首页> 美国卫生研究院文献>The Journal of Veterinary Medical Science >ELISA using a recombinant chimera of ESAT-6/MPB70/MPB83 for Mycobacterium bovis diagnosis in naturally infected cattle
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ELISA using a recombinant chimera of ESAT-6/MPB70/MPB83 for Mycobacterium bovis diagnosis in naturally infected cattle

机译:使用ESAT-6 / MPB70 / MPB83重组嵌合体的ELISA诊断自然感染牛的牛分枝杆菌

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摘要

Bovine tuberculosis (bTB) control programs generally rely on intradermal tuberculin tests for the antemortem diagnosis of Mycobacterium bovis infection in cattle, but these tests detect only a portion of the infected animals. The aim of the present study was to evaluate the diagnostic coverage of a combination of the bTB antemortem techniques known as the comparative intradermal tuberculin test (CITT) and an ELISA based on a recombinant chimera of ESAT-6/MPB70/MPB83 as the antigen in cattle. The results were compared to postmortem findings based on M. bovis culturing and PCR. Paired comparisons of all data (n=92) demonstrated that ELISA and LST results compared to the culturing results did not present significant differences (P=0.27 on McNemar’s test and P=0.12 on Fisher’s exact test, respectively). Using culturing as the gold standard, the sensitivity and specificity of ELISA were 79.5% (95% CI: 64.5–89.2%) and 75.5% (95% CI: 62.4–85.1%), respectively, whereas LST demonstrated 100% sensitivity (95% CI: 91.03–100%) and 92.5% specificity (95% CI: 82.1–97.0%). The ELISA results did not reveal significant differences in relation to the LST results (P>0.99 on Fisher’s exact test). Using the latter as the gold standard, the sensitivity and specificity of ELISA were 79.1% (95% CI: 64.8–88.6%) and 79.6% (95% CI: 66.4–88.5%), respectively. The use of ELISA with the recombinant chimera of ESAT-6/MPB70/MPB83 as the antigen complements the diagnostic coverage provided by CITT and increases the removal of infected animals from herds.
机译:牛结核病(bTB)控制程序通常依靠皮内结核菌素检测来对牛的牛分枝杆菌感染进行死前诊断,但是这些检测仅检测到一部分感染动物。本研究的目的是评估被称为比较皮内结核菌素试验(CITT)的bTB死前技术和基于ESAT-6 / MPB70 / MPB83重组嵌合体作为抗原的ELISA的诊断覆盖率。牛。将结果与基于牛分枝杆菌培养和PCR的验尸结果进行比较。所有数据的配对比较(n = 92)表明,ELISA和LST结果与培养结果相比没有显着差异(分别为McNemar试验的P = 0.27和Fisher精确试验的P = 0.12)。以培养为金标准,ELISA的灵敏度和特异性分别为79.5%(95%CI:64.5-89.2%)和75.5%(95%CI:62.4-85.1%),而LST的灵敏度为100%(95 %CI:91.03–100%)和92.5%特异性(95%CI:82.1–97.0%)。 ELISA结果与LST结果之间没有显着差异(Fisher精确检验的P> 0.99)。使用后者作为金标准,ELISA的灵敏度和特异性分别为79.1%(95%CI:64.8–88.6%)和79.6%(95%CI:66.4–88.5%)。将ELISA与ESAT-6 / MPB70 / MPB83的重组嵌合体作为抗原配合使用,可补充CITT提供的诊断范围,并增加从畜群中清除受感染动物的能力。

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