• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
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
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
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 @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

临床分离株的分子钟速率低于每年每个基因组1个单核苷酸多态性。

Clinical isolates exhibit a molecular clock rate below 1 SNP per genome per year.

作者信息

Wang Jun-Li, Chen Ya-Li, Guan Cui-Ping, Yu Kan, Wang Mao-Shui

机构信息

Department of Lab Medicine, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.

Guangxi Engineering Research Center for Precise Genetic Testing of Long-Dwelling Nationalities, Guangxi, China.

出版信息

Front Microbiol. 2025 Jun 13;16:1591792. doi: 10.3389/fmicb.2025.1591792. eCollection 2025.

DOI:10.3389/fmicb.2025.1591792
PMID:40584032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12202658/
Abstract

PURPOSE

Tuberculosis (TB) remains a significant global health concern, necessitating effective measures to control the epidemic. Understanding the evolution of () through molecular clock analysis is crucial for tracing outbreaks, managing transmission, and ultimately improving TB management in practice.

RESULTS

A total of 27 studies were included for analysis. The pooled mutation rate was estimated at 0.63 single nucleotide polymorphisms (SNPs) per genome per year [95% confidence interval (CI): 0.51-0.75; 95% predictive interval (PI): 0.04-1.22], significant heterogeneity (I = 92.7%,  < 0.001) was observed. Clinical strains had a mutation rate of 0.55 SNPs per year (95% CI: 0.45-0.65; 95% PI: 0.12-0.98), while model strains showed a higher rate of 1.14 SNPs per year (95% CI: 0.68-1.60; 95% PI: -0.22-2.50; Meta-regression analysis,  = 0.006). Mutation rates did not significantly differ between transmission events and reactivation or single episodes ( = 0.497).

CONCLUSION

The mutation rate of clinical strains is below 1 SNP per genome per year, indicating evolutionary stability in clinical settings. This finding is important for TB outbreak reconstructions and public health strategies. Future research should refine subgroup analyses based on infection characteristics for more precise molecular clock estimates.

SYSTEMATIC REVIEW REGISTRATION

PROSPERO, identifier CRD42024595161.

摘要

目的

结核病仍然是全球重大的公共卫生问题,需要采取有效措施来控制疫情。通过分子钟分析了解()的演变对于追踪疫情暴发、管理传播以及最终改善结核病的实际管理至关重要。

结果

共纳入27项研究进行分析。估计每年每个基因组的合并突变率为0.63个单核苷酸多态性(SNP)[95%置信区间(CI):0.51 - 0.75;95%预测区间(PI):0.04 - 1.22],观察到显著的异质性(I² = 92.7%,P < 0.001)。临床菌株的突变率为每年0.55个SNP(95% CI:0.45 - 0.65;95% PI:0.12 - 0.98),而模型菌株的突变率较高,为每年1.14个SNP(95% CI:0.68 - 1.60;95% PI: - 0.22 - 2.50;Meta回归分析,P = 0.006)。传播事件与再激活或单次发作之间的突变率无显著差异(P = 0.497)。

结论

临床()菌株的突变率低于每年每个基因组1个SNP,表明临床环境中的进化稳定性。这一发现对于结核病疫情暴发的重建和公共卫生策略很重要。未来的研究应根据感染特征完善亚组分析,以获得更精确的分子钟估计。

系统评价注册

PROSPERO,标识符CRD42024595161。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c429/12202658/7ea7d146fd37/fmicb-16-1591792-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c429/12202658/dd8340ef3268/fmicb-16-1591792-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c429/12202658/7ea7d146fd37/fmicb-16-1591792-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c429/12202658/dd8340ef3268/fmicb-16-1591792-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c429/12202658/7ea7d146fd37/fmicb-16-1591792-g002.jpg

