期刊
CLINICAL INFECTIOUS DISEASES
卷 74, 期 10, 页码 1722-1728出版社
OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciab691
关键词
severe acute respiratory syndrome coronavirus 2; SARS-CoV-2; aerosol transmission; airborne transmission; COVID-19
资金
- Singapore National Medical Research Council [MOH-000443, NMRC/CG/M009/2017 NUH/NUHS]
- National University of Singapore (NUS)
The study found that fine aerosols generated during talking and singing contain more SARS-CoV-2 copies than coarse aerosols, potentially playing a key role in virus transmission. Patients in earlier stages of illness were more likely to emit detectable RNA, highlighting the importance of addressing fine aerosol exposure, especially in indoor settings. Challenges remain in isolating viable SARS-CoV-2 from respiratory aerosol samples, prompting the need for larger-scale studies on emerging variants.
We sampled respiratory aerosols emitted by COVID-19 patients and discovered that fine aerosols (<= 5 mu m) generated during talking and singing contain more SARS-CoV-2 copies than coarse aerosols (>5 mu m) and may play a significant role in the transmission of SARS-CoV-2. Background Multiple severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) superspreading events suggest that aerosols play an important role in driving the coronavirus disease 2019 (COVID-19) pandemic. To better understand how airborne SARS-CoV-2 transmission occurs, we sought to determine viral loads within coarse (>5 mu m) and fine (<= 5 mu m) respiratory aerosols produced when breathing, talking, and singing. Methods Using a G-II exhaled breath collector, we measured viral RNA in coarse and fine respiratory aerosols emitted by COVID-19 patients during 30 minutes of breathing, 15 minutes of talking, and 15 minutes of singing. Results Thirteen participants (59%) emitted detectable levels of SARS-CoV-2 RNA in respiratory aerosols, including 3 asymptomatic and 1 presymptomatic patient. Viral loads ranged from 63-5821 N gene copies per expiratory activity per participant, with high person-to-person variation. Patients earlier in illness were more likely to emit detectable RNA. Two participants, sampled on day 3 of illness, accounted for 52% of total viral load. Overall, 94% of SARS-CoV-2 RNA copies were emitted by talking and singing. Interestingly, 7 participants emitted more virus from talking than singing. Overall, fine aerosols constituted 85% of the viral load detected in our study. Virus cultures were negative. Conclusions Fine aerosols produced by talking and singing contain more SARS-CoV-2 copies than coarse aerosols and may play a significant role in SARS-CoV-2 transmission. Exposure to fine aerosols, especially indoors, should be mitigated. Isolating viable SARS-CoV-2 from respiratory aerosol samples remains challenging; whether this can be more easily accomplished for emerging SARS-CoV-2 variants is an urgent enquiry necessitating larger-scale studies.
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