RT-LAMP as Diagnostic Tool for Influenza—A Virus Detection in Swine

Author:

Storms Suzanna M.1ORCID,Shisler Joanna2,Nguyen Thanh H.3ORCID,Zuckermann Federico A.4,Lowe James F.1ORCID

Affiliation:

1. Department of Veterinary Clinical Medicine, University of Illinois at Urbana-Champaign, Urbana, IL 61802, USA

2. Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, IL 61802, USA

3. Department of Civil Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61802, USA

4. Department of Pathobiology, University of Illinois at Urbana-Champaign, Urbana, IL 61802, USA

Abstract

Point-of-care diagnostic technologies are becoming more widely available for production species. Here, we describe the application of reverse transcription loop-mediated isothermal amplification (RT-LAMP) to detect the matrix (M) gene of influenza A virus in swine (IAV-S). M-specific LAMP primers were designed based on M gene sequences from IAV-S isolated in the USA between 2017 and 2020. The LAMP assay was incubated at 65 °C for 30 min, with the fluorescent signal read every 20 s. The assay’s limit of detection (LOD) was 20 M gene copies for direct LAMP of the matrix gene standard, and 100 M gene copies when using spiked extraction kits. The LOD was 1000 M genes when using cell culture samples. Detection in clinical samples showed a sensitivity of 94.3% and a specificity of 94.9%. These results show that the influenza M gene RT-LAMP assay can detect the presence of IAV in research laboratory conditions. With the appropriate fluorescent reader and heat block, the assay could be quickly validated as a low-cost, rapid, IAV-S screening tool for use on farms or in clinical diagnostic labs.

Funder

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services

Publisher

MDPI AG

Subject

General Veterinary

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