畜牧兽医学报 ›› 2026, Vol. 57 ›› Issue (1): 369-377.doi: 10.11843/j.issn.0366-6964.2026.01.032

• 预防兽医 • 上一篇    下一篇

布鲁菌双重TaqMan荧光定量PCR检测方法的建立及初步应用

彭海涛(), 高阳, 刘雨欣, 顾德媛, 张东, 张如, 许会会, 陈思(), 杨艳玲()   

  1. 中国农业科学院特产研究所,长春 130000
  • 收稿日期:2025-01-22 出版日期:2026-01-23 发布日期:2026-01-26
  • 通讯作者: 陈思,杨艳玲 E-mail:735184279@qq.com;374582512@qq.com;m1804321339@163.com
  • 作者简介:彭海涛,硕士生,主要从事布鲁菌病诊断试剂研制,E-mail:735184279@qq.com
  • 基金资助:
    “十四五”国家重点研发计划(2023YFD1800703);“十四五”国家重点研发计划(2023YFD1802501);中国农业科学院重大科技任务项目(CAAS-ZDRW202410);吉林省发展与改革委员会基本建设资金产业技术与开发专项(2024C015-3)

Establishment and Preliminary Application of a Duplex TaqMan Real-time PCR Assay for Brucella

PENG Haitao(), GAO Yang, LIU Yuxin, GU Deyuan, ZHANG Dong, ZHANG Ru, XU Huihui, CHEN Si(), YANG Yanling()   

  1. Institute of Special Animal and Plant Sciences,Chinese Academy of Agricultural Sciences,Changchun 130000,China
  • Received:2025-01-22 Online:2026-01-23 Published:2026-01-26
  • Contact: CHEN Si, YANG Yanling E-mail:735184279@qq.com;374582512@qq.com;m1804321339@163.com

摘要:

旨在建立一种经济高效的布鲁菌双重TaqMan荧光定量PCR鉴别检测方法,用于布鲁菌感染的动物及动物产品的快速检测并区分牛种布鲁菌和其他种布鲁菌感染的动物,为临床常的疫苗和研发的新型疫苗提供科学有效的鉴别诊断方法。本研究根据GenBank公布的galUOmp31的序列设计检测引物和探针,构建重组质粒,对方法特异性、灵敏性及重复性评价,检测实验室制备和临床动物布病血清及组织样品。结果表明,成功建立了布鲁菌双重TaqMan荧光定量PCR检测方法,该方法最低检测限为1.93×100 copies·μL-1,与其他革兰阴性菌无交叉反应,批内及批间变异系数均小于2%。利用本研究建立的方法检测实验室制备样品和临床采集样品共156份,与BCSP31-PCR相比,两者阳性符合率为69.75%;与PCR和虎红凝集试验相比,灵敏性更高,双重TaqMan荧光定量PCR的敏感性为100%,PCR的敏感性为69.75%,虎红凝集试验的敏感性为58.65%。本研究建立的布鲁菌双重TaqMan荧光定量PCR检测方法,为布鲁菌临床鉴别检测、流行病学调查及净化提供技术支持。

关键词: 布鲁菌, 双重Taq Man荧光定量PCR, 检测方法, 鉴别诊断

Abstract:

This study aimed to establish a cost-effective duplex TaqMan real-time quantitative PCR (qPCR) assay for the rapid detection of Brucella infection in animals and animal products, and to differentiate B.abortus from other Brucella species. This method provides a scientifically valid diagnostic tool for distinguishing currently used vaccine strains and novel vaccines under development. Specific primers and TaqMan probes targeting the galU and Omp31 genes were designed based on GenBank sequences. Recombinant plasmids were constructed. The assay's specificity, sensitivity, and repeatability were rigorously evaluated. Clinical serum and tissue samples from animals with brucellosis were tested. A duplex TaqMan qPCR assay for Brucella detection was successfully developed. The limit of detection (LOD) for recombinant plasmid standards was 1.93×100copies·μL-1. The assay exhibited no cross-reactivity with other Gram-negative bacteria. Both intra-assay and inter-assay reproducibility were excellent, with coefficients of variation (CV) consistently below 2%. Testing of 156 samples (including laboratory-prepared and clinical specimens) revealed a positive agreement rate of 69.75% compared to BCSP31-PCR. Furthermore, the duplex TaqMan qPCR demonstrated significantly higher sensitivity (100%) than conventional PCR (69.75%) and the RBPT (58.65%). The established duplex TaqMan qPCR assay provides a robust technical foundation for the clinical differential diagnosis, epidemiological surveillance, and eradication programs of brucellosis.

Key words: Brucella, duplex TaqMan real-time PCR, detection method, differential diagnosis

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