Genomic surveillance of SARS-CoV-2 variants in Guangzhou, China, from April 2023 to March 2024

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES
Zhuoyun Li , Liya Li , Yuyi Min , Yaqing Lin , Yingfen Wen , Ruiying He , Jiaojiao Li , Quanyang Gao , Fengyu Hu , Feng Li , Yun Lan
{"title":"Genomic surveillance of SARS-CoV-2 variants in Guangzhou, China, from April 2023 to March 2024","authors":"Zhuoyun Li ,&nbsp;Liya Li ,&nbsp;Yuyi Min ,&nbsp;Yaqing Lin ,&nbsp;Yingfen Wen ,&nbsp;Ruiying He ,&nbsp;Jiaojiao Li ,&nbsp;Quanyang Gao ,&nbsp;Fengyu Hu ,&nbsp;Feng Li ,&nbsp;Yun Lan","doi":"10.1016/j.meegid.2025.105747","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>After the relaxation of stringent control measures, nationwide large-scale SARS-CoV-2 surveillance was gradually phased out post-2023, transitioning to focused monitoring of Influenza-like Illness (ILI) through sentinel hospitals and laboratory networks. Nationally, surveillance of respiratory pathogens was performed via random sampling, resulting in a lack of microbial monitoring results in Guangzhou China. A crucial area of scientific inquiry is whether the current cases are attributable to the emergence of a novel SARS-CoV-2 variant.</div></div><div><h3>Methods</h3><div>Throat swab samples were obtained from 1478 outpatients and 337 hospitalized patients with fever (temperature ≥ 38 °C) and cough or sore throat to detect SARS-CoV-2. The positive samples were subjected to viral whole-genome sequencing and phylogenetic analysis. Respiratory pathogen multiplex PCR tests were performed on stratified random samples.</div></div><div><h3>Results</h3><div>SARS-CoV-2 was detected in 517 (28.48 %) patients. There were higher rates of SARS-CoV-2 infection among women, older patients and those who were hospitalized. A total of 299 high-quality SARS-CoV-2 sequences were obtained, including 12 clades and 71 pango lineages. The advantageous clades evolved over three peak periods of infection, from BA.5 (April 2023) to XBB (June to July 2023) and then to JN.1 (February 2024). A total of 590 distinct amino acid mutations were identified across the sequences. The highest prevalence of mutations was observed for spike protein mutations, with more than 50 % of the three epidemic peaks detected. Epidemiological profiles of interactions between SARS-CoV-2 and other respiratory pathogens exhibit considerable variation across different seasons, with a tendency toward suppression within each.</div></div><div><h3>Conclusion</h3><div>Surveillance by Guangzhou Eighth People's Hospital provides a snapshot of the epidemic in Guangzhou, which is consistent with the national epidemic and offers important data for understanding the spread of SARS-CoV-2 in southern China.</div></div>","PeriodicalId":54986,"journal":{"name":"Infection Genetics and Evolution","volume":"130 ","pages":"Article 105747"},"PeriodicalIF":2.6000,"publicationDate":"2025-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infection Genetics and Evolution","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S156713482500036X","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Background

After the relaxation of stringent control measures, nationwide large-scale SARS-CoV-2 surveillance was gradually phased out post-2023, transitioning to focused monitoring of Influenza-like Illness (ILI) through sentinel hospitals and laboratory networks. Nationally, surveillance of respiratory pathogens was performed via random sampling, resulting in a lack of microbial monitoring results in Guangzhou China. A crucial area of scientific inquiry is whether the current cases are attributable to the emergence of a novel SARS-CoV-2 variant.

Methods

Throat swab samples were obtained from 1478 outpatients and 337 hospitalized patients with fever (temperature ≥ 38 °C) and cough or sore throat to detect SARS-CoV-2. The positive samples were subjected to viral whole-genome sequencing and phylogenetic analysis. Respiratory pathogen multiplex PCR tests were performed on stratified random samples.

Results

SARS-CoV-2 was detected in 517 (28.48 %) patients. There were higher rates of SARS-CoV-2 infection among women, older patients and those who were hospitalized. A total of 299 high-quality SARS-CoV-2 sequences were obtained, including 12 clades and 71 pango lineages. The advantageous clades evolved over three peak periods of infection, from BA.5 (April 2023) to XBB (June to July 2023) and then to JN.1 (February 2024). A total of 590 distinct amino acid mutations were identified across the sequences. The highest prevalence of mutations was observed for spike protein mutations, with more than 50 % of the three epidemic peaks detected. Epidemiological profiles of interactions between SARS-CoV-2 and other respiratory pathogens exhibit considerable variation across different seasons, with a tendency toward suppression within each.

Conclusion

Surveillance by Guangzhou Eighth People's Hospital provides a snapshot of the epidemic in Guangzhou, which is consistent with the national epidemic and offers important data for understanding the spread of SARS-CoV-2 in southern China.
2023 年 4 月至 2024 年 3 月期间在中国广州对 SARS-CoV-2 变种进行基因组监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信