使用液滴数字 PCR 通过定期监测污水处理厂环境样本检测致病性肠道 RNA 病毒的规程

Ram Kumar Nema , Surya Singh , Ashutosh Kumar Singh , Devojit Kumar Sarma , Vishal Diwan , Rajnarayan R. Tiwari , Rajesh Kumar Mondal , Pradyumna Kumar Mishra
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引用次数: 0

摘要

背景本综合方案主要是通过液滴数字 PCR(ddPCR)技术检测污水处理厂中的致病性肠道 RNA 病毒,特别是诺如病毒第Ⅱ基因组(GⅡ)、星状病毒、轮状病毒、爱知病毒、沙波病毒、甲型肝炎病毒和戊型肝炎病毒。肠道病毒是导致肠胃炎等疾病的主要原因,因此备受公众健康关注。定期监测环境样本,特别是来自污水处理厂的样本,对于早期检测和控制这些病毒至关重要。这项研究旨在加深人们对印度城市肠道病毒流行和动态的了解,并将为其他地区的类似研究树立典范。我们的方案旨在建立一种基于 ddPCR 的新型方法,用于检测和分子鉴定印度博帕尔废水样本中的肠道病毒。我们的检测方法无需标准曲线即可准确量化病毒浓度,最大限度地减少了大量优化工作,提高了灵敏度和精确度,尤其是针对低丰度目标。我们的研究创新性地将 ddPCR 应用于同时检测和量化废水中的肠道病毒,这是一种更先进的技术。结论这项研究将有助于了解这些病毒的遗传多样性和变异率,这对于制定有针对性的干预策略至关重要。研究结果将有助于制定公共卫生对策和改进流行病学监测,尤其是在污水管网密集的地区。
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Protocol for detection of pathogenic enteric RNA viruses by regular monitoring of environmental samples from wastewater treatment plants using droplet digital PCR

Background

The present comprehensive protocol is focused on the detection of pathogenic enteric RNA viruses, explicitly focusing on norovirus genogroup Ⅱ (GⅡ), astrovirus, rotavirus, Aichi virus, sapovirus, hepatitis A and E viruses in wastewater treatment plants through droplet digital PCR (ddPCR). Enteric viruses are of significant public health concern, as they are the leading cause of diseases like gastroenteritis. Regular monitoring of environmental samples, particularly from wastewater treatment plants, is crucial for early detection and control of these viruses. This research aims to improve the understanding of the prevalence and dynamics of enteric viruses in urban India and will serve as a model for similar studies in other regions. Our protocol's objective is to establish a novel ddPCR-based methodology for the detection and molecular characterization of enteric viruses present in wastewater samples sourced from Bhopal, India. Our assay is capable of accurately quantifying virus concentrations without standard curves, minimizing extensive optimization, and enhancing sensitivity and precision, especially for low-abundance targets.

Methods

The study involves fortnightly collecting and analyzing samples from nine wastewater treatment plants over two years, ensuring comprehensive coverage and consistent data. Our study innovatively applies ddPCR to simultaneously detect and quantify enteric viruses in wastewater, a more advanced technique. Additionally, we will employ next-generation sequencing for detailed viral genome identification in samples tested positive for pathogenic viruses.

Conclusion

This study will aid in understanding these viruses’ genetic diversity and mutation rates, which is crucial for developing tailored intervention strategies. The findings will be instrumental in shaping public health responses and improving epidemiological surveillance, especially in localities heaving sewage networks.
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