Domanska-Blicharz K, Lisowska A, Pikuła A, Sajewicz-Krukowska J
Department of Poultry Diseases, National Veterinary Research Institute, Pulawy, Poland.
Lett Appl Microbiol. 2017 Aug;65(2):141-146. doi: 10.1111/lam.12753. Epub 2017 Jul 3.
Infectious bronchitis virus (IBV) is a worldwide prevalent RNA virus that causes highly contagious and economically devastating disease in chicken. The virus exists in many different genetic forms which made the disease control very difficult. The present study describes the development and validation of TaqMan probe-based real-time reverse transcription-polymerase chain reaction (real-time RT-PCR) targeting the S1 coding region of S gene characteristic for the GII-1 lineage (formerly the D1466-like variant) of IBV. These strains are quite different from other European IBV belonging to different lineages of the GI genotype. The developed method was 30-fold more sensitive than used so far for standard nested RT-PCR with detection limit of 56 RNA copies per reaction. The specificity of the assay was also evaluated with a panel of different poultry pathogens. Repeatability and reproducibility of the method was very high with coefficients of variation lower than 4%. One hundred and twenty-seven IBV-positive samples were tested by this method and GII-1 strains were detected in four of them (3·15%) which indicate a decrease in the GII-1 IBV prevalence in Poland. The assay was proven to be a valuable tool for rapid diagnosis of GII-1 lineage of IBV strains and moreover it enabled the monitoring of viral loads which can be used to assess disease progression.
This study reports a TaqMan probe-based real-time reverse transcription-polymerase chain reaction (real-time RT-PCR) for rapid and accurate identification of GII-1 lineage (formerly D1466-like variant) of infectious bronchitis virus (IBV). The assay revealed to be more sensitive than standard nested RT-PCR assay, previously used for this purpose. The developed assay has been tested on numerous field samples and revealed 3·15% prevalence of this lineage of IBV in Polish chicken population. Moreover, this new assay enables the assessment of viral load measurement which might be useful for epidemiology and pathogenesis studies.
传染性支气管炎病毒(IBV)是一种在全球流行的RNA病毒,可在鸡群中引发高传染性且造成经济损失的疾病。该病毒存在多种不同的基因形式,这使得疾病防控极具难度。本研究描述了一种基于TaqMan探针的实时逆转录-聚合酶链反应(实时RT-PCR)方法的开发与验证,该方法靶向针对IBV GII-1谱系(以前的D1466样变异株)S基因特征性的S1编码区。这些毒株与属于GI基因型不同谱系的其他欧洲IBV毒株有很大差异。所开发的方法比目前用于标准巢式RT-PCR的方法灵敏30倍,检测限为每个反应56个RNA拷贝。还使用一组不同的家禽病原体评估了该检测方法的特异性。该方法的重复性和再现性非常高,变异系数低于4%。用该方法检测了127份IBV阳性样本,其中4份(3.15%)检测到GII-1毒株,这表明波兰GII-1 IBV的流行率有所下降。该检测方法被证明是快速诊断IBV毒株GII-1谱系的有价值工具,此外,它还能监测病毒载量,可用于评估疾病进展。
本研究报告了一种基于TaqMan探针的实时逆转录-聚合酶链反应(实时RT-PCR),用于快速准确鉴定传染性支气管炎病毒(IBV)的GII-1谱系(以前的D1466样变异株)。该检测方法比以前用于此目的的标准巢式RT-PCR检测方法更灵敏。所开发的检测方法已在众多现场样本上进行了测试,结果显示该IBV谱系在波兰鸡群中的流行率为3.15%。此外,这种新的检测方法能够评估病毒载量测量,这可能对流行病学和发病机制研究有用。