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Development of a Novel Nested–Rt–Lamp Assay for the Rapid and Accurate Coronavirus Disease-2019 Diagnosis Publisher



Mirzaei H1 ; Sepahi N2 ; Ghasemian A2 ; Ranjbar R2 ; Samsami S3 ; Mansoori Y2 ; Chenari M4 ; Montaseri Z5 ; Namavari N6 ; Namavari S7 ; Ghanbariasad A7
Authors
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Authors Affiliations
  1. 1. Department of Medical Genetics, School of Medicine, Zabol University of Medical Sciences, Zabol, Iran
  2. 2. Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran
  3. 3. Student Research Committee, Fasa University of Medical Sciences, Fasa, Iran
  4. 4. Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Infectious Diseases, School of Medicine, Fasa University of Medical Sciences, Fasa, Iran
  6. 6. School of Medicine Grenada, St. George’s University, St. George’s, Grenada
  7. 7. Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Fasa University of Medical Sciences, Fasa, Iran

Source: Canadian Journal of Infectious Diseases and Medical Microbiology Published:2025


Abstract

Background and Aims: Coronavirus disease 2019 (COVID-19), an emerging life-threatening viral disease, has rapidly spread worldwide, exerting a detrimental impact on public health. We aimed to devise an innovative platform based on the loop-mediated isothermal amplification (LAMP) method, having priorities over real-time PCR (RT–PCR) in terms of sensitivity, specificity, and low running costs. Methods: To develop a novel assay, a new primer set plus four primer sets were designed targeting the N gene of the COVID-19 agent, resulting in the sensitivity reinforcement. The limit of detection (LOD) of the developed approach was determined and compared to those of the standard RT–LAMP and RT–PCR. Two hundred confirmed positive and negative samples initially tested by RT–PCR were recruited to assess the nested–RT–LAMP assay. Furthermore, for the one-step nested–RT–LAMP assay, positive samples were tested directly without the need for RNA extraction. Results: The LOD of nested–RT–LAMP, LAMP, and RT–PCR were 5, 15, and 15 copies/μL, respectively. The findings of the investigation illustrated 100% sensitivity and 98% specificity for both LAMP assays. Moreover, respectively, 94% and 97% sensitivity and specificity were determined regarding the one-step nested–RT–LAMP assay. Conclusion: We offered a novel approach with more sensitivity compared to RT–PCR and common RT–LAMP, not only being a simple, accurate, cost-effective alternative diagnostic tool for RT–PCR but also being able to detect asymptomatic or mildly symptomatic patients more accurately in 2 h by naked eyes. Copyright © 2025 Hadi Mirzaei et al. Canadian Journal of Infectious Diseases and Medical Microbiology published by John Wiley & Sons Ltd.