Department of Biological Sciences and Biotechnology, College of Natural Sciences, Chungbuk National University, Cheongju, 28644, South Korea.
College of Veterinary Medicine, Chonnam National University, Gwangju, 61186, South Korea.
Arch Virol. 2023 Oct 6;168(11):267. doi: 10.1007/s00705-023-05887-3.
Genotype 4 (G4) Eurasian avian-like lineage swine H1N1 influenza A viruses, which are reassortants containing sequences from the pandemic 2009 H1N1 virus lineage, triple-reassortant-lineage internal genes, and EA-lineage external genes, have been reported in China since 2013. These have been predominant in pig populations since 2016 and have exhibited pandemic potential. In this study, we developed a one-step multiplex RT-qPCR assay targeting the M, HA1, and PB2 genes to detect G4 and related EA H1N1 viruses, with detection limits of 1.5 × 10 copies/μL and 1.15 × 10 ng/μL for the purified PCR products and RNA templates, respectively. The specificity of the detection method was confirmed using various influenza virus subtypes. When the one-step multiplex RT-qPCR assay was applied to swine respiratory samples collected between 2020 and 2022 in Korea, a virus related to G4 EA H1N1 strains was detected. Phylogenetic analysis based on portions of all eight genome segments showed that the positive sample contained HA, NA, PB2, NS, and NP genes closely related to those of G4 EA H1N1 viruses, confirming the ability of our assay to accurately detect G4 EA H1N1 viruses in the field.
自 2013 年以来,中国已报告了基因型 4(G4)欧亚禽源样谱系猪 H1N1 流感 A 病毒,这些病毒是由大流行 2009 年 H1N1 病毒谱系、三重重配谱系内部基因和 EA 谱系外部基因重组而成的。自 2016 年以来,这些病毒一直是猪群中的主要病毒,并表现出大流行的潜力。在本研究中,我们开发了一种针对 M、HA1 和 PB2 基因的一步多重 RT-qPCR 检测方法,用于检测 G4 和相关的 EA H1N1 病毒,其对纯化 PCR 产物和 RNA 模板的检测限分别为 1.5×10 拷贝/μL 和 1.15×10 ng/μL。该检测方法的特异性已通过各种流感病毒亚型得到证实。当一步多重 RT-qPCR 检测方法应用于 2020 年至 2022 年期间在韩国收集的猪呼吸道样本时,检测到与 G4 EA H1N1 株相关的病毒。基于所有 8 个基因组片段的部分进行的系统发育分析表明,阳性样本含有 HA、NA、PB2、NS 和 NP 基因,与 G4 EA H1N1 病毒密切相关,证实了我们的检测方法能够在现场准确检测 G4 EA H1N1 病毒的能力。