Please use this identifier to cite or link to this item: https://cris.library.msu.ac.zw//handle/11408/4664
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dc.contributor.authorMarembo, Takudzwa-
dc.contributor.authorChimbunde, Prosper-
dc.contributor.authorChipendo, Tendai-
dc.contributor.authorMunemo, Clayton-
dc.contributor.authorManangazira, Portia-
dc.contributor.authorBangure, Donewell-
dc.date.accessioned2022-01-25T11:21:06Z-
dc.date.available2022-01-25T11:21:06Z-
dc.date.issued2022-
dc.identifier.issn0887-8013-
dc.identifier.issn1098-2825-
dc.identifier.uri10.1002/jcla.24161-
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/34882825/-
dc.identifier.urihttp://hdl.handle.net/11408/4664-
dc.description.abstractBackground: Various nucleic acid amplification assays for the diagnosis of SARS-CoV-2 infection have been developed, and there is a need to assess their test performance relative to one another. The aim of this study was to compare the performance characteristics of the Biosewoom Real-Q 2019-nCoV assay targeting the E and RdRP genes to DaAn Gene 2019-nCoV kit targeting the N gene and ORF1ab in the diagnosis of SARS-CoV-2. Methods: We performed a diagnostic comparison study by testing nasopharyngeal samples for SARS-CoV-2 using the two reverse transcription polymerase chain reaction (RT-PCR) assays. Assay agreement was assessed by overall percent agreement, negative percent agreement, positive percent agreement, and Cohen's kappa coefficient. Results: A total of 48 nasopharyngeal samples were tested using the two assays. One sample was invalid, and three showed inconclusive results with Real-Q; hence, 44 were included for the comparative analysis. Overall, percent agreement between the assays was 93.2% (95% CI 81.3%-98.6%), Positive percent agreement (PPA) was 86.4% (95% CI 65.1%-97.1%) and negative percent agreement (NPA) was 100% (95% CI 84.6%-100%). The kappa coefficient was 0.86 (95% CI 0.72-1.01). Three samples (6.8%) were positive with DaAn gene kit and negative with Real-Q. The fluorescence intensity for Real-Q reporter dyes was low. Conclusion: The two kits showed high levels of concordance in their detection of SARS-CoV-2 despite having different gene targets. The Biosewoom kit can be improved through addressing the fluorescence intensity of the target dyes, and feedback was given to the manufacturer.en_US
dc.language.isoenen_US
dc.publisherWiley Open Accessen_US
dc.relation.ispartofseriesJournal of Clinical Laboratory Analysis;Vol. 36; No. 1-
dc.subjectCOVID-19en_US
dc.subjectPCRen_US
dc.subjectSARS-CoV-2en_US
dc.subjectCoronavirusen_US
dc.subjectZimbabween_US
dc.titleComparison of Real-Q 2019-nCoV and DaAn Gene 2019-nCoV polymerase chain reaction assays for the detection of SARS-CoV-2en_US
dc.typeArticleen_US
item.openairetypeArticle-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.grantfulltextopen-
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