A blueprint for the implementation of a validated approach for the detection of SARS-Cov2 in clinical samples in academic facilities

The COVID-19 pandemic is expanding at an unprecedented rate. As a result, diagnostic services are stretched to their limit, and there is a clear need for the provision of additional diagnostic capacity. Academic laboratories, many of which are closed due to governmental lockdowns, may be in a positi...

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Glavni autori: Sridhar, S, Forrest, S, Kean, I, Young, J, Bartholdson Scott, J, Maes, M, Pereira-Dias, J, Parmar, S, Routledge, M, Sparkes, D, Rivett, L, Dougan, G, Weekes, M, Curran, M, Goodfellow, I, Baker, S
Format: Journal article
Jezik:English
Izdano: F1000Research 2020
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author Sridhar, S
Forrest, S
Kean, I
Young, J
Bartholdson Scott, J
Maes, M
Pereira-Dias, J
Parmar, S
Routledge, M
Sparkes, D
Rivett, L
Dougan, G
Weekes, M
Curran, M
Goodfellow, I
Baker, S
author_facet Sridhar, S
Forrest, S
Kean, I
Young, J
Bartholdson Scott, J
Maes, M
Pereira-Dias, J
Parmar, S
Routledge, M
Sparkes, D
Rivett, L
Dougan, G
Weekes, M
Curran, M
Goodfellow, I
Baker, S
author_sort Sridhar, S
collection OXFORD
description The COVID-19 pandemic is expanding at an unprecedented rate. As a result, diagnostic services are stretched to their limit, and there is a clear need for the provision of additional diagnostic capacity. Academic laboratories, many of which are closed due to governmental lockdowns, may be in a position to support local screening capacity by adapting their current laboratory practices. Here, we describe the process of developing a SARS-Cov2 diagnostic workflow in a conventional academic Containment Level 2 laboratory. Our outline includes simple SARS-Cov2 deactivation upon contact, the method for a quantitative real-time reverse transcriptase PCR detecting SARS-Cov2, a description of process establishment and validation, and some considerations for establishing a similar workflow elsewhere. This was achieved under challenging circumstances through the collaborative efforts of scientists, clinical staff, and diagnostic staff to mitigate to the ongoing crisis. Within 14 days, we created a validated COVID-19 diagnostics service for healthcare workers in our local hospital. The described methods are not exhaustive, but we hope may offer support to other academic groups aiming to set up something comparable in a short time frame.
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spelling oxford-uuid:7d32d173-ec5b-4e97-9b7f-c559f8c81d162022-03-26T21:02:03ZA blueprint for the implementation of a validated approach for the detection of SARS-Cov2 in clinical samples in academic facilitiesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:7d32d173-ec5b-4e97-9b7f-c559f8c81d16EnglishSymplectic Elements F1000Research2020Sridhar, SForrest, SKean, IYoung, JBartholdson Scott, JMaes, MPereira-Dias, JParmar, SRoutledge, MSparkes, DRivett, LDougan, GWeekes, MCurran, MGoodfellow, IBaker, SThe COVID-19 pandemic is expanding at an unprecedented rate. As a result, diagnostic services are stretched to their limit, and there is a clear need for the provision of additional diagnostic capacity. Academic laboratories, many of which are closed due to governmental lockdowns, may be in a position to support local screening capacity by adapting their current laboratory practices. Here, we describe the process of developing a SARS-Cov2 diagnostic workflow in a conventional academic Containment Level 2 laboratory. Our outline includes simple SARS-Cov2 deactivation upon contact, the method for a quantitative real-time reverse transcriptase PCR detecting SARS-Cov2, a description of process establishment and validation, and some considerations for establishing a similar workflow elsewhere. This was achieved under challenging circumstances through the collaborative efforts of scientists, clinical staff, and diagnostic staff to mitigate to the ongoing crisis. Within 14 days, we created a validated COVID-19 diagnostics service for healthcare workers in our local hospital. The described methods are not exhaustive, but we hope may offer support to other academic groups aiming to set up something comparable in a short time frame.
spellingShingle Sridhar, S
Forrest, S
Kean, I
Young, J
Bartholdson Scott, J
Maes, M
Pereira-Dias, J
Parmar, S
Routledge, M
Sparkes, D
Rivett, L
Dougan, G
Weekes, M
Curran, M
Goodfellow, I
Baker, S
A blueprint for the implementation of a validated approach for the detection of SARS-Cov2 in clinical samples in academic facilities
title A blueprint for the implementation of a validated approach for the detection of SARS-Cov2 in clinical samples in academic facilities
title_full A blueprint for the implementation of a validated approach for the detection of SARS-Cov2 in clinical samples in academic facilities
title_fullStr A blueprint for the implementation of a validated approach for the detection of SARS-Cov2 in clinical samples in academic facilities
title_full_unstemmed A blueprint for the implementation of a validated approach for the detection of SARS-Cov2 in clinical samples in academic facilities
title_short A blueprint for the implementation of a validated approach for the detection of SARS-Cov2 in clinical samples in academic facilities
title_sort blueprint for the implementation of a validated approach for the detection of sars cov2 in clinical samples in academic facilities
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