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一种通过荧光熔解曲线分析检测呼吸道病原体的新型多重PCR检测方法的开发与临床验证。

Development and clinical validation of a novel multiplex PCR test for detection of respiratory pathogens via fluorescence melting curve analysis.

作者信息

Jiang Yaping, Wang Haifeng, Bai Guanghong, Wei Zihan, Zhong Guowei, Shi Jie, Wang Xiaolin, Wang Zhuo, Zou YuanWu

机构信息

Department of Clinical Laboratory, Xi'an No. 3 Hospital, The Affiliated Hospital of Northwest University, Xi'an, 710018, China.

Department of Clinical Laboratory, Shaanxi Provincial Hospital of Tuberculosis Prevention and Treatment Hospital, The Fifth People's Hospital of Shaanxi Province, Xi'an, 710100, China.

出版信息

Sci Rep. 2025 Aug 20;15(1):30503. doi: 10.1038/s41598-025-16434-2.

Abstract

Respiratory infections caused by pathogens such as SARS-CoV-2, influenza viruses, and Mycoplasma pneumoniae pose significant diagnostic challenges due to overlapping clinical symptoms, particularly during seasonal outbreaks. Conventional single-pathogen tests and commercial multiplex PCR kits are often costly, time-consuming, and lack flexibility for resource-limited settings. To address these limitations, we developed a novel fluorescence melting curve analysis-based (FMCA-based) multiplex PCR assay for simultaneous detection of six respiratory pathogens, including SARS-CoV-2, influenza A virus (IAV), influenza B virus (IBV), M. pneumoniae, respiratory syncytial virus (RSV), and human adenovirus (hADV). The method was evaluated for its limit of detection (LOD), precision and specificity before clinical validation, followed by a prospective single-center study in patients with presumptive acute respiratory infections. Analytical validation revealed high sensitivity with limits of detection (LOD) between 4.94 and 14.03 copies/µL, exceptional precision (intra-/inter-assay CVs ≤ 0.70% and ≤ 0.50%), and no cross-reactivity. Clinical evaluation using 1005 samples demonstrated 98.81% agreement with RT-qPCR, identifying 51.54% pathogen-positive cases, including 6.07% co-infections. The assay resolved 12 discordant results via sanger sequencing, confirming superior sensitivity in low viral load scenarios. With a turnaround time of 1.5 h and a cost of $5/sample (86.5% cheaper than commercial kits), this scalable platform enables high-throughput screening during outbreaks. Our findings highlight its potential as a cost-effective, rapid diagnostic tool for differentiating respiratory pathogens, guiding clinical management, and enhancing surveillance in diverse healthcare settings. Further adaptations to include emerging variants and sample types could strengthen global preparedness for respiratory epidemics.

摘要

由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)、流感病毒和肺炎支原体等病原体引起的呼吸道感染,由于临床症状重叠,尤其是在季节性暴发期间,带来了重大的诊断挑战。传统的单病原体检测和商业多重聚合酶链反应(PCR)试剂盒通常成本高昂、耗时,并且在资源有限的环境中缺乏灵活性。为了解决这些局限性,我们开发了一种基于新型荧光熔解曲线分析(FMCA)的多重PCR检测方法,用于同时检测六种呼吸道病原体,包括SARS-CoV-2、甲型流感病毒(IAV)、乙型流感病毒(IBV)、肺炎支原体、呼吸道合胞病毒(RSV)和人腺病毒(hADV)。在临床验证之前,对该方法的检测限(LOD)、精密度和特异性进行了评估,随后在疑似急性呼吸道感染患者中进行了一项前瞻性单中心研究。分析验证显示出高灵敏度,检测限在4.94至14.03拷贝/微升之间,精密度极佳(批内/批间变异系数分别≤0.70%和≤0.50%),且无交叉反应。使用1005份样本进行的临床评估表明,与逆转录定量PCR(RT-qPCR)的一致性为98.81%,确定了51.54%的病原体阳性病例,包括6.07%的合并感染病例。该检测方法通过桑格测序解决了12个不一致的结果,证实了在低病毒载量情况下具有更高的灵敏度。周转时间为1.5小时,每个样本成本为5美元(比商业试剂盒便宜86.5%),这个可扩展的平台能够在疫情暴发期间进行高通量筛查。我们的研究结果突出了其作为一种经济高效、快速诊断工具的潜力,可用于区分呼吸道病原体、指导临床管理以及加强在不同医疗环境中的监测。进一步调整以纳入新出现的变异株和样本类型,可以增强全球对呼吸道疫情的防范能力。

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