Characterization of SARS-CoV-2 Omicron BA.2.75 clinical isolates

Author:

Uraki RyutaORCID,Iida ShunORCID,Halfmann Peter J.,Yamayoshi SeiyaORCID,Hirata Yuichiro,Iwatsuki-Horimoto KiyokoORCID,Kiso Maki,Ito Mutsumi,Furusawa Yuri,Ueki HiroshiORCID,Sakai-Tagawa Yuko,Kuroda Makoto,Maemura Tadashi,Kim Taksoo,Mine Sohtaro,Iwamoto Noriko,Li Rong,Liu Yanan,Larson Deanna,Fukushi Shuetsu,Watanabe Shinji,Maeda KenORCID,Wang ZhongdeORCID,Ohmagari Norio,Theiler James,Fischer WillORCID,Korber BetteORCID,Imai MasakiORCID,Suzuki TadakiORCID,Kawaoka YoshihiroORCID

Abstract

AbstractThe prevalence of the Omicron subvariant BA.2.75 rapidly increased in India and Nepal during the summer of 2022, and spread globally. However, the virological features of BA.2.75 are largely unknown. Here, we evaluated the replicative ability and pathogenicity of BA.2.75 clinical isolates in Syrian hamsters. Although we found no substantial differences in weight change among hamsters infected with BA.2, BA.5, or BA.2.75, the replicative ability of BA.2.75 in the lungs is higher than that of BA.2 and BA.5. Of note, BA.2.75 causes focal viral pneumonia in hamsters, characterized by patchy inflammation interspersed in alveolar regions, which is not observed in BA.5-infected hamsters. Moreover, in competition assays, BA.2.75 replicates better than BA.5 in the lungs of hamsters. These results suggest that BA.2.75 can cause more severe respiratory disease than BA.5 and BA.2 in a hamster model and should be closely monitored.

Funder

Japan Agency for Medical Research and Development

Division of Intramural Research, National Institute of Allergy and Infectious Diseases

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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