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タイトル: Virological characteristics of the SARS-CoV-2 XBB variant derived from recombination of two Omicron subvariants
著者: Tamura, Tomokazu
Ito, Jumpei
Uriu, Keiya
Zahradnik, Jiri
Kida, Izumi
Anraku, Yuki
Nasser, Hesham
Shofa, Maya
Oda, Yoshitaka
Lytras, Spyros
Nao, Naganori
Itakura, Yukari
Deguchi, Sayaka
Suzuki, Rigel
Wang, Lei
Begum, MST Monira
Kita, Shunsuke
Yajima, Hisano
Sasaki, Jiei
Sasaki-Tabata, Kaori
Shimizu, Ryo
Tsuda, Masumi
Kosugi, Yusuke
Fujita, Shigeru
Pan, Lin
Sauter, Daniel
Yoshimatsu, Kumiko
Suzuki, Saori
Asakura, Hiroyuki
Nagashima, Mami
Sadamasu, Kenji
Yoshimura, Kazuhisa
Yamamoto, Yuki
Nagamoto, Tetsuharu
Schreiber, Gideon
Maenaka, Katsumi
The Genotype to Phenotype Japan (G2P-Japan)
Hashiguchi, Takao  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0001-7578-7571 (unconfirmed)
Ikeda, Terumasa
Fukuhara, Takasuke
Saito, Akatsuki
Tanaka, Shinya
Matsuno, Keita
Takayama, Kazuo  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-1132-2457 (unconfirmed)
Sato, Kei
著者名の別形: 田村, 友和
伊東, 潤平
瓜生, 慧也
紀田, 泉
安楽, 佑樹
小田, 義崇
直, 亨則
板倉, 友香里
出口, 清香
鈴木, 理滋
王, 磊
喜多, 俊介
矢島, 久乃
佐々木, 慈英
田畑, 香織
清水, 凌
津田, 真寿美
小杉, 優介
藤田, 滋
潘, 琳
吉松, 組子
鈴木, 紗織
浅倉, 弘幸
長島, 真美
貞升, 健志
吉村, 和久
山本, 佑樹
永元, 哲治
前仲, 勝実
橋口, 隆生
池田, 輝政
福原, 崇介
齊藤, 暁
田中, 伸哉
松野, 啓太
高山, 和雄
佐藤, 佳
キーワード: SARS-CoV-2
Viral evolution
Virus–host interactions
発行日: 2023
出版者: Springer Nature
誌名: Nature Communications
巻: 14
論文番号: 2800
抄録: In late 2022, SARS-CoV-2 Omicron subvariants have become highly diversified, and XBB is spreading rapidly around the world. Our phylogenetic analyses suggested that XBB emerged through the recombination of two cocirculating BA.2 lineages, BJ.1 and BM.1.1.1 (a progeny of BA.2.75), during the summer of 2022. XBB.1 is the variant most profoundly resistant to BA.2/5 breakthrough infection sera to date and is more fusogenic than BA.2.75. The recombination breakpoint is located in the receptor-binding domain of spike, and each region of the recombinant spike confers immune evasion and increases fusogenicity. We further provide the structural basis for the interaction between XBB.1 spike and human ACE2. Finally, the intrinsic pathogenicity of XBB.1 in male hamsters is comparable to or even lower than that of BA.2.75. Our multiscale investigation provides evidence suggesting that XBB is the first observed SARS-CoV-2 variant to increase its fitness through recombination rather than substitutions.
記述: オミクロンXBB株の進化経路とウイルス学的特性の解明 --遺伝子組換えによる更なる免疫逃避能力の獲得--. 京都大学プレスリリース. 2023-05-22.
著作権等: © The Author(s) 2023
This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
URI: http://hdl.handle.net/2433/282776
DOI(出版社版): 10.1038/s41467-023-38435-3
PubMed ID: 37193706
関連リンク: https://www.kyoto-u.ac.jp/ja/research-news/2023-05-22-1
出現コレクション:学術雑誌掲載論文等

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