Virological characteristics of the SARS-CoV-2 Omicron EG.5.1 variant

Author:

Tsujino Shuhei,Deguchi Sayaka,Nomai Tomo,Padilla-Blanco Miguel,Plianchaisuk Arnon,Wang Lei,Begum MST Monira,Uriu Keiya,Mizuma Keita,Nao Naganori,Kojima Isshu,Tsubo Tomoya,Li Jingshu,Matsumura YasufumiORCID,Nagao Miki,Oda Yoshitaka,Tsuda Masumi,Anraku Yuki,Kita Shunsuke,Yajima Hisano,Sasaki-Tabata Kaori,Guo Ziyi,Hinay Alfredo A,Yoshimatsu Kumiko,Yamamoto Yuki,Nagamoto Tetsuharu,Asakura Hiroyuki,Nagashima Mami,Sadamasu Kenji,Yoshimura Kazuhisa,Nasser Hesham,Jonathan Michael,Putri Olivia,Kim Yoonjin,Chen Luo,Suzuki Rigel,Tamura Tomokazu,Maenaka KatsumiORCID,Irie Takashi,Matsuno Keita,Tanaka ShinyaORCID,Ito Jumpei,Ikeda Terumasa,Takayama Kazuo,Zahradnik Jiri,Hashiguchi Takao,Fukuhara Takasuke,Sato Kei,

Abstract

AbstractIn middle-late 2023, a sublineage of SARS-CoV-2 Omicron XBB, EG.5.1 (a progeny of XBB.1.9.2), is spreading rapidly around the world. Here, we performed multiscale investigations to reveal virological features of newly emerging EG.5.1 variant. Our phylogenetic-epidemic dynamics modeling suggested that two hallmark substitutions of EG.5.1, S:F456L and ORF9b:I5T, are critical to the increased viral fitness. Experimental investigations addressing the growth kinetics, sensitivity to clinically available antivirals, fusogenicity and pathogenicity of EG.5.1 suggested that the virological features of EG.5.1 is comparable to that of XBB.1.5. However, the cryo-electron microscopy reveals the structural difference between the spike proteins of EG.5.1 and XBB.1.5. We further assessed the impact of ORF9b:I5T on viral features, but it was almost negligible at least in our experimental setup. Our multiscale investigations provide the knowledge for understanding of the evolution trait of newly emerging pathogenic viruses in the human population.

Publisher

Cold Spring Harbor Laboratory

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