Comparison of loop-mediated isothermal amplification (LAMP) and real-time PCR method targeting a 529-bp repeat element for diagnosis of toxoplasmosis
文献类型: 外文期刊
第一作者: Lin, Zhibing
作者: Lin, Zhibing;Zhang, Yanlei;Zhang, Houshuang;Zhou, Yongzhi;Cao, Jie;Zhou, Jinlin
作者机构:
关键词: Toxoplasma gondii;Conventional PCR;Loop-mediated isothermal amplification (LAMP);Real-time PCR;529 bp element
期刊名称:VETERINARY PARASITOLOGY ( 影响因子:2.738; 五年影响因子:2.951 )
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年卷期:
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收录情况: SCI
摘要: Loop-mediated isothermal amplification (LAMP) is a simple method that can amplify DNA with high specificity, sensitivity, and rapidity. In this study, we compared the performance of LAMP and real-time PCR assays for diagnosis of toxoplasmosis. We designed a real-time PCR assay targeting a 529 bp element repeated 200-300 times in the Toxoplasma gondii genome. The detection limits of the LAMP and real-time PCR assays were 10 fg/mu L and 1 fg/mu L of T. gondii DNA, respectively. Conventional PCR, LAMP, and real-time PCR methods were applied to detect T. gondii DNA in blood samples from 284 pigs and 292 sheep. Positive results were obtained with 0.4%, 3.2%, and 4.2% of the pig samples and 3.8%,17.1%, and 17.8% of the sheep samples with conventional PCR, LAMP, and real-time PCR analyses, respectively. The real-time PCR assay provided the most sensitive diagnosis of toxoplasmosis, but the LAMP assay has potential as an alternative tool for detection of T. gondii in the field
分类号: S85
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