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首页> 外文期刊>Preventive Veterinary Medicine >Diagnostic performance measures of ELISA and quantitative PCR tests for porcine circovirus type 2 exposure using Bayesian latent class analysis.
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Diagnostic performance measures of ELISA and quantitative PCR tests for porcine circovirus type 2 exposure using Bayesian latent class analysis.

机译:使用贝叶斯潜伏类分析的2型猪圆环病毒暴露的ELISA和定量PCR测试的诊断性能指标。

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Porcine circovirus 2 (PCV2) is believed to be a necessary but not sufficient underlying cause of porcine circovirus associated disease (PCVAD) in swine (Opriessnig et al., 2007). Since the potential threat of PCVAD is dependent on the prevalence of PCV2 in swine populations, accurate diagnostic tests are important for epidemiologic surveillance. Therefore, we evaluated the diagnostic sensitivity (Se) and specificity (Sp) of a new indirect ELISA and two quantitative PCR tests for PCV2 in a series of latent class models that used Bayesian estimation procedures. A total of 4140 samples from finisher pigs were tested for evidence of PCV2 by the ELISA and a TaqMan (TM) quantitative PCR, 995 by the ELISA and a SYBR Green (SG) dye-binding PCR, 998 by both PCRs and 993 by all three tests. Overall, the median (95% probability interval) ELISA Se and Sp was 0.85 (0.83-0.87) and 0.74 (0.68-0.79), respectively, when all three tests were analyzed together at an ELISA absorbance (optical density or OD) cutoff of >=0.3. The TM PCR Se and Sp was 0.86 (0.84-0.88) and 0.94 (0.87-0.97), respectively, and the SG PCR Se and Sp was 0.83 (0.81-0.85) and 0.98 (0.94-1.00), respectively when all three tests were analyzed together at an ELISA OD cutoff of >=0.3. Sensitivity analysis revealed that Sp estimates in general had less stability than Se estimates, but the SG PCRSp was the most stable. Limited conditional dependence between the two PCR tests was detected. We conclude that the ELISA had the highest diagnostic Se at an absorbance cutoff of >=0.3, while the SG PCR had the highest diagnostic Sp. The prevalence levels for exposure to PCV2 in finishing swine populations across all analyses ranged from 58 to 100%.
机译:猪圆环病毒2(PCV2)被认为是猪猪圆环病毒相关疾病(PCVAD)的必要但不充分的根本原因(Opriessnig et al。,2007)。由于PCVAD的潜在威胁取决于猪群中PCV2的流行,因此准确的诊断检测对于流行病学监测非常重要。因此,我们在一系列使用贝叶斯估计程序的潜在分类模型中,评估了新的间接ELISA的诊断敏感性(Se)和特异性(Sp)和PCV2的两次定量PCR测试。通过ELISA和TaqMan(TM)定量PCR检验了来自育肥猪的总共4140个样品的PCV2证据,通过ELISA和SYBR Green(SG)染料结合PCR检验了PCV2的证据,通过PCR和PCR均检测了998,对993所有三个测试。总体而言,当以ELISA吸光度(光学密度或OD)截止值将所有三个测试一起分析时,ELISA Se和Sp的中位数(95%概率区间)分别为0.85(0.83-0.87)和0.74(0.68-0.79)。 > = 0.3。在所有三个测试中,TM PCR Se和Sp分别为0.86(0.84-0.88)和0.94(0.87-0.97),而SG PCR Se和Sp分别为0.83(0.81-0.85)和0.98(0.94-1.00)。将ELISA OD截止值> = 0.3一起分析。敏感性分析表明,Sp估计值总体上比Se估计值稳定性差,但SG PCR Sp 最为稳定。在两个PCR测试之间检测到有限的条件依赖性。我们得出的结论是,ELISA在吸光度截止值> = 0.3时具有最高的诊断Se,而SG PCR的诊断Sp最高。在所有分析中,最终猪群中PCV2的暴露水平为58%至100%。

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