首页> 外文期刊>The Veterinary Record >COMPARISON OF FIVE TESTS FOR THE DETECTION OF ANTIBODIES AGAINST CHLAMYDIAL (ENZOOTIC) ABORTION OF EWES
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COMPARISON OF FIVE TESTS FOR THE DETECTION OF ANTIBODIES AGAINST CHLAMYDIAL (ENZOOTIC) ABORTION OF EWES

机译:五种检测母婴感染性(共生)败血症的抗体的比较

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Five tests for antibodies against chlamydial (enzootic) abortion of ewes were compared using 255 sera from experimentally (group 1) or naturally (group 2) infected animals, flocks free of the disease (group 3) and individual animals testing positively by the complement fixation test but from flocks with no evidence of chlamydial abortion (group 4) Sera from five specific pathogen-free lambs vaccinated with two different subtypes of Chlamydia pecorum were also included (group 5), AU tests used some form of processed culture of C psittaci as antigen, Specificities, established with groups 3 and 4 sera, ranged between 96 per cent (ELISA using lipopolysaccharide antigen) and 59 per cent (Immunocomb). Reactions with group 5 sera suggested that the cause of false positive results in the field might be cross-reactive antibodies against tile arthritogenic subtype of C pecorum. Sensitivities, Established with groups 1 and 2 sera, ranged between 81 per cent (Immunocomb) and 51 per cent (ELISA using solubilised protein antigen), The minimum sample sizes required to be 95 per cent certain of detecting at least five seropositives in two infected flocks (combined data) were 15 to 48, dependent on the test applied, The Western blot test, applied to a proportion of samples, yielded no false positives with group 3 sera bat 31.7 per cent with group 4 sera, Thus, none of the tests in this comparison emerged as sufficiently satisfactory in all respects, suggesting that further improvements in chlamydial serology must come through the use of non-native antigens or in the form of a competitive ELISA.
机译:使用来自实验性感染(第1组)或自然感染(第2组),无疾病的鸡群(第3组)和个体动物通过补体固定呈阳性的255个血清,比较了五种针对衣原体(动物性)流产的抗体的测试试验,但没有证明衣原体流产的鸡群(第4组),还包括来自用两种不同亚型衣原体接种的5种无特定病原体羔羊的血清(第5组),AU试验使用了某种形式的鹦鹉热C.抗原,由第3组和第4组血清确定的特异性,介于96%(使用脂多糖抗原的ELISA)和59%(免疫腔)之间。与第5组血清的反应表明,该领域假阳性结果的原因可能是针对C pecorum的关节炎形成亚型的交叉反应抗体。灵敏度由第1组和第2组血清确定,范围在81%(免疫腔)至51%(使用溶解的蛋白抗原的ELISA)之间,至少要能够检测到两个感染者中至少五种血清阳性的样本的最小样本量才能达到95%。鸡群(合并数据)为15到48,取决于所应用的测试。对一部分样品进行的蛋白质印迹测试表明,第3组血清蝙蝠未产生假阳性,而第4组血清则为31.7%,因此,没有该比较中的测试在各个方面都令人满意,这表明衣原体血清学的进一步改善必须通过使用非天然抗原或竞争性ELISA的形式来实现。

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