Although the unprecedented efforts the world has been taking to control the spread of the human coronavirus disease (COVID‐19) and its causative aetiology [severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2)], the number of confirmed cases has been increasing drastically. Therefore, there is an urgent need for devising more efficient preventive measures, to limit the spread of the infection until an effective treatment or vaccine is available. The preventive measures depend mainly on the understanding of the transmission routes of this virus, its environmental stability, and its persistence on common touch surfaces. Due to the very limited knowledge about SARS‐CoV‐2, we can speculate its stability in the light of previous studies conducted on other human and animal coronaviruses. In this review, we present the available data on the stability of coronaviruses (CoVs), including SARS‐CoV‐2, from previous reports to help understand its environmental survival. According to available data, possible airborne transmission of SARS‐CoV‐2 has been suggested. SARS‐CoV‐2 and other human and animal CoVs have remarkably short persistence on copper, latex and surfaces with low porosity as compared to other surfaces like stainless steel, plastics, glass and highly porous fabrics. It has also been reported that SARS‐CoV‐2 is associated with diarrhoea and that it is shed in the faeces of COVID‐19 patients. Some CoVs show persistence in human excrement, sewage and waters for a few days. These findings suggest a possible risk of faecal–oral, foodborne and waterborne transmission of SARS‐CoV‐2 in developing countries that often use sewage‐polluted waters in irrigation and have poor water treatment systems. CoVs survive longer in the environment at lower temperatures and lower relative humidity. It has been suggested that large numbers of COVID‐19 cases are associated with cold and dry climates in temperate regions of the world and that seasonality of the virus spread is suspected.

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Minimal food-processing methods are not effective against foodborne viruses, such as human norovirus (NV). It is important, therefore, to explore novel nonthermal technologies for decontamination of foods eaten fresh, minimally processed and ready-to-eat foods, and food contact surfaces. We studied the in vitro virucidal activity of cold atmospheric gaseous plasma (CGP) against feline calicivirus (FCV), a surrogate of NV. Factors affecting the virucidal activity of CGP (a socalled radio frequency atmospheric pressure plasma jet) were the plasma generation power, the exposure time and distance, the plasma feed gas mixture, and the virus suspension medium. Exposure to 2.5-W argon (Ar) plasma caused a 5.55 log 10 unit reduction in the FCV titer within 120 s. The reduction in the virus titer increased with increasing exposure time and decreasing exposure distance. Of the four plasma gas mixtures studied (Ar, Ar plus 1% O 2 , Ar plus 1% dry air, and Ar plus 0.27% water), Ar plus 1% O 2 plasma treatment had the highest virucidal effect: more than 6.0 log 10 units of the virus after 15 s of exposure. The lowest virus reduction was observed with Ar plus 0.27% water plasma treatment (5 log 10 unit reduction after 120 s). The highest reduction in titer was observed when the virus was suspended in distilled water. Changes in temperature and pH and formation of H 2 O 2 were not responsible for the virucidal effect of plasma. The oxidation of viral capsid proteins by plasma-produced reactive oxygen and nitrogen species in the solution was thought to be responsible for the virucidal effect. In conclusion, CGP exhibits virucidal activity in vitro and has the potential to combat viral contamination in foods and on food preparation surfaces. Foodborne illnesses continue to plague public health, as well as world economies, costing approximately $152 billion in the United States alone (1). Enteric viruses, particularly human norovirus (NV) and hepatitis A virus (HAV), are the leading causes of viral foodborne illnesses (2). Human NV, one of the top five pathogens with respect to the total cost of foodborne illnesses in the United States, belongs to the family Caliciviridae and is a wellknown cause of "winter vomiting disease" or "stomach flu" (3). NV causes 19 to 21 million cases of acute gastroenteritis annually in the United States and leads to 1.7 to 1.9 million outpatient visits, 400,000 emergency room visits, 56,000 to 71,000 hospitalizations, and 570 to 800 deaths, mostly among young children (4). More than half of all foodborne disease outbreaks due to a known cause reported to the CDC from 2006 to 2010 were attributed to NV. In the European Union in 2007, caliciviruses (primarily NV) were responsible for 507 of 675 foodborne viral disease outbreaks (5).Multiple issues related to the quality of thermally processed foods, e.g., nutritional losses and adverse effects on organoleptic quality, have led to the emergence of so-called nonthermal technologies, which consist of preservation treatments that are effective at ambient o...

