We used a Sioutas personal cascade impactor sampler (PCIS) to screen for SARS-CoV-2 in a car driven by a COVID-19 patient. SARS-CoV-2 was detectable at all PCIS stages by PCR and was cultured from the section of the sampler collecting particles in the 0.25 to 0.50 □μm size range.

While we have learned a great deal about transmission of SARS-CoV-2 since the beginning of the current pandemic, questions remain about the exposure risk in different settings, and the contribution of various modes of transmission to virus spread.1 In particular, there is continuing uncertainty about the relative contribution of larger virus-laden respiratory particles at close distances, compared with virions in aerosols at close or longer ranges, to spread of the virus. There are now multiple epidemiology studies consistent with aerosol spread of SARS-CoV-2 within closed spaces,2,3 and the virus has been shown to remain infective in laboratory-generated aerosols for at least 16 hours.4 Data from our group and others have documented the presence of the virus in aerosols in patient settings by RT-PCR.5–7 However, molecular detection of SARS-CoV-2 RNA does not necessarily correlate with risk of developing COVID-19, since only viable virions can cause disease. Subsequently, we have reported isolation of viable SARS-CoV-2 from the air within the room of hospitalized COVID-19 patients.8

Credit: Trinks’ Images


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