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首页> 外文期刊>Journal of Clinical Microbiology >Development and Evaluation of a Test for Tuberculosis in Live European Badgers (Meles meles) Based on Measurement of Gamma Interferon mRNA by Real-Time PCR
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Development and Evaluation of a Test for Tuberculosis in Live European Badgers (Meles meles) Based on Measurement of Gamma Interferon mRNA by Real-Time PCR

机译:基于实时PCR测量γ干扰素mRNA的活欧洲Live(Meles meles)结核病检测方法的开发和评估

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A real-time PCR assay for the measurement of gamma interferon (IFN-γ) mRNA in European badger (Meles meles) blood cultures was developed. The levels of IFN-γ mRNA in blood cultures stimulated with either bovine or avian tuberculin or specific mycobacterial antigens were compared with those in a nonstimulated control blood culture as the basis for determining the tuberculosis (TB) status of live badgers. The assay was validated by testing 247 animals for which there were matching data from postmortem examination and culture of tissues. Relative changes in the levels of IFN-γ mRNA in response to bovine tuberculin and specific antigens were found to be greater among badgers with tissues positive for TB on culture. The test was at its most accurate (87% of test results were correct) by using blood cultures containing bovine tuberculin as the antigen and when the response to avian tuberculin was taken into account by subtracting the avian tuberculin response from the bovine tuberculin response. At a specificity of 90.7%, the test was 70.6% sensitive. At the same specificity, the current serological enzyme-linked immunosorbent assay for TB in badgers was only 53% sensitive. This work demonstrates that measurement of IFN-γ mRNA by real-time PCR is a valid method for the detection of TB in live badgers and may provide an alternative to the current serological methods of diagnosis, the Brock test. The testing procedure can be completed within 5 h of receipt of the blood culture samples. In addition, the use of a molecular biology-based test offers the potential to fully automate the testing procedure through the use of robotics.
机译:开发了一种实时PCR检测欧洲for( Meles meles )血液培养物中γ-干扰素(IFN-γ)mRNA的方法。将牛或禽结核菌素或特定分枝杆菌抗原刺激的血液培养物中的IFN-γmRNA水平与非刺激性对照血液培养物中的IFN-γmRNA水平进行比较,以此作为确定badge的结核(TB)状态的基础。通过测试247只动物的死后检查和组织培养数据,验证了该分析方法的有效性。发现在badge培养组织中结核阳性的badge中,对牛结核菌素和特定抗原的应答,IFN-γmRNA的相对变化更大。通过使用包含牛结核菌素作为抗原的血液培养物,以及从牛结核菌素应答中减去禽结核菌素应答来考虑对禽结核菌素的应答时,该测试是最准确的(87%的测试结果是正确的)。在90.7%的特异性下,测试的敏感度为70.6%。在相同的特异性下,目前ser中TB的血清学酶联免疫吸附测定仅53%灵敏。这项工作表明,通过实时PCR测量IFN-γmRNA是检测live中TB的有效方法,并且可以为当前的血清学诊断方法Brock测试提供替代方法。可以在收到血培养样本后5小时内完成测试程序。另外,基于分子生物学的测试的使用提供了通过使用机器人技术使测试过程完全自动化的潜力。

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