文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

社论:奥密克戎 SARS-CoV-2 的 XBB.1.5(“Kraken”)亚变体及其快速全球传播。

Editorial: The XBB.1.5 ('Kraken') Subvariant of Omicron SARS-CoV-2 and its Rapid Global Spread.

机构信息

Science Editor, Medical Science Monitor, International Scientific Information, Inc., Melville, NY, USA.

出版信息

Med Sci Monit. 2023 Feb 1;29:e939580. doi: 10.12659/MSM.939580.


DOI:10.12659/MSM.939580
PMID:36722047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9901170/
Abstract

In November 2021, the World Health Organization (WHO) first identified the Omicron variant of SARS-CoV-2, B.1.1.529, as a variant of concern (VOC). By early 2022, the Omicron variant and its five lineages, BA.1, BA.2, BA.3, BA.4. and BA.5, had become the predominant cause of COVID-19 in most countries. The Omicron XBB.1.5 subvariant is a sublineage of the XBB variant, a recombinant of two BA.2 sublineages, with the F486P mutation in the spike protein that increases infectivity due to increased binding affinity to the angiotensin-converting enzyme 2 (ACE2) receptor. On the week ending 21 January 2023, the XBB.1.5 subvariant caused 49.1% of cases of COVID-19 in the US. The rapid rise in the prevalence of this subvariant may be explained by immune escape to previous infection or vaccines, spike mutations in F486P, and increased affinity for the ACE2 receptor. Also, current booster vaccines may not provide adequate protection from infection from this subvariant, which has been named by the media as the 'Kraken' subvariant. This Editorial aims to present the current status of the XBB.1.5 subvariant of Omicron SARS-CoV-2 and the reasons for, and implications of, its rapid global spread.

摘要

2021 年 11 月,世界卫生组织(WHO)首次将 SARS-CoV-2 的奥密克戎变异株 B.1.1.529 鉴定为关注变异株(VOC)。到 2022 年初,奥密克戎变异株及其五个谱系,BA.1、BA.2、BA.3、BA.4 和 BA.5,已成为大多数国家 COVID-19 的主要致病原因。奥密克戎 XBB.1.5 亚谱系是 XBB 变异株的一个亚谱系,是两个 BA.2 亚谱系的重组体,其刺突蛋白中的 F486P 突变增加了与血管紧张素转换酶 2(ACE2)受体的结合亲和力,从而提高了感染力。截至 2023 年 1 月 21 日当周,XBB.1.5 亚谱系导致美国 COVID-19 病例的 49.1%。这种亚谱系的快速流行可能归因于先前感染或疫苗的免疫逃逸、刺突蛋白中的 F486P 突变以及对 ACE2 受体的亲和力增加。此外,目前的加强疫苗可能无法为感染这种亚谱系提供充分的保护,这种亚谱系已被媒体命名为“Kraken”亚谱系。本社论旨在介绍奥密克戎 SARS-CoV-2 的 XBB.1.5 亚谱系的现状及其快速全球传播的原因和影响。

相似文献

[1]
Editorial: The XBB.1.5 ('Kraken') Subvariant of Omicron SARS-CoV-2 and its Rapid Global Spread.

Med Sci Monit. 2023-2-1

[2]
Ensemble-Based Mutational Profiling and Network Analysis of the SARS-CoV-2 Spike Omicron XBB Lineages for Interactions with the ACE2 Receptor and Antibodies: Cooperation of Binding Hotspots in Mediating Epistatic Couplings Underlies Binding Mechanism and Immune Escape.

Int J Mol Sci. 2024-4-12

[3]
Relative vaccine protection, disease severity, and symptoms associated with the SARS-CoV-2 omicron subvariant BA.2.86 and descendant JN.1 in Denmark: a nationwide observational study.

Lancet Infect Dis. 2024-9

[4]
Balancing Functional Tradeoffs between Protein Stability and ACE2 Binding in the SARS-CoV-2 Omicron BA.2, BA.2.75 and XBB Lineages: Dynamics-Based Network Models Reveal Epistatic Effects Modulating Compensatory Dynamic and Energetic Changes.

Viruses. 2023-5-10

[5]
Early Estimates of Bivalent mRNA Booster Dose Vaccine Effectiveness in Preventing Symptomatic SARS-CoV-2 Infection Attributable to Omicron BA.5- and XBB/XBB.1.5-Related Sublineages Among Immunocompetent Adults - Increasing Community Access to Testing Program, United States, December 2022-January 2023.

