首页|期刊导航|分析化学|炭疽芽孢生物标志物2,6-吡啶二羧酸检测技术的研究进展

炭疽芽孢生物标志物2,6-吡啶二羧酸检测技术的研究进展OA

Research Progress on Detection Techniques for Anthrax Spore Biomarker Dipicolinic Acid

中文摘要英文摘要

炭疽病是由炭疽芽孢杆菌引起的人畜共患严重传染病,其产生的芽孢具有极强的传染性和环境抵抗力,对公共健康与生物安全构成重大威胁.2,6-吡啶二羧酸(DPA)是炭疽芽孢特有的生物标志物,对其开展痕量和高特异性检测对炭疽病早期诊断、疫情预警及生物安全防控至关重要.近年来,DPA化学检测技术因具有操作简便、成本低、灵敏度高和响应快速等优势,已成为该领域的研究热点.本文首先简要介绍了炭疽杆菌及其芽孢的生物检测技术(聚合酶链式反应、环介导等温扩增和 CRISPR-Cas技术)的研究现状,然后重点总结了基于化学技术检测DPA的最新研究进展,包括光学检测、电化学检测及检测技术联用方法等,最后,结合当前技术瓶颈,对DPA检测技术的应用前景与未来发展方向进行了展望.

Anthrax is a severe zoonotic infectious disease caused by Bacillus anthracis,whose spores possess extremely strong infectivity and environmental resistance,posing a major threat to public health and biosecurity.As a unique biomarker of anthrax spores,trace and highly specific detection of 2,6-pyridinedicarboxylic acid(DPA)is crucial for early diagnosis of anthrax,epidemic early warning,and biosecurity prevention and control.In recent years,DPA chemical detection techniques have become a research hotspot in this field due to their advantages of simple operation,low cost,high sensitivity and rapid response.Firstly,this review briefly introduced the research status of biological detection techniques for Bacillus anthracis and its spores,including polymerase chain reaction,loop-mediated isothermal amplification and CRISPR-Cas techniques.Subsequently,it focused on summarizing the latest research progress of DPA detection based on chemical techniques,including principles,advantages,disadvantages,and differences in limit of detection of optical,electrochemical and hyphenated detection techniques.Finally,combined with the current technical bottlenecks,future optimization directions and application prospects of DPA detection technologies were prospected.

王鑫;高梅梅;杨婉琪;周金荣;赵世强;陈玮;常春

郑州大学化工学院,郑州 450001郑州大学第一附属医院药学部,郑州 450052郑州大学化工学院,郑州 450001郑州大学化工学院,郑州 450001郑州大学化工学院,郑州 450001宏业控股集团有限公司,濮阳 457004郑州大学化工学院,郑州 450001

炭疽病2,6-吡啶二羧酸生物标志物检测技术评述

AnthraxDipicolinic acidBiomarkerDetection techniquesReview

《分析化学》 2026 (5)

814-824,11

国家自然科学基金项目(No.22203079)、河南省重点研发与推广项目(科技攻关)(No.252102310047)和河南省研究生教育改革与质量提升工程项目(No.YJS2024JD04)资助. Supported by the National Natural Science Foundation of China(No.22203079),the Key Research and Development Program of Henan Province(Science and Technology Project)(No.252102310047)and the Graduate Education Reform and Quality Improvement Project of Henan Province(No.YJS2024JD04).

10.19756/j.issn.0253-3820.251333

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