Frontiers in Microbiology (Nov 2023)

Rapid detection of H5 subtype avian influenza virus using CRISPR Cas13a based-lateral flow dipstick

  • Yang Li,
  • Jiajing Shang,
  • Jiajing Shang,
  • Juan Luo,
  • Juan Luo,
  • Fuyou Zhang,
  • Ge Meng,
  • Ge Meng,
  • Yingjie Feng,
  • Yingjie Feng,
  • Wenming Jiang,
  • Xiaohui Yu,
  • Chunran Deng,
  • Chunran Deng,
  • Guanhui Liu,
  • Hualei Liu

DOI
https://doi.org/10.3389/fmicb.2023.1283210
Journal volume & issue
Vol. 14

Abstract

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Due to its high mortality rate, highly pathogenic avian influenza (HPAI), a notifiable animal illness designated by the World Organisation for Animal Health (WOAH), has caused enormous financial losses to the poultry sector. The H5 subtype of avian influenza virus (H5-AIV) is regarded as the most common highly pathogenic avian influenza virus (HPAIV) that threatens public health and safety. Virus isolation and reverse transcription quantitative PCR (RT-qPCR) are usually used to detect H5-AIV and are important for the timely diagnosis and control of H5-AIV. However, these methods are time-consuming and require a significant amount of effort. In this study, we established a recombinase-aided amplification (RAA) combined with CRISPR-Cas13a and lateral flow dipstick (LFD) assay for the detection of H5-AIV. The results showed that the process can be completed within 40 min at 37°C. The method had a detection limit of 0.1 copy/μL, which was comparable to the RT-qPCR. There was no cross-reactivity with H3-AIV, H7-AIV, H9-AIV, H10-AIV, IBV, NDV, RVA and DAstV. The kappa value of RT-RAA-Cas13a-LFD and RT-qPCR in 380 clinical samples was 0.89 (κ>0.75). In conclusion, we established a convenient, efficient and accurate method to detect H5-AIV, and the results can be visualized and interpreted using LFD, which can be adapted to the needs of grassroots laboratories and field-deployable assays. This approach provides a new perspective for clinical H5-AIV diagnosis and has great potential for application in clinical quarantine of the poultry farming.

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