Viral Load of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in Respiratory Aerosols Emitted by Patients With Coronavirus Disease 2019 (COVID-19) While Breathing, Talking, and Singing

© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissionsoup.com..

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 μm) and fine (≤5 μm) 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.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:74

Enthalten in:

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America - 74(2022), 10 vom: 30. Mai, Seite 1722-1728

Sprache:

Englisch

Beteiligte Personen:

Coleman, Kristen K [VerfasserIn]
Tay, Douglas Jie Wen [VerfasserIn]
Tan, Kai Sen [VerfasserIn]
Ong, Sean Wei Xiang [VerfasserIn]
Than, The Son [VerfasserIn]
Koh, Ming Hui [VerfasserIn]
Chin, Yi Qing [VerfasserIn]
Nasir, Haziq [VerfasserIn]
Mak, Tze Minn [VerfasserIn]
Chu, Justin Jang Hann [VerfasserIn]
Milton, Donald K [VerfasserIn]
Chow, Vincent T K [VerfasserIn]
Tambyah, Paul Anantharajah [VerfasserIn]
Chen, Mark [VerfasserIn]
Tham, Kwok Wai [VerfasserIn]

Links:

Volltext

Themen:

Aerosol transmission
Aerosols
Airborne transmission
COVID-19
Journal Article
RNA, Viral
Research Support, Non-U.S. Gov't
SARS-CoV-2
Severe acute respiratory syndrome coronavirus 2

Anmerkungen:

Date Completed 02.06.2022

Date Revised 21.06.2022

published: Print

Citation Status MEDLINE

doi:

10.1093/cid/ciab691

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM329025600