TY - JOUR
T1 - DRUL for school
T2 - Opening Pre-K with safe, simple, sensitive saliva testing for SARS-CoV-2
AU - Frank, Mayu O.
AU - Blachere, Nathalie E.
AU - Parveen, Salina
AU - Hacisuleyman, Ezgi
AU - Fak, John
AU - Luna, Joseph M.
AU - Michailidis, Eleftherios
AU - Wright, Samara
AU - Stark, Pamela
AU - Campbell, Ann
AU - Foo, Ashley
AU - Sakmar, Thomas P.
AU - Huffman, Virginia
AU - Bergh, Marissa
AU - Goldfarb, Audrey
AU - Mansisidor, Andres
AU - Patriotis, Agata L.
AU - Palmquist, Karl H.
AU - Poulton, Nicolas
AU - Leicher, Rachel
AU - Vargas, Cesar D.M.
AU - Duba, Irene
AU - Hurley, Arlene
AU - Colagreco, Joseph
AU - Pagane, Nicole
AU - Orange, Dana E.
AU - Mora, Kevin
AU - Rakeman, Jennifer L.
AU - Fowler, Randal C.
AU - Fernandes, Helen
AU - Lamendola-Essel, Michelle F.
AU - Didkovsky, Nicholas
AU - Silvera, Leopolda
AU - Masci, Joseph
AU - Allen, MacHelle
AU - Rice, Charles M.
AU - Darnell, Robert B.
N1 - Publisher Copyright:
© 2021 Frank et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2021/6
Y1 - 2021/6
N2 - To address the need for simple, safe, sensitive, and scalable SARS-CoV-2 tests, we validated and implemented a PCR test that uses a saliva collection kit use at home. Individuals self-collected 300 μl saliva in vials containing Darnell Rockefeller University Laboratory (DRUL) buffer and extracted RNA was assayed by RT-PCR (the DRUL saliva assay). The limit of detection was confirmed to be 1 viral copy/μl in 20 of 20 replicate extractions. Viral RNA was stable in DRUL buffer at room temperature up to seven days after sample collection, and safety studies demonstrated that DRUL buffer immediately inactivated virus at concentrations up to 2.75x106 PFU/ml. Results from SARS-CoV-2 positive nasopharyngeal (NP) swab samples collected in viral transport media and assayed with a standard FDA Emergency Use Authorization (EUA) test were highly correlated with samples placed in DRUL buffer. Direct comparison of results from 162 individuals tested by FDA EUA oropharyngeal (OP) or NP swabs with co-collected saliva samples identified four otherwise unidentified positive cases in DRUL buffer. Over six months, we collected 3, 724 samples from individuals ranging from 3 months to 92 years of age. This included collecting weekly samples over 10 weeks from teachers, children, and parents from a pre-school program, which allowed its safe reopening while at-risk pods were quarantined. In sum, we validated a simple, sensitive, stable, and safe PCR-based test using a self-collected saliva sample as a valuable tool for clinical diagnosis and screening at workplaces and schools.
AB - To address the need for simple, safe, sensitive, and scalable SARS-CoV-2 tests, we validated and implemented a PCR test that uses a saliva collection kit use at home. Individuals self-collected 300 μl saliva in vials containing Darnell Rockefeller University Laboratory (DRUL) buffer and extracted RNA was assayed by RT-PCR (the DRUL saliva assay). The limit of detection was confirmed to be 1 viral copy/μl in 20 of 20 replicate extractions. Viral RNA was stable in DRUL buffer at room temperature up to seven days after sample collection, and safety studies demonstrated that DRUL buffer immediately inactivated virus at concentrations up to 2.75x106 PFU/ml. Results from SARS-CoV-2 positive nasopharyngeal (NP) swab samples collected in viral transport media and assayed with a standard FDA Emergency Use Authorization (EUA) test were highly correlated with samples placed in DRUL buffer. Direct comparison of results from 162 individuals tested by FDA EUA oropharyngeal (OP) or NP swabs with co-collected saliva samples identified four otherwise unidentified positive cases in DRUL buffer. Over six months, we collected 3, 724 samples from individuals ranging from 3 months to 92 years of age. This included collecting weekly samples over 10 weeks from teachers, children, and parents from a pre-school program, which allowed its safe reopening while at-risk pods were quarantined. In sum, we validated a simple, sensitive, stable, and safe PCR-based test using a self-collected saliva sample as a valuable tool for clinical diagnosis and screening at workplaces and schools.
UR - https://www.scopus.com/pages/publications/85108680525
U2 - 10.1371/journal.pone.0252949
DO - 10.1371/journal.pone.0252949
M3 - Article
C2 - 34170927
AN - SCOPUS:85108680525
SN - 1932-6203
VL - 16
JO - PLoS ONE
JF - PLoS ONE
IS - 6 June
M1 - e0252949
ER -