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


Journal

ACS omega
ISSN: 2470-1343
Titre abrégé: ACS Omega
Pays: United States
ID NLM: 101691658

Informations de publication

Date de publication:
16 Mar 2021
Historique:
received: 11 01 2021
accepted: 12 02 2021
entrez: 22 3 2021
pubmed: 23 3 2021
medline: 23 3 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 33748564
doi: 10.1021/acsomega.1c00166
pmc: PMC7970463
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

6528-6536

Informations de copyright

© 2021 The Authors. Published by American Chemical Society.

Déclaration de conflit d'intérêts

The authors declare no competing financial interest.

Références

Infect Genet Evol. 2020 Jul;81:104260
pubmed: 32092483
Clin Infect Dis. 2020 Dec 17;71(10):2663-2666
pubmed: 32442256
Science. 2020 Jul 3;369(6499):77-81
pubmed: 32376603
Euro Surveill. 2020 Jul;25(30):
pubmed: 32734855
Diagnostics (Basel). 2021 Mar 03;11(3):
pubmed: 33802451
Nature. 2020 May;581(7809):465-469
pubmed: 32235945
J Clin Microbiol. 2020 May 26;58(6):
pubmed: 32269100
Diagn Microbiol Infect Dis. 2018 May;91(1):27-33
pubmed: 29463426
Nat Med. 2020 May;26(5):672-675
pubmed: 32296168
iScience. 2020 Aug 21;23(8):101406
pubmed: 32771976
J Clin Microbiol. 2020 Oct 21;58(11):
pubmed: 32839250
Euro Surveill. 2020 Aug;25(32):
pubmed: 32794447
Nature. 2020 Dec;588(7838):498-502
pubmed: 32805734
Anal Bioanal Chem. 2021 Jan;413(1):49-71
pubmed: 33073312
Lancet. 2021 Jan 9;397(10269):99-111
pubmed: 33306989
ACS Infect Dis. 2020 Aug 14;6(8):1998-2016
pubmed: 32677821
EBioMedicine. 2020 Aug;58:102916
pubmed: 32711256
Clin Infect Dis. 2020 Nov 19;71(16):2249-2251
pubmed: 32306036
BMJ Open. 2020 Aug 5;10(8):e039856
pubmed: 32759252
N Engl J Med. 2020 Nov 12;383(20):1920-1931
pubmed: 32663912
J Clin Microbiol. 2020 Sep 22;58(10):
pubmed: 32554479
J Clin Med. 2021 Jan 17;10(2):
pubmed: 33477365
ACS Nano. 2020 Apr 28;14(4):5135-5142
pubmed: 32293168
N Engl J Med. 2021 Mar 18;384(11):1015-1027
pubmed: 33523609
Cell. 2020 May 28;181(5):1004-1015.e15
pubmed: 32375025
Nat Microbiol. 2020 Oct;5(10):1299-1305
pubmed: 32651556
Viruses. 2020 Oct 23;12(11):
pubmed: 33114233
J Gen Virol. 2021 Mar;102(3):
pubmed: 33416462
Diagnostics (Basel). 2021 Jan 01;11(1):
pubmed: 33401392
Lancet Microbe. 2021 Jan;2(1):e13-e22
pubmed: 33521734
Viruses. 2020 Jun 06;12(6):
pubmed: 32517266
J Infect Dis. 2020 Oct 1;222(9):1462-1467
pubmed: 32798217
Int J Infect Dis. 2020 Jun;95:441-443
pubmed: 32376309
Structure. 2020 Nov 3;28(11):1218-1224.e4
pubmed: 33058760
Life Sci. 2020 Jul 15;253:117592
pubmed: 32222463
J Infect. 2020 Sep;81(3):357-371
pubmed: 32615199
Thorax. 2021 Jan;76(1):86-88
pubmed: 33097604
Anal Bioanal Chem. 2022 Jan;414(1):103-113
pubmed: 33616686
Eur J Clin Microbiol Infect Dis. 2020 Jun;39(6):1059-1061
pubmed: 32342252
Biologicals. 2005 Jun;33(2):95-9
pubmed: 15939287
Arch Pathol Lab Med. 2020 Apr 16;:
pubmed: 32298137
J Clin Virol. 2020 Jun;127:104384
pubmed: 32361285
J Med Virol. 2020 Jun;92(6):660-666
pubmed: 32159237
Clin Infect Dis. 2021 Dec 6;73(11):e3884-e3899
pubmed: 33270107
J Virol Methods. 2004 Oct;121(1):85-91
pubmed: 15350737
J Clin Microbiol. 2021 Mar 19;59(4):
pubmed: 33509809
ACS Nano. 2020 Apr 28;14(4):3822-3835
pubmed: 32223179
N Engl J Med. 2021 Feb 18;384(7):610-618
pubmed: 33406353
J Pharm Anal. 2020 Apr;10(2):97-101
pubmed: 32292623
J Transl Med. 2020 Apr 22;18(1):179
pubmed: 32321524
EClinicalMedicine. 2021 Jan;31:100677
pubmed: 33521610

Auteurs

Ilka Engelmann (I)

Univ. Lille, CHU Lille, Laboratoire de Virologie ULR3610, F-59000 Lille, France.

Enagnon Kazali Alidjinou (EK)

Univ. Lille, CHU Lille, Laboratoire de Virologie ULR3610, F-59000 Lille, France.

Judith Ogiez (J)

Univ. Lille, CHU Lille, Laboratoire de Virologie ULR3610, F-59000 Lille, France.

Quentin Pagneux (Q)

Univ. Lille, CNRS, Centrale Lille, University Polytechnique Hauts-de-France, UMR 8520-IEMN, F-59000 Lille, France.

Sana Miloudi (S)

Univ. Lille, CHU Lille, Laboratoire de Virologie ULR3610, F-59000 Lille, France.

Ilyes Benhalima (I)

Univ. Lille, CHU Lille, Laboratoire de Virologie ULR3610, F-59000 Lille, France.

Mahdi Ouafi (M)

Univ. Lille, CHU Lille, Laboratoire de Virologie ULR3610, F-59000 Lille, France.

Famara Sane (F)

Univ. Lille, CHU Lille, Laboratoire de Virologie ULR3610, F-59000 Lille, France.

Didier Hober (D)

Univ. Lille, CHU Lille, Laboratoire de Virologie ULR3610, F-59000 Lille, France.

Alain Roussel (A)

Architecture et Fonction des Macromolécules Biologiques, Aix-Marseille Université, Campus de Luminy, CEDEX 20, 13020 Marseille, France.
Architecture et Fonction des Macromolécules Biologiques, Centre National de la Recherche Scientifique (CNRS), Campus de Luminy, CEDEX 20, 13020 Marseille, France.

Christian Cambillau (C)

Architecture et Fonction des Macromolécules Biologiques, Aix-Marseille Université, Campus de Luminy, CEDEX 20, 13020 Marseille, France.
Architecture et Fonction des Macromolécules Biologiques, Centre National de la Recherche Scientifique (CNRS), Campus de Luminy, CEDEX 20, 13020 Marseille, France.

David Devos (D)

Univ. Lille, CHU-Lille, Inserm, U1172, Lille Neuroscience & Cognition, LICEND, F-59000 Lille, France.

Rabah Boukherroub (R)

Univ. Lille, CNRS, Centrale Lille, University Polytechnique Hauts-de-France, UMR 8520-IEMN, F-59000 Lille, France.

Sabine Szunerits (S)

Univ. Lille, CNRS, Centrale Lille, University Polytechnique Hauts-de-France, UMR 8520-IEMN, F-59000 Lille, France.

Classifications MeSH