Zhao Xiangna, He Xiaoming, Li Huan, Zhao Jiangtao, Huang Simo, Liu Wei, Wei Xiao, Ding Yiwei, Wang Zhaoyan, Zou Dayang, Wang Xuesong, Dong Derong, Yang Zhan, Yan Xiabei, Huang Liuyu, Du Shuangkui, Yuan Jing
Institute of Disease Control and Prevention, Academy of Military Medical Sciences, Beijing 100071, China.
College of Food Science and Engineering, Northwest A & F University, Yangling 712100, China.
FEMS Microbiol Lett. 2015 Sep;362(18):fnv148. doi: 10.1093/femsle/fnv148. Epub 2015 Aug 27.
Streptococcus pyogenes is an increasingly important pathogen in many parts of the world. Rapid and accurate detection of S. pyogenes aids in the control of the infection. In this study, a loop-mediated isothermal amplification (LAMP) assay was developed and validated for the specific detection of S. pyogenes. The assay incorporates two methods: a chromogenic analysis using a calcein/Mn(2+) complex and real-time turbidity monitoring to assess the reaction. Both methods detected the target DNA within 60 min under 64°C isothermal conditions. The assay used specifically designed primers to target spy1258, and correctly identified 111 strains of S. pyogenes and 32 non-S. pyogenes strains, including other species of the genus Streptococcus. Tests using reference strains showed that the LAMP assay was highly specific. The sensitivity of the assay, with a detection limit of 1.49 pg DNA, was 10-fold greater than that of PCR. The LAMP assay established in this study is simple, fast and sensitive, and does not rely upon any special equipment; thus, it could be employed in clinical diagnosis.
化脓性链球菌在世界许多地区正成为一种日益重要的病原体。快速准确地检测化脓性链球菌有助于控制感染。在本研究中,开发并验证了一种环介导等温扩增(LAMP)检测法,用于特异性检测化脓性链球菌。该检测法包含两种方法:使用钙黄绿素/Mn(2+)复合物的显色分析和实时浊度监测来评估反应。两种方法均在64°C等温条件下60分钟内检测到目标DNA。该检测法使用专门设计的引物靶向spy1258,并正确鉴定了111株化脓性链球菌菌株和32株非化脓性链球菌菌株,包括链球菌属的其他物种。使用参考菌株进行的测试表明,LAMP检测法具有高度特异性。该检测法的灵敏度检测限为1.49 pg DNA,比PCR高10倍。本研究建立的LAMP检测法简单、快速且灵敏,不依赖任何特殊设备;因此,可用于临床诊断。