相似文献

1
Clinical isolates exhibit a molecular clock rate below 1 SNP per genome per year.临床分离株的分子钟速率低于每年每个基因组1个单核苷酸多态性。
Front Microbiol. 2025 Jun 13;16:1591792. doi: 10.3389/fmicb.2025.1591792. eCollection 2025.
2
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.系统性药理学治疗慢性斑块状银屑病:网络荟萃分析。
Cochrane Database Syst Rev. 2021 Apr 19;4(4):CD011535. doi: 10.1002/14651858.CD011535.pub4.
3
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.慢性斑块状银屑病的全身药理学治疗:一项网状Meta分析。
Cochrane Database Syst Rev. 2020 Jan 9;1(1):CD011535. doi: 10.1002/14651858.CD011535.pub3.
4
Intravenous magnesium sulphate and sotalol for prevention of atrial fibrillation after coronary artery bypass surgery: a systematic review and economic evaluation.静脉注射硫酸镁和索他洛尔预防冠状动脉搭桥术后房颤:系统评价与经济学评估
Health Technol Assess. 2008 Jun;12(28):iii-iv, ix-95. doi: 10.3310/hta12280.
5
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.慢性斑块状银屑病的全身药理学治疗:一项网状荟萃分析。
Cochrane Database Syst Rev. 2017 Dec 22;12(12):CD011535. doi: 10.1002/14651858.CD011535.pub2.
6
Molecular clustering of patients with diabetes and pulmonary tuberculosis: A systematic review and meta-analysis.糖尿病合并肺结核患者的分子聚类:系统评价与荟萃分析
PLoS One. 2017 Sep 13;12(9):e0184675. doi: 10.1371/journal.pone.0184675. eCollection 2017.
7
Xpert MTB/RIF assay for extrapulmonary tuberculosis and rifampicin resistance.用于肺外结核病和利福平耐药性的Xpert MTB/RIF检测
Cochrane Database Syst Rev. 2018 Aug 27;8(8):CD012768. doi: 10.1002/14651858.CD012768.pub2.
8
Home treatment for mental health problems: a systematic review.心理健康问题的居家治疗:一项系统综述
Health Technol Assess. 2001;5(15):1-139. doi: 10.3310/hta5150.
9
Intensive case management for severe mental illness.严重精神疾病的强化个案管理。
Cochrane Database Syst Rev. 2010 Oct 6(10):CD007906. doi: 10.1002/14651858.CD007906.pub2.
10
Computer and mobile technology interventions for self-management in chronic obstructive pulmonary disease.用于慢性阻塞性肺疾病自我管理的计算机和移动技术干预措施。
Cochrane Database Syst Rev. 2017 May 23;5(5):CD011425. doi: 10.1002/14651858.CD011425.pub2.

本文引用的文献

1
Genetic factors associated with acquired phenotypic drug resistance and its compensatory evolution during tuberculosis treatment.与获得性表型药物耐药性相关的遗传因素及其在结核病治疗期间的代偿性进化。
Clin Microbiol Infect. 2024 May;30(5):637-645. doi: 10.1016/j.cmi.2024.01.016. Epub 2024 Jan 28.
2
Systematic comparison of variant calling pipelines of target genome sequencing cross multiple next-generation sequencers.跨多个下一代测序仪对目标基因组测序变异检测流程的系统比较。
Front Genet. 2024 Jan 4;14:1293974. doi: 10.3389/fgene.2023.1293974. eCollection 2023.
3
Global-scale GWAS associates a subset of SNPs with animal-adapted variants in M. tuberculosis complex.
全球范围的 GWAS 将一小部分 SNP 与结核分枝杆菌复合群中的动物适应变体相关联。
BMC Med Genomics. 2023 Oct 24;16(1):260. doi: 10.1186/s12920-023-01695-5.
4
Advantages of analysing both pairwise SNV-distance and differing SNVs between isolates for recurrent tuberculosis cause determination.分析重复结核病因确定中两种配对 SNV 距离和不同 SNV 的优势。
Microb Genom. 2023 Mar;9(3). doi: 10.1099/mgen.0.000956.
5
Estimation of the mutation rate of Mycobacterium tuberculosis in cases with recurrent tuberculosis using whole genome sequencing.使用全基因组测序估计复发性结核病例中结核分枝杆菌的突变率。
Sci Rep. 2022 Oct 6;12(1):16728. doi: 10.1038/s41598-022-21144-0.
6
Variant calling: Considerations, practices, and developments.变异调用:考虑因素、实践和发展。
Hum Mutat. 2022 Aug;43(8):976-985. doi: 10.1002/humu.24311. Epub 2021 Dec 16.
7
complex lineage 5 exhibits high levels of within-lineage genomic diversity and differing gene content compared to the type strain H37Rv.与 H37Rv 相比,谱系 5 表现出较高的谱系内基因组多样性和不同的基因组成。
Microb Genom. 2021 Jul;7(7). doi: 10.1099/mgen.0.000437.
8
Meta-analysis of variation suggests that embracing variability improves both replicability and generalizability in preclinical research.元分析表明,在临床前研究中,接受变异性可以提高可重复性和普遍性。
PLoS Biol. 2021 May 19;19(5):e3001009. doi: 10.1371/journal.pbio.3001009. eCollection 2021 May.
9
Genomic epidemiology of tuberculosis in eastern Malaysia: insights for strengthening public health responses.马来西亚东部的结核病基因组流行病学:加强公共卫生应对措施的见解。
Microb Genom. 2021 May;7(5). doi: 10.1099/mgen.0.000573.
10
PRISMA 2020 explanation and elaboration: updated guidance and exemplars for reporting systematic reviews.PRISMA 2020 解释和说明:系统评价报告的更新指南和范例。
BMJ. 2021 Mar 29;372:n160. doi: 10.1136/bmj.n160.