Biodiversity Division, Ecological Risk Assessment and Control Section, National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki, 305-8506, Japan.
Biodiversity Division, Ecological Risk Assessment and Control Section, National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki, 305-8506, Japan; Animal Research Center of Hokkaido Research Organization, 5-39 Shintoku, Hokkaido, 081-0038, Japan.
Comp Immunol Microbiol Infect Dis. 2023 Nov;102:102076. doi: 10.1016/j.cimid.2023.102076. Epub 2023 Oct 4.
We developed a method to determine the sequences of hemagglutinin (HA) and neuraminidase (NA) from RNA extracted directly from wild bird fecal samples, using Nanopore Flongle. We determined the nucleotide sequences and subtypes of HA and NA in 16 and 15 samples respectively, using Flongle. The results of HA and NA subtyping determined by the conventional method were consistent with their subtypes determined by our method, thereby the applicability of this method in the identification of HA and NA subtypes. In addition, the homology between the HA fragments in this and the Sanger methods ranged from 98.5 % to 100 %. Compared with conventional PCR with the Sanger method, this method can easily determine HA and NA subtypes and sequences directly from the fecal samples. It is easier to implement and has lower running costs (USD100$) than other NGS-based methods, making it a useful tool for avian influenza surveillance in wild birds.
我们开发了一种方法,使用 Nanopore Flongle 从直接从野生鸟类粪便样本中提取的 RNA 中确定血凝素 (HA) 和神经氨酸酶 (NA) 的序列。我们使用 Flongle 分别确定了 16 个和 15 个样本中的 HA 和 NA 的核苷酸序列和亚型。通过常规方法确定的 HA 和 NA 亚型的结果与我们方法确定的亚型一致,从而证明了该方法在鉴定 HA 和 NA 亚型方面的适用性。此外,本方法与 Sanger 方法中 HA 片段之间的同源性为 98.5%至 100%。与传统的 Sanger 方法的 PCR 相比,该方法可以直接从粪便样本中轻松确定 HA 和 NA 亚型和序列。它比其他基于 NGS 的方法更容易实施,运行成本更低(100 美元),是监测野生鸟类中禽流感的有用工具。