Virological characteristics of the SARS-CoV-2 BA.2.86 variant
Author
Tamura, Tomokazu
Mizuma, Keita
Nasser, Hesham
Deguchi, Sayaka
Padilla-Blanco, Miguel
Oda, Yoshitaka
Uriu, Keiya
Tolentino, Jarel E. M.
Tsujino, Shuhei
Suzuki, Rigel
Kojima, Isshu
Nao, Naganori
Shimizu, Ryo
Wang, Lei
Tsuda, Masumi
Jonathan, Michael
Kosugi, Yusuke
Guo, Ziyi
Hinay, Alfredo A.
Putri, Olivia
Kim, Yoonjin
Tanaka, Yuri L.
Asakura, Hiroyuki
Nagashima, Mami
Sadamasu, Kenji
Yoshimura, Kazuhisa
Saito, Akatsuki
Ito, Jumpei
Irie, Takashi
Tanaka, Shinya
Ikeda, Terumasa
Takayama, Kazuo
Matsuno, Keita
Fukuhara, Takasuke
Sato, Kei
Publication date
2024Published in
Cell Host and MicrobeVolume / Issue
32 (2)ISBN / ISSN
ISSN: 1931-3128ISBN / ISSN
eISSN: 1934-6069Metadata
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This publication has a published version with DOI 10.1016/j.chom.2024.01.001
Abstract
In late 2023, several SARS-CoV-2 XBB descendants, notably EG.5.1, were predominant worldwide. However, a distinct SARS-CoV-2 lineage, the BA.2.86 variant, also emerged. BA.2.86 is phylogenetically distinct from other Omicron sublineages, accumulating over 30 amino acid mutations in its spike protein. Here, we examined the virological characteristics of the BA.2.86 variant. Our epidemic dynamics modeling suggested that the relative reproduction number of BA.2.86 is significantly higher than that of EG.5.1. Additionally, four clinically available antivirals were effective against BA.2.86. Although the fusogenicity of BA.2.86 spike is similar to that of the parental BA.2 spike, the intrinsic pathogenicity of BA.2.86 in hamsters was significantly lower than that of BA.2. Since the growth kinetics of BA.2.86 are significantly lower than those of BA.2 both in vitro and in vivo, the attenuated pathogenicity of BA.2.86 is likely due to its decreased replication capacity. These findings uncover the features of BA.2.86, providing insights for control and treatment.
Keywords
SARS-CoV-2, COVID-19, BA.2.86, pathogenicity
Permanent link
https://hdl.handle.net/20.500.14178/2693License
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