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基于CRISPR-Cas12b技术的登革病毒检测方法的建立

马银双 刘静 谢晓霞 李娟娟 杨阳 张富强 张蕾 胡挺松

中国人兽共患病学报2026,Vol.42Issue(3):263-268,284,7.
中国人兽共患病学报2026,Vol.42Issue(3):263-268,284,7.DOI:10.3969/j.issn.1002-2694.2026.00.062

基于CRISPR-Cas12b技术的登革病毒检测方法的建立

Establishment of a dengue virus detection method based on CRISPR-Cas12b

马银双 1刘静 1谢晓霞 2李娟娟 3杨阳 1张富强 1张蕾 1胡挺松1

作者信息

  • 1. 中国人民解放军南部战区疾病预防控制中心,广州 510507
  • 2. 广州医科大学公共卫生学院,广州 511436
  • 3. 暨南大学基础医学与公共卫生学院,广州 510632
  • 折叠

摘要

Abstract

This study was aimed at establishing a detection method for dengue virus(DENV)based on RPA-CRISPR/Cas12b tech-nology.We designed and synthesized RPA primers and sgRNAs targeting the conserved 3'-UTR region of the DENV genome,screened for optimal sgRNA and RPA primer combinations,and established the RPA-CRISPR/Cas12b detection system.Plasmid standards were constructed to evaluate sensitivity with varying plasmid concentrations.The established method was validated in 16 blood samples.The re-sults demonstrated a minimum detection limit of 1 copies/µL for DENV plasmid.The results for the 16 blood samples exhibited 100%con-cordance with RT-qPCR results.The established RPA-CRISPR/Cas12b-based DENV detection method is simple and rapid,and it exhib-its favorable specificity and sensitivity,thereby offering a novel strategy for faster,more portable identification of DENV.

关键词

CRISPR-Cas12b/登革病毒/检测

Key words

CRISPR-Cas12b/dengue virus/detection

分类

医药卫生

引用本文复制引用

马银双,刘静,谢晓霞,李娟娟,杨阳,张富强,张蕾,胡挺松..基于CRISPR-Cas12b技术的登革病毒检测方法的建立[J].中国人兽共患病学报,2026,42(3):263-268,284,7.

中国人兽共患病学报

1002-2694

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