Virological characteristics of the SARS-CoV-2 Omicron EG.5.1 variant

IF 1.9 4区 医学 Q4 IMMUNOLOGY
Shuhei Tsujino, Sayaka Deguchi, Tomo Nomai, Miguel Padilla-Blanco, Arnon Plianchaisuk, Lei Wang, MST Monira Begum, Keiya Uriu, Keita Mizuma, Naganori Nao, Isshu Kojima, Tomoya Tsubo, Jingshu Li, Yasufumi Matsumura, Miki Nagao, Yoshitaka Oda, Masumi Tsuda, Yuki Anraku, Shunsuke Kita, Hisano Yajima, Kaori Sasaki-Tabata, Ziyi Guo, Alfredo A. Hinay Jr., Kumiko Yoshimatsu, Yuki Yamamoto, Tetsuharu Nagamoto, Hiroyuki Asakura, Mami Nagashima, Kenji Sadamasu, Kazuhisa Yoshimura, Hesham Nasser, Michael Jonathan, Olivia Putri, Yoonjin Kim, Luo Chen, Rigel Suzuki, Tomokazu Tamura, Katsumi Maenaka, Takashi Irie, Keita Matsuno, Shinya Tanaka, Jumpei Ito, Terumasa Ikeda, Kazuo Takayama, Jiri Zahradnik, Takao Hashiguchi, Takasuke Fukuhara, Kei Sato, The Genotype to Phenotype Japan (G2P-Japan) Consortium
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Abstract

In middle to late 2023, a sublineage of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron XBB, EG.5.1 (a progeny of XBB.1.9.2), is spreading rapidly around the world. We performed multiscale investigations, including phylogenetic analysis, epidemic dynamics modeling, infection experiments using pseudoviruses, clinical isolates, and recombinant viruses in cell cultures and experimental animals, and the use of human sera and antiviral compounds, to reveal the virological features of the newly emerging EG.5.1 variant. Our phylogenetic analysis and epidemic dynamics modeling suggested that two hallmark substitutions of EG.5.1, S:F456L and ORF9b:I5T are critical to its increased viral fitness. Experimental investigations on the growth kinetics, sensitivity to clinically available antivirals, fusogenicity, and pathogenicity of EG.5.1 suggested that the virological features of EG.5.1 are comparable to those of XBB.1.5. However, cryo-electron microscopy revealed structural differences between the spike proteins of EG.5.1 and XBB.1.5. We further assessed the impact of ORF9b:I5T on viral features, but it was almost negligible in our experimental setup. Our multiscale investigations provide knowledge for understanding the evolutionary traits of newly emerging pathogenic viruses, including EG.5.1, in the human population.

Abstract Image

SARS-CoV-2 Omicron EG.5.1 变体的病毒学特征。
2023 年中后期,严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)的一个亚系 Omicron XBB、EG.5.1(XBB.1.9.2 的后代)正在全球迅速传播。为了揭示新出现的 EG.5.1 变体的病毒学特征,我们进行了多尺度研究,包括系统进化分析、流行动力学建模、使用假病毒、临床分离株和重组病毒在细胞培养物和实验动物中进行感染实验,以及使用人类血清和抗病毒化合物。我们的系统发育分析和流行动力学建模表明,EG.5.1的两个标志性取代,即S:F456L和ORF9b:I5T,是其提高病毒适应性的关键。对 EG.5.1 的生长动力学、对临床可用抗病毒药物的敏感性、致熔性和致病性进行的实验研究表明,EG.5.1 的病毒学特征与 XBB.1.5 相当。然而,低温电子显微镜显示 EG.5.1 和 XBB.1.5 的尖峰蛋白在结构上存在差异。我们进一步评估了 ORF9b:I5T 对病毒特征的影响,但在我们的实验装置中几乎可以忽略不计。我们的多尺度研究为了解包括EG.5.1在内的新出现的致病病毒在人类群体中的进化特征提供了知识。
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来源期刊
Microbiology and Immunology
Microbiology and Immunology 医学-免疫学
CiteScore
5.20
自引率
3.80%
发文量
78
审稿时长
1 months
期刊介绍: Microbiology and Immunology is published in association with Japanese Society for Bacteriology, Japanese Society for Virology, and Japanese Society for Host Defense Research. It is peer-reviewed publication that provides insight into the study of microbes and the host immune, biological and physiological responses. Fields covered by Microbiology and Immunology include:Bacteriology|Virology|Immunology|pathogenic infections in human, animals and plants|pathogenicity and virulence factors such as microbial toxins and cell-surface components|factors involved in host defense, inflammation, development of vaccines|antimicrobial agents and drug resistance of microbes|genomics and proteomics.
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