Simultaneous detection of influenza A, B and respiratory syncytial virus in wastewater samples by one-step multiplex RT-ddPCR assay.

IF 3.8 3区 医学 Q2 GENETICS & HEREDITY
Anastasia Zafeiriadou, Lazaros Kaltsis, Nikolaos S Thomaidis, Athina Markou
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引用次数: 0

Abstract

Background: After the occurrence of the COVID-19 pandemic, detection of other disseminated respiratory viruses using highly sensitive molecular methods was declared essential for monitoring the spread of health-threatening viruses in communities. The development of multiplex molecular assays are essential for the simultaneous detection of such viruses even at low concentrations. In the present study, a highly sensitive and specific multiplex one-step droplet digital PCR (RT-ddPCR) assay was developed for the simultaneous detection and absolute quantification of influenza A (IAV), influenza B (IBV), respiratory syncytial virus (RSV), and beta-2-microglobulin transcript as an endogenous internal control (IC B2M).

Results: The assay was first evaluated for analytical sensitivity and specificity, linearity, reproducibility, and recovery rates with excellent performance characteristics and then applied to 37 wastewater samples previously evaluated with commercially available and in-house quantitative real-time reverse transcription PCR (RT-qPCR) assays. IAV was detected in 16/37 (43%), IBV in 19/37 (51%), and RSV in 10/37 (27%) of the wastewater samples. Direct comparison of the developed assay with real-time RT-qPCR assays showed statistically significant high agreement in the detection of IAV (kappa Cohen's correlation coefficient: 0.834, p = 0.001) and RSV (kappa: 0.773, p = 0.001) viruses between the two assays, while the results for the detection of IBV (kappa: 0.355, p = 0.27) showed good agreement without statistical significance.

Conclusions: Overall, the developed one-step multiplex ddPCR assay is cost-effective, highly sensitive and specific, and can simultaneously detect three common respiratory viruses in the complex matrix of wastewater samples even at low concentrations. Due to its high sensitivity and resistance to PCR inhibitors, the developed assay could be further used as an early warning system for wastewater monitoring.

利用一步法多重 RT-ddPCR 分析法同时检测废水样本中的甲型、乙型流感病毒和呼吸道合胞病毒。
背景:COVID-19 大流行发生后,使用高灵敏度的分子方法检测其他传播的呼吸道病毒被认为是监测威胁健康的病毒在社区传播的关键。开发多重分子检测方法对于同时检测低浓度的此类病毒至关重要。本研究开发了一种高灵敏度和特异性的多重一步式液滴数字 PCR(RT-ddPCR)检测方法,用于同时检测和绝对定量甲型流感病毒(IAV)、乙型流感病毒(IBV)、呼吸道合胞病毒(RSV)以及作为内源性内对照(IC B2M)的β-2-微球蛋白转录本:首先对该检测方法的分析灵敏度和特异性、线性度、重现性和回收率进行了评估,结果表明该检测方法性能优异,然后将其应用于 37 个废水样本,这些样本之前曾用市售和内部的定量实时反转录 PCR(RT-qPCR)检测方法进行过评估。在 16/37 份(43%)废水样本中检测到了 IAV,在 19/37 份(51%)废水样本中检测到了 IBV,在 10/37 份(27%)废水样本中检测到了 RSV。将所开发的检测方法与实时 RT-qPCR 检测方法进行直接比较后发现,两种检测方法在检测 IAV(卡帕科恩相关系数:0.834,p = 0.001)和 RSV(卡帕:0.773,p = 0.001)病毒方面具有统计学意义的高度一致性,而检测 IBV(卡帕:0.355,p = 0.27)的结果显示出良好的一致性,但无统计学意义:总之,所开发的一步法多重 ddPCR 检测方法具有成本效益高、灵敏度高和特异性强的特点,即使在低浓度下也能同时检测废水样本复杂基质中的三种常见呼吸道病毒。由于其高灵敏度和对 PCR 抑制剂的抗性,所开发的检测方法可进一步用作废水监测的预警系统。
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来源期刊
Human Genomics
Human Genomics GENETICS & HEREDITY-
CiteScore
6.00
自引率
2.20%
发文量
55
审稿时长
11 weeks
期刊介绍: Human Genomics is a peer-reviewed, open access, online journal that focuses on the application of genomic analysis in all aspects of human health and disease, as well as genomic analysis of drug efficacy and safety, and comparative genomics. Topics covered by the journal include, but are not limited to: pharmacogenomics, genome-wide association studies, genome-wide sequencing, exome sequencing, next-generation deep-sequencing, functional genomics, epigenomics, translational genomics, expression profiling, proteomics, bioinformatics, animal models, statistical genetics, genetic epidemiology, human population genetics and comparative genomics.
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