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Simulated Sunlight Rapidly Inactivates SARS-CoV-2 on Surfaces

Abstract

Previous studies have demonstrated that SARS-CoV-2 is stable on surfaces for extended periods under indoor conditions. In the present study, simulated sunlight rapidly inactivated SARS-CoV-2 suspended in either simulated saliva or culture media and dried on stainless steel coupons. Ninety percent of infectious virus was inactivated every 6.8 minutes in simulated saliva and every 14.3 minutes in culture media when exposed to simulated sunlight representative of the summer solstice at 40°N latitude at sea level on a clear day. Significant inactivation also occurred, albeit at a slower rate, under lower simulated sunlight levels. The present study provides the first evidence that sunlight may rapidly inactivate SARS-CoV-2 on surfaces, suggesting that persistence, and subsequently exposure risk, may vary significantly between indoor and outdoor environments. Additionally, these data indicate that natural sunlight may be effective as a disinfectant for contaminated nonporous materials.

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References
1.
Thomas Y, Boquete-Suter P, Koch D, Pittet D, Kaiser L . Survival of influenza virus on human fingers. Clin Microbiol Infect. 2013; 20(1):O58-64. DOI: 10.1111/1469-0691.12324. View

2.
Nelson K, Boehm A, Davies-Colley R, Dodd M, Kohn T, Linden K . Sunlight-mediated inactivation of health-relevant microorganisms in water: a review of mechanisms and modeling approaches. Environ Sci Process Impacts. 2018; 20(8):1089-1122. PMC: 7064263. DOI: 10.1039/c8em00047f. View

3.
Beck S, Rodriguez R, Hawkins M, Hargy T, Larason T, Linden K . Comparison of UV-Induced Inactivation and RNA Damage in MS2 Phage across the Germicidal UV Spectrum. Appl Environ Microbiol. 2015; 82(5):1468-1474. PMC: 4771313. DOI: 10.1128/AEM.02773-15. View

4.
Darnell M, Taylor D . Evaluation of inactivation methods for severe acute respiratory syndrome coronavirus in noncellular blood products. Transfusion. 2006; 46(10):1770-7. PMC: 7201869. DOI: 10.1111/j.1537-2995.2006.00976.x. View

5.
Heimbuch B, Wallace W, Kinney K, Lumley A, Wu C, Woo M . A pandemic influenza preparedness study: use of energetic methods to decontaminate filtering facepiece respirators contaminated with H1N1 aerosols and droplets. Am J Infect Control. 2010; 39(1):e1-9. DOI: 10.1016/j.ajic.2010.07.004. View