Caliskan-Aydogan Oznur, Sharief Saad Asadullah, Alocilja Evangelyn C
Department of Biosystems and Agricultural Engineering, Michigan State University, East Lansing, MI 48824, USA.
Global Alliance for Rapid Diagnostics, Michigan State University, East Lansing, MI 48824, USA.
Diagnostics (Basel). 2023 Feb 9;13(4):656. doi: 10.3390/diagnostics13040656.
Antimicrobial resistance (AMR) is a global public health issue, and the rise of carbapenem-resistant bacteria needs attention. While progress is being made in the rapid detection of resistant bacteria, affordability and simplicity of detection still need to be addressed. This paper presents a nanoparticle-based plasmonic biosensor for detecting the carbapenemase-producing bacteria, particularly the beta-lactam carbapenemase () gene. The biosensor used dextrin-coated gold nanoparticles (GNPs) and an oligonucleotide probe specific to to detect the target DNA in the sample within 30 min. The GNP-based plasmonic biosensor was tested in 47 bacterial isolates: 14 KPC-producing target bacteria and 33 non-target bacteria. The stability of GNPs, confirmed by the maintenance of their red appearance, indicated the presence of target DNA due to probe-binding and GNP protection. The absence of target DNA was indicated by the agglomeration of GNPs, corresponding to a color change from red to blue or purple. The plasmonic detection was quantified with absorbance spectra measurements. The biosensor successfully detected and differentiated the target from non-target samples with a detection limit of 2.5 ng/μL, equivalent to ~10 CFU/mL. The diagnostic sensitivity and specificity were found to be 79% and 97%, respectively. The GNP plasmonic biosensor is simple, rapid, and cost-effective in detecting -positive bacteria.
抗菌药物耐药性(AMR)是一个全球公共卫生问题,耐碳青霉烯类细菌的出现需要引起关注。虽然在耐药菌的快速检测方面取得了进展,但检测的可负担性和简易性仍需解决。本文介绍了一种基于纳米颗粒的等离子体生物传感器,用于检测产碳青霉烯酶的细菌,特别是β-内酰胺碳青霉烯酶()基因。该生物传感器使用糊精包被的金纳米颗粒(GNPs)和针对的特异性寡核苷酸探针,在30分钟内检测样品中的目标DNA。基于GNP的等离子体生物传感器在47株细菌分离株中进行了测试:14株产KPC的目标细菌和33株非目标细菌。GNPs的稳定性通过其红色外观得以维持来证实,这表明由于探针结合和GNP保护而存在目标DNA。GNPs的团聚表明不存在目标DNA,这对应于颜色从红色变为蓝色或紫色。通过吸光光谱测量对等离子体检测进行定量。该生物传感器成功地检测并区分了目标样品和非目标样品,检测限为2.5 ng/μL,相当于约10 CFU/mL。诊断敏感性和特异性分别为79%和97%。GNP等离子体生物传感器在检测阳性细菌方面简单、快速且具有成本效益。