• 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

利用扩增子深度测序分析、PvAmpSeq、同源性和基于模型的分类来理解复发性感染。

Understanding recurrent infections using an amplicon deep sequencing assay, PvAmpSeq, identity-by-descent and model-based classification.

作者信息

Rosado Jason, Han Jiru, Obadia Thomas, Munro Jacob, Traore Zeinabou, Schoffer Kael, Brewster Jessica, Bourke Caitlin, Vinetz Joseph M, White Michael, Bahlo Melanie, Gamboa Dionicia, Mueller Ivo, Ruybal-Pesántez Shazia

机构信息

Institut Pasteur, Université Paris Cité, Infectious Diseases Epidemiology and Analytics G5 Unit, Institut Pasteur, Paris, France.

Université Paris Cité, Institut de Recherche pour le Développement, MERIT, Paris, France.

出版信息

medRxiv. 2025 Jun 13:2025.05.26.25327775. doi: 10.1101/2025.05.26.25327775.

DOI:10.1101/2025.05.26.25327775
PMID:40492072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12148277/
Abstract

infections are characterised by recurrent bouts of blood-stage parasitaemia. Understanding the genetic relatedness of recurrences can distinguish whether these are caused by relapse, reinfection, or recrudescence, which is critical to understand treatment efficacy and transmission dynamics. We developed PvAmpseq, an amplicon sequencing assay targeting 11 SNP-rich regions of the genome. PvAmpSeq was validated on field isolates from a clinical trial in the Solomon Islands and a longitudinal observational cohort in Peru, and statistical models were applied for genetic classification of infection pairs. In the Solomon Islands trial, where participants received antimalarials at baseline, half of the recurrent infections were caused by parasites with >50% relatedness to the baseline infection, with statistical models classifying 25% and 25% as probable relapses and recrudescences, respectively. In the Peruvian cohort, 26% of recurrences were likely relapses. PvAmpSeq provides high-resolution genotyping to characterise recurrences, offering insights into transmission and treatment outcomes.

摘要

感染的特征是反复出现血期寄生虫血症。了解复发的遗传相关性可以区分这些复发是由复发、再感染还是再燃引起的,这对于理解治疗效果和传播动态至关重要。我们开发了PvAmpseq,这是一种针对基因组11个富含单核苷酸多态性(SNP)区域的扩增子测序检测方法。PvAmpSeq在来自所罗门群岛一项临床试验和秘鲁一个纵向观察队列的现场分离株上得到验证,并应用统计模型对感染对进行基因分类。在所罗门群岛的试验中,参与者在基线时接受抗疟药治疗,一半的复发性感染是由与基线感染相关性>50%的寄生虫引起的,统计模型分别将25%和25%分类为可能的复发和再燃。在秘鲁队列中,26%的复发可能是复发。PvAmpSeq提供高分辨率基因分型以表征复发情况,为传播和治疗结果提供见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/4086233a5560/nihpp-2025.05.26.25327775v2-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/4fbb50d440ce/nihpp-2025.05.26.25327775v2-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/1d65317b0bfe/nihpp-2025.05.26.25327775v2-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/b73cc2d6974f/nihpp-2025.05.26.25327775v2-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/d814074c626d/nihpp-2025.05.26.25327775v2-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/4086233a5560/nihpp-2025.05.26.25327775v2-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/4fbb50d440ce/nihpp-2025.05.26.25327775v2-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/1d65317b0bfe/nihpp-2025.05.26.25327775v2-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/b73cc2d6974f/nihpp-2025.05.26.25327775v2-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/d814074c626d/nihpp-2025.05.26.25327775v2-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/12169163/4086233a5560/nihpp-2025.05.26.25327775v2-f0006.jpg

