Surveillance of human adenoviruses in water environments: Assessing the suitability of a locally developed quenching of unincorporated amplification signal reporters-loop-mediated isothermal amplification assay

IF 2.2 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS
Joy Ann P. Santos , Elchin Juanico , Joseth Jermaine Abello , Jonah L. Bondoc , Windell L. Rivera
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引用次数: 0

Abstract

The human adenovirus (HAdV) has shown greater environmental persistence, more water treatment resistance than bacteria, and cause infection even at low concentrations. HAdV causes gastrointestinal illnesses and is abundant in various environmental samples such as groundwater, surface water, recreational water, and drinking water. The detection of these pathogens calls for a more practical and affordable approach. A recent technology based on the quenching of unincorporated amplification signal reporters (QUASR) was adapted for the detection of human adenoviruses. This technology allows for non-inhibitory, single-step DNA detection in a closed tube. The QUASR-(loop-mediated isothermal amplification (LAMP) assay was previously optimized and was tested for its applicability to detect enteric HAdV in two areas where people can unintentionally be exposed to contaminated water. A total of 203 water samples were collected and tested using both real-time PCR and QUASR-LAMP assays. Results showed a higher positivity rate of 78.82 % (160/203) for QUASR-LAMP compared to qPCR with only 58.62 % (119/203). The sensitivity and specificity rates for QUASR-LAMP were calculated at 86.55 % and 32.14 %, respectively, when compared to qPCR. The QUASR-LAMP assay's ability to detect target analytes even at low concentrations can be attributed to its increased diagnostic sensitivity but lower specificity since there were samples that were positive in PCR but negative in the QUASR-LAMP assay. However, this characteristic does not diminish its utility as a valuable tool for the detection of HAdV. In fact, this attribute enhances its advantages in situations with constrained space and instrumentation requirements, making it suitable for rapid surveillance of important viruses. Finally, the capacity of the QUASR-LAMP assay to differentiate between positive and negative samples at a defined endpoint is highly beneficial for laboratory technicians who possess limited molecular biology expertise or experience. The QUASR-LAMP platform has demonstrated its usefulness as a diagnostic tool for surveillance of enteric adenoviruses in water sources.
监测水环境中的人类腺病毒:评估本地开发的未结合扩增信号淬灭报告器-环介导等温扩增测定法的适用性。
人类腺病毒(HAdV)在环境中的持久性更强,比细菌更耐水处理,即使在低浓度下也会造成感染。HAdV 可导致胃肠道疾病,并大量存在于地下水、地表水、娱乐用水和饮用水等各种环境样本中。检测这些病原体需要一种更实用、更经济的方法。最近,一种基于未结合扩增信号报告器(QUASR)淬火的技术被用于检测人类腺病毒。该技术可在封闭的试管中进行无抑制、单步 DNA 检测。QUASR-(loop-mediated isothermal amplification (LAMP)) 检测方法之前已经过优化,并在两个人们可能无意中接触到受污染水源的地区进行了适用性测试,以检测肠道 HAdV。共采集了 203 份水样,并使用实时 PCR 和 QUASR-LAMP 检测法进行了检测。结果显示,QUASR-LAMP 的阳性率为 78.82%(160/203),而 qPCR 的阳性率仅为 58.62%(119/203)。与 qPCR 相比,QUASR-LAMP 的灵敏度和特异性分别为 86.55% 和 32.14%。QUASR-LAMP 检测法即使在低浓度下也能检测到目标分析物,这可能是由于它的诊断灵敏度较高,但特异性较低,因为有些样本在 PCR 检测中呈阳性,但在 QUASR-LAMP 检测中呈阴性。不过,这一特点并没有削弱它作为检测 HAdV 的重要工具的作用。事实上,在空间和仪器要求有限的情况下,这一特性增强了它的优势,使其适用于重要病毒的快速监测。最后,QUASR-LAMP 检测能在确定的终点区分阳性和阴性样本,这对分子生物学专业知识或经验有限的实验室技术人员非常有益。QUASR-LAMP 平台已证明它是监测水源中肠道腺病毒的有用诊断工具。
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来源期刊
CiteScore
5.80
自引率
0.00%
发文量
209
审稿时长
41 days
期刊介绍: The Journal of Virological Methods focuses on original, high quality research papers that describe novel and comprehensively tested methods which enhance human, animal, plant, bacterial or environmental virology and prions research and discovery. The methods may include, but not limited to, the study of: Viral components and morphology- Virus isolation, propagation and development of viral vectors- Viral pathogenesis, oncogenesis, vaccines and antivirals- Virus replication, host-pathogen interactions and responses- Virus transmission, prevention, control and treatment- Viral metagenomics and virome- Virus ecology, adaption and evolution- Applied virology such as nanotechnology- Viral diagnosis with novelty and comprehensive evaluation. We seek articles, systematic reviews, meta-analyses and laboratory protocols that include comprehensive technical details with statistical confirmations that provide validations against current best practice, international standards or quality assurance programs and which advance knowledge in virology leading to improved medical, veterinary or agricultural practices and management.
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