First cases of infection with the 21L/BA.2 Omicron variant in Marseille, France

被引:17
作者
Colson, Philippe [1 ,2 ,3 ]
Delerce, Jeremy [1 ]
Beye, Mamadou [1 ]
Levasseur, Anthony [1 ,2 ]
Boschi, Celine [1 ,2 ,3 ]
Houhamdi, Linda [1 ,3 ]
Tissot-Dupont, Herve [1 ,2 ,3 ]
Yahi, Nouara [4 ]
Million, Matthieu [1 ,2 ,3 ]
La Scola, Bernard [1 ,2 ,3 ]
Fantini, Jacques [4 ]
Raoult, Didier [1 ,2 ]
Fournier, Pierre-Edouard [1 ,3 ,5 ]
机构
[1] IHU Mediterranee Infect, 19-21 Blvd Jean Moulin, F-13005 Marseille, France
[2] Aix Marseille Univ, Inst Rech Dev, Microbes Evolut Phylogeny & Infect, Marseille, France
[3] AP HM, Marseille, France
[4] Aix Marseille Univ, INSERM, UMR S 1072, Marseille, France
[5] Aix Marseille Univ, Inst Rech Dev, Vecteurs Infect Trop & Mediterranee, Marseille, France
关键词
emergence; Omicron; SARS-CoV-2; southern France; travel; variant;
D O I
10.1002/jmv.27695
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 13 cases using variant-specific qPCR and next-generation sequencing between 28/11/2021 and 31/01/2022, the first two cases being diagnosed in travelers 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 highlighted a significant enlargement and flattening of the surface of the 21L/BA.2 N-terminal domain of the spike protein compared to that of the 21K/BA.1 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.
引用
收藏
页码:3421 / 3430
页数:10
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