Kao Kaily, Alocilja Evangelyn C
Department of Biosystems and Agricultural Engineering, Michigan State University, East Lansing, MI 48824, USA.
Global Alliance for Rapid Diagnostics (GARD), Michigan State University, East Lansing, MI 48824, USA.
Biosensors (Basel). 2025 Feb 14;15(2):112. doi: 10.3390/bios15020112.
Antimicrobial resistance (AMR) is a rapidly growing global concern resulting from the overuse of antibiotics in agricultural and clinical settings. The challenge is exacerbated by the lack of rapid surveillance for resistant bacteria in clinical, environmental, and food supply settings. The increasing resistance to carbapenems, an important sub-class of beta-lactam antibiotics, is a major concern in the healthcare community. Carbapenem resistance (CR) has been found in the environment and food supply chain, where it has the potential to spread to pathogens, animals, and humans through direct or indirect contact. Rapid detection for preventative and control measures should be developed. This study utilized a gold nanoparticle-based plasmonic biosensor for the parallel detection of the CR genes and . To explore the field portability, DNA was extracted using two methods: a commercial extraction kit and a boiling method. The results were compared between the two methods using a spectrophotometer and a cellphone application for RGB values to quantify the visual results. The results showed that the boiling method of extraction was more effective than extraction with a commercial kit for this analysis. The parallel detection of unamplified genes extracted via the boiling method is novel. When combined with other portable testing equipment, the approach has the potential to be an inexpensive, rapid, and simple on-site CR gene detection protocol.
抗菌药物耐药性(AMR)是一个在全球范围内迅速加剧的问题,这是由农业和临床环境中抗生素的过度使用导致的。临床、环境和食品供应环境中缺乏对抗耐药菌的快速监测,使这一挑战更加严峻。对碳青霉烯类(β-内酰胺类抗生素的一个重要子类)的耐药性不断增加,是医疗界的一个主要担忧。在环境和食品供应链中已发现碳青霉烯类耐药性(CR),它有可能通过直接或间接接触传播到病原体、动物和人类。应开发用于预防和控制措施的快速检测方法。本研究利用基于金纳米颗粒的等离子体生物传感器对CR基因 和 进行平行检测。为了探索现场便携性,使用两种方法提取DNA:商业提取试剂盒和煮沸法。使用分光光度计和用于RGB值的手机应用程序对两种方法的结果进行比较,以量化视觉结果。结果表明,对于该分析,煮沸提取法比使用商业试剂盒提取更有效。通过煮沸法提取未扩增基因的平行检测是新颖的。当与其他便携式检测设备结合使用时,该方法有可能成为一种廉价、快速且简单的现场CR基因检测方案。