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首页> 外文期刊>Journal of applied microbiology >Comparative analysis of different TaqMan real-time RT-PCR assays for the detection of swine Hepatitis E virus and integration of Feline calicivirus as internal control
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Comparative analysis of different TaqMan real-time RT-PCR assays for the detection of swine Hepatitis E virus and integration of Feline calicivirus as internal control

机译:TaqMan实时RT-PCR检测猪戊型肝炎病毒和猫杯状病毒整合为内部对照的比较分析

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摘要

The aim of this study was to compare the performance of four TaqMan RT-PCR assays with a commonly used nested RT-PCR and to include the Feline calicivirus (FCV) as an internal control.RNA extracted from 87 swine faecal samples and 103 swine blood samples was subjected to different detection systems. Faecal samples naturally contaminated with Hepatitis E virus (HEV) and negative samples were artificially inoculated with 3.2 x 10(3) PFU of FCV. Detection results obtained on faecal and plasma samples were 35.6% and 4.9% with the nested RT-PCR assay, 8.0% and 0%, 0% and 0%, 13.8% and 0% and 36.8% and 3.9% with TaqMan systems A, B, C and D respectively. The Ct means obtained with the multiplex TaqMan assay were 30.11 and 30.43 for the detection of FCV with HEV contaminated samples and negative samples.The TaqMan system D was more suitable for the detection of swine HEV strains than the three others and FCV was integrated successfully as an internal control.FCV was demonstrated as an efficient control to monitor the RNA extraction process and HEV amplification procedure in a multiplex HEV/FCV TaqMan assay. This control would be helpful in limiting false negative results.
机译:这项研究的目的是比较四种TaqMan RT-PCR分析与常用嵌套式RT-PCR的性能,并包括猫杯状病毒(FCV)作为内部对照。从87头猪粪便样品和103头猪血中提取RNA样品经受了不同的检测系统。用3.2 x 10(3)PFU的FCV人工接种自然感染了戊型肝炎病毒(HEV)的粪便样品和阴性样品。巢式RT-PCR法检测粪便和血浆样品的检测结果分别为35.6%和4.9%,TaqMan系统A分别为8.0%和0%,0%和0%,13.8%和0%和36.8%和3.9%, B,C和D分别。通过多重TaqMan测定获得的Ct平均值分别为30.11和30.43,用于检测HEV污染样品和阴性样品的FCV.TaqMan系统D比其他三个更适合检测猪HEV菌株,并且FCV成功整合FCV被证明是在多重HEV / FCV TaqMan分析中监测RNA提取过程和HEV扩增程序的有效对照。这种控制将有助于限制假阴性结果。

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