Evaluation of the RT-LAMP/CRISPR-Cas12 diagnostic method for SARS-COV-2

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Abstract

Brazil is one of the countries that least performs detection tests for SARS-COV-2, even though diagnosing cases is the most effective way to control epidemics, which is crucial to guide public policies. From this perspective, this study aimed to evaluate the RT-LAMP/CRISPR-Cas12 detection method using synthetic and natural SARS-COV-2 sequences. A total of 84 reactions of RT-LAMP/CRISPR-Cas12 resulted in the colorimetric results: 55 reactions turned pink, 18 turned orange, and 11 turned yellow. This result showed that, in the RT-LAMP colorimetric criterion, most reactions (65.4%) were classified as negative, followed by inconclusive (21.4%), and a minority (13%) was classified as positive. The colorimetric results showed instabilities such as reaction sensitivity to heating and ambient temperatures at the reaction preparation site. The use of CRISPR/Cas12 proved unnecessary in this experiment and for the RT-LAMP methodology since its reagent is used only for the detection mix and for lateral flow strip analysis. The flow/detection strips in this experiment were ineffective for a retest as they were dependent on the Reporter reagent solution, and their result was not validated with the presence or absence of genetic material.

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Peduti, G. P., & Diniz, M. C. (2023). Evaluation of the RT-LAMP/CRISPR-Cas12 diagnostic method for SARS-COV-2. Acta Scientiarum - Health Sciences, 45. https://doi.org/10.4025/ACTASCIHEALTHSCI.V45I1.62103

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