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用于检测田间样本中猪细小病毒的实时荧光定量PCR方法

Real-time PCR protocol for the detection of porcine parvovirus in field samples.

作者信息

Wilhelm Sonja, Zimmermann Pia, Selbitz Hans Joachim, Truyen Uwe

机构信息

Institute for Animal Hygiene and Veterinary Public Health, An den Tierkliniken 1, 04103 Leipzig, Germany.

出版信息

J Virol Methods. 2006 Jun;134(1-2):257-60. doi: 10.1016/j.jviromet.2006.01.004. Epub 2006 Feb 9.

Abstract

This report describes a real-time polymerase chain reaction assay with SYBR Green for detection of a broad range of porcine parvoviruses (PPV) and accurate virus quantification in porcine tissues. The assay targets the VP2 gene of PPV and the porcine genomic c-myc gene for normalization. The detection limit of the SYBR Green reaction was shown to be equivalent to 6 x 10(0) to 6 x 10(1) PPV copies/reaction and the overall detection limit equivalent to 0.1 TCID(50)/100 microl. The assay was linear over a 10(7) dilution range of template concentrations. Other porcine pathogens involved in reproductive disorders such as porcine circovirus 2 (PCV-2), porcine reproductive and respiratory virus (PRRSV), Aujeszky's disease virus (PRV) and other parvoviruses such as feline parvovirus (FPV), canine parvovirus (CPV), minute virus of canines (MVC) and a human parvovirus (B19) were not detected by this assay.

摘要

本报告描述了一种使用SYBR Green的实时聚合酶链反应检测方法,用于检测多种猪细小病毒(PPV)并对猪组织中的病毒进行准确定量。该检测方法以PPV的VP2基因和猪基因组c-myc基因作为内参进行标准化。SYBR Green反应的检测限相当于6×10(0)至6×10(1)个PPV拷贝/反应,总体检测限相当于0.1 TCID(50)/100微升。该检测方法在模板浓度10(7)的稀释范围内呈线性。此检测方法未检测到其他与繁殖障碍有关的猪病原体,如猪圆环病毒2型(PCV-2)、猪繁殖与呼吸综合征病毒(PRRSV)、伪狂犬病病毒(PRV),以及其他细小病毒,如猫细小病毒(FPV)、犬细小病毒(CPV)、犬微小病毒(MVC)和人细小病毒(B19)。

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