James Joe, Slomka Marek J, Reid Scott M, Thomas Saumya S, Mahmood Sahar, Byrne Alexander M P, Cooper Jayne, Russell Christine, Mollett Benjamin C, Agyeman-Dua Eric, Essen Steve, Brown Ian H, Brookes Sharon M
Virology Department, Animal and Plant Health Agency-Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, United Kingdom,
Virology Department, Animal and Plant Health Agency-Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, United Kingdom.
Avian Dis. 2019 Mar 1;63(sp1):209-218. doi: 10.1637/11900-051518-Reg.1.
Previously published NA subtype-specific real-time reverse-transcriptase PCRs (RRT-PCRs) were further validated for the detection of five avian influenza virus (AIV) NA subtypes, namely N5, N6, N7, N8, and N9. Testing of 30 AIV isolates of all nine NA subtypes informed the assay assessments, with the N5 and N9 RRT-PCRs retained as the original published assays while the N7 and N8 assays were modified in the primer-probe sequences to optimize detection of current threats. The preferred N6 RRT-PCR was either the original or the modified variant, depending on the specific H5N6 lineage. Clinical specimen ( = 137) testing revealed the ability of selected N5, N6, and N8 RRT-PCRs to sensitively detect clade 2.3.4.4b highly pathogenic AIV (HPAIV) infections due to H5N5, H5N6, and H5N8 subtypes, respectively, all originating from European poultry and wild bird cases during 2016-2018. Similar testing ( = 32 clinical specimens) also showed the ability of N7 and N9 RRT-PCRs to sensitively detect European H7N7 HPAIV and China-origin H7N9 low pathogenicity AIV infections, respectively.
先前发表的针对特定NA亚型的实时逆转录聚合酶链反应(RRT-PCR)方法,针对5种禽流感病毒(AIV)NA亚型,即N5、N6、N7、N8和N9的检测进行了进一步验证。对所有9种NA亚型的30株AIV分离株进行检测,为分析评估提供了依据。N5和N9的RRT-PCR方法保留为最初发表的方法,而N7和N8的方法在引物-探针序列上进行了修改,以优化对当前威胁的检测。根据特定的H5N6谱系,首选的N6 RRT-PCR方法为原始方法或修改后的变体。临床样本(n = 137)检测显示,所选的N5、N6和N8 RRT-PCR方法分别能够灵敏地检测出2016 - 2018年期间源自欧洲家禽和野鸟病例的H5N5、H5N6和H5N8亚型的2.3.4.4b分支高致病性禽流感病毒(HPAIV)感染。类似检测(n = 32份临床样本)还表明,N7和N9 RRT-PCR方法分别能够灵敏地检测出欧洲H7N7 HPAIV和源自中国的H7N9低致病性AIV感染。