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Longitudinal Assessment of Diagnostic Test Performance Over the Course of Acute SARS-CoV-2 Infection
Author(s) -
Rebecca L. Smith,
Laura Gibson,
Pamela P. Martinez,
Ruian Ke,
Agha Zeeshan Mirza,
Madison Conte,
Nicholas Gallagher,
Abigail Conte,
Leyi Wang,
Richard Fredrickson,
Darci C. Edmonson,
Melinda E. Baughman,
Karen Chiu,
Hannah Choi,
Tor Jensen,
Kevin R. Scardina,
Shan Bradley,
Stacy L Gloss,
Crystal Reinhart,
Jagadeesh Yedetore,
Alyssa N. Owens,
John Broach,
Bruce Barton,
Péter Lázár,
Darcy Henness,
Todd Young,
Alastair Dunnett,
Matthew L. Robinson,
Heba H. Mostafa,
Andrew Pekosz,
Yukari C. Manabe,
William Heetderks,
David D. McManus,
Christopher B. Brooke
Publication year - 2021
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1093/infdis/jiab337
Subject(s) - viral culture , virology , immunoassay , covid-19 , antigen , viral shedding , medicine , saliva , transmission (telecommunications) , incubation period , virus , real time polymerase chain reaction , reverse transcription polymerase chain reaction , biology , immunology , coronavirus , antibody , infectious disease (medical specialty) , disease , incubation , biochemistry , messenger rna , gene , electrical engineering , engineering
Background Serial screening is critical for restricting spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by facilitating timely identification of infected individuals to interrupt transmission. Variation in sensitivity of different diagnostic tests at different stages of infection has not been well documented. Methods In a longitudinal study of 43 adults newly infected with SARS-CoV-2, all provided daily saliva and nasal swabs for quantitative reverse transcription polymerase chain reaction (RT-qPCR), Quidel SARS Sofia antigen fluorescent immunoassay (FIA), and live virus culture. Results Both RT-qPCR and Quidel SARS Sofia antigen FIA peaked in sensitivity during the period in which live virus was detected in nasal swabs, but sensitivity of RT-qPCR tests rose more rapidly prior to this period. We also found that serial testing multiple times per week increases the sensitivity of antigen tests. Conclusions RT-qPCR tests are more effective than antigen tests at identifying infected individuals prior to or early during the infectious period and thus for minimizing forward transmission (given timely results reporting). All tests showed >98% sensitivity for identifying infected individuals if used at least every 3 days. Daily screening using antigen tests can achieve approximately 90% sensitivity for identifying infected individuals while they are viral culture positive.

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