The use of low‐temperature plasmas for bio‐decontamination and sterilization has been gaining increased attention. In this study, a two‐dimensional array of integrated coaxial microhollow micro‐discharges generated in dry air at atmospheric pressure is used to treat metal surfaces (gas‐phase) and solution (liquid‐phase) contaminated with a known concentration of feline calicivirus (FCV). FCV acts as a surrogate for human norovirus, which is responsible for causing outbreaks of acute gastroenteritis in humans. The decontamination efficacy as well as the primary chemical pathways leading to virus inactivation in both the treatments are studied and compared. It is found that the humidity of the bio‐sample for gas‐phase treatment in dry air is required to achieve >5 log10 reduction in FCV titer within 3 min. The gas‐phase FCV inactivation is found to be due to a combination of ozone (O3) and reactive nitrogen species (RNS), most likely NOx. The liquid‐phase FCV inactivation mechanism is pH‐dependent and is primarily due to RNS, most likely acidified nitrites. O3 has a negligible effect on FCV suspended in solution. Previous studies performed in a batch reactor have shown that the inactivation pathways through O3 and RNS are mutually exclusive due to ozone poisoning at high NxOy concentrations. The present study employs a flow‐through system which avoids accumulation of reactive species and allows for the coexistence of NOx and O3 for the gas residence times used in this study, giving rise to these specific inactivation pathways.

Control technologies to inactivate airborne viruses effectively are needed during the ongoing SARS-CoV-2 pandemic, and to guard against airborne transmitted diseases. We demonstrate that sealed UV–C flow reactors operating with fluences near 253 ± 1 nm of 13.9–49.6 mJ cm –2 efficiently inactivate coronaviruses in an aerosol. For measurements, porcine respiratory coronavirus (PRCV) was nebulized in a custom-built, 3.86 m wind tunnel housed in a biosafety level class II facility. The single pass log 10 reduction of active coronavirus was in excess of 2.2 at a flow rate of 2439 L min –1 (13.9 mJ cm –2 ) and in excess of 3.7 (99.98% removal efficiency) at 684 L min –1 (49.6 mJ cm –2 ). Because virus titers resulting from sampling downstream of the UV–C reactor were below the limit of detection, the true log reduction is likely even higher than measured. Comparison of virus titration results to reverse transcriptase quantitative PCR and measurement of fluorescein concentrations (doped into the nebulized aerosol) reveals that the reduction in viable PRCV is primarily due to UV–C based inactivation, as opposed to physical collection of virus. The results confirm that UV–C flow reactors can efficiently inactivate coronaviruses through incorporation into HVAC ducts or recirculating air purifiers.

Possible mechanisms that lead to inactivation of feline calicivirus (FCV) by cold atmospheric-pressure plasma (CAP) generated in 99% argon-1% O2 admixture were studied. We evaluated the impact of CAP exposure on the FCV viral capsid protein and RNA employing several cultural, molecular, proteomic and morphologic characteristics techniques. In the case of long exposure (2 min) to CAP, the reactive species of CAP strongly oxidized the major domains of the viral capsid protein (VP1) leading to disintegration of a majority of viral capsids. In the case of short exposure (15 s), some of the virus particles retained their capsid structure undamaged but failed to infect the host cells in vitro. In the latter virus particles, CAP exposure led to the oxidation of specific amino acids located in functional peptide residues in the P2 subdomain of the protrusion (P) domain, the dimeric interface region of VP1 dimers, and the movable hinge region linking the S and P domains. These regions of the capsid are known to play an essential role in the attachment and entry of the virus to the host cell. These observations suggest that the oxidative effect of CAP species inactivates the virus by hindering virus attachment and entry into the host cell. Furthermore, we found that the oxidative impact of plasma species led to oxidation and damage of viral RNA once it becomes unpacked due to capsid destruction. The latter effect most likely plays a secondary role in virus inactivation since the intact FCV genome is infectious even after damage to the capsid.

Cold atmospheric pressure plasma has potential as a non-thermal processing technology to decontaminate food and food contact surfaces due to its ability to generate an abundance of reactive oxygen and nitrogen species with antimicrobial attributes at ambient conditions. In this study, we present a comparison on the effectiveness of surface decontamination against feline calicivirus (FCV) and Salmonella spp using four different plasma sources, a dielectric barrier discharge (DBD) in direct contact with the substrate and three remote plasma treatment sources: a 2D DBD, a volumetric DBD and a gliding arc discharge. The plasma sources were all operated in air at atmospheric pressure. The decontamination efficacy was enhanced by the presence of humidity on the sample surface and only direct contact between plasma and samples allowed the inactivation of pathogens on dry substrates. Across all sources, FCV was seen to be more susceptible to the plasma-generated species than Salmonella spp. The diminished effectiveness of the gliding arc discharge compared to the DBDs operating at the same power is most likely due to the low Henry’s law constant of NO, the dominant reactive species generated by the gliding arc. Control experiments illustrate that the co-existence of O3 and NO2, as in the afterglow of the remote DBDs enhances the inactivation compared to the inactivation by O3 or NO2 only. A chemical kinetics model of the plasma effluent and the plasma treatments show a strong correlation between the gas-phase concentration of N2O5 and inactivation of the virus. We experimentally show that the production of N2O5 coincides with the enhanced generation of reactive nitrogen species in the liquid phase.