Budiarto Bugi Ratno, Mustopa Apon Zaenal, Ningrum Ratih Asmana, Amilia Nurul, Saepudin Endang
Research Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Raya Bogor Street KM.46, Cibinong, Bogor, West Java, 16911, Indonesia.
Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Indonesia, Depok, 16424, Indonesia.
Mol Biol Rep. 2022 Oct;49(10):9355-9363. doi: 10.1007/s11033-022-07786-3. Epub 2022 Jul 27.
Diarrhea is a major cause of severe gastrointestinal illness in the infant especially in many developing countries. Although this molecular technique has been accepted as standard technique to detect Diarrhea-causing EPEC, the practical aspect of this technique for in-site rapid screening purposes is still facing a major challenge. In this study, we characterized EPEC specific aptamers and applied it as an AuNP-based aptasensor for point of care (POC) diagnosis purpose.
As many as six selected DNA aptamers was screened using target bacteria and the bound aptamer was measured by qPCR technique. Moreover, Kd value for each optimal bound aptamer was measured by using the same technique. Colorimetry assay was applied to test specificity and LOD of AuNP-based aptasensor.
Two DNA aptamers have been successfully obtained to detect Enteropathogenic Escherichia coli K.1.1. DNA aptamer S8-7 exhibited constant dissociation (Kd) value of 17.08 nM, while DNA aptamer S10-5 exhibited Kd value of 34.14 nM. AuNP-based aptasensor showed high selectivity and specificity for EPEC K.1.1 with a limit of detection (LOD) value of 10 CFU/mL. Truncation study on DNA aptamer S8-7 showed that elimination of primer binding sequence only slightly increased both performance of detection and LOD value of AuNP-based aptasensor.
Further study is necessary to improve AuNP-aptasensor performance such as through mutagenesis approach on targeted DNA aptamers before AuNP-based aptasensor can be applied as a biosensor in point of care (POC) diagnosis.
腹泻是婴儿严重胃肠道疾病的主要原因,在许多发展中国家尤其如此。尽管这种分子技术已被公认为检测致腹泻肠致病性大肠杆菌(EPEC)的标准技术,但该技术用于现场快速筛查的实际应用仍面临重大挑战。在本研究中,我们对EPEC特异性适体进行了表征,并将其应用于基于金纳米颗粒(AuNP)的适体传感器,用于即时检测(POC)诊断。
使用目标细菌筛选多达六种选定的DNA适体,并通过qPCR技术测量结合的适体。此外,使用相同技术测量每个最佳结合适体的解离常数(Kd)值。采用比色法检测基于AuNP的适体传感器的特异性和检测限(LOD)。
已成功获得两种DNA适体,用于检测肠致病性大肠杆菌K.1.1。DNA适体S8-7的解离常数(Kd)值恒定为17.08 nM,而DNA适体S10-5的Kd值为34.14 nM。基于AuNP的适体传感器对EPEC K.1.1具有高选择性和特异性,检测限(LOD)值为10 CFU/mL。对DNA适体S8-7的截短研究表明,去除引物结合序列仅略微提高了基于AuNP的适体传感器的检测性能和LOD值。
在基于AuNP的适体传感器可作为即时检测(POC)诊断中的生物传感器应用之前,有必要进一步研究以提高其性能,例如通过对靶向DNA适体进行诱变的方法。