Assessment of Specimen Pooling to Conserve SARS CoV-2 Testing Resources

Author:

Abdalhamid Baha12,Bilder Christopher R3ORCID,McCutchen Emily L12,Hinrichs Steven H1,Koepsell Scott A1ORCID,Iwen Peter C12

Affiliation:

1. Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha

2. Nebraska Public Health Laboratory, University of Nebraska Medical Center, Omaha

3. Department of Statistics, University of Nebraska-Lincoln, Lincoln, NE

Abstract

Abstract Objectives To establish the optimal parameters for group testing of pooled specimens for the detection of SARS-CoV-2. Methods The most efficient pool size was determined to be five specimens using a web-based application. From this analysis, 25 experimental pools were created using 50 µL from one SARS-CoV-2 positive nasopharyngeal specimen mixed with 4 negative patient specimens (50 µL each) for a total volume of 250 µL. Viral RNA was subsequently extracted from each pool and tested using the CDC SARS-CoV-2 RT-PCR assay. Positive pools were consequently split into individual specimens and tested by extraction and PCR. This method was also tested on an unselected group of 60 nasopharyngeal specimens grouped into 12 pools. Results All 25 pools were positive with cycle threshold (Ct) values within 0 and 5.03 Ct of the original individual specimens. The analysis of 60 specimens determined that 2 pools were positive followed by identification of 2 individual specimens among the 60 tested. This testing was accomplished while using 22 extractions/PCR tests, a savings of 38 reactions. Conclusions When the incidence rate of SARS-CoV-2 infection is 10% or less, group testing will result in the saving of reagents and personnel time with an overall increase in testing capability of at least 69%.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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