Collection of SARS-CoV-2 Virus from the Air of a Clinic within a University Student Health Care Center and Analyses of the Viral Genomic Sequence
The progression of COVID-19 worldwide can be tracked by identifying mutations within the genomic sequence of SARS-CoV-2 that occur as a function of time. Such efforts currently rely on sequencing the genome of SARS-CoV-2 in patient specimens (direct sequencing) or of virus isolated from patient spec...
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Published in | Aerosol and air quality research Vol. 20; no. 6; pp. 1167 - 1171 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cham
Springer International Publishing
01.06.2020
Taiwan Association of Aerosol Research Springer |
Subjects | |
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Abstract | The progression of COVID-19 worldwide can be tracked by identifying mutations within the genomic sequence of SARS-CoV-2 that occur as a function of time. Such efforts currently rely on sequencing the genome of SARS-CoV-2 in patient specimens (direct sequencing) or of virus isolated from patient specimens in cell cultures. A pilot SARS-CoV-2 air sampling study conducted at a clinic within a university student health care center detected the virus vRNA, with an estimated concentration of 0.87 virus genomes L
−1
air. To determine whether the virus detected was viable (‘live’), attempts were made to isolate the virus in cell cultures. Virus-induced cytopathic effects (CPE) were observed within two days post-inoculation of Vero E6 cells with collection media from air samples; however, rtRT-PCR tests for SARS-CoV-2 vRNA from cell culture were negative. Instead, three other fast-growing human respiratory viruses were isolated and subsequently identified, illustrating the challenge in isolating SARS-CoV-2 when multiple viruses are present in a test sample. The complete SAR-CoV-2 genomic sequence was nevertheless determined by Sanger sequencing and most closely resembles SARS-CoV-2 genomes previously described in Georgia, USA. Results of this study illustrate the feasibility of tracking progression of the COVID-19 pandemic using environmental aerosol samples instead of human specimens. Collection of a positive sample from a distance more than 2 m away from the nearest patient traffic implies the virus was in an aerosol. |
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AbstractList | The progression of COVID-19 worldwide can be tracked by identifying mutations within the genomic sequence of SARS-CoV-2 that occur as a function of time. Such efforts currently rely on sequencing the genome of SARS-CoV-2 in patient specimens (direct sequencing) or of virus isolated from patient specimens in cell cultures. A pilot SARS-CoV-2 air sampling study conducted at a clinic within a university student health care center detected the virus vRNA, with an estimated concentration of 0.87 virus genomes L
−1
air. To determine whether the virus detected was viable (‘live’), attempts were made to isolate the virus in cell cultures. Virus-induced cytopathic effects (CPE) were observed within two days post-inoculation of Vero E6 cells with collection media from air samples; however, rtRT-PCR tests for SARS-CoV-2 vRNA from cell culture were negative. Instead, three other fast-growing human respiratory viruses were isolated and subsequently identified, illustrating the challenge in isolating SARS-CoV-2 when multiple viruses are present in a test sample. The complete SAR-CoV-2 genomic sequence was nevertheless determined by Sanger sequencing and most closely resembles SARS-CoV-2 genomes previously described in Georgia, USA. Results of this study illustrate the feasibility of tracking progression of the COVID-19 pandemic using environmental aerosol samples instead of human specimens. Collection of a positive sample from a distance more than 2 m away from the nearest patient traffic implies the virus was in an aerosol. Abstract The progression of COVID-19 worldwide can be tracked by identifying mutations within the genomic sequence of SARS-CoV-2 that occur as a function of time. Such efforts currently rely on sequencing the genome of SARS-CoV-2 in patient specimens (direct sequencing) or of virus isolated from patient specimens in cell cultures. A pilot SARS-CoV-2 air sampling study conducted at a clinic within a university student health care center detected the virus vRNA, with an estimated concentration of 0.87 virus genomes L−1 air. To determine whether the virus detected was viable (‘live’), attempts were made to isolate the virus in cell cultures. Virus-induced cytopathic effects (CPE) were observed within two days post-inoculation of Vero E6 cells with collection media from air samples; however, rtRT-PCR tests for SARS-CoV-2 vRNA from cell culture were negative. Instead, three other fast-growing human respiratory viruses were isolated and subsequently identified, illustrating the challenge in isolating SARS-CoV-2 when multiple viruses are present in a test sample. The complete SAR-CoV-2 genomic sequence was nevertheless determined by Sanger sequencing and most closely resembles SARS-CoV-2 genomes previously described in Georgia, USA. Results of this