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SARS-CoV-2 infection and transmission via the skin to oro-nasal route with the production of bioaerosols in the ferret model

  • Rebecca Shipley
  • , Amanda H. Seekings*
  • , Alexander M.P. Byrne
  • , Shweta Shukla
  • , Joe James
  • , Hooman Goharriz
  • , Fabian Z.X. Lean
  • , Alejandro Núñez
  • , Anthony R. Fooks
  • , Lorraine M. McElhinney
  • , Sharon M. Brookes
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

Direct and indirect transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been attributed to virus survival in droplets, bioaerosols and on fomites including skin and surfaces. Survival of SARS-CoV-2 variants of concern (Alpha, Beta, Gamma, and Delta) on the skin and virus transference following rounds of skin-to-skin contact were assessed on porcine skin as a surrogate for human skin. SARS-CoV-2 variants were detectable on skin by RT-qPCR after 72 h at biologically relevant temperatures (35.2 °C) with viral RNA (vRNA) detected after ten successive skin-to-skin contacts. Skin-to-skin virus transmission to establish infection in ferrets as a model for mild/asymptomatic SARS-CoV-2 infection in mustelids and humans was also investigated and compared to intranasal ferret inoculation. Naïve ferrets exposed to Delta variant SARS-CoV-2 in a ‘wet’ or ‘dry’ form on porcine skin resulted in robust infection with shedding detectable for up to 14 days post-exposure, at comparable viral loads to ferrets inoculated intranasally. Transmission of SARS-CoV-2 to naïve ferrets in direct contact with infected ferrets was achieved, with environmental contamination detected from ferret fur swabs and air samples. Genetic substitutions were identified in bioaerosol samples acquired following single contact passage in ferrets, including Spike, ORF1ab, and ORF3a protein sequences, suggesting a utility for monitoring host adaptation and virus evolution via air sampling. The longevity of SARS-CoV-2 variants survival directly on the skin and skin-to-skin transference, enabling subsequent infection via the skin to oro-nasal contact route, could represent a pathway for SARS-CoV-2 infection with implications to public and veterinary health. © 2024 Crown copyright

Original languageEnglish
Article number002022
Number of pages15
JournalJournal of General Virology
Volume105
Issue number9
Online published18 Sept 2024
DOIs
Publication statusPublished - 2024
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2024 Crown copyright.

Funding

This work was funded by the Health and Safety Executive as part of the National Core Studies – PROTECT programme. The SARS-CoV-2 research programme at APHA was supported by the Department for Environment, Food and Rural Affairs (Defra) and the devolved governments (Wales and Scotland) via research projects SE0557, SE0558, SE0562 and SE0575. The study was co-funded by OneHealth EJP COVRIN and has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 773830. The SARS-CoV-2 in vitro transcribed RNA used for RNA quantification was acquired by the European Virus Archive Global (EVAG) that has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 871029.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Keywords

  • Alpha
  • Beta
  • bioaerosol
  • Delta
  • ferret
  • Gamma
  • SARS-CoV-2
  • skin transference
  • transmission
  • zoonoses

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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