Virological characteristics of the SARS-CoV-2 XBB variant derived from recombination of two Omicron subvariants

Author:

Tamura Tomokazu,Ito Jumpei,Uriu Keiya,Zahradnik Jiri,Kida Izumi,Nasser Hesham,Shofa Maya,Oda Yoshitaka,Lytras SpyrosORCID,Nao Naganori,Itakura Yukari,Deguchi Sayaka,Suzuki Rigel,Wang Lei,Begum MST Monira,Tsuda Masumi,Kosugi Yusuke,Fujita Shigeru,Yoshimatsu Kumiko,Suzuki Saori,Asakura Hiroyuki,Nagashima Mami,Sadamasu Kenji,Yoshimura Kazuhisa,Yamamoto Yuki,Nagamoto Tetsuharu,Schreiber Gideon,Ikeda Terumasa,Fukuhara Takasuke,Saito AkatsukiORCID,Tanaka ShinyaORCID,Matsuno Keita,Takayama Kazuo,Sato KeiORCID,

Abstract

AbstractIn late 2022, the SARS-CoV-2 Omicron subvariants have highly diversified, and XBB is spreading rapidly around the world. Our phylogenetic analyses suggested that XBB emerged by recombination of two co-circulating BA.2 lineages, BJ.1 and BM.1.1.1 (a progeny of BA.2.75), during the summer of 2022 around India.In vitroexperiments revealed that XBB is the most profoundly resistant variant to BA.2/5 breakthrough infection sera ever and is more fusogenic than BA.2.75. Notably, the recombination breakpoint is located in the receptor-binding domain of spike, and each region of recombined spike conferred immune evasion and augmented fusogenicity to the XBB spike. Finally, the intrinsic pathogenicity of XBB in hamsters is comparable to or even lower than that of BA.2.75. Our multiscale investigation provided evidence suggesting that XBB is the first documented SARS-CoV-2 variant increasing its fitness through recombination rather than single mutations.

Publisher

Cold Spring Harbor Laboratory

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