study illustrate the feasibility of tracking progression of the COVID-19 pandemic using environmental aerosol samples instead of human specimens. Collection of a positive sample from a distance more than 2 m away from the nearest patient traffic implies the virus was in an aerosol. The progression of COVID-19 worldwide can be tracked by identifying mutations within the genomic sequence of SARS-CoV-2 that occur as a function of time. Such efforts currently rely on sequencing the genome of SARS-CoV-2 in patient specimens (direct sequencing) or of virus isolated from patient specimens in cell cultures. A pilot SARS-CoV-2 air sampling study conducted at a clinic within a university student health care center detected the virus vRNA, with an estimated concentration of 0.87 virus genomes L–1 air. To determine whether the virus detected was viable (‘live’), attempts were made to isolate the virus in cell cultures. Virus-induced cytopathic effects (CPE) were observed within two days post-inoculation of Vero E6 cells with collection media from air samples; however, rtRT-PCR tests for SARS-CoV-2 vRNA from cell culture were negative. Instead, three other fast-growing human respiratory viruses were isolated and subsequently identified, illustrating the challenge in isolating SARS-CoV-2 when multiple viruses are present in a test sample. The complete SAR-CoV-2 genomic sequence was nevertheless determined by Sanger sequencing and most closely resembles SARS-CoV-2 genomes previously described in Georgia, USA. Results of this study illustrate the feasibility of tracking progression of the COVID-19 pandemic using environmental aerosol samples instead of human specimens. Collection of a positive sample from a distance more than 2 m away from the nearest patient traffic implies the virus was in an aerosol. |
Author | Mavian, Carla N. Elbadry, Maha A. Alam, Md. Mahbubul Lednicky, John A. Morris, J. Glenn Salemi, Marco Gibson, Julia C. Shankar, Sripriya N. Stephenson, Caroline J. Eiguren-Fernandez, Arantzazu Wu, Chang-Yu Clugston, James R. |
Author_xml | – sequence: 1 givenname: John A. surname: Lednicky fullname: Lednicky, John A. organization: Department of Environmental and Global Health, University of Florida, Emerging Pathogens Institute, University of Florida – sequence: 2 givenname: Sripriya N. surname: Shankar fullname: Shankar, Sripriya N. organization: Department of Environmental Engineering Sciences, University of Florida – sequence: 3 givenname: Maha A. surname: Elbadry fullname: Elbadry, Maha A. organization: Department of Environmental and Global Health, University of Florida, Emerging Pathogens Institute, University of Florida – sequence: 4 givenname: Julia C. surname: Gibson fullname: Gibson, Julia C. organization: Department of Environmental and Global Health, University of Florida, Emerging Pathogens Institute, University of Florida – sequence: 5 givenname: Md. Mahbubul surname: Alam fullname: Alam, Md. Mahbubul organization: Department of Environmental and Global Health, University of Florida, Emerging Pathogens Institute, University of Florida – sequence: 6 givenname: Caroline J. surname: Stephenson fullname: Stephenson, Caroline J. organization: Department of Environmental and Global Health, University of Florida, Emerging Pathogens Institute, University of Florida – sequence: 7 givenname: Arantzazu surname: Eiguren-Fernandez fullname: Eiguren-Fernandez, Arantzazu organization: Aerosol Dynamics Inc – sequence: 8 givenname: J. Glenn surname: Morris fullname: Morris, J. Glenn organization: Emerging Pathogens Institute, University of Florida, College of Medicine, University of Florida – sequence: 9 givenname: Carla N. surname: Mavian fullname: Mavian, Carla N. organization: Emerging Pathogens Institute, University of Florida, Department of Pathology, Immunology, and Laboratory Medicine, College of Medicine, University of Florida – sequence: 10 givenname: Marco surname: Salemi fullname: Salemi, Marco organization: Emerging Pathogens Institute, University of Florida, Department of Pathology, Immunology, and Laboratory Medicine, College of Medicine, University of Florida – sequence: 11 givenname: James R. surname: Clugston fullname: Clugston, James R. organization: Student Health Care Center, University of Florida, Department of Community Health and Family Medicine, University of Florida – sequence: 12 givenname: Chang-Yu surname: Wu fullname: Wu, Chang-Yu email: cywu@ufl.edu organization: Department of Environmental Engineering Sciences, University of Florida |
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SubjectTerms | Aerosol Aerosols Air sampling Cell culture Collection Coronaviruses COVID-19 Feasibility studies Gene sequencing Genomes Genomics Health care Impacts and Mitigation (II) Inoculation Masks Mutation Pandemics Patients Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Special Issue on COVID-19 Aerosol Drivers Students Viral diseases Viruses |
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Title | Collection of SARS-CoV-2 Virus from the Air of a Clinic within a University Student Health Care Center and Analyses of the Viral Genomic Sequence |
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