Fisher Mathew, Ali Jennifer, Giesbrecht Shayna, Roopra Raveena, Carroll Veronica, Papineau Amber, Buchanan Cody, Duan Nicholas, Landgraff Chrystal
Wastewater Genomics Unit, Bacterial Pathogens, AMR, and Wastewater, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada.
Department of Food Science, Ontario Agricultural College, University of Guelph, Guelph, ON, Canada.
Sci Rep. 2025 Aug 11;15(1):29361. doi: 10.1038/s41598-025-13927-y.
Wastewater-based surveillance (WBS) has modernized in recent years and emerged as an important tool for the monitoring of viral pathogens, including monkeypox virus (MPXV). Here we describe a novel targeted amplicon sequencing method developed for clade and subclade characterization of MPXV from municipal wastewater. This new method addresses the limitations of PCR-based methods and the challenges of sequencing a pathogen displaying low viral load in municipal wastewater samples. A tiled amplicon scheme composed of 11 primer pairs targeting a 4.2 kb portion of the inverted terminal repeat (ITR) region of the MPXV genome was designed and tested. In silico analysis demonstrated high accuracy for clade and subclade calls using the full target region, with specific amplicons also exhibiting strong performance individually. An MPXV consensus sequence representing the entire target region was successfully sequenced from a wastewater sample and differentiated from positive controls by a distinct deletion within a short homopolymeric region. Notably, clade-informing data was also achieved from partial sequences recovered from lower abundance samples. This study presents a new sequencing method targeting MPXV with enhanced genomic resolution compared to existing PCR-based approaches, providing critical genomic-level information informing MPXV surveillance and public health interventions.
近年来,基于废水的监测(WBS)已实现现代化,并成为监测包括猴痘病毒(MPXV)在内的病毒病原体的重要工具。在此,我们描述了一种新开发的靶向扩增子测序方法,用于对城市废水中的MPXV进行分支和亚分支特征分析。这种新方法解决了基于PCR方法的局限性以及对城市废水样本中病毒载量较低的病原体进行测序的挑战。设计并测试了一种由11对引物组成的平铺扩增子方案,这些引物靶向MPXV基因组反向末端重复(ITR)区域的4.2 kb部分。计算机分析表明,使用整个目标区域进行分支和亚分支分类的准确性很高,特定扩增子单独也表现出很强的性能。从废水样本中成功测序出代表整个目标区域的MPXV共有序列,并通过一个短同聚物区域内的明显缺失与阳性对照区分开来。值得注意的是,从低丰度样本中回收的部分序列也获得了分支信息数据。本研究提出了一种针对MPXV的新测序方法,与现有的基于PCR的方法相比,具有更高的基因组分辨率,为MPXV监测和公共卫生干预提供了关键的基因组水平信息。