Wilhelm Sonja, Zimmermann Pia, Selbitz Hans Joachim, Truyen Uwe
Institute for Animal Hygiene and Veterinary Public Health, An den Tierkliniken 1, 04103 Leipzig, Germany.
J Virol Methods. 2006 Jun;134(1-2):257-60. doi: 10.1016/j.jviromet.2006.01.004. Epub 2006 Feb 9.
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.
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)。