Virological characteristics of the SARS-CoV-2 BA.2.86 variant

Author:

Tamura Tomokazu,Mizuma Keita,Nasser Hesham,Deguchi Sayaka,Padilla-Blanco Miguel,Uriu Keiya,Tolentino Jarel Elgin M.,Tsujino Shuhei,Suzuki Rigel,Kojima Isshu,Nao Naganori,Shimizu Ryo,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 AkatsukiORCID,Ito Jumpei,Irie Takashi,Zahradnik Jiri,Ikeda Terumasa,Takayama Kazuo,Matsuno Keita,Fukuhara Takasuke,Sato Kei,

Abstract

AbstractIn late 2023, a lineage of SARS-CoV-2 emerged and was named the BA.2.86 variant. BA.2.86 is phylogenetically distinct from other Omicron sublineages identified so far, displaying an accumulation of over 30 amino acid mutations in its spike protein. Here, we performed multiscale investigations to reveal 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. Experimental studies showed that 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 is significantly lower than that of BA.2 in bothin vitrocell cultures andin vivo, it is suggested that the attenuated pathogenicity of BA.2.86 is due to its decreased replication capacity.

Publisher

Cold Spring Harbor Laboratory

Reference51 articles.

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