首页> 外文期刊>Bulletin of Animal Health and Production in Africa >COMPARISON BETWEEN VIRUS NEUTRALISATION TESTS AND AN INDIRECT ENZYME-LINKED IMMUNOSORBENT ASSAY FOR DETECTING ANTIBODIES TO RINDERPEST VIRUS IN CATTLE SERA
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COMPARISON BETWEEN VIRUS NEUTRALISATION TESTS AND AN INDIRECT ENZYME-LINKED IMMUNOSORBENT ASSAY FOR DETECTING ANTIBODIES TO RINDERPEST VIRUS IN CATTLE SERA

机译:病毒中和测试与间接酶联免疫吸附法检测牛血清中林德病毒的比较

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Sera from 1916 cattle were screened for antibodies to rinderpest virus using the microtitre virus neutralisation test (MVNT) and an indirect enzyme-linked immunosorbent assay (ELISA). Eleven sera (0.6%) could not be assayed in the MVNT due to contamination or non-specific cytotoxicity and another 177 (9%) required retesting in the MVNT due to difficulties in reading the initial screening results. Comparison of the 1905 fully testable sera showed agreement for 1414 (74,2%) and disagreement for 491 (25.8%) of the sera. One hundred and fourteen of the 491 sera with discrepant results were then assayed by the tube neutralisation test (VNT) and the results extrapolated to reinterpret the results of the original screen. Overall the MVNT was more sensitivebut less specific than the indirect ELISA for detecting antibodies to rinderpest virus. This study also showed that the MVNT was more sensitive but less specific than the ELISA when compared to the tu be neutralisation test. In contrast, pre-vaccinationsera from 44 cattle were free of rinderpest virus neutralising antibodies in seven of these sera. Three weeks after vaccination of 31 of these cattle the MVNT and VNT detected antibodies in all of the vaccinated cattle but the ELISA detected antibodiesin the sera of only 27. Following virulent challenge all of the 31 vaccinates survived while the 13 unvaccinated cattle died from clinical rinderpest. The indirect ELISA offers a practical alternative tothe MVNT for mass sero-monitoring of cattle populations with expected high antibody prevalences. However, neutralisation tests are more reliable when assaying small numbers of sera especially for detecting antibody negative animals.
机译:使用微量滴定病毒中和试验(MVNT)和间接酶联免疫吸附测定(ELISA),对1916头牛的血清进行了牛瘟病毒抗体的筛选。由于污染或非特异性细胞毒性,无法在MVNT中测定11个血清(0.6%),而由于难以读取初始筛选结果,因此需要在MVNT中重新测试另外177个血清(9%)。对1905年可完全测试的血清进行比较,结果显示同意1414(74,2%)和491(25.8%)血清。然后用试管中和试验(VNT)对491份血清中的114份结果进行了差异分析,并推断出结果以重新解释原始筛选的结果。总体而言,MVNT与间接ELISA相比对牛瘟病毒抗体更敏感,但特异性更低。这项研究还表明,与中和试验相比,MVNT比ELISA更具敏感性,但特异性较低。相比之下,来自44头牛的疫苗接种前血清中有7株不含牛瘟病毒中和抗体。在对其中31头牛进行疫苗接种三周后,MVNT和VNT在所有已接种牛中检测到抗体,但ELISA在仅27例血清中检测到抗体。在强力攻击后,所有31株疫苗都存活了下来,而13例未接种牛则死于临床牛瘟。间接ELISA为MVNT的大规模血清学监测提供了一种实用的替代方法,可以对牛血清进行高抗体流行率的监测。但是,中和测试在检测少量血清时更可靠,尤其是用于检测抗体阴性动物时。

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