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Enhanced fusogenicity and pathogenicity of SARS-CoV-2 Delta P681R mutation

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Title: Enhanced fusogenicity and pathogenicity of SARS-CoV-2 Delta P681R mutation
Authors: Saito, Akatsuki Browse this author
Irie, Takashi Browse this author
Suzuki, Rigel Browse this author
Maemura, Tadashi Browse this author
Nasser, Hesham Browse this author
Uriu, Keiya Browse this author
Kosugi, Yusuke Browse this author
Shirakawa, Kotaro Browse this author
Sadamasu, Kenji Browse this author
Kimura, Izumi Browse this author
Ito, Jumpei Browse this author
Wu, Jiaqi Browse this author
Iwatsuki-Horimoto, Kiyoko Browse this author
Ito, Mutsumi Browse this author
Yamayoshi, Seiya Browse this author
Loeber, Samantha Browse this author
Tsuda, Masumi Browse this author
Wang, Lei Browse this author
Ozono, Seiya Browse this author
Butlertanaka, Erika P. Browse this author
Tanaka, Yuri L. Browse this author
Shimizu, Ryo Browse this author
Shimizu, Kenta Browse this author
Yoshimatsu, Kumiko Browse this author
Kawabata, Ryoko Browse this author
Sakaguchi, Takemasa Browse this author
Tokunaga, Kenzo Browse this author
Yoshida, Isao Browse this author
Asakura, Hiroyuki Browse this author
Nagashima, Mami Browse this author
Kazuma, Yasuhiro Browse this author
Nomura, Ryosuke Browse this author
Horisawa, Yoshihito Browse this author
Yoshimura, Kazuhisa Browse this author
Takaori-Kondo, Akifumi Browse this author
Imai, Masaki Browse this author
Tanaka, Shinya Browse this author →KAKEN DB
Nakagawa, So Browse this author
Ikeda, Terumasa Browse this author
Fukuhara, Takasuke Browse this author →KAKEN DB
Kawaoka, Yoshihiro Browse this author
Sato, Kei Browse this author
Issue Date: 10-Feb-2022
Publisher: Nature Portfolio
Journal Title: Nature
Volume: 602
Issue: 7896
Start Page: 300
End Page: 306
Publisher DOI: 10.1038/s41586-021-04266-9
Abstract: During the current coronavirus disease 2019 (COVID-19) pandemic, a variety of mutations have accumulated in the viral genome of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and, at the time of writing, four variants of concern are considered to be potentially hazardous to human society(1). The recently emerged B.1.617.2/Delta variant of concern is closely associated with the COVID-19 surge that occurred in India in the spring of 2021 (ref.(2)). However, the virological properties of B.1.617.2/Delta remain unclear. Here we show that the B.1.617.2/Delta variant is highly fusogenic and notably more pathogenic than prototypic SARS-CoV-2 in infected hamsters. The P681R mutation in the spike protein, which is highly conserved in this lineage, facilitates cleavage of the spike protein and enhances viral fusogenicity. Moreover, we demonstrate that the P681R-bearing virus exhibits higher pathogenicity compared with its parental virus. Our data suggest that the P681R mutation is a hallmark of the virological phenotype of the B.1.617.2/Delta variant and is associated with enhanced pathogenicity.
Type: article
URI: http://hdl.handle.net/2115/84468
Appears in Collections:医学院・医学研究院 (Graduate School of Medicine / Faculty of Medicine) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

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