Coronavirus and Herpes simplex virus type 1 stability in surgical masks and gowns
Bioquímica y Patología Clínica (ByPC)
pdf (Spanish)

Keywords

viral infectivity
coronavirus
surgical masks
gown

How to Cite

Coronavirus and Herpes simplex virus type 1 stability in surgical masks and gowns. (2022). Biochemistry and Clinical Pathology Journal, 86(3), 39-44. https://doi.org/10.62073/bypc.v86i3.228

Abstract

Introduction. During the current COVID-19 pandemic, many controversies and questions have arisen regarding the persistence of viral activity on different surfaces. In particular, for the health area, it has been a great challenge to optimize the uses of the personal protective equipment, even more so taking into account the uncertainty about the stability of viral particles on different surfaces. Objectives. To analyze viral stability in surgical masks and disposable gowns. Materials and methods. Commercial three-layer surgical masks and gowns approved by the Argentine Agency of Medicines, Food and Medical Technology (ANMAT) were artificially inoculated with defined amounts of herpes simplex virus type I (HSV-1) and bovine coronavirus (BCoV) under strictly established environmental conditions, or exposed to COVID-positive patients. Then, residual or remnant viral infectivity was evaluated using the PFU technique and by the appearance of cytopathic effects in cell cultures infected with residual virus. Results. The inactivation time was dependent on the initial infective dose.
For the maximum doses studied, the artificially inoculated viruses remained viable for up to 72 hours. However, in the gowns exposed to COVID-positive patients, no viral activity was recovered after 4 h. Conclusions. Under the same environmental conditions, the viral inactivation time depends on the initial infective dose. The higher the infective dose, the longer it will take for the inoculum to become inactivated. With doses higher than those  naturally expected, the inactivation time of viral activity is 72 hours.

pdf (Spanish)

References

Boone SA, Gerba CP. Significance of Fomites in the Spread of Respiratory and Enteric Viral Disease. Appl. Environ. Microbiol. 2007; 73: 1687–1696.

Killingley B, Nguyen-Van-Tam J. Routes of Influenza Transmission. Influ. Other Respir. Viruses 2013;7: 42–51.

Otter JA, Yezli S, Salkeld JA, French GL. Evidence That Contaminated Surfaces Contribute to the Transmission of Hospital Pathogens and an Overview of Strategies to Address Contaminated Surfaces in Hospital Settings. Am. J. Infect. Control 2013; 41: S6–S11.

Fernstrom A, Goldblatt M. Aerobiology and Its Role in the Transmission of Infectious Diseases. J. Pathog. 2013; 1–13.

Boone SA, Gerba CP. Significance of Fomites in the Spread of Respiratory and Enteric Viral Disease. Appl. Environ. Microbiol. 2007; 73:1687-96.

World Health Organization (WHO) Shortage of personal protective equipment endangering health workers worldwide [WWW Document]. URL 2020.

Ayala-Peña V, Santillán G, Scolaro L. Experimental in vitro infection of rat osteoblasts with measles virus stimulates osteogenic differentiation. Biochem. Biophys. Res. Commun. 2014; 451: 609–614.

Kasloff SB, Strong JE, Funk D, Cutts TA. Stability of SARS-CoV-2 on Critical Personal Protective Equipment. medRxiv. 2020;11:984.

Warnes SL, Little ZR, Keevil CW. Human Coronavirus 229E Remains Infectious on Common Touch Surface Materials. MBio. 2015; 10:6:e01697-15.

Morens DM, Halstead SB, Repik PM, Putvatana R, Raybourne N. Simplified plaque reduction neutralization assay for dengue viruses by semimicro methods in BHK-21 cells: comparison of the BHK suspension test with standard plaque reduction neutralization. J Clin Microbiol. 1985; 22:250-4.

Knipe DM, Howley PM. Fields Virology. 5th Edición. Holanda, Lippincott Williams & Wilkins. 2006.

Atkinson B, Petersen, E. SARS-CoV-2 Shedding and Infectivity. Lancet 2020; 395: 1339–1340.

Córdoba‑Lanús E, García‑Pérez O, Cazorla‑Rivero S, Rodríguez‑Esparragón F, Piñero JE, Clavo B, y col., Persistence of SARS‑CoV‑2 infection on personal protective equipment (PPE). BMC Infect Dis. 2021;19:21,1169.

Shahi AK, Ahmed-Saeed N, Taylor I, Kiernan S, Mahobia N, Pelosi E, Saeed K. Environmental contamination and personal protective equipment contamination with SARS-CoV-2 virus in a real-life clinical setting. J Infect Prev. 2022;23:7-10.

Xue X,Ball JK, Alexander C, Morgan RA. All Surfaces Are Not Equal in Contact Transmission of SARS-CoV-2. Matter 2020; 3:1433-1441.

Colaneri M, Seminari E, Piralla A, Zuccaro V, Di Filippo F, Baldanti,R, y col. Lack of SARS-CoV-2 RNA environmental contamination in a tertiary referral hospital for infectious diseases in Northern Italy. J Hosp Infect 2020; 105: 474–76. 5

Colaneri M, Seminari E, Novati S, Asperges E, Biscarini S, Piralla E, y col. Severe acute respiratory syndrome coronavirus 2 RNA contamination of inanimate surfaces and virus viability in a health care emergency unit. Clin Microbiol Infect. 2020; 26: 1094.e1–e5.

Haddow AD, Watt T, Bloomfield H, Fetterer DP, Harbourt DE. Modeling the Stability of SARS-CoV-2 on Personal Protective Equipment (PPE). Am J Trop Med Hyg. 2020;104:549-551.

Goldman E. Exaggerated risk of transmission of COVID-19 by fomites. Lancet Infect Dis. 2020;20:892-893 20. Mondelli MU, Colaneri M, Seminari EM, Baldanti F, Brunob R. Low risk of SARS-CoV-2 transmission by fomites in real-life conditions. Lancet Infect Dis. 2021; 21: e112.

Weissman DN, de Perio MA, Radonovich LJ. COVID-19 and risks posed to personnel during endotracheal intubation. JAMA 2020; 323: 2027–2028.

Lindsley WG, Blachere FM, Thewlis RE, Vishnu A, Davis KA, Cao K, Palmer J, Clark K, Fisher MA, Kakoo R, Beezhold DH. Measurements of airborne influenza virus in aerosol particles from human coughs. PLoS One 2010; 5: e15100.

Brady MT, Evans J, Cuartas J. Survival and disinfection of parainfluenza viruses on environmental surfaces. Am. J. Infect.1990;18:18–23.

Eccles, R. Respiratory Mucus and Persistence of Virus on Surfaces. J. Hosp. Infect. 2020; 105: 350.