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Volume 32, Number 10—October 2026

Research

Detection of Influenza D Virus using Reverse Transcription Loop-Mediated Isothermal Amplification

Carlos Abelardo dos Santos, Jialu Li, Pauline M. van Diemen, Andrew McMahon, Benjamin C. Mollett, Andrew M. Ramsay, Meshach M. Maina, Joe James, Helen E. Everett, Janet M. Daly, and Nicole C. RobbComments to Author 
Author affiliation: Warwick Medical School, University of Warwick, Coventry, UK (C.A. dos Santos, J. Li, N.C. Robb); Animal and Plant Health Agency Weybridge, Addlestone, UK (P.M. van Diemen, B.C. Mollett, A.M. Ramsay, J. James, H.E. Everett); School of Life Sciences, University of Warwick, Coventry (A. McMahon); One Virology, Wolfson Centre for Global Virus Research, University of Nottingham, Nottingham, UK (M.M. Maina, J.M. Daly)

Main Article

Figure 3

Mean amplification curves from reverse transcription loop-mediated isothermal amplification reaction triplicates showing the onset of amplification in study of isothermal detection of influenza D virus. All influenza D virus isolate RNAs at 104 and 103 copies per µL amplified within the first 20 minutes regardless of the lineage. NTC, nontemplate control.

Figure 3. Mean amplification curves from reverse transcription loop-mediated isothermal amplification reaction triplicates showing the onset of amplification in study of isothermal detection of influenza D virus. All influenza D virus isolate RNAs at 104 and 103 copies per µL amplified within the first 20 minutes regardless of the lineage. NTC, nontemplate control.

Main Article

Page created: August 13, 2026
Page updated: September 28, 2026
Page reviewed: September 28, 2026
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