Comparison of a novel antigen detection test with reverse transcription polymerase chain reaction assay for laboratory diagnosis of SARS-CoV-2 infection

dc.contributor.authorCirit, Osman Sezer
dc.contributor.authorMutlu, Esvet
dc.contributor.authorSancak, Banu
dc.contributor.authorKocagoz, Tanil
dc.contributor.authorCan, Ozge
dc.contributor.authorCicek, Candan
dc.contributor.authorSayiner, Ayca Arzu
dc.contributor.authorAppak, Ozgur
dc.contributor.authorUyar, Neval Yurttutan
dc.contributor.authorKulah, Canan
dc.contributor.authorCicek, Aysegul Copur
dc.contributor.authorOzgumus, Osman Birol
dc.contributor.authorAltintop, Yasemin Ay
dc.contributor.authorSaatci, Esma
dc.contributor.authorKarsligil, Tekin
dc.contributor.authorZer, Yasemin
dc.contributor.authorOzen, Nevgun Sepin
dc.contributor.authorCekin, Yesim
dc.contributor.authorKarahan, Zeynep Ceren
dc.contributor.authorEvren, Ebru
dc.contributor.authorKarakoc, Ayse Esra
dc.contributor.authorOrhan, Sultan Gulbahce
dc.contributor.authorMutlu, Derya
dc.contributor.authorBozdemir, Tugba
dc.contributor.authorCayci, Yeliz Tanriverdi
dc.contributor.authorCinar, Canberk
dc.contributor.authorTasbakan, Meltem
dc.contributor.authorMert, Merve
dc.contributor.authorCinar, Ece
dc.contributor.authorKutsoylu, Oya Ozlem Eren
dc.contributor.authorKocagoz, Sesin
dc.contributor.authorErturk, Ayse
dc.contributor.authorCelik, Ilhami
dc.contributor.authorMete, Ayse Ozlem
dc.contributor.authorEneyli, Muge Gunalp
dc.contributor.authorAkdemir, Irem
dc.contributor.authorKarakok, Taliha
dc.contributor.authorInan, Dilara
dc.contributor.authorAtilla, Aynur
dc.contributor.authorTaflan, Sevket Onur
dc.contributor.authorYoruk, Kagan Etka
dc.date.accessioned2023-02-21T12:41:51Z
dc.date.available2023-02-21T12:41:51Z
dc.date.issued2022-01-01
dc.description.abstractMolecular diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by real-time reverse transcription polymerase chain reaction (RT-PCR) in respiratory specimens is considered the gold standard method. This method is highly sensitive and specific but it has some limitations such as being expensive and requiring special laboratory equipment and skilled personnel. RapidFor (TM) Antigen Rapid Test Kit is a commercially available Ag-RDT which is produced in Turkey and designed to detect the nucleocapsid antigen of SARS-CoV-2 in nasopharyngeal swab samples. The aim of this study was to evaluate the performance of this novel SARS-CoV-2 antigen detection considering the RT-PCR method as the gold standard. Four hundred forty-four nasopharyngeal swab samples which were collected from the patients who met clinical criteria of COVID-19 from ten centers in Turkey between September 2020 and February 2021 were included in the study. All the nasopharyngeal swab samples were tested for SARS-CoV-2 RNA using commercial RT-PCR kits (Bioeksen and A1 Lifesciences, Istanbul, Turkey) according to the manufacturer's instructions. Viral loads were assessed according to the cycle threshold (Ct) values. RapidFor (TM) SARS-CoV-2 antigen test (Vitrosens Biotechnology, Istanbul, Turkey) was used to investigate the presence of SARS-CoV-2 antigen in all samples following the manufacturer's instructions. Out of 444 nasopharyngeal swab samples tested, 346 (77.9\%) were positive and 98 (22.1\%) were negative for SARS-CoV-2 RNA by RTPCR. Overall sensitivity of the RapidFor (TM). Antigen Rapid Test Kit was 80.3\% whereas specificity was found to be 87.8\%. Positivity rate of rapid antigen test in samples with Ct values over 25 and below 30 was 82.7\%, while it increased to 95.7\% in samples 20 <= Ct < 25 and reached 100\% in samples with Ct values below 20. RapidFor (TM) SARS-CoV-2 Ag test might be a good choice in the screening of symptomatic and asymptomatic patients and their contacts for taking isolation measures early, with advantages over RT-PCR as being rapid, easy and being applicable in every laboratory and even at point of care.
dc.identifier.doi10.1007/s15010-022-01832-9
dc.identifier.urihttps://hdl.handle.net/11443/2758
dc.identifier.urihttp://dx.doi.org/10.1007/s15010-022-01832-9
dc.identifier.wosWOS:000791075000001
dc.publisherSPRINGER HEIDELBERG
dc.relation.ispartofINFECTION
dc.subjectCOVID-19
dc.subjectNasopharyngeal swab samples
dc.subjectRapid antigen test
dc.subjectRT-PCR
dc.subjectSARS-CoV-2
dc.titleComparison of a novel antigen detection test with reverse transcription polymerase chain reaction assay for laboratory diagnosis of SARS-CoV-2 infection
dc.typeArticle

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