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Sequencing using a two-steps strategy reveals high genetic diversity in the S gene of SARS-CoV-2 after a high transmission period in Tunis, Tunisia.
Wasfi Fares; Kais Ghedira; Mariem Gdoura; Anissa Chouikha; Sondos Haddad-Boubaker; Marwa Khediri; Kaouthar Ayouni; Asma Lamari; Henda Touzi; Walid Hammemi; Zina Medeb; Nahed Hogga; Nissaf Ben Aleya; Henda Triki.
Afiliação
  • Wasfi Fares; Institut Pasteur de Tunis
  • Kais Ghedira; Institut Pasteur de Tunis
  • Mariem Gdoura; Charles Nicolle Hospital
  • Anissa Chouikha; Institut Pasteur de Tunis
  • Sondos Haddad-Boubaker; Institut Pasteur de Tunis
  • Marwa Khediri; Institut Pasteur de Tunis
  • Kaouthar Ayouni; Institut Pasteur de Tunis
  • Asma Lamari; Institut Pasteur de Tunis
  • Henda Touzi; Institut Pasteur de Tunis
  • Walid Hammemi; Institut Pasteur de Tunis
  • Zina Medeb; Institut Pasteur de Tunis
  • Nahed Hogga; Institut Pasteur de Tunis
  • Nissaf Ben Aleya; Ministry of Public Health
  • Henda Triki; Institut Pasteur de Tunis
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-449083
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ABSTRACT
Recent efforts have reported numerous variants that influence SARS-CoV-2 viral characteristics including pathogenicity, transmission rate and ability of detection by molecular tests. Whole genome sequencing based on NGS technologies is the method of choice to identify all viral variants; however, the resources needed to use these techniques for a representative number of specimens remain limited in many low and middle income countries. To decrease sequencing cost, we developed a couple of primers allowing to generate partial sequences in the viral S gene allowing rapid detection of numerous variants of concern (VOCs) and variants of interest (VOIs); whole genome sequencing is then performed on a selection of viruses based on partial sequencing results. Two hundred and one nasopharyngeal specimens collected during the decreasing phase of a high transmission COVID-19 wave in T unisia were analyzed. The results reveal high genetic variability within the sequenced fragment and allowed the detection of first introduction in the country of already known VOCs and VOIs as well as others variants that have interesting genomic mutations and need to be kept under surveillance. ImportanceThe method of choice for SARS-CoV-2 variants detection is whole genome sequencing using NGS technologies. Resources for this technology remain limited in many low and middle income countries where it is not possible to perform whole genome sequencing for representative number of SARS-CoV-2 positive cases. In the present work, we developed a novel strategy based on a first partial sanger screening in the S gene including key mutations of the already known VOCs and VOIs for rapid identification of these VOCs and VOIs and helps to better select specimens that need to be sequenced by NGS technologies. The second step consisting in whole genome sequencing allowed to have a holistic view of all variants within the selected viral strains and confirmed the initial classification of the strains based on partial S gene sequencing.
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Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Estudo diagnóstico Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Estudo diagnóstico Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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