Cargando…

Preanalytical Issues and Cycle Threshold Values in SARS-CoV-2 Real-Time RT-PCR Testing: Should Test Results Include These?

[Image: see text] Since the emergence of SARS-CoV-2 pandemic, clinical laboratories worldwide are overwhelmed with SARS-CoV-2 testing using the current gold standard: real-time reverse-transcription polymerase chain reaction (RT-PCR) assays. The large numbers of suspected cases led to shortages in n...

Descripción completa

Detalles Bibliográficos
Autores principales: Engelmann, Ilka, Alidjinou, Enagnon Kazali, Ogiez, Judith, Pagneux, Quentin, Miloudi, Sana, Benhalima, Ilyes, Ouafi, Mahdi, Sane, Famara, Hober, Didier, Roussel, Alain, Cambillau, Christian, Devos, David, Boukherroub, Rabah, Szunerits, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970463/
https://www.ncbi.nlm.nih.gov/pubmed/33748564
http://dx.doi.org/10.1021/acsomega.1c00166
_version_ 1783666429630873600
author Engelmann, Ilka
Alidjinou, Enagnon Kazali
Ogiez, Judith
Pagneux, Quentin
Miloudi, Sana
Benhalima, Ilyes
Ouafi, Mahdi
Sane, Famara
Hober, Didier
Roussel, Alain
Cambillau, Christian
Devos, David
Boukherroub, Rabah
Szunerits, Sabine
author_facet Engelmann, Ilka
Alidjinou, Enagnon Kazali
Ogiez, Judith
Pagneux, Quentin
Miloudi, Sana
Benhalima, Ilyes
Ouafi, Mahdi
Sane, Famara
Hober, Didier
Roussel, Alain
Cambillau, Christian
Devos, David
Boukherroub, Rabah
Szunerits, Sabine
author_sort Engelmann, Ilka
collection PubMed
description [Image: see text] Since the emergence of SARS-CoV-2 pandemic, clinical laboratories worldwide are overwhelmed with SARS-CoV-2 testing using the current gold standard: real-time reverse-transcription polymerase chain reaction (RT-PCR) assays. The large numbers of suspected cases led to shortages in numerous reagents such as specimen transport and RNA extraction buffers. We try to provide some answers on how strongly preanalytical issues affect RT-PCR results by reviewing the utility of different transport buffer media and virus inactivation procedures and comparing the literature data with our own recent findings. We show that various viral inactivation procedures and transport buffers are available and are less of a bottleneck for PCR-based methods. However, efficient alternative lysis buffers remain more difficult to find, and several fast RT-PCR assays are not compatible with guanidine-containing media, making this aspect more of a challenge in the current crisis. Furthermore, the availability of different SARS-CoV-2-specific RT-PCR kits with different sensitivities makes the definition of a general cutoff level for the cycle threshold (Ct) value challenging. Only a few studies have considered how Ct values relate to viral infectivity and how preanalytical issues might affect viral infectivity and RNA detection. We review the current data on the correlation between Ct values and viral infectivity. The presence of the SARS-CoV-2 viral genome in its own is not sufficient proof of infectivity and caution is needed in evaluation of the infectivity of samples. The correlation between Ct values and viral infectivity revealed an RT-PCR cutoff value of 34 cycles for SARS-CoV-2 infectivity using a laboratory-developed RT-PCR assay targeting the RdRp gene. While ideally each clinical laboratory should perform its own correlation, we believe this perspective article could be a reference point for others, in particular medical doctors and researchers interested in COVID-19 diagnostics, and a first step toward harmonization.
format Online
Article
Text
id pubmed-7970463
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-79704632021-03-19 Preanalytical Issues and Cycle Threshold Values in SARS-CoV-2 Real-Time RT-PCR Testing: Should Test Results Include These? Engelmann, Ilka Alidjinou, Enagnon Kazali Ogiez, Judith Pagneux, Quentin Miloudi, Sana Benhalima, Ilyes Ouafi, Mahdi Sane, Famara Hober, Didier Roussel, Alain Cambillau, Christian Devos, David Boukherroub, Rabah Szunerits, Sabine ACS Omega [Image: see text] Since the emergence of SARS-CoV-2 pandemic, clinical laboratories worldwide are overwhelmed with SARS-CoV-2 testing using the current gold standard: real-time reverse-transcription polymerase chain reaction (RT-PCR) assays. The large numbers of suspected cases led to shortages in numerous reagents