Department of Biological Systems Engineering, Virginia Tech, Blacksburg, Virginia 24061, United States.
Department of Bioengineering, University of California, Riverside, California 92521, United States.
Anal Chem. 2024 Feb 13;96(6):2676-2683. doi: 10.1021/acs.analchem.3c05459. Epub 2024 Jan 30.
Sepsis is an extremely dangerous medical condition that emanates from the body's response to a pre-existing infection. Early detection of sepsis-inducing bacterial infections can greatly enhance the treatment process and potentially prevent the onset of sepsis. However, current point-of-care (POC) sensors are often complex and costly or lack the ideal sensitivity for effective bacterial detection. Therefore, it is crucial to develop rapid and sensitive biosensors for the on-site detection of sepsis-inducing bacteria. Herein, we developed a graphene oxide CRISPR-Cas12a (GO-CRISPR) biosensor for the detection of sepsis-inducing bacteria in human serum. In this strategy, single-stranded (ssDNA) FAM probes were quenched with single-layer graphene oxide (GO). Target-activated Cas12a -cleavage was utilized for the degradation of the ssDNA probes, detaching the short ssDNA probes from GO and recovering the fluorescent signals. Under optimal conditions, we employed our GO-CRISPR system for the detection of Typhimurium (. Typhimurium) with a detection sensitivity of as low as 3 × 10 CFU/mL in human serum, as well as a good detection specificity toward other competing bacteria. In addition, the GO-CRISPR biosensor exhibited excellent sensitivity to the detection of . Typhimurium in spiked human serum. The GO-CRISPR system offers superior rapidity for the detection of sepsis-inducing bacteria and has the potential to enhance the early detection of bacterial infections in resource-limited settings, expediting the response for patients at risk of sepsis.
脓毒症是一种极其危险的医学病症,源于人体对先前存在的感染的反应。早期发现引发脓毒症的细菌感染可以极大地改善治疗过程,并有可能预防脓毒症的发生。然而,目前的即时检测(POC)传感器往往复杂且昂贵,或者缺乏有效细菌检测的理想灵敏度。因此,开发用于现场检测引发脓毒症的细菌的快速和敏感的生物传感器至关重要。在此,我们开发了一种用于检测人血清中引发脓毒症的细菌的氧化石墨烯 CRISPR-Cas12a(GO-CRISPR)生物传感器。在该策略中,单链(ssDNA) FAM 探针被单层氧化石墨烯(GO)猝灭。靶标激活的 Cas12a 切割用于 ssDNA 探针的降解,将短 ssDNA 探针从 GO 上脱离并恢复荧光信号。在最佳条件下,我们采用我们的 GO-CRISPR 系统以低至 3×10 CFU/mL 的浓度在人血清中检测鼠伤寒沙门氏菌(Salmonella enterica serovar Typhimurium,. Typhimurium),并且对其他竞争细菌具有良好的检测特异性。此外,GO-CRISPR 生物传感器在人血清中检测到污染的. Typhimurium 时表现出优异的灵敏度。GO-CRISPR 系统在检测引发脓毒症的细菌方面具有卓越的快速性,有可能在资源有限的环境中增强对细菌感染的早期检测,为处于脓毒症风险中的患者加快响应速度。