4.7 Article

Boosting SARS-CoV-2 detection combining pooling and multiplex strategies

Journal

SCIENTIFIC REPORTS
Volume 12, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-022-12747-8

Keywords

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Funding

  1. Conselho Nacional de Pesquisa (CNPq)
  2. Carlos Chagas Filho Foundation for Research Support of Rio de Janeiro State (FAPERJ), Brazil
  3. Industry Federation of Rio de Janeiro FIRJAN
  4. CENPES/PETROBRAS

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RT-qPCR is the gold standard for SARS-CoV-2 detection, but it has long run times and high costs. In this study, a pooling strategy was evaluated and validated using samples from a mass testing program. The results showed that pooling can increase testing capacity and save costs without sacrificing sensitivity.
RT-qPCR is the gold standard technique available for SARS-CoV-2 detection. However, the long test run time and costs associated with this type of molecular testing are a challenge in a pandemic scenario. Due to high testing demand, especially for monitoring highly vaccinated populations facing the emergence of new SARS-CoV-2 variants, strategies that allow the increase in testing capacity and cost savings are needed. We evaluated a RT-qPCR pooling strategy either as a simplex and multiplex assay, as well as performed in-silico statistical modeling analysis validated with specimen samples obtained from a mass testing program of Industry Federation of the State of Rio de Janeiro (Brazil). Although the sensitivity reduction in samples pooled with 32 individuals in a simplex assay was observed, the high-test sensitivity was maintained even when 16 and 8 samples were pooled. This data was validated with the results obtained in our mass testing program with a cost saving of 51.5% already considering the expenditures with pool sampling that were analyzed individually. We also demonstrated that the pooling approach using 4 or 8 samples tested with a triplex combination in RT-qPCR is feasible to be applied without sensitivity loss, mainly combining Nucleocapsid (N) and Envelope (E) gene targets. Our data shows that the combination of pooling in a RT-qPCR multiplex assay could strongly contribute to mass testing programs with high-cost savings and low-reagent consumption while maintaining test sensitivity. In addition, the test capacity is predicted to be considerably increased which is fundamental for the control of the virus spread in the actual pandemic scenario.

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