Colorimetric RT-LAMP SARS-CoV-2 diagnostic sensitivity relies on color interpretation and viral load

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作者
Mateus Nóbrega Aoki
Bruna de Oliveira Coelho
Luiz Gustavo Bentim Góes
Paola Minoprio
Edison Luiz Durigon
Luis Gustavo Morello
Fabricio Klerynton Marchini
Irina Natassja Riediger
Maria do Carmo Debur
Helder I. Nakaya
Lucas Blanes
机构
[1] Carlos Chagas Institute,Laboratory for Applied Science and Technology in Health
[2] Oswaldo Cruz Foundation (Fiocruz),Departamento de Microbiologia – ICB‐II
[3] Scientific Platform Pasteur - University of São Paulo,Department of Clinical and Toxicological Analyses, School of Pharmaceutical Sciences
[4] Universidade de São Paulo,undefined
[5] University of São Paulo,undefined
[6] Paraná´s Central Laboratory (LACEN-PR),undefined
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摘要
The use of RT-LAMP (reverse transcriptase—loop mediated isothermal amplification) has been considered as a promising point-of-care method to diagnose COVID-19. In this manuscript we show that the RT-LAMP reaction has a sensitivity of only 200 RNA virus copies, with a color change from pink to yellow occurring in 100% of the 62 clinical samples tested positive by RT-qPCR. We also demonstrated that this reaction is 100% specific for SARS-CoV-2 after testing 57 clinical samples infected with dozens of different respiratory viruses and 74 individuals without any viral infection. Although the majority of manuscripts recently published using this technique describe only the presence of two-color states (pink = negative and yellow = positive), we verified by naked-eye and absorbance measurements that there is an evident third color cluster (orange), in general related to positive samples with low viral loads, but which cannot be defined as positive or negative by the naked eye. Orange colors should be repeated or tested by RT-qPCR to avoid a false diagnostic. RT-LAMP is therefore very reliable for samples with a RT-qPCR Ct < 30 being as sensitive and specific as a RT-qPCR test. All reactions were performed in 30 min at 65 °C. The use of reaction time longer than 30 min is also not recommended since nonspecific amplifications may cause false positives.
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