Suppr超能文献

H9 亚型禽流感病毒实时 RT-PCR 方法的重新设计与验证。

Redesign and Validation of a Real-Time RT-PCR to Improve Surveillance for Avian Influenza Viruses of the H9 Subtype.

机构信息

EU/OIE/National Reference Laboratory for Avian Influenza and Newcastle Disease, FAO Reference Centre for Animal Influenza and Newcastle Disease, Division of Comparative Biomedical Sciences, Istituto Zooprofilattico Sperimentale delle Venezie (IZSVe), 35020 Legnaro, Italy.

OIE Reference Laboratory for Avian Influenza, Faculty of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan.

出版信息

Viruses. 2022 Jun 10;14(6):1263. doi: 10.3390/v14061263.

Abstract

Avian influenza viruses of the H9 subtype cause significant losses to poultry production in endemic regions of Asia, Africa and the Middle East and pose a risk to human health. The availability of reliable and updated diagnostic tools for H9 surveillance is thus paramount to ensure the prompt identification of this subtype. The genetic variability of H9 represents a challenge for molecular-based diagnostic methods and was the cause for suboptimal detection and false negatives during routine diagnostic monitoring. Starting from a dataset of sequences related to viruses of different origins and clades (Y439, Y280, G1), a bioinformatics workflow was optimized to extract relevant sequence data preparatory for oligonucleotides design. Analytical and diagnostic performances were assessed according to the OIE standards. To facilitate assay deployment, amplification conditions were optimized with different nucleic extraction systems and amplification kits. Performance of the new real-time RT-PCR was also evaluated in comparison to existing H9-detection methods, highlighting a significant improvement of sensitivity and inclusivity, in particular for G1 viruses. Data obtained suggest that the new assay has the potential to be employed under different settings and geographic areas for a sensitive detection of H9 viruses.

摘要

H9 亚型禽流感病毒在亚洲、非洲和中东的流行地区给家禽养殖业造成了重大损失,对人类健康构成了威胁。因此,获得可靠和最新的 H9 监测诊断工具对于确保及时识别该亚型至关重要。H9 的遗传变异性给基于分子的诊断方法带来了挑战,也是常规诊断监测中检测不佳和出现假阴性的原因。本研究从与不同起源和分支(Y439、Y280、G1)的病毒相关的序列数据集出发,优化了生物信息学工作流程,以提取相关的序列数据,为寡核苷酸设计做准备。根据 OIE 标准评估了分析和诊断性能。为了便于检测的应用,我们使用不同的核酸提取系统和扩增试剂盒优化了扩增条件。还将新的实时 RT-PCR 与现有的 H9 检测方法进行了比较,结果表明,新方法在敏感性和包容性方面有了显著提高,特别是对 G1 病毒。这些数据表明,新的检测方法具有在不同环境和地理区域下用于敏感检测 H9 病毒的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/567b/9227555/e6840ec5f372/viruses-14-01263-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验