Abstract

Viral diseases can spread through a variety of routes including aerosols. Yet, limited data are available on the efficacy of aerosolized chemicals to reduce viral loads in the air. Bacteriophages (phages) are often used as surrogates for hazardous viruses in aerosol studies because they are inexpensive, easy to handle, and safe for laboratory workers. Moreover, several of these bacterial viruses display physical characteristics similar to pathogenic human and animal viruses, like morphological size, type of nucleic acids, capsid morphology, and the presence of an envelope. In this study, the efficacy of four chemicals was evaluated on four airborne phages at two different relative humidity levels. Non-tailed bacteriophages MS2 (single-stranded RNA), ϕ6 (double-stranded RNA, enveloped), PR772 (double-stranded DNA), and ϕX174 (single-stranded DNA) were first aerosolized in a 55L rotative environmental chamber at 19°C with 25% and 50% relative humidity. Then, hydrogen peroxide, Eugenol (phenylpropene used in commercial perfumes and flavorings), Mist® (automobile disinfectant containing Triethylene glycol), and Pledge® (multisurface disinfectant containing Isopropanol, n-Alkyl Dimethyl Benzyl Amonium Chlorides, and n-Alkyl Dimethyl Ethylbenzyl Ammonium Chloride) were nebulized with the phages using a separate nebulizer. Aerosols were maintained in suspension during 10 minutes, 1 hour, and 2 hours. Viral aerosols were sampled using an SKC BioSampler and samples were analyzed using qPCR and plaque assays. The resistance levels of the four phages varied depending on the relative humidity (RH) and germicidal products tested. Phage MS2 was the most stable airborne virus under the environmental conditions tested while phage PR772 was the least stable. Pledge® and Eugenol reduced the infectivity of all airborne phages tested. At 25% RH, Pledge® and Eugenol were more effective at reducing infectivity of RNA phages ϕ6 and MS2. At 50% RH, Pledge® was the most effective agent against phage MS2. These findings illustrate that various airborne viruses should be tested to demonstrate the effectiveness of germicidal treatments. This research also provides a set of parameters for testing germicidal products in large-scale settings to reduce the risk of virus transmission.

Highlights

  • Viral diseases can spread through a variety of routes such as direct contact with an infected person or indirect contact with fomites, exposure to large droplets, and inhalation of aerosolized droplets nuclei

  • Tryptic soy broth (TSB) and tryptic soy agar (TSA) culture media were purchased from Difco Laboratory (Detroit, MI)

  • Phage φ6 was grown on its host on TSA soft agar (0.75%) plates as reported elsewhere [27] while phage PR772 was amplified on TSB soft agarose (0.75%) plates [30]

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Summary

Introduction

Viral diseases can spread through a variety of routes such as direct contact with an infected person or indirect contact with fomites, exposure to large droplets, and inhalation of aerosolized droplets nuclei. The latter is of interest as they can stay in the air for an extended period of time and travel long distances. Airborne transmission of viruses has been demonstrated for some diseases, including measles [1] and smallpox [2]. The airborne transmission of other well-known viruses like Influenza virus and Norovirus is still under investigation [3, 4]. Other public or occupational spaces such as day care centers and wastewater treatment plants are suspected to represent occupational hazards with respect to viral diseases [7, 8]

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