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Virological characteristics of the SARS-CoV-2 Omicron BA.2.75 variant

Authors :
80728270
50632098
10759509
Saito, Akatsuki
Tamura, Tomokazu
Zahradnik, Jiri
Deguchi, Sayaka
Tabata, Koshiro
Anraku, Yuki
Kimura, Izumi
Ito, Jumpei
Yamasoba, Daichi
Nasser, Hesham
Toyoda, Mako
Nagata, Kayoko
Uriu, Keiya
Kosugi, Yusuke
Fujita, Shigeru
Shofa, Maya
Monira Begum, M.S.T.
Shimizu, Ryo
Oda, Yoshitaka
Suzuki, Rigel
Ito, Hayato
Nao, Naganori
Wang, Lei
Tsuda, Masumi
Yoshimatsu, Kumiko
Kuramochi, Jin
Kita, Shunsuke
Sasaki-Tabata, Kaori
Fukuhara, Hideo
Maenaka, Katsumi
Yamamoto, Yuki
Nagamoto, Tetsuharu
Asakura, Hiroyuki
Nagashima, Mami
Sadamasu, Kenji
Yoshimura, Kazuhisa
Ueno, Takamasa
Schreiber, Gideon
Takaori-Kondo, Akifumi
The Genotype to Phenotype Japan (G2P-Japan) Consortium
Shirakawa, Kotaro
Sawa, Hirofumi
Irie, Takashi
Hashiguchi, Takao
Takayama, Kazuo
Matsuno, Keita
Tanaka, Shinya
Ikeda, Terumasa
Fukuhara, Takasuke
Sato, Kei
80728270
50632098
10759509
Saito, Akatsuki
Tamura, Tomokazu
Zahradnik, Jiri
Deguchi, Sayaka
Tabata, Koshiro
Anraku, Yuki
Kimura, Izumi
Ito, Jumpei
Yamasoba, Daichi
Nasser, Hesham
Toyoda, Mako
Nagata, Kayoko
Uriu, Keiya
Kosugi, Yusuke
Fujita, Shigeru
Shofa, Maya
Monira Begum, M.S.T.
Shimizu, Ryo
Oda, Yoshitaka
Suzuki, Rigel
Ito, Hayato
Nao, Naganori
Wang, Lei
Tsuda, Masumi
Yoshimatsu, Kumiko
Kuramochi, Jin
Kita, Shunsuke
Sasaki-Tabata, Kaori
Fukuhara, Hideo
Maenaka, Katsumi
Yamamoto, Yuki
Nagamoto, Tetsuharu
Asakura, Hiroyuki
Nagashima, Mami
Sadamasu, Kenji
Yoshimura, Kazuhisa
Ueno, Takamasa
Schreiber, Gideon
Takaori-Kondo, Akifumi
The Genotype to Phenotype Japan (G2P-Japan) Consortium
Shirakawa, Kotaro
Sawa, Hirofumi
Irie, Takashi
Hashiguchi, Takao
Takayama, Kazuo
Matsuno, Keita
Tanaka, Shinya
Ikeda, Terumasa
Fukuhara, Takasuke
Sato, Kei
Publication Year :
2022

Abstract

The SARS-CoV-2 Omicron BA.2.75 variant emerged in May 2022. BA.2.75 is a BA.2 descendant but is phylogenetically distinct from BA.5, the currently predominant BA.2 descendant. Here, we show that BA.2.75 has a greater effective reproduction number and different immunogenicity profile than BA.5. We determined the sensitivity of BA.2.75 to vaccinee and convalescent sera as well as a panel of clinically available antiviral drugs and antibodies. Antiviral drugs largely retained potency but antibody sensitivity varied depending on several key BA.2.75-specific substitutions. The BA.2.75 spike exhibited a profoundly higher affinity for its human receptor, ACE2. Additionally, the fusogenicity, growth efficiency in human alveolar epithelial cells, and intrinsic pathogenicity in hamsters of BA.2.75 were greater than those of BA.2. Our multilevel investigations suggest that BA.2.75 acquired virological properties independent of BA.5, and the potential risk of BA.2.75 to global health is greater than that of BA.5.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1458642143
Document Type :
Electronic Resource