Academic Thesis

Basic information

Name Kojima Isshu
Belonging department
Occupation name
researchmap researcher code R000055330
researchmap agency Okayama University of Science

Title

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

Bibliography Type

Joint Author

Author

Tomokazu Tamura/Keita Mizuma/Hesham Nasser/Sayaka Deguchi/Miguel Padilla-Blanco/Yoshitaka Oda/Keiya Uriu/Jarel E M Tolentino/Shuhei Tsujino/Rigel Suzuki/Isshu Kojima/Naganori Nao/Ryo Shimizu/Lei Wang/Masumi Tsuda/Michael Jonathan/Yusuke Kosugi/Ziyi Guo/Alfredo A Hinay Jr/Olivia Putri/Yoonjin Kim/Yuri L Tanaka/Hiroyuki Asakura/Mami Nagashima/Kenji Sadamasu/Kazuhisa Yoshimura; Genotype to Phenotype Japan (G2P-Japan) Consortium; Akatsuki Saito/Jumpei Ito/Takashi Irie/Shinya Tanaka/Jiri Zahradnik/Terumasa Ikeda/Kazuo Takayama/Keita Matsuno/Takasuke Fukuhara/Kei Sato

Summary

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.

Magazine(name)

Cell host & microbe

Publisher

Volume

32

Number Of Pages

2

StartingPage

170

EndingPage

180

Date of Issue

2024/02

Referee

Exist

Invited

Language

Thesis Type

ISSN

DOI

10.1016/j.chom.2024.01.001.

NAID

PMID

J-GLOBAL ID

arXiv ID

ORCID Put Code

DBLP ID