期刊
JOURNAL OF CLINICAL VIROLOGY
卷 162, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.jcv.2023.105426
关键词
SARS-CoV-2; Sequencing; COVID-19; Rapid test; RT-PCR
类别
The widespread use of over-the-counter rapid diagnostic tests for SARS-CoV-2 has resulted in a shortage of clinical samples for viral genomic surveillance. In this study, we assessed the RNA isolated from BinaxNOW swabs stored at room temperature for SARS-CoV-2 rRT-PCR and complete viral genome sequencing. Out of 103 samples, 81 (78.6%) yielded detectable RNA, and out of 57 samples, 46 (80.7%) produced complete genome sequences. Our findings demonstrate that SARS-CoV-2 RNA extracted from used Binax test swabs presents an important opportunity for enhancing SARS-CoV-2 genomic surveillance, investigating transmission clusters, and monitoring within-host evolution.
Widespread use of over-the-counter rapid diagnostic tests for SARS-CoV-2 has led to a decrease in availability of clinical samples for viral genomic surveillance. As an alternative sample source, we evaluated RNA isolated from BinaxNOW swabs stored at ambient temperature for SARS-CoV-2 rRT-PCR and full viral genome sequencing. 81 of 103 samples (78.6%) yielded detectable RNA, and 46 of 57 samples (80.7 %) yielded complete genome se-quences. Our results illustrate that SARS-CoV-2 RNA extracted from used Binax test swabs provides an important opportunity for improving SARS-CoV-2 genomic surveillance, evaluating transmission clusters, and monitoring within-patient evolution.
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