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Validation of a direct-to-PCR COVID-19 detection protocol utilizing mechanical homogenization: A model for reducing resources needed for accurate testing

Efficient and effective viral detection methodologies are a critical piece in the global response to COVID-19, with PCR-based nasopharyngeal and oropharyngeal swab testing serving as the current gold standard. With over 100 million confirmed cases globally, the supply chains supporting these PCR tes...

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Bibliographic Details
Published in:PloS one 2021-08, Vol.16 (8), p.e0256316-e0256316
Main Authors: Morehouse, Zachary P, Samikwa, Lyson, Proctor, Caleb M, Meleke, Harry, Kamdolozi, Mercy, Ryan, Gabriella L, Chaima, David, Ho, Antonia, Nash, Rodney J, Nyirenda, Tonney S
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Language:English
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Summary:Efficient and effective viral detection methodologies are a critical piece in the global response to COVID-19, with PCR-based nasopharyngeal and oropharyngeal swab testing serving as the current gold standard. With over 100 million confirmed cases globally, the supply chains supporting these PCR testing efforts are under a tremendous amount of stress, driving the need for innovative and accurate diagnostic solutions. Herein, the utility of a direct-to-PCR method of SARS-CoV-2 detection grounded in mechanical homogenization is examined for reducing resources needed for testing while maintaining a comparable sensitivity to the current gold standard workflow of nasopharyngeal and oropharyngeal swab testing. In a head-to-head comparison of 30 patient samples, this initial clinical validation study of the proposed homogenization-based workflow demonstrated significant agreeability with the current extraction-based method utilized while cutting the total resources needed in half.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0256316