Frontiers in Medicine (Jan 2022)

Setting-Up a Rapid SARS-CoV-2 Genome Assessment by Next-Generation Sequencing in an Academic Hospital Center (LPCE, Louis Pasteur Hospital, Nice, France)

  • Paul Hofman,
  • Paul Hofman,
  • Paul Hofman,
  • Olivier Bordone,
  • Olivier Bordone,
  • Emmanuel Chamorey,
  • Jonathan Benzaquen,
  • Jonathan Benzaquen,
  • Renaud Schiappa,
  • Virginie Lespinet-Fabre,
  • Virginie Lespinet-Fabre,
  • Elisabeth Lanteri,
  • Patrick Brest,
  • Baharia Mograbi,
  • Charlotte Maniel,
  • Virginie Tanga,
  • Virginie Tanga,
  • Maryline Allegra,
  • Maryline Allegra,
  • Myriam Salah,
  • Julien Fayada,
  • Jacques Boutros,
  • Sylvie Leroy,
  • Simon Heeke,
  • Véronique Hofman,
  • Véronique Hofman,
  • Véronique Hofman,
  • Charles-Hugo Marquette,
  • Charles-Hugo Marquette,
  • Marius Ilié,
  • Marius Ilié,
  • Marius Ilié

DOI
https://doi.org/10.3389/fmed.2021.730577
Journal volume & issue
Vol. 8

Abstract

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Introduction: Aside from the reverse transcription-PCR tests for the diagnosis of the COVID-19 in routine clinical care and population-scale screening, there is an urgent need to increase the number and the efficiency for full viral genome sequencing to detect the variants of SARS-CoV-2. SARS-CoV-2 variants assessment should be easily, rapidly, and routinely available in any academic hospital.Materials and Methods: SARS-CoV-2 full genome sequencing was performed retrospectively in a single laboratory (LPCE, Louis Pasteur Hospital, Nice, France) in 103 SARS-CoV-2 positive individuals. An automated workflow used the Ion Ampliseq SARS-CoV-2 panel on the Genexus Sequencer. The analyses were made from nasopharyngeal swab (NSP) (n = 64) and/or saliva (n = 39) samples. All samples were collected in the metropolitan area of the Nice city (France) from September 2020 to March 2021.Results: The mean turnaround time between RNA extraction and result reports was 30 h for each run of 15 samples. A strong correlation was noted for the results obtained between NSP and saliva paired samples, regardless of low viral load and high (>28) Ct values. After repeated sequencing runs, complete failure of obtaining a valid sequencing result was observed in 4% of samples. Besides the European strain (B.1.160), various variants were identified, including one variant of concern (B.1.1.7), and different variants under monitoring.Discussion: Our data highlight the current feasibility of developing the SARS-CoV-2 next-generation sequencing approach in a single hospital center. Moreover, these data showed that using the Ion Ampliseq SARS-CoV-2 Assay, the SARS-CoV-2 genome sequencing is rapid and efficient not only in NSP but also in saliva samples with a low viral load. The advantages and limitations of this setup are discussed.

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