Adenosine Triphosphate Bioluminescence-Based Bacteria Detection Using Targeted Photothermal Lysis by Gold Nanorods

细菌 化学 溶解 生物发光 单核细胞增生李斯特菌 致病菌 三磷酸腺苷 微生物学 大肠杆菌 光热治疗 沙门氏菌 纳米技术 生物化学 生物 材料科学 基因 遗传学
作者
Seong U. Kim,Eun‐Jung Jo,Yuseon Noh,Hyoyoung Mun,Young-Deok Ahn,Min‐Gon Kim
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:90 (17): 10171-10178 被引量:54
标识
DOI:10.1021/acs.analchem.8b00254
摘要

Bacterial infections are common causes of morbidity and mortality worldwide; therefore, environmental contamination by bacterial pathogens represents a global public health concern. Consequently, a selective, rapid, sensitive, and in-field detection platform for detecting significant bacterial contamination is required to ensure hygiene and protect public health. Here, we developed a fast and simple platform for the selective and sensitive detection of bacteria by measuring adenosine triphosphate (ATP) bioluminescence following targeted photothermal lysis mediated by antibody-conjugated gold nanorods. This method employed both targeted photothermal lysis of bacteria by near-infrared (NIR) irradiation and highly selective detection of the lysed bacteria via ATP bioluminescence within 36 min (incubation, 30 min; NIR irradiation, 6 min). The use of the proposed method allowed limits of detection in pure solution of 12.7, 70.7, and 5.9 CFU for Escherichia coli O157:H7, Salmonella typhimurium, and Listeria monocytogenes, respectively. Additionally, bacteria were successfully detected on artificially inoculated plastic cutting boards. Furthermore, this method was highly specific, without cross-reaction among pathogenic bacteria. We believe that the proposed method has significant potential as an on-site diagnostic tool for applications associated with public health and environmental pollution monitoring.
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