TEDA School of Biological Sciences and Biotechnology, Nankai University, 23# HongDa Street, TEDA, Tianjin 300457, China.
Int J Food Microbiol. 2011 Jan 31;145(1):293-300. doi: 10.1016/j.ijfoodmicro.2011.01.014. Epub 2011 Jan 13.
The safety and accessibility of drinking water are major concerns throughout the world. Consumption of water contaminated with infectious agents, toxic chemicals or radiological hazards represents a significant health risk and is strongly associated with mortality. Therefore, we have developed an oligonucleotide-based microarray using the sequences of 16S-23S rDNA internal transcribed spacer regions (ITS) and the gyrase subunit B gene (gyrB) found in the most prevalent and devastating waterborne pathogenic agents. This new diagnostic contains 26 specific probes and can simultaneously detect Aeromonas hydrophila, Klebsiella pneumoniae, Legionella pneumophila, Pseudomonas aeruginosa, Salmonella spp., Shigella spp., Staphylococcus aureus, Vibrio choleraeo, Vibrio parahaemolyticus, Yersinia enterocolitica and Leptospira interrogans. Testing was carried out against a total of 218 bacterial strains, including 53 representative strains, 103 clinical isolates and 62 strains of other bacterial species belonging to 10 genera and 48 species. The results were specific and reproducible, with a detection sensitivity of 0.1 ng DNA or 10(4)CFU/ml achieved for pure cultures of each target organism. The diluted cultures and real drinking water samples were tested by the microarray with 100% accuracy. This novel diagnostic method is superior in time- and labor-efficiency to conventional bacterial culture and antiserum agglutination, and can be readily applied to epidemiological surveillance and other food safety applications.
饮用水的安全性和可及性是全世界关注的主要问题。饮用水受到感染性病原体、有毒化学物质或放射性危害物的污染会带来严重的健康风险,并且与死亡率密切相关。因此,我们开发了一种基于寡核苷酸的微阵列,使用了最普遍和最具破坏性的水源性病原体中发现的 16S-23S rDNA 内部转录间隔区(ITS)和拓扑异构酶亚基 B 基因(gyrB)的序列。这个新的诊断方法包含 26 个特定的探针,可以同时检测气单胞菌、肺炎克雷伯菌、嗜肺军团菌、铜绿假单胞菌、沙门氏菌、志贺氏菌、金黄色葡萄球菌、霍乱弧菌、副溶血性弧菌、肠侵袭性大肠杆菌和问号钩端螺旋体。对总共 218 株细菌进行了测试,包括 53 株代表性菌株、103 株临床分离株和 62 株其他细菌,属于 10 个属和 48 个种。结果具有特异性和可重复性,对于每种目标生物的纯培养物,检测灵敏度达到 0.1ng DNA 或 10(4)CFU/ml。该微阵列可对稀释培养物和实际饮用水样本进行 100%准确的检测。与传统的细菌培养和抗血清凝集相比,这种新的诊断方法在时间和劳动力效率上具有优势,并且可以很容易地应用于流行病学监测和其他食品安全应用。