Biosensors for Klebsiella pneumoniae with Molecularly Imprinted Polymer (MIP) Technique

肺炎克雷伯菌 粪肠球菌 微生物学 铜绿假单胞菌 屎肠球菌 肺炎克雷伯菌 抗生素 肺炎 医学 检出限 金黄色葡萄球菌 细菌 生物 内科学 大肠杆菌 化学 色谱法 生物化学 遗传学 基因
作者
Chuchart Pintavirooj,Naphatsawan Vongmanee,Wannisa Sukjee,Chak Sangma,Sarinporn Visitsattapongse
出处
期刊:Sensors [Multidisciplinary Digital Publishing Institute]
卷期号:22 (12): 4638-4638 被引量:2
标识
DOI:10.3390/s22124638
摘要

Nosocomial infection is one of the most important problems that occurs in hospitals, as it directly affects susceptible patients or patients with immune deficiency. Klebsiella pneumoniae (K. pneumoniae) is the most common cause of nosocomial infections in hospitals. K. pneumoniae can cause various diseases such as pneumonia, urinary tract infections, septicemias, and soft tissue infections, and it has also become highly resistant to antibiotics. The principal routes for the transmission of K. pneumoniae are via the gastrointestinal tract and the hands of hospital personnel via healthcare workers, patients, hospital equipment, and interventional procedures. These bacteria can spread rapidly in the hospital environment and tend to cause nosocomial outbreaks. In this research, we developed a MIP-based electrochemical biosensor to detect K. pneumoniae. Quantitative detection was performed using an electrochemical technique to measure the changes in electrical signals in different concentrations of K. pneumoniae ranging from 10 to 105 CFU/mL. Our MIP-based K. pneumoniae sensor was found to achieve a high linear response, with an R2 value of 0.9919. A sensitivity test was also performed on bacteria with a similar structure to that of K. pneumoniae. The sensitivity results show that the MIP-based K. pneumoniae biosensor with a gold electrode was the most sensitive, with a 7.51 (% relative current/log concentration) when compared with the MIP sensor applied with Pseudomonas aeruginosa and Enterococcus faecalis, where the sensitivity was 2.634 and 2.226, respectively. Our sensor was also able to achieve a limit of detection (LOD) of 0.012 CFU/mL and limit of quantitation (LOQ) of 1.61 CFU/mL.
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