Host and viral determinants of airborne transmission of SARS-CoV-2 in the Syrian hamster

Author:

Port Julia R1ORCID,Morris Dylan H2,Riopelle Jade C1,Yinda Claude Kwe1ORCID,Avanzato Victoria A1,Holbrook Myndi G1,Bushmaker Trenton1ORCID,Schulz Jonathan E1,Saturday Taylor A1,Barbian Kent3,Russell Colin A4,Perry-Gottschalk Rose5,Shaia Carl6,Martens Craig3,Lloyd-Smith James O2ORCID,Fischer Robert J1ORCID,Munster Vincent J1ORCID

Affiliation:

1. Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health

2. Department of Ecology and Evolutionary Biology, University of California, Los Angeles

3. Rocky Mountain Research and Technologies Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health

4. Department of Medical Microbiology | Amsterdam University Medical Center, University of Amsterdam

5. Rocky Mountain Visual and Medical Arts Unit, Research Technologies Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health

6. Rocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health

Abstract

It remains poorly understood how SARS-CoV-2 infection influences the physiological host factors important for aerosol transmission. We assessed breathing pattern, exhaled droplets, and infectious virus after infection with Alpha and Delta variants of concern (VOC) in the Syrian hamster. Both VOCs displayed a confined window of detectable airborne virus (24–48 hr), shorter than compared to oropharyngeal swabs. The loss of airborne shedding was linked to airway constriction resulting in a decrease of fine aerosols (1–10 µm) produced, which are suspected to be the major driver of airborne transmission. Male sex was associated with increased viral replication and virus shedding in the air. Next, we compared the transmission efficiency of both variants and found no significant differences. Transmission efficiency varied mostly among donors, 0–100% (including a superspreading event), and aerosol transmission over multiple chain links was representative of natural heterogeneity of exposure dose and downstream viral kinetics. Co-infection with VOCs only occurred when both viruses were shed by the same donor during an increased exposure timeframe (24–48 hr). This highlights that assessment of host and virus factors resulting in a differential exhaled particle profile is critical for understanding airborne transmission.

Funder

National Institutes of Health

Defense Advanced Research Projects Agency

National Science Foundation

National Institute of Allergy and Infectious Diseases

Publisher

eLife Sciences Publications, Ltd

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