such as specimen transport and RNA extraction buffers. We try to provide some answers on how strongly preanalytical issues affect RT-PCR results by reviewing the utility of different transport buffer media and virus inactivation procedures and comparing the literature data with our own recent findings. We show that various viral inactivation procedures and transport buffers are available and are less of a bottleneck for PCR-based methods. However, efficient alternative lysis buffers remain more difficult to find, and several fast RT-PCR assays are not compatible with guanidine-containing media, making this aspect more of a challenge in the current crisis. Furthermore, the availability of different SARS-CoV-2-specific RT-PCR kits with different sensitivities makes the definition of a general cutoff level for the cycle threshold (Ct) value challenging. Only a few studies have considered how Ct values relate to viral infectivity and how preanalytical issues might affect viral infectivity and RNA detection. We review the current data on the correlation between Ct values and viral infectivity. The presence of the SARS-CoV-2 viral genome in its own is not sufficient proof of infectivity and caution is needed in evaluation of the infectivity of samples. The correlation between Ct values and viral infectivity revealed an RT-PCR cutoff value of 34 cycles for SARS-CoV-2 infectivity using a laboratory-developed RT-PCR assay targeting the RdRp gene. While ideally each clinical laboratory should perform its own correlation, we believe this perspective article could be a reference point for others, in particular medical doctors and researchers interested in COVID-19 diagnostics, and a first step toward harmonization. American Chemical Society 2021-03-06 /pmc/articles/PMC7970463/ /pubmed/33748564 http://dx.doi.org/10.1021/acsomega.1c00166 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Engelmann, Ilka
Alidjinou, Enagnon Kazali
Ogiez, Judith
Pagneux, Quentin
Miloudi, Sana
Benhalima, Ilyes
Ouafi, Mahdi
Sane, Famara
Hober, Didier
Roussel, Alain
Cambillau, Christian
Devos, David
Boukherroub, Rabah
Szunerits, Sabine
Preanalytical Issues and Cycle Threshold Values in SARS-CoV-2 Real-Time RT-PCR Testing: Should Test Results Include These?
title Preanalytical Issues and Cycle Threshold Values in SARS-CoV-2 Real-Time RT-PCR Testing: Should Test Results Include These?
title_full Preanalytical Issues and Cycle Threshold Values in SARS-CoV-2 Real-Time RT-PCR Testing: Should Test Results Include These?
title_fullStr Preanalytical Issues and Cycle Threshold Values in SARS-CoV-2 Real-Time RT-PCR Testing: Should Test Results Include These?
title_full_unstemmed Preanalytical Issues and Cycle Threshold Values in SARS-CoV-2 Real-Time RT-PCR Testing: Should Test Results Include These?
title_short Preanalytical Issues and Cycle Threshold Values in SARS-CoV-2 Real-Time RT-PCR Testing: Should Test Results Include These?
title_sort preanalytical issues and cycle threshold values in sars-cov-2 real-time rt-pcr testing: should test results include these?
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970463/
https://www.ncbi.nlm.nih.gov/pubmed/33748564
http://dx.doi.org/10.1021/acsomega.1c00166
work_keys_str_mv AT engelmannilka preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT alidjinouenagnonkazali preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT ogiezjudith preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT pagneuxquentin preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT miloudisana preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT benhalimailyes preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT ouafimahdi preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT sanefamara preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT hoberdidier preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT rousselalain preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT cambillauchristian preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT devosdavid preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT boukherroubrabah preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese
AT szuneritssabine preanalyticalissuesandcyclethresholdvaluesinsarscov2realtimertpcrtestingshouldtestresultsincludethese