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Sponge Whirl-Pak Sampling Method and Droplet Digital RT-PCR Assay for Monitoring of SARS-CoV-2 on Surfaces in Public and Working Environments
The SARS-CoV-2 can spread directly via saliva, respiratory aerosols and droplets, and indirectly by contact through contaminated objects and/or surfaces and by air. In the context of COVID-19 fomites can be an important vehicle of virus transmission and contribute to infection risk in public environ...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9141805/ https://www.ncbi.nlm.nih.gov/pubmed/35627397 http://dx.doi.org/10.3390/ijerph19105861 |
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author | Cardinale, Davide Tafuro, Maria Mancusi, Andrea Girardi, Santa Capuano, Federico Proroga, Yolande Thérèse Rose Corrado, Federica D’Auria, Jacopo Luigi Coppola, Annachiara Rofrano, Giuseppe Volzone, Palmiero Galdi, Pio De Vita, Sabato Gallo, Alfonso Suffredini, Elisabetta Pierri, Biancamaria Cerino, Pellegrino Morgante, Maria |
author_facet | Cardinale, Davide Tafuro, Maria Mancusi, Andrea Girardi, Santa Capuano, Federico Proroga, Yolande Thérèse Rose Corrado, Federica D’Auria, Jacopo Luigi Coppola, Annachiara Rofrano, Giuseppe Volzone, Palmiero Galdi, Pio De Vita, Sabato Gallo, Alfonso Suffredini, Elisabetta Pierri, Biancamaria Cerino, Pellegrino Morgante, Maria |
author_sort | Cardinale, Davide |
collection | PubMed |
description | The SARS-CoV-2 can spread directly via saliva, respiratory aerosols and droplets, and indirectly by contact through contaminated objects and/or surfaces and by air. In the context of COVID-19 fomites can be an important vehicle of virus transmission and contribute to infection risk in public environments. The aim of the study was to analyze through surface sampling (sponge method) the presence of SARS-CoV-2 in public and working environments, in order to evaluate the risk for virus transmission. Seventy-seven environmental samples were taken using sterile sponges in 17 animal farms, 4 public transport buses, 1 supermarket and 1 hotel receptive structure. Furthermore, 246 and 93 swab samples were taken in the farms from animals and from workers, respectively. SARS-CoV-2 detection was conducted by real-time RT-PCR and by digital droplet RT-PCR (dd RT-PCR) using RdRp, gene E and gene N as targets. None of the human and animal swab samples were positive for SARS-CoV-2, while detection was achieved in 20 of the 77 sponge samples (26%) using dd RT-PCR. Traces of the RdRp gene, gene E and gene N were found in 17/77 samples (22%, average concentration 31.2 g.c./cm(2), range 5.6 to 132 g.c./cm(2)), 8/77 samples (10%, average concentration 15.1 g.c./cm(2), range 6 to 36 g.c./cm(2)), and in 1/77 (1%, concentration 7.2 g.c./cm(2)). Higher detection rates were associated with sampling in animal farms and on public transport buses (32% and 30%) compared to the supermarket (21%) and the hotel (no detection). The result of the study suggests that the risk of contamination of surfaces with SARS-CoV-2 increases in environments in which sanitation strategies are not suitable and/or in highly frequented locations, such as public transportation. Considering the analytical methods, the dd RT-PCR was the only approach achieving detection of SARS-CoV-2 traces in environmental samples. Thus, dd RT-PCR emerges as a reliable tool for sensitive SARS-CoV-2 detection. |
format | Online Article Text |
