Abstract

There is little doubt that aerosols play a major role in the transmission of SARS-CoV-2. The significance of the presence and infectivity of this virus on environmental surfaces, especially in a hospital setting, remains less clear. We aimed to analyze surface swabs for SARS-CoV-2 RNA and infectivity, and to determine their suitability for sequence analysis. Samples were collected during two waves of COVID-19 at the University of California, Davis Medical Center, in COVID-19 patient serving and staff congregation areas. qRT-PCR positive samples were investigated in Vero cell cultures for cytopathic effects and phylogenetically assessed by whole genome sequencing. Improved cleaning and patient management practices between April and August 2020 were associated with a substantial reduction of SARS-CoV-2 qRT-PCR positivity (from 11% to 2%) in hospital surface samples. Even though we recovered near-complete genome sequences in some, none of the positive samples (11 of 224 total) caused cytopathic effects in cultured cells suggesting this nucleic acid was either not associated with intact virions, or they were present in insufficient numbers for infectivity. Phylogenetic analysis suggested that the SARS-CoV-2 genomes of the positive samples were derived from hospitalized patients. Genomic sequences isolated from qRT-PCR negative samples indicate a superior sensitivity of viral detection by sequencing. This study confirms the low likelihood that SARS-CoV-2 contamination on hospital surfaces contains infectious virus, disputing the importance of fomites in COVID-19 transmission. Ours is the first report on recovering near-complete SARS-CoV-2 genome sequences directly from environmental surface swabs.

Highlights

  • This study confirms the low likelihood that SARS-CoV-2 contamination on hospital surfaces contains infectious virus, disputing the importance of fomites in COVID-19 transmission

  • Ours is the first report on recovering near-complete SARS-CoV-2 genome sequences directly from environmental surface swabs

  • There is a paucity of data regarding survival and infectivity of the SARS-CoV-2 virus on surfaces in closed environments, some data are available for other coronaviruses [1, 2]

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Summary

Introduction

There is a paucity of data regarding survival and infectivity of the SARS-CoV-2 virus on surfaces in closed environments, some data are available for other coronaviruses [1, 2]. Another study examining survival on PPE showed that the virus decayed rapidly on cotton but survived for up to 21 days on some other surface material [4]. More recent evaluation of a variety of surfaces showed that infectious virions could survive for up to 28 days in laboratory conditions including high titer virus and in the dark [5]. It is unclear in all of these cases how this relates to virus survival and the potential for its transmission outside the laboratory. It is known that SARS-CoV-2 can survive on skin for about nine hours and may allow or extend viral survival on surfaces following contact [7]

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