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10.1016/j.ijid.2020.06.027

http://scihub22266oqcxt.onion/10.1016/j.ijid.2020.06.027
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suck abstract from ncbi


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pmid32535302      Int+J+Infect+Dis 2020 ; 97 (ä): 225-229
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  • Multiple assays in a real-time RT-PCR SARS-CoV-2 panel can mitigate the risk of loss of sensitivity by new genomic variants during the COVID-19 outbreak #MMPMID32535302
  • Penarrubia L; Ruiz M; Porco R; Rao SN; Juanola-Falgarona M; Manissero D; Lopez-Fontanals M; Pareja J
  • Int J Infect Dis 2020[Aug]; 97 (ä): 225-229 PMID32535302show ga
  • OBJECTIVES: In this study, five SARS-CoV-2 PCR assay panels were evaluated against the accumulated genetic variability of the virus to assess the effect on sensitivity of the individual assays. DESIGN OR METHODS: As of week 21, 2020, the complete set of available SARS-CoV-2 genomes from GISAID and GenBank databases were used in this study. SARS-CoV-2 primer sequences from publicly available panels (WHO, CDC, NMDC, and HKU) and QIAstat-Dx were included in the alignment, and accumulated genetic variability affecting any oligonucleotide annealing was annotated. RESULTS: A total of 11,627 (34.38%) genomes included single mutations affecting annealing of any PCR assay. Variations in 8,773 (25.94%) genomes were considered as high risk, whereas additional 2,854 (8.43%) genomes presented low frequent single mutations and were predicted to yield no impact on sensitivity. In case of the QIAstat-Dx SARS-CoV-2 Panel, 99.11% of the genomes matched with a 100% coverage all oligonucleotides, and critical variations were tested in vitro corroborating no loss of sensitivity. CONCLUSIONS: This analysis stresses the importance of targeting more than one region in the viral genome for SARS-CoV-2 detection to mitigate the risk of loss of sensitivity due to the unknown mutation rate during this SARS-CoV-2 outbreak.
  • |*Genome, Viral[MESH]
  • |*Real-Time Polymerase Chain Reaction[MESH]
  • |*Reverse Transcriptase Polymerase Chain Reaction[MESH]
  • |Betacoronavirus/*genetics[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*diagnosis/epidemiology[MESH]
  • |Disease Outbreaks[MESH]
  • |Genetic Variation[MESH]
  • |Genomics[MESH]
  • |Humans[MESH]
  • |Mutation[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*diagnosis/epidemiology[MESH]
  • |Risk Factors[MESH]


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