Virological characteristics of the SARS-CoV-2 Omicron XBB.1.5 variant
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Published:2024-02-08
Issue:1
Volume:15
Page:
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ISSN:2041-1723
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Container-title:Nature Communications
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language:en
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Short-container-title:Nat Commun
Author:
Tamura TomokazuORCID, Irie TakashiORCID, Deguchi Sayaka, Yajima HisanoORCID, Tsuda MasumiORCID, Nasser HeshamORCID, Mizuma Keita, Plianchaisuk ArnonORCID, Suzuki SaoriORCID, Uriu Keiya, Begum Mst Monira, Shimizu Ryo, Jonathan MichaelORCID, Suzuki Rigel, Kondo Takashi, Ito Hayato, Kamiyama Akifumi, Yoshimatsu KumikoORCID, Shofa Maya, Hashimoto RinaORCID, Anraku YukiORCID, Kimura Kanako Terakado, Kita ShunsukeORCID, Sasaki Jiei, Sasaki-Tabata Kaori, Maenaka KatsumiORCID, Nao Naganori, Wang LeiORCID, Oda Yoshitaka, , Sawa Hirofumi, Kawabata Ryoko, Watanabe Yukio, Sakamoto Ayaka, Yasuhara Naoko, Suzuki Tateki, Nakajima Yukari, Ferdous Zannatul, Shishido Kenji, Mugita Yuka, Takahashi Otowa, Ichihara Kimiko, Kaku Yu, Misawa Naoko, Guo Ziyi, Hinay Alfredo, Kosugi Yusuke, Fujita Shigeru, Tolentino Jarel M., Chen Luo, Pan Lin, Suganami Mai, Chiba Mika, Yoshimura Ryo, Yasuda Kyoko, Iida Keiko, Ohsumi Naomi, Strange Adam P., Shibatani Yuki, Nishiuchi Tomoko, Tanaka Shiho, Putri Olivia, Joas Gustav, Kim Yoonjin, Yamasoba Daichi, Yoshimura Kazuhisa, Sadamasu Kenji, Nagashima Mami, Asakura Hiroyuki, Yoshida Isao, Nakagawa So, Takaori-Kondo Akifumi, Shirakawa Kotaro, Nagata Kayoko, Nomura Ryosuke, Horisawa Yoshihito, Tashiro Yusuke, Kawai Yugo, Ueno Takamasa, Motozono Chihiro, Toyoda Mako, Ikeda TerumasaORCID, Saito AkatsukiORCID, Matsuno KeitaORCID, Ito JumpeiORCID, Tanaka ShinyaORCID, Sato KeiORCID, Hashiguchi TakaoORCID, Takayama KazuoORCID, Fukuhara TakasukeORCID
Abstract
AbstractCirculation of SARS-CoV-2 Omicron XBB has resulted in the emergence of XBB.1.5, a new Variant of Interest. Our phylogenetic analysis suggests that XBB.1.5 evolved from XBB.1 by acquiring the S486P spike (S) mutation, subsequent to the acquisition of a nonsense mutation in ORF8. Neutralization assays showed similar abilities of immune escape between XBB.1.5 and XBB.1. We determine the structural basis for the interaction between human ACE2 and the S protein of XBB.1.5, showing similar overall structures between the S proteins of XBB.1 and XBB.1.5. We provide the intrinsic pathogenicity of XBB.1 and XBB.1.5 in hamsters. Importantly, we find that the ORF8 nonsense mutation of XBB.1.5 resulted in impairment of MHC suppression. In vivo experiments using recombinant viruses reveal that the XBB.1.5 mutations are involved with reduced virulence of XBB.1.5. Together, our study identifies the two viral functions defined the difference between XBB.1 and XBB.1.5.
Funder
Japan Agency for Medical Research and Development MEXT | Japan Society for the Promotion of Science Takeda Medical Research Foundation Hokkaido University Hirose Fundation
Publisher
Springer Science and Business Media LLC
Reference68 articles.
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