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一种用于“同一健康”检测流感 A 病毒的通用 RT-qPCR 检测方法。

A universal RT-qPCR assay for "One Health" detection of influenza A viruses.

机构信息

State Veterinary Institute Prague, Prague, Czech Republic.

National Institute of Public Health, National Reference Laboratory for Influenza, Prague, Czech Republic.

出版信息

PLoS One. 2021 Jan 20;16(1):e0244669. doi: 10.1371/journal.pone.0244669. eCollection 2021.

Abstract

The mutual dependence of human and animal health is central to the One Health initiative as an integrated strategy for infectious disease control and management. A crucial element of the One Health includes preparation and response to influenza A virus (IAV) threats at the human-animal interface. The IAVs are characterized by extensive genetic variability, they circulate among different hosts and can establish host-specific lineages. The four main hosts are: avian, swine, human and equine, with occasional transmission to other mammalian species. The host diversity is mirrored in the range of the RT-qPCR assays for IAV detection. Different assays are recommended by the responsible health authorities for generic IAV detection in birds, swine or humans. In order to unify IAV monitoring in different hosts and apply the One Health approach, we developed a single RT-qPCR assay for universal detection of all IAVs of all subtypes, species origin and global distribution. The assay design was centred on a highly conserved region of the IAV matrix protein (MP)-segment identified by a comprehensive analysis of 99,353 sequences. The reaction parameters were effectively optimised with efficiency of 93-97% and LOD95% of approximately ten IAV templates per reaction. The assay showed high repeatability, reproducibility and robustness. The extensive in silico evaluation demonstrated high inclusivity, i.e. perfect sequence match in the primers and probe binding regions, established as 94.6% for swine, 98.2% for avian and 100% for human H3N2, pandemic H1N1, as well as other IAV strains, resulting in an overall predicted detection rate of 99% on the analysed dataset. The theoretical predictions were confirmed and extensively validated by collaboration between six veterinary or human diagnostic laboratories on a total of 1970 specimens, of which 1455 were clinical and included a diverse panel of IAV strains.

摘要

人类健康和动物健康相互依存,是作为传染病控制和管理综合战略的“同一健康”倡议的核心。“同一健康”的一个关键要素包括在人类-动物界面为应对甲型流感病毒 (IAV) 威胁做好准备和做出反应。IAV 的特点是具有广泛的遗传变异性,它们在不同宿主之间传播,并能建立宿主特异性谱系。四个主要宿主是:禽类、猪、人类和马,偶尔也会传播给其他哺乳动物。宿主多样性反映在用于检测 IAV 的 RT-qPCR 检测方法的范围上。负责的卫生当局为通用 IAV 检测推荐了不同的检测方法,用于检测鸟类、猪或人类的 IAV。为了统一不同宿主的 IAV 监测并应用“同一健康”方法,我们开发了一种用于普遍检测所有 IAV 亚型、物种来源和全球分布的通用 RT-qPCR 检测方法。该检测方法的设计以综合分析 99353 个序列确定的 IAV 基质蛋白 (MP) 片段的高度保守区域为中心。通过对大约 10 个 IAV 模板进行反应效率优化,获得了 93-97%的效率和 95%的 LOD。该检测方法显示出高重复性、重现性和稳健性。广泛的计算机评估证明了高包容性,即在引物和探针结合区域的完美序列匹配,在猪中为 94.6%,在禽类中为 98.2%,在人类 H3N2、大流行性 H1N1 以及其他 IAV 株中为 100%,导致分析数据集的总体预测检出率为 99%。理论预测通过六个兽医或人类诊断实验室之间的合作得到了证实和广泛验证,总共对 1970 个标本进行了分析,其中 1455 个为临床标本,包括多样化的 IAV 株。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d03/7817021/3cf28bca23c3/pone.0244669.g001.jpg

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