Validation of saline, PBS and a locally produced VTM at varying storage conditions to detect the SARS-CoV-2 virus by qRT-PCR.
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2023
2023
Historique:
received:
19
09
2022
accepted:
05
01
2023
entrez:
13
2
2023
pubmed:
14
2
2023
medline:
16
2
2023
Statut:
epublish
Résumé
Coronavirus Disease-2019 tests require a Nasopharyngeal (NP) and/or Oropharyngeal (OP) specimen from the upper airway, from which virus RNA is extracted and detected through quantitative reverse transcription-Polymerase Chain Reaction (qRT-PCR). The viability of the virus is maintained after collection by storing the NP/OP swabs in Viral Transport Media (VTM). We evaluated the performance of four transport media: locally manufactured ("REVITAL") Viral Transport Media (RVTM), Standard Universal Transport Media (SUTM), PBS and 0.9% (w/v) NaCl (normal saline). We used laboratory cultured virus to evaluate: i) viral recovery and maintaining integrity at different time periods and temperatures; ii) stability in yielding detectable RNA consistently for all time points and conditions; and iii) their overall accuracy. Four vials of SARS-CoV-2 cultured virus (2 high and 2 low concentration samples) and 1 negative control sample were prepared for each media type (SUTM, RVTM, PBS and normal saline) and stored at the following temperatures, -80°C, 4°C, 25°C and 37°C for 7 days. Viral RNA extractions and qRT-PCR were performed at 1, 2, 3, 4 and 7 days after inoculation with the cultured virus to assess virus stability and viral recovery. Ct values fell over time at 25°C and 37°C, but normal saline, PBS, RVTM and SUTM all showed comparable performance in maintaining virus integrity and stability allowing for the detection of SARS-CoV-2 RNA. Overall, this study demonstrated that normal saline, PBS and the locally manufactured VTM can be used for COVID-19 sample collection and testing, thus expanding the range of SARS-CoV-2 viral collection media.
Identifiants
pubmed: 36780469
doi: 10.1371/journal.pone.0280685
pii: PONE-D-22-25994
pmc: PMC9924993
doi:
Substances chimiques
Saline Solution
0
RNA, Viral
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0280685Subventions
Organisme : Wellcome Trust
Pays : United Kingdom
Informations de copyright
Copyright: © 2023 Ngetsa et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
Références
Innovation (Camb). 2021 May 28;2(2):100114
pubmed: 33942035
J Clin Microbiol. 2012 Mar;50(3):1064-5
pubmed: 22205810
Wellcome Open Res. 2020 Jul 7;5:162
pubmed: 35330938
Eur J Clin Microbiol Infect Dis. 2004 Apr;23(4):289-99
pubmed: 15015033
Surv Immunol Res. 1982;1(4):371-4
pubmed: 6764850
J Clin Microbiol. 2020 May 26;58(6):
pubmed: 32229604
J Clin Microbiol. 2020 Jul 23;58(8):
pubmed: 32341141
J Med Virol. 2022 Mar;94(3):1167-1174
pubmed: 34755352
J Clin Microbiol. 2020 Jul 23;58(8):
pubmed: 32414839
J Med Virol. 2021 May;93(5):2774-2781
pubmed: 33128389
J Virol Methods. 2020 Nov;285:113947
pubmed: 32781008
Indian J Med Res. 2021 May&Jun;153(5&6):684-688
pubmed: 34643568
Nat Mater. 2021 May;20(5):593-605
pubmed: 33589798