MMWR Morb Mortal Wkly Rep. 2023-2-3

[6]
Temperature-dependent Spike-ACE2 interaction of Omicron subvariants is associated with viral transmission.

mBio. 2024-8-14

[7]
EG.5 (Eris) and BA.2.86 (Pirola) two new subvariants of SARS-CoV-2: a new face of old COVID-19.

Infection. 2024-4

[8]
Comprehensive Analysis of Omicron Subvariants: EG.5 Rise, Vaccination Strategies, and Global Impact.

Curr Drug Targets. 2024

[9]
Comparative Analysis of Conformational Dynamics and Systematic Characterization of Cryptic Pockets in the SARS-CoV-2 Omicron BA.2, BA.2.75 and XBB.1 Spike Complexes with the ACE2 Host Receptor: Confluence of Binding and Structural Plasticity in Mediating Networks of Conserved Allosteric Sites.

Viruses. 2023-10-10

[10]
Editorial: A Rapid Global Increase in COVID-19 is Due to the Emergence of the EG.5 (Eris) Subvariant of Omicron SARS-CoV-2.

Med Sci Monit. 2023-9-1

引用本文的文献

[1]
Multiscale Modeling and Dynamic Mutational Profiling of Binding Energetics and Immune Escape for Class I Antibodies with SARS-CoV-2 Spike Protein: Dissecting Mechanisms of High Resistance to Viral Escape Against Emerging Variants.

Viruses. 2025-7-23

[2]
4-Hydroxychalcone Inhibits Human Coronavirus HCoV-OC43 by Targeting EGFR/AKT/ERK1/2 Signaling Pathway.

Viruses. 2025-7-23

[3]
Conformational Dynamics and Binding Interactions of SARS-CoV-2 Spike Protein Variants: Omicron, XBB.1.9.2, and EG.5.

J Chem Inf Model. 2025-7-11

[4]
In silico genomic surveillance by CoVerage predicts and characterizes SARS-CoV-2 variants of interest.

Nat Commun. 2025-7-8

[5]
Emergence and transmission dynamics of the FY.4 Omicron variant in Kenya.

Virus Evol. 2025-5-11

[6]
Beyond the Pandemic Era: Recent Advances and Efficacy of SARS-CoV-2 Vaccines Against Emerging Variants of Concern.

Vaccines (Basel). 2025-4-17

[7]
Conformational and Stability Analysis of SARS-CoV-2 Spike Protein Variants by Molecular Simulation.

Pathogens. 2025-3-12

[8]
Early 2022 breakthrough infection sera from India target the conserved cryptic class 5 epitope to counteract immune escape by SARS-CoV-2 variants.

J Virol. 2025-4-15

[9]
Quantitative Characterization and Prediction of the Binding Determinants and Immune Escape Hotspots for Groups of Broadly Neutralizing Antibodies Against Omicron Variants: Atomistic Modeling of the SARS-CoV-2 Spike Complexes with Antibodies.

Biomolecules. 2025-2-8

[10]
Genomic Epidemiology of the Main SARS-CoV-2 Variants Circulating in Italy During the Omicron Era.

J Med Virol. 2025-2

本文引用的文献

[1]
Substantial Neutralization Escape by SARS-CoV-2 Omicron Variants BQ.1.1 and XBB.1.

N Engl J Med. 2023-2-16

[2]
Daily briefing: Is subvariant XBB.1.5 a global threat?

Nature. 2023-1-10

[3]
Coronavirus variant XBB.1.5 rises in the United States - is it a global threat?

Nature. 2023-1

[4]
Characterization of SARS-CoV-2 recombinants and emerging Omicron sublineages.

Int J Med Sci. 2023

[5]
Antibody evasion by SARS-CoV-2 Omicron subvariants BA.2.12.1, BA.4 and BA.5.

Nature. 2022-8

[6]
Neutralization Escape by SARS-CoV-2 Omicron Subvariants BA.2.12.1, BA.4, and BA.5.

N Engl J Med. 2022-7-7

[7]
Are COVID surges becoming more predictable? New Omicron variants offer a hint.

Nature. 2022-5

[8]
Editorial: The 2022 World Health Organization (WHO) Priority Recommendations and Response to the Omicron Variant (B.1.1.529) of SARS-CoV-2.

Med Sci Monit. 2022-2-1

[9]
Editorial: Revised World Health Organization (WHO) Terminology for Variants of Concern and Variants of Interest of SARS-CoV-2.

Med Sci Monit. 2021-6-21

[10]
Genetic Variants of SARS-CoV-2-What Do They Mean?

JAMA. 2021-2-9

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索