相似文献

1
Understanding recurrent infections using an amplicon deep sequencing assay, PvAmpSeq, identity-by-descent and model-based classification.利用扩增子深度测序分析、PvAmpSeq、同源性和基于模型的分类来理解复发性感染。
medRxiv. 2025 Jun 13:2025.05.26.25327775. doi: 10.1101/2025.05.26.25327775.
2
Artemisinin-based combination therapy for treating uncomplicated Plasmodium vivax malaria.以青蒿素为基础的联合疗法治疗无并发症间日疟原虫疟疾。
Cochrane Database Syst Rev. 2013 Oct 25;2013(10):CD008492. doi: 10.1002/14651858.CD008492.pub3.
3
Microhaplotype deep sequencing assays to capture Plasmodium vivax infection lineages.用于捕获间日疟原虫感染谱系的微单倍型深度测序分析。
Nat Commun. 2025 Aug 5;16(1):7192. doi: 10.1038/s41467-025-62357-x.
4
Mass drug administration for malaria.大规模药物治疗疟疾。
Cochrane Database Syst Rev. 2021 Sep 29;9(9):CD008846. doi: 10.1002/14651858.CD008846.pub3.
5
Primaquine or other 8-aminoquinoline for reducing P. falciparum transmission.伯氨喹或其他8-氨基喹啉用于减少恶性疟原虫传播。
Cochrane Database Syst Rev. 2014 Jun 30(6):CD008152. doi: 10.1002/14651858.CD008152.pub3.
6
Comparison of Two Modern Survival Prediction Tools, SORG-MLA and METSSS, in Patients With Symptomatic Long-bone Metastases Who Underwent Local Treatment With Surgery Followed by Radiotherapy and With Radiotherapy Alone.两种现代生存预测工具 SORG-MLA 和 METSSS 在接受手术联合放疗和单纯放疗治疗有症状长骨转移患者中的比较。
Clin Orthop Relat Res. 2024 Dec 1;482(12):2193-2208. doi: 10.1097/CORR.0000000000003185. Epub 2024 Jul 23.
7
Primaquine or other 8-aminoquinoline for reducing Plasmodium falciparum transmission.伯氨喹或其他8-氨基喹啉用于减少恶性疟原虫传播。
Cochrane Database Syst Rev. 2015 Feb 19(2):CD008152. doi: 10.1002/14651858.CD008152.pub4.
8
Mass drug administration for malaria.疟疾群体服药
Cochrane Database Syst Rev. 2013 Dec 9;2013(12):CD008846. doi: 10.1002/14651858.CD008846.pub2.
9
Primaquine for preventing relapse in people with Plasmodium vivax malaria treated with chloroquine.伯氨喹用于预防接受氯喹治疗的间日疟患者复发。
Cochrane Database Syst Rev. 2013 Oct 26;2013(10):CD004389. doi: 10.1002/14651858.CD004389.pub3.
10
Aural toilet (ear cleaning) for chronic suppurative otitis media.慢性化脓性中耳炎的耳道清理(耳部清洁)
Cochrane Database Syst Rev. 2025 Jun 9;6(6):CD013057. doi: 10.1002/14651858.CD013057.pub3.

本文引用的文献

1
Microhaplotype deep sequencing assays to capture Plasmodium vivax infection lineages.用于捕获间日疟原虫感染谱系的微单倍型深度测序分析。
Nat Commun. 2025 Aug 5;16(1):7192. doi: 10.1038/s41467-025-62357-x.
2
Molecular epidemiology and genetic diversity of disappearing Plasmodium vivax in southern Thailand.泰国南部间日疟原虫消失的分子流行病学与遗传多样性
Sci Rep. 2025 Jan 21;15(1):2620. doi: 10.1038/s41598-025-86578-8.
3
High-throughput genotyping of Plasmodium vivax in the Peruvian Amazon via molecular inversion probes.高通量基因分型玻利维亚亚马逊流域间日疟 via 分子反转探针。
Nat Commun. 2024 Nov 25;15(1):10219. doi: 10.1038/s41467-024-54731-y.
4
AmpSeqR: an R package for amplicon deep sequencing data analysis.AmpSeqR:一个用于扩增子高通量测序数据分析的 R 包。
F1000Res. 2023 Mar 23;12:327. doi: 10.12688/f1000research.129581.1. eCollection 2023.
5
Genetic diversity of Plasmodium vivax population in northeast Myanmar assessed by amplicon sequencing of PvMSP1 and PvMSP3α.通过间日疟原虫 merozoite surface protein 1(PvMSP1)和 PvMSP3α 的扩增子测序评估缅甸东北部间日疟原虫种群的遗传多样性。
Acta Trop. 2024 Dec;260:107461. doi: 10.1016/j.actatropica.2024.107461. Epub 2024 Nov 12.
6
Lineage-informative microhaplotypes for recurrence classification and spatio-temporal surveillance of Plasmodium vivax malaria parasites.用于间日疟原虫疟疾寄生虫复发分类和时空监测的谱系信息微单倍型
Nat Commun. 2024 Aug 8;15(1):6757. doi: 10.1038/s41467-024-51015-3.
7
Plasmodium vivax genomic surveillance in the Peruvian Amazon with Pv AmpliSeq assay.采用 PvAmpliSeq assay 对秘鲁亚马逊地区的间日疟原虫进行基因组监测。
PLoS Negl Trop Dis. 2024 Jul 11;18(7):e0011879. doi: 10.1371/journal.pntd.0011879. eCollection 2024 Jul.
8
Using a mobile nanopore sequencing lab for end-to-end genomic surveillance of Plasmodium falciparum: A feasibility study.使用移动纳米孔测序实验室对恶性疟原虫进行端到端基因组监测:一项可行性研究。
PLOS Glob Public Health. 2024 Feb 1;4(2):e0002743. doi: 10.1371/journal.pgph.0002743. eCollection 2024.
9
Molecular markers for malaria genetic epidemiology: progress and pitfalls.疟疾遗传流行病学的分子标记:进展与问题
Trends Parasitol. 2024 Feb;40(2):147-163. doi: 10.1016/j.pt.2023.11.006. Epub 2023 Dec 20.
10
Amplicon deep sequencing of five highly polymorphic markers of Plasmodium falciparum reveals high parasite genetic diversity and moderate population structure in Ethiopia.对恶性疟原虫五个高度多态性标记物的扩增子深度测序揭示了埃塞俄比亚寄生虫遗传多样性高和种群结构中等。
Malar J. 2023 Dec 12;22(1):376. doi: 10.1186/s12936-023-04814-w.