Aya Abu Rumaila, Basima Abu Rumaila, Wafa Masoud, Antonio Ruiz-Canales, Nawaf Abu-Khalaf
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The partial least square (PLS) regression model detected the limit of detection (LOD) of the concentration that was monitored to grow the bacteria with different incubation periods (from 4 to 24 h). The measured data were analysed by principal component analysis (PCA) and followed by projecting unknown bacterial samples (at specific concentrations and time of incubation) to examine the recognition ability of the ET. Astree II ET was able to track bacterial proliferation and metabolic changes in the media at very low concentrations (between the dilutions 10<sup>-11</sup> and 10<sup>-10</sup> for both bacteria). <i>S.aureus</i> was detected after 6 h incubation period and between 6 and 8 h for <i>E.coli</i>. After creating the strains' models, ET was also able to classify unknown samples according to their foot-printing characteristics in the media (<i>S.aureus</i>, <i>E.coli</i> or neither of them). 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引用次数: 0
摘要
电子舌(ET)已被用作医疗部门的诊断技术。它由具有高交叉灵敏度和低选择性的多传感器阵列组成。本研究利用Astree II Alpha MOS ET确定食源性人类致病菌的早期检测和诊断限度,并利用预先储存的模型识别未知细菌样本。金黄色葡萄球菌(ATCC 25923)和大肠杆菌(ATCC25922)在原始接种量(约107*105 CFU/mL)的营养液(NB)培养基中增殖。将它们稀释至10-14,并使用ET测量10-14至10-4的稀释度。偏最小二乘(PLS)回归模型检测不同孵育期(4至24小时)细菌生长监测浓度的检出限(LOD)。测量数据通过主成分分析(PCA)进行分析,然后投影未知细菌样本(特定浓度和孵育时间)以检验识别Astree II ET能够在极低浓度(两种细菌的稀释倍数在10-11和10-10之间)的培养基中跟踪细菌的增殖和代谢变化。金黄色葡萄球菌潜伏期为6 h,大肠杆菌潜伏期为6 ~ 8 h。在创建菌株模型后,ET还能够根据它们在培养基中的足迹特征(金黄色葡萄球菌、大肠杆菌或两者都没有)对未知样本进行分类。结果认为,ET是一种强大的电位测定工具,可在复杂系统中早期识别处于天然状态的食源性微生物,从而挽救患者的生命。
Electronic tongue for determining the limit of detection of human pathogenic bacteria.
The Electronic tongue (ET) has been used as a diagnostic technique in the medical sector. It is composed of a multisensor array set with high cross-sensitivity and low selectivity characteristics. The research investigated using Astree II Alpha MOS ET to determine the limit of early detection and diagnosis of food-borne human pathogenic bacteria and to recognize unknown bacterial samples relying on pre-stored models. Staphylococcus aureus (ATCC 25923) and Escherichia coli (ATCC25922) were proliferated in nutrient broth (NB) medium with original inoculum (approximately 107*105 CFU/mL). They were diluted up to 10-14 and the dilutions ranging from 10-14 to 10-4 were measured using ET. The partial least square (PLS) regression model detected the limit of detection (LOD) of the concentration that was monitored to grow the bacteria with different incubation periods (from 4 to 24 h). The measured data were analysed by principal component analysis (PCA) and followed by projecting unknown bacterial samples (at specific concentrations and time of incubation) to examine the recognition ability of the ET. Astree II ET was able to track bacterial proliferation and metabolic changes in the media at very low concentrations (between the dilutions 10-11 and 10-10 for both bacteria). S.aureus was detected after 6 h incubation period and between 6 and 8 h for E.coli. After creating the strains' models, ET was also able to classify unknown samples according to their foot-printing characteristics in the media (S.aureus, E.coli or neither of them). The results considered ET a powerful potentiometric tool for the early identification of food-borne microorganisms in their native state within a complex system to save patients' lives.
期刊介绍:
ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study