Evaluation of a microfluidic-based point-of-care prototype with customized chip for detection of bacterial clusters.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2024-11-06 DOI:10.1128/spectrum.00862-24
Janina Treffon, Nicole Isserstedt-John, Richard Klemm, Claudia Gärtner, Alexander Mellmann
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Abstract

Bacterial infection clusters cause high mortality rates and healthcare costs due to excessive therapy and hygiene measures. The aim of this study was to develop an automated real-time PCR-based point-of-care (POC) system with a customized microfluidic chip that facilitates fast detection of bacterial cluster isolates by targeting cluster-specific single-nucleotide polymorphisms (SNPs). For cluster detection of Acinetobacter baumannii, Staphylococcus aureus, and Escherichia coli, nine TaqMan real-time PCR assays targeting cluster-specific SNPs were designed. Additionally, for DNA input control, a universal PCR amplifying the 16S rDNA was constructed. All reactions were implemented into a microfluidic chip that was analyzed by a POC prototype enabling automated sample processing, fluid handling, and signal detection. Performance of the prototype was evaluated using 45 chips loaded with defined bacterial solutions, including swab eluates. For seven PCRs, implementation into the microfluidic chip was successful, leading to correct identification of all SNPs specific for A. baumannii and E. coli cluster isolates and delineation of all non-cluster strains within 70 min. The remaining three reactions failed in the chip, which resulted in misidentification of the S. aureus cluster. Sensitivity, specificity, and accuracy of the prototype were 43%, 88%, and 55%, respectively. The detection limit was PCR dependent and ranged between 103 and 105 colony-forming units/mL. Once optimized, the microfluidic POC system for cluster detection could be applied as time-saving and easy-to-use method to complement whole-genome sequencing efforts during screening for bacterial clusters.

Importance: Especially in medical facilities, where morbid people are nursed in close distance to each other, pathogenic bacteria can accumulate and spread. To contain such infection clusters, usually time- and labor-intensive large-scale screening assays are conducted, where patients and patient-side surfaces are sampled, and PCR or whole-genome sequencing analyses are conducted to confirm or deny cluster affiliation of cultivated bacteria. Hence, fast solutions with easy application are required to complement the current state-of-the-art technology for cluster surveillance. Here, we developed a fully automated microfluidic point-of-care prototype that identified bacterial cluster isolates within 70 min from bacterial solutions, including swab eluates. The system requires only low hands-on time and can be applied apart from laboratory infrastructures near the patient, which considerably reduces the time from sampling to result. This ensures fast implementation of hygiene measures and quick containment of the infection cluster, which would enhance patients' safety and outcome.

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评估基于微流控的护理点原型,该原型带有定制芯片,用于检测细菌集群。
由于过度治疗和卫生措施,细菌感染集群导致了很高的死亡率和医疗成本。本研究的目的是开发一种基于实时 PCR 的自动护理点 (POC) 系统,该系统采用定制的微流控芯片,可通过针对集群特异性单核苷酸多态性 (SNP) 快速检测细菌集群分离物。针对鲍曼不动杆菌、金黄色葡萄球菌和大肠埃希菌的集群检测,设计了九种针对集群特异性 SNP 的 TaqMan 实时 PCR 检测方法。此外,为了控制 DNA 输入,还构建了扩增 16S rDNA 的通用 PCR。所有反应都在一个微流控芯片中进行,该芯片由一个 POC 原型进行分析,可实现自动样本处理、液体处理和信号检测。使用 45 个装有确定细菌溶液(包括拭子洗脱液)的芯片对原型的性能进行了评估。在微流控芯片中成功实施了七项 PCR,在 70 分钟内正确识别了鲍曼尼氏菌和大肠杆菌集群分离物的所有特异 SNP,并确定了所有非集群菌株。芯片中其余三个反应失败,导致金黄色葡萄球菌集群识别错误。原型的灵敏度、特异性和准确性分别为 43%、88% 和 55%。检测限取决于 PCR,介于 103 和 105 菌落形成单位/毫升之间。一旦优化,用于集群检测的微流控 POC 系统可作为一种省时、易用的方法,在细菌集群筛查过程中补充全基因组测序工作:特别是在医疗机构中,患病者之间的护理距离很近,致病菌可能会聚集和传播。为遏制此类感染集群,通常需要进行耗时耗力的大规模筛查,即对患者和患者体表进行采样,然后进行 PCR 或全基因组测序分析,以确认或否认培养细菌的集群归属。因此,需要应用简便的快速解决方案来补充目前最先进的集群监测技术。在此,我们开发了一种全自动微流控护理点原型,可在 70 分钟内从细菌溶液(包括拭子洗脱液)中鉴定细菌集群分离物。该系统只需较少的动手时间,而且可以在病人附近的实验室基础设施之外使用,从而大大缩短了从采样到得出结果的时间。这确保了卫生措施的快速实施和感染群的快速遏制,从而提高了病人的安全和治疗效果。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
期刊最新文献
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