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First cases of infection with the 21L/BA.2 Omicron variant in Marseille, France
Philippe Colson; Jeremy Delerce; Mamadou Beye; Anthony LEVASSEUR; Celine Boschi; Linda Houhamdi; Herve Tissot-Dupont; Nouara Yahi; Matthieu Million; Bernard LA SCOLA; Jacques Fantini; Didier Raoult; Pierre-Edouard Fournier.
Affiliation
  • Philippe Colson; IHU Mediterranee Infection
  • Jeremy Delerce; IHU Mediterranee Infection
  • Mamadou Beye; IHU Mediterranee Infection
  • Anthony LEVASSEUR; Aix-Marseille University
  • Celine Boschi; IHU Mediterranee Infection
  • Linda Houhamdi; IHU Mediterranee Infection
  • Herve Tissot-Dupont; IHU Mediterranee Infection
  • Nouara Yahi; Aix-Marseille university
  • Matthieu Million; IHU Mediterranee Infection
  • Bernard LA SCOLA; IHU Mediterranee Infection
  • Jacques Fantini; Aix-Marseille University
  • Didier Raoult; Aix Marseille Universite IHU Mediterranee Infection
  • Pierre-Edouard Fournier; IHU Mediterranee Infection
Preprint in En | PREPRINT-MEDRXIV | ID: ppmedrxiv-22270495
ABSTRACT
The SARS-CoV-2 21K/BA.1, 21L/BA.2, and BA.3 Omicron variants have recently emerged worldwide. To date, the 21L/BA.2 Omicron variant has remained very minority globally but became predominant in Denmark instead of the 21K/BA.1 variant. Here we describe the first cases diagnosed with this variant in south-eastern France. We identified thirteen cases using variant-specific qPCR and next-generation sequencing between 28/11/2021 and 31/01/2022, the first two cases being diagnosed in travellers returning from Tanzania. Overall, viral genomes displayed a mean ({+/-}standard deviation) number of 65.9{+/-}2.5 (range, 61-69) nucleotide substitutions and 31.0{+/-}8.3 (27-50) nucleotide deletions, resulting in 49.6{+/-}2.2 (45-52) amino acid substitutions (including 28 in the spike protein) and 12.4{+/-}1.1 (12-15) amino acid deletions. Phylogeny showed the distribution in three different clusters of these genomes, which were most closely related to genomes from England and South Africa, from Singapore and Nepal, or from France and Denmark. Structural predictions pointed out a significant enlargement and flattening of the 21L/BA.2 N-terminal domain surface compared with that of the 21K/BA.2 Omicron variant, which may facilitate initial viral interactions with lipid rafts. Close surveillance is needed at global, country and center scales to monitor the incidence and clinical outcome of the 21L/BA.2 Omicron variant.
License
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Full text: 1 Collection: 09-preprints Database: PREPRINT-MEDRXIV Type of study: Observational_studies / Prognostic_studies Language: En Year: 2022 Type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-MEDRXIV Type of study: Observational_studies / Prognostic_studies Language: En Year: 2022 Type: Preprint