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Tytuł pozycji:

Overcoming Supply Shortage for SARS-CoV-2 Detection by RT-qPCR.

Tytuł:
Overcoming Supply Shortage for SARS-CoV-2 Detection by RT-qPCR.
Autorzy:
Barra GB; Research and Development Section, Sabin Medicina Diagnóstica, 70632-340 Brasília, Brazil.
Santa Rita TH; Research and Development Section, Sabin Medicina Diagnóstica, 70632-340 Brasília, Brazil.
Mesquita PG; Research and Development Section, Sabin Medicina Diagnóstica, 70632-340 Brasília, Brazil.
Jácomo RH; Research and Development Section, Sabin Medicina Diagnóstica, 70632-340 Brasília, Brazil.
Nery LFA; Research and Development Section, Sabin Medicina Diagnóstica, 70632-340 Brasília, Brazil.
Źródło:
Genes [Genes (Basel)] 2021 Jan 13; Vol. 12 (1). Date of Electronic Publication: 2021 Jan 13.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Original Publication: Basel : MDPI
MeSH Terms:
COVID-19*/diagnosis
COVID-19*/genetics
COVID-19 Nucleic Acid Testing*
RNA, Viral*/genetics
RNA, Viral*/metabolism
Real-Time Polymerase Chain Reaction*
Reverse Transcriptase Polymerase Chain Reaction*
SARS-CoV-2*/genetics
SARS-CoV-2*/metabolism
Female ; Humans ; Male
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Contributed Indexing:
Keywords: RT-qPCR*; SARS-CoV-2*; validation*
Substance Nomenclature:
0 (RNA, Viral)
Entry Date(s):
Date Created: 20210116 Date Completed: 20210125 Latest Revision: 20231110
Update Code:
20240105
PubMed Central ID:
PMC7828326
DOI:
10.3390/genes12010090
PMID:
33450867
Czasopismo naukowe
In February 2020, our laboratory started to offer a RT-qPCR assay for the qualitative detection of severe acute respiratory syndrome coronavirus 2. A few months after the assay was released to our patients, some materials, reagents, and equipment became in short supply. Alternative protocols were necessary in order to avoid stopping testing to the population. However, the suitability of these alternatives needs to be validated before their use. Here, we investigated if saliva is a reliable alternative specimen to nasopharyngeal swabs; if 0.45% saline is a reliable alternative to guanidine hydrochloride as a collection viral transport media; the stability of SARS-COV-2 in guanidine hydrochloride and in 0.45% saline for 10 and 50 days at room temperature; and if the primers/probe concentration and thermocycling times could be reduced so as to overcome the short supply of these reagents and equipment, without a significant loss of the assay performance. We found that saliva is not an appropriated specimen for our method-nasopharyngeal swabs perform better. Saline (0.45%) and guanidine hydrochloride have a similar SARS-CoV-2 diagnostic capability as tube additives. Reliable SARS-CoV-2 RNA detection can be performed after sample storage for 10 days at room temperature (18-23 °C) in both 0.45% saline and guanidine hydrochloride. Using synthetic RNA, and decreasing the concentration of primers by five-fold and probes by 2.5-fold, changed the assay limit of detection (LOD) from 7.2 copies/reaction to 23.7 copies/reaction and the subsequent reducing of thermocycling times changed the assay LOD from 23.7 copies/reaction to 44.2 copies/reaction. However, using real clinical samples with Cq values ranging from ~12.15 to ~36.46, the results of the three tested conditions were almost identical. These alterations will not affect the vast majority of diagnostics and increase the daily testing capability in 30% and increase primers and probe stocks in 500% and 250%, respectively. Taken together, the alternative protocols described here overcome the short supply of tubes, reagents and equipment during the SARS-CoV-2 pandemic, avoiding the collapse of test offering for the population: 105,757 samples were processed, and 25,156 SARS-CoV-2 diagnostics were performed from 9 May 2020 to 30 June 2020.

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