SARS-CoV-2 RNA Detection on Environmental Surfaces in a University Setting of Central Italy

Int J Environ Res Public Health. 2022 May 3;19(9):5560. doi: 10.3390/ijerph19095560.

Abstract

The transmission of SARS-CoV-2 occurs through direct contact (person to person) and indirect contact by means of objects and surfaces contaminated by secretions from individuals with COVID-19 or asymptomatic carriers. In this study, we evaluated the presence of SARS-CoV-2 RNA on surfaces made of different materials located in university environments frequented by students and staff involved in academy activity during the fourth pandemic wave (December 2021). A total of 189 environmental samples were collected from classrooms, the library, computer room, gym and common areas and subjected to real-time PCR assay to evaluate the presence of SARS-CoV-2 RNA by amplification of the RNA-dependent RNA polymerase (RdRp) gene. All samples gave a valid result for Internal Process Control and nine (4.8%) tested very low positive for SARS-CoV-2 RNA amplification with a median Ct value of 39.44 [IQR: 37.31-42.66] (≤1 copy of viral genome). Our results show that, despite the prevention measures implemented, the presence of infected subjects cannot be excluded, as evidenced by the recovery of SARS-CoV-2 RNA from surfaces. The monitoring of environmental SARS-CoV-2 RNA could support public health prevention strategies in the academic and school world.

Keywords: SARS-CoV-2 RNA; environmental surfaces; high-touch surface; real-time RT-PCR multiplex assay; university setting.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • COVID-19* / epidemiology
  • Humans
  • Pandemics
  • RNA, Viral / genetics
  • SARS-CoV-2* / genetics
  • Universities

Substances

  • RNA, Viral

Grants and funding

This research was partially funded by DISB—Hygiene section, Ricerca FanoAteneo, and Fondi d’Ateneo Covid Lab.