Exhaled SARS-CoV-2 quantified by face-mask sampling in hospitalised patients with COVID-19

•We present a novel method to detect SARS-CoV-2 in exhaled breath using sampling strips fixed within facemasks that can be readily removed and analysed using RT-qPCR (face-mask sampling, FMS).•In 66 hospitalised patients 38% were FMS positive within 24 h of a routinely positive SARS-CoV-2 PCR by nas...

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Veröffentlicht in:The Journal of infection 2021-06, Vol.82 (6), p.253-259
Hauptverfasser: Williams, Caroline M., Pan, Daniel, Decker, Jonathan, Wisniewska, Anika, Fletcher, Eve, Sze, Shirley, Assadi, Sara, Haigh, Richard, Abdulwhhab, Mohamad, Bird, Paul, Holmes, Christopher W, Al-Taie, Alaa, Saleem, Baber, Pan, Jingzhe, Garton, Natalie J, Pareek, Manish, Barer, Michael R
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Sprache:eng
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Zusammenfassung:•We present a novel method to detect SARS-CoV-2 in exhaled breath using sampling strips fixed within facemasks that can be readily removed and analysed using RT-qPCR (face-mask sampling, FMS).•In 66 hospitalised patients 38% were FMS positive within 24 h of a routinely positive SARS-CoV-2 PCR by nasopharyngeal swab.•Higher FMS viral loads were associated with higher ISARIC deterioration and mortality scores, respiratory symptoms at time of sampling and shorter intervals between symptom onset and sampling. Human to human transmission of SARS-CoV-2 is driven by the respiratory route but little is known about the pattern and quantity of virus output from exhaled breath. We have previously shown that face-mask sampling (FMS) can detect exhaled tubercle bacilli and have adapted its use to quantify exhaled SARS-CoV-2 RNA in patients admitted to hospital with Coronavirus Disease-2019 (COVID-19). Between May and December 2020, we took two concomitant FMS and nasopharyngeal samples (NPS) over two days, starting within 24 h of a routine virus positive NPS in patients hospitalised with COVID-19, at University Hospitals of Leicester NHS Trust, UK. Participants were asked to wear a modified duckbilled facemask for 30 min, followed by a nasopharyngeal swab. Demographic, clinical, and radiological data, as well as International Severe Acute Respiratory and emerging Infections Consortium (ISARIC) mortality and deterioration scores were obtained. Exposed masks were processed by removal, dissolution and analysis of sampling matrix strips fixed within the mask by RT-qPCR. Viral genome copy numbers were determined and results classified as Negative; Low: ≤999 copies; Medium: 1000–99,999 copies and High ≥ 100,000 copies per strip for FMS or per 100 µl for NPS. 102 FMS and NPS were collected from 66 routinely positive patients; median age: 61 (IQR 49 - 77), of which FMS was positive in 38% of individuals and concomitant NPS was positive in 50%. Positive FMS viral loads varied over five orders of magnitude (
ISSN:0163-4453
1532-2742
DOI:10.1016/j.jinf.2021.03.018