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基于流式细胞术的尿路感染活细菌快速准确测量技术研究
王润润, 王蒙, 刘思渊, 王梓权, 张雅芬, 隋志伟
计量学报 ›› 2025, Vol. 46 ›› Issue (10) : 1527-1535.
PDF(2247 KB)
PDF(2247 KB)
基于流式细胞术的尿路感染活细菌快速准确测量技术研究
Rapid and Accurate Quantification of Total Viable Bacteria in Urinary Tract Infection Using a Flow Cytometry Method
为了实现对尿路感染中活细菌数的快速准确测量,建立了一种基于流式细胞术(flow cytometry,FCM)结合叠氮溴化丙锭(propidium monoazide,PMA)以及荧光原位杂交技术(fluorescence in situ hybridization,FISH)的新型测量方法,并验证了其测量效果。首先利用PMA标记膜破损的死菌 DNA;然后基于 FISH 的寡核苷酸探针特异结合细菌核酸序列,实现细菌广谱标记;最后通过 FCM 检测双重荧光信号从而实现对尿路感染中活细菌的准确测量。经技术参数优化后,该方法能在 1.5 h 内准确表征尿路感染中细菌的活性,检测结果与传统平板计数方法的结果具有良好的线性关系(R 2= 0.999),测量范围为104~108 cells/mL。该方法还可高效回收磷酸盐缓冲液和人工尿液中的活细菌,回收率分别为 94.46% 和 95.85%,表明PMA-FISH-FCM 方法具有准确测量真实样品的潜力。
To rapidly and accurately quantify viable bacteria in UTI, a method combining flow cytometry (FCM) with propidium monoazide (PMA) and fluorescence in situ hybridization (FISH) was established. Firstly, PMA is used to stain the DNA of all dead bacteria with compromised membranes; Secondly, the oligonucleotide probe based on FISH enables specific fluorescence labeling of target bacteria. Finally, dual fluorescence signals are detected by FCM to achieve quantitative detection of viable bacteria in UTI. Upon optimization of its technical parameters, the results demonstrated that the method can accurately quantify viable bacteria within 1.5 h and exhibits an excellent linear relationship with the traditional plate counting method (104 to 108 cells/mL, R 2 = 0.999). 7、 The method also efficiently recovered live bacteria in phosphate buffer and artificial urine, with recoveries of 94.46% and 95.85%, respectively, indicating that the PMA-FISH-FCM method has the potential to accurately measure real samples.
生物计量 / 尿路感染 / 流式细胞术 / 荧光原位杂交 / 活菌计数 / 叠氮溴化丙锭
biometrology / urinary tract infection / flow cytometry / fluorescence in situ hybridization / viable bacteria quantification / propidium monoazide
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