id | pubmed-9141805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91418052022-05-28 Sponge Whirl-Pak Sampling Method and Droplet Digital RT-PCR Assay for Monitoring of SARS-CoV-2 on Surfaces in Public and Working Environments Cardinale, Davide Tafuro, Maria Mancusi, Andrea Girardi, Santa Capuano, Federico Proroga, Yolande Thérèse Rose Corrado, Federica D’Auria, Jacopo Luigi Coppola, Annachiara Rofrano, Giuseppe Volzone, Palmiero Galdi, Pio De Vita, Sabato Gallo, Alfonso Suffredini, Elisabetta Pierri, Biancamaria Cerino, Pellegrino Morgante, Maria Int J Environ Res Public Health Article The SARS-CoV-2 can spread directly via saliva, respiratory aerosols and droplets, and indirectly by contact through contaminated objects and/or surfaces and by air. In the context of COVID-19 fomites can be an important vehicle of virus transmission and contribute to infection risk in public environments. The aim of the study was to analyze through surface sampling (sponge method) the presence of SARS-CoV-2 in public and working environments, in order to evaluate the risk for virus transmission. Seventy-seven environmental samples were taken using sterile sponges in 17 animal farms, 4 public transport buses, 1 supermarket and 1 hotel receptive structure. Furthermore, 246 and 93 swab samples were taken in the farms from animals and from workers, respectively. SARS-CoV-2 detection was conducted by real-time RT-PCR and by digital droplet RT-PCR (dd RT-PCR) using RdRp, gene E and gene N as targets. None of the human and animal swab samples were positive for SARS-CoV-2, while detection was achieved in 20 of the 77 sponge samples (26%) using dd RT-PCR. Traces of the RdRp gene, gene E and gene N were found in 17/77 samples (22%, average concentration 31.2 g.c./cm(2), range 5.6 to 132 g.c./cm(2)), 8/77 samples (10%, average concentration 15.1 g.c./cm(2), range 6 to 36 g.c./cm(2)), and in 1/77 (1%, concentration 7.2 g.c./cm(2)). Higher detection rates were associated with sampling in animal farms and on public transport buses (32% and 30%) compared to the supermarket (21%) and the hotel (no detection). The result of the study suggests that the risk of contamination of surfaces with SARS-CoV-2 increases in environments in which sanitation strategies are not suitable and/or in highly frequented locations, such as public transportation. Considering the analytical methods, the dd RT-PCR was the only approach achieving detection of SARS-CoV-2 traces in environmental samples. Thus, dd RT-PCR emerges as a reliable tool for sensitive SARS-CoV-2 detection. MDPI 2022-05-11 /pmc/articles/PMC9141805/ /pubmed/35627397 http://dx.doi.org/10.3390/ijerph19105861 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cardinale, Davide Tafuro, Maria Mancusi, Andrea Girardi, Santa Capuano, Federico Proroga, Yolande Thérèse Rose Corrado, Federica D’Auria, Jacopo Luigi Coppola, Annachiara Rofrano, Giuseppe Volzone, Palmiero Galdi, Pio De Vita, Sabato Gallo, Alfonso Suffredini, Elisabetta Pierri, Biancamaria Cerino, Pellegrino Morgante, Maria Sponge Whirl-Pak Sampling Method and Droplet Digital RT-PCR Assay for Monitoring of SARS-CoV-2 on Surfaces in Public and Working Environments |
title | Sponge Whirl-Pak Sampling Method and Droplet Digital RT-PCR Assay for Monitoring of SARS-CoV-2 on Surfaces in Public and Working Environments |
title_full | Sponge Whirl-Pak Sampling Method and Droplet Digital RT-PCR Assay for Monitoring of SARS-CoV-2 on Surfaces in Public and Working Environments |
title_fullStr | Sponge Whirl-Pak Sampling Method and Droplet Digital RT-PCR Assay for Monitoring of SARS-CoV-2 on Surfaces in Public and Working Environments |
title_full_unstemmed | Sponge Whirl-Pak Sampling Method and Droplet Digital RT-PCR Assay for Monitoring of SARS-CoV-2 on Surfaces in Public and Working Environments |
title_short | Sponge Whirl-Pak Sampling Method and Droplet Digital RT-PCR Assay for Monitoring of SARS-CoV-2 on Surfaces in Public and Working Environments |
title_sort | sponge whirl-pak sampling method and droplet digital rt-pcr assay for monitoring of sars-cov-2 on surfaces in public and working environments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9141805/ https://www.ncbi.nlm.nih.gov/pubmed/35627397 http://dx.doi.org/10.3390/ijerph19105861 |
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