物喂食无卵囊的肉丸。每周收集一次接种后血样,直到接种后35-63天(DPI)安乐死。死后从diaphragm肌,心脏和胸骨肌获得组织液。通过16 DPI,使用ELISA在血清学检测中以1:50的血清稀释度检测了10只接种猪中的9头,并通过MAT在血清稀释度为1:25的条件下检测了所有十只猪。最后一头猪通过21 DPI在ELISA上呈阳性,并且10头猪在实验过程中保持其血清学状态。心肌是用于ELISA的最佳总体体液来源,并且使用隔膜或心脏组织液样本,接种500或1000个卵囊的所有六头猪均为阳性。但是,使用ELISA未检测到来自接受≤300个卵囊的猪的18份液体样本中的10份,其中包括6份来自胸骨肌的肌肉。在组织液按1:10的预测试稀释比例使用的MAT可以正确识别所有10头接种的猪,而无需考虑源肌肉。根据这些数据,我们得出结论认为,两种测定法都可用于使用血清进行牛群评估或监视测试,而MAT则是用于出于相同目的测试组织液的良好候选测定法。数字对象标识符http://dx.doi .org / 10.1016 / j.vetpar.2012.06.040

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