Convergent evolution of the SARS-CoV-2 Omicron subvariants leading to the emergence of BQ.1.1 variant

Author:

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

Abstract

AbstractIn late 2022, although the SARS-CoV-2 Omicron subvariants have highly diversified, some lineages have convergently acquired amino acid substitutions at five critical residues in the spike protein. Here, we illuminated the evolutionary rules underlying the convergent evolution of Omicron subvariants and the properties of one of the latest lineages of concern, BQ.1.1. Our phylogenetic and epidemic dynamics analyses suggest that Omicron subvariants independently increased their viral fitness by acquiring the convergent substitutions. Particularly, BQ.1.1, which harbors all five convergent substitutions, shows the highest fitness among the viruses investigated. Neutralization assays show that BQ.1.1 is more resistant to breakthrough BA.2/5 infection sera than BA.5. The BQ.1.1 spike exhibits enhanced binding affinity to human ACE2 receptor and greater fusogenicity than the BA.5 spike. However, the pathogenicity of BQ.1.1 in hamsters is comparable to or even lower than that of BA.5. Our multiscale investigations provide insights into the evolutionary trajectory of Omicron subvariants.

Publisher

Cold Spring Harbor Laboratory

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