Skip to Main Content (Press Enter)

Logo UNISR
  • ×
  • Home
  • Persone
  • Pubblicazioni
  • Facoltà
  • Ambiti Di Ricerca

UNIFIND
Logo UNISR

|

UNIFIND

unisr.it
  • ×
  • Home
  • Persone
  • Pubblicazioni
  • Facoltà
  • Ambiti Di Ricerca
  1. Pubblicazioni

Multiplex real-time reverse-transcription polymerase chain reaction assays for diagnostic testing of severe acute respiratory syndrome coronavirus 2 and seasonal influenza viruses: A challenge of the phase 3 pandemic setting

Articolo
Data di Pubblicazione:
2021
Citazione:
Multiplex real-time reverse-transcription polymerase chain reaction assays for diagnostic testing of severe acute respiratory syndrome coronavirus 2 and seasonal influenza viruses: A challenge of the phase 3 pandemic setting / Mancini, F.; Barbanti, F.; Scaturro, M.; Fontana, S.; Di Martino, A.; Marsili, G.; Puzelli, S.; Calzoletti, L.; Facchini, M.; Di Mario, G.; Fabiani, C.; Bella, A.; Riccardo, F.; Pezzotti, P.; Stefanelli, P.; Rezza, G.; Ciervo, A.; Villa, L.; Fortini, D.; Iacobino, A.; Fiore, S.; Benedetti, E.; Marchi, A.; Venturi, G.; Fortuna, C.; Amendola, A.; Toma, L.; Di Luca, M.; Severini, F.. - In: THE JOURNAL OF INFECTIOUS DISEASES. - ISSN 0022-1899. - 223:(2021), pp. 765-774. [10.1093/infdis/jiaa658]
Abstract:
Background. Pandemic coronavirus disease 2019 (COVID-19) disease represents a challenge for healthcare structures. The molecular confirmation of samples from infected individuals is crucial and therefore guides public health decision making. Clusters and possibly increased diffuse transmission could occur in the context of the next influenza season. For this reason, a diagnostic test able to discriminate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) from influenza viruses is urgently needed. Methods. A multiplex real-time reverse-transcription polymerase chain reaction (PCR) assay was assessed using 1 laboratory protocol with different real-time PCR instruments. Overall, 1000 clinical samples (600 from samples SARS-CoV-2-infected patients, 200 samples from influenza-infected patients, and 200 negative samples) were analyzed. Results. The assay developed was able to detect and discriminate each virus target and to intercept coinfections. The limit of quantification of each assay ranged between 5 and 10 genomic copy numbers, with a cutoff value of 37.7 and 37.8 for influenza and SARS-CoV-2 viruses, respectively. Only 2 influenza coinfections were detected in COVID-19 samples. Conclusions. This study suggests that multiplex assay is a rapid, valid, and accurate method for the detection of SARS-CoV-2 and influenza viruses in clinical samples. The test may be an important diagnostic tool for both diagnostic and surveillance purposes during the seasonal influenza activity period.
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
Mancini, F.; Barbanti, F.; Scaturro, M.; Fontana, S.; Di Martino, A.; Marsili, G.; Puzelli, S.; Calzoletti, L.; Facchini, M.; Di Mario, G.; Fabiani, C.; Bella, A.; Riccardo, F.; Pezzotti, P.; Stefanelli, P.; Rezza, G.; Ciervo, A.; Villa, L.; Fortini, D.; Iacobino, A.; Fiore, S.; Benedetti, E.; Marchi, A.; Venturi, G.; Fortuna, C.; Amendola, A.; Toma, L.; Di Luca, M.; Severini, F.
Autori di Ateneo:
REZZA GIOVANNI
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/157396
Link al Full Text:
https://iris.unisr.it//retrieve/handle/20.500.11768/157396/201464/jiaa658.pdf
Pubblicato in:
THE JOURNAL OF INFECTIOUS DISEASES
Journal
  • Dati Generali

Dati Generali

URL

https://academic.oup.com/jid/article/223/5/765/5932324?login=true
  • Utilizzo dei cookie

Realizzato con VIVO | Designed by Cineca | 26.5.1.0