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国家规模的污水中抗菌药物耐药性监测:HT qPCR 和宏基因组方法的比较分析。

National-scale antimicrobial resistance surveillance in wastewater: A comparative analysis of HT qPCR and metagenomic approaches.

机构信息

School of Environmental & Natural Sciences, Bangor University, Bangor, LL57 2UW, Wales, UK.

Microbiomes, Microbes and Informatics Group, Organisms and Environment Division, School of Biosciences, Museum Avenue, Cardiff University, Cardiff, CF10 3AX, Wales, UK.

出版信息

Water Res. 2024 Sep 15;262:121989. doi: 10.1016/j.watres.2024.121989. Epub 2024 Jun 22.

Abstract

Wastewater serves as an important reservoir of antimicrobial resistance (AMR), and its surveillance can provide insights into population-level trends in AMR to inform public health policy. This study compared two common high-throughput screening approaches, namely (i) high-throughput quantitative PCR (HT qPCR), targeting 73 antimicrobial resistance genes, and (ii) metagenomic sequencing. Weekly composite samples of wastewater influent were taken from 47 wastewater treatment plants (WWTPs) across Wales, as part of a national AMR surveillance programme, alongside 4 weeks of daily wastewater effluent samples from a large municipal hospital. Metagenomic analysis provided more comprehensive resistome coverage, detecting 545 genes compared to the targeted 73 genes by HT qPCR. It further provided contextual information critical to risk assessment (i.e. potential bacterial hosts). In contrast, HT qPCR exhibited higher sensitivity, quantifying all targeted genes including those of clinical relevance present at low abundance. When limited to the HT qPCR target genes, both methods were able to reflect the spatiotemporal dynamics of the complete metagenomic resistome, distinguishing that of the hospital and the WWTPs. Both approaches revealed correlations between resistome compositional shifts and environmental variables like ammonium wastewater concentration, though differed in their interpretation of some potential influencing factors. Overall, metagenomics provides more comprehensive resistome profiling, while qPCR permits sensitive quantification of genes significant to clinical resistance. We highlight the importance of selecting appropriate methodologies aligned to surveillance aims to guide the development of effective wastewater-based AMR monitoring programmes.

摘要

污水是抗菌药物耐药性(AMR)的重要储存库,对其进行监测可以了解人群中 AMR 的趋势,为公共卫生政策提供信息。本研究比较了两种常见的高通量筛选方法,即(i)针对 73 种抗菌药物耐药基因的高通量定量 PCR(HT qPCR),和(ii)宏基因组测序。作为国家 AMR 监测计划的一部分,每周从威尔士的 47 个污水处理厂(WWTP)采集污水进水的综合样本,以及从一家大型市立医院采集 4 周的每日污水出水样本。宏基因组分析提供了更全面的耐药组覆盖,检测到 545 个基因,而 HT qPCR 仅检测到 73 个靶向基因。它还提供了对风险评估至关重要的背景信息(即潜在的细菌宿主)。相比之下,HT qPCR 表现出更高的灵敏度,定量检测到所有靶向基因,包括那些低丰度存在的临床相关基因。当仅限于 HT qPCR 靶向基因时,两种方法都能够反映完整宏基因组耐药组的时空动态,区分医院和 WWTP 的耐药组。两种方法都揭示了耐药组组成变化与环境变量(如氨废水浓度)之间的相关性,但在解释一些潜在影响因素方面存在差异。总体而言,宏基因组学提供了更全面的耐药组分析,而 qPCR 则允许对与临床耐药性相关的基因进行敏感定量。我们强调选择与监测目标相匹配的适当方法的重要性,以指导有效的基于污水的 AMR 监测计划的制定。

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