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首页> 外文期刊>Scientific reports. >Riems influenza a typing array (RITA): An RT-qPCR-based low density array for subtyping avian and mammalian influenza a viruses
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Riems influenza a typing array (RITA): An RT-qPCR-based low density array for subtyping avian and mammalian influenza a viruses

机译:Riems流感分型阵列(RITA):基于RT-qPCR的低密度阵列,用于亚型禽流感和哺乳动物a型流感病毒

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摘要

Rapid and sensitive diagnostic approaches are of the utmost importance for the detection of humans and animals infected by specific influenza virus subtype(s). Cascade-like diagnostics starting with the use of pan-influenza assays and subsequent subtyping devices are normally used. Here, we demonstrated a novel low density array combining 32 TaqMan(?) real-time RT-PCR systems in parallel for the specific detection of the haemagglutinin (HA) and neuraminidase (NA) subtypes of avian and porcine hosts. The sensitivity of the newly developed system was compared with that of the pan-influenza assay, and the specificity of all RT-qPCRs was examined using a broad panel of 404 different influenza A virus isolates representing 45 different subtypes. Furthermore, we analysed the performance of the RT-qPCR assays with diagnostic samples obtained from wild birds and swine. Due to the open format of the array, adaptations to detect newly emerging influenza A virus strains can easily be integrated. The RITA array represents a competitive, fast and sensitive subtyping tool that requires neither new machinery nor additional training of staff in a lab where RT-qPCR is already established.
机译:快速灵敏的诊断方法对于检测被特定流感病毒亚型感染的人类和动物至关重要。通常使用从泛流感检测和后续亚型分析设备开始的级联式诊断。在这里,我们展示了一种新颖的低密度阵列,可同时结合32个TaqMan(?)实时RT-PCR系统,用于禽和猪宿主的血凝素(HA)和神经氨酸酶(NA)亚型的特异性检测。将新开发的系统的敏感性与全流感检测的敏感性进行了比较,并使用代表45种不同亚型的404种不同的甲型流感病毒分离株检测了所有RT-qPCR的特异性。此外,我们用野生鸟类和猪的诊断样品分析了RT-qPCR分析的性能。由于阵列的开放格式,因此可以很容易地整合检测新出现的甲型流感病毒株的方法。 RITA阵列代表了一种竞争性,快速且灵敏的分型工具,在已经建立了RT-qPCR的实验室中,不需要新的设备,也不需要额外的人员培训。

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