建立一个实用的方法来监测下水道的抗菌素耐药基因和生物在医疗机构。

Rachel S Poretsky,Dolores Sanchez Gonzalez,Adam Horton,Michael Schoeny,Chi-Yu Lin,Modou Lamin Jarju,Michael Secreto,Cecilia Chau,Ellen Gough,Erin Newcomer,Adit Chaudhary,Lisa Duffner,Nidhi Undevia,Angela Coulliette-Salmond,Amanda K Lyons,Florence Whitehill,Mary K Hayden,Stefan J Green,Michael Y Lin
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引用次数: 0

摘要

背景:对卫生保健设施废水的监测有可能发现具有公共卫生重要性的多药耐药(MDR)基因的出现。具体而言,废水监测(WWS)可以为医疗机构中的新型耐多药基因或生物体提供哨点监测,帮助指导有针对性的预防工作并监测纵向影响。在WWS常规用于耐多药监测之前,需要解决一些知识空白,包括确定采样、处理和测试废水的最佳方法。为此,我们在芝加哥的一家长期急性护理医院评估了多种废水收集(被动、复合和抓取)、浓缩(纳米颗粒、过滤和离心)和PCR定量(实时定量PCR与数字PCR)对念珠菌和5种碳青霉烯酶基因(blaKPC、blaNDM、blaVIM、blaIMP和blaoxa -48样)的方法,每周两次,持续6个月。我们还测试了不同运输和样品储存条件对PCR定量的影响。结果设施废水中检测到所有基因,其中以blaKPC含量最高。实验在三个重复中进行,用基因拷贝、变异和三个重复之间的检测次数来确定方法的有效性。我们发现,立即进行离心处理的被动样品,在检测耐多药基因和金黄色葡萄球菌时,采用打珠和dPCR的方法可以提供最可靠的结果。我们还提出了不同方法的权衡,并使用培养和宏基因组学来阐明临床相关性。结论本研究建立了一种实用的方法,将WWS作为卫生保健机构耐多药负担公共卫生监测的潜在工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Establishing a Practical Approach to Sewer Monitoring for Antimicrobial Resistance Genes and Organisms at Healthcare Facilities.
BACKGROUND Surveillance of wastewater from healthcare facilities has the potential to identify the emergence of multidrug-resistance (MDR) genes of public health importance. Specifically, wastewater surveillance (WWS) can provide sentinel surveillance of novel MDR genes or organisms in healthcare facilities, helping to direct targeted prevention efforts and monitor longitudinal effects. Several knowledge gaps need to be addressed before WWS can be used routinely for MDR surveillance, including determining optimal approaches to sampling, processing, and testing wastewater. METHODS To this end, we evaluated multiple methods for wastewater collection (passive, composite, and grab), concentration (nanoparticles, filtration, and centrifugation), and PCR quantification (real-time quantitative PCR vs. digital PCR) for Candida auris and 5 carbapenemase genes (blaKPC, blaNDM, blaVIM, blaIMP, and blaOXA-48-like) twice weekly for 6 months at a long-term acute care hospital in Chicago, IL. We also tested the effects of different transport and sample storage conditions on PCR quantification. RESULTS All genes were detected in facility wastewater, with blaKPC being the most consistently abundant. Experiments were done in triplicate with gene copy, variance, and number of detections between triplicates used to determine method efficacy. We found that passive samples processed immediately by centrifugation followed by bead-beating and dPCR provided the most reliable results for detecting MDR genes and C. auris. We also present the tradeoffs of different approaches and use culture and metagenomics to elucidate clinical relevance. CONCLUSIONS This study establishes a practical approach for WWS as a potential tool for public health monitoring of MDR burden in healthcare facilities.
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