基于CRISPR/Cas13a系统编码mcr-1基因的多素耐药性检测试验
Yingjie Song1, Qiang Hu1, Yao Han1
1State Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, China.
Frontiers in cellular and infection microbiology
|June 20, 2025
概括
一个新的CRISPR/Cas13a测定与侧向流带可以检测多素抗性基因mcr-1. 这种便携式方法适用于初级卫生保健和对多药耐药细菌的现场监测.
科学领域:
- 微生物学 微生物学
- 分子生物学分子生物学
- 抗微生物耐药性 抗微生物耐药性
背景情况:
- 聚米克辛对于治疗多药耐药的格拉姆阴性细菌感染至关重要.
- 在mcr-1基因的出现赋予了多素耐药性,对公众健康构成重大威胁.
- 准确和快速检测mcr-1对于指导治疗和控制耐药性传播至关重要.
研究的目的:
- 开发一种灵敏,便携式的检测mcr-1基因的方法.
- 与定量实时PCR (qPCR) 相比,评估开发的试验的性能.
主要方法:
- 为了检测mcr-1基因,使用了CRISPR/Cas13a系统与侧向流带相结合.
- 测试优化和验证使用大肠杆菌的临床分离物进行.
- 与qPCR进行了比较,以评估准确性和一致性.
主要成果:
- 对mcr-1基因的检测极限为100拷贝/毫升.
- 该试验显示出高分析特异性,没有观察到交叉反应性.
- 对36个临床隔离物观察到与qPCR结果100%的一致性,正确识别了31个mcr-1阳性菌株.
结论:
- 成功建立了一种基于CRISPR/Cas13a的mcr-1基因新型检测方法.
- 该测试提供了视觉读数,而不需要专门的设备,提高了便携性.
- 这种方法有可能在初级医疗保健机构和对多素耐药性的现场监测中应用.
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