Du Shuheng, Yan Chao, Du Bing, Zhao Hanqing, Xue Guanhua, Zheng Ping, Feng Yanling, Cui Jinghua, Gan Lin, Feng Junxia, Fan Zheng, Xu Ziying, Fu Tongtong, Fu Hanyu, Zhang Qun, Li Nannan, Zhang Rui, Liu Shiyu, Li Xiaoran, Cui Xiaohu, Zhou Yao, Zhang Qi, Chen Yaodong, Yuan Jing
Department of Bacteriology, Capital Institute of Pediatrics, Beijing, China.
Key Laboratory of Resources Biology and Biotechnology in Western China, Ministry of Education, College of Life Sciences, Northwest University, Xi'an, China.
Front Microbiol. 2022 Jan 17;12:816997. doi: 10.3389/fmicb.2021.816997. eCollection 2021.
() is a common major human pathogen associated with community-acquired pneumonia, septicemia, meningitis, and otitis media. It is difficult to isolate and identify form clinical samples. To evaluate a novel, rapid, sensitive, and specific loop-mediated isothermal amplification (LAMP) assay to detect pneumonia in children, we designed specific LAMP primers targeting and genes. We optimized the reaction time and reaction system, and evaluated its sensitivity and specificity of detection using real-time turbidity monitoring and visual observation. We also analyzed the molecular characteristics of the isolates obtained from the positive samples. The primer sets LytA-1 and PsaA-2 amplified the genes in the shortest times, and 63°C was confirmed as the optimum reaction temperature. The detection sensitivity of each reaction was 10 and 100 copies/μL with primer sets LytA-1 and PsaA-2, respectively. This LAMP assay showed no cross-reactivity with other 27 pathogens. To describe the availability of this method, we collected 748 clinical samples from children with pneumonia. Among them, 135 were confirmed to be positive by LAMP. The sensitivity was 100% (95% CI 96.4-100%), specificity 99.0% (95% CI 97.8-99.6%). Including them, 50 were co-infected with . This LAMP assay detected in 1 h and the results can be identified with visual naked eyes. Thus, it will be a powerful tool for early diagnosis and effective antibiotic therapy.
()是一种常见的主要人类病原体,与社区获得性肺炎、败血症、脑膜炎和中耳炎相关。从临床样本中分离和鉴定它很困难。为了评估一种新型、快速、灵敏且特异的环介导等温扩增(LAMP)检测法用于检测儿童肺炎,我们设计了针对和基因的特异性LAMP引物。我们优化了反应时间和反应体系,并使用实时浊度监测和肉眼观察评估其检测的灵敏度和特异性。我们还分析了从阳性样本中获得的分离株的分子特征。引物组LytA-1和PsaA-2在最短时间内扩增了基因,并且63°C被确认为最佳反应温度。引物组LytA-1和PsaA-2的每个反应的检测灵敏度分别为10和100拷贝/μL。这种LAMP检测法与其他27种病原体无交叉反应。为了描述这种方法的实用性,我们收集了748份肺炎儿童临床样本。其中,135份经LAMP确认为阳性。灵敏度为100%(95%CI 96.4 - 100%),特异性为99.0%(95%CI 97.8 - 99.6%)。其中,50份同时感染了。这种LAMP检测法在1小时内检测到,结果可用肉眼识别。因此,它将成为早期诊断和有效抗生素治疗的有力工具。