Department of Bioengineering, Santa Clara University, Santa Clara, CA 95053, USA.
Department of Biology, Santa Clara University, Santa Clara, CA 95053, USA.
Sensors (Basel). 2020 Feb 19;20(4):1145. doi: 10.3390/s20041145.
There are no existing affordable diagnostics for sensitive, rapid, and on-site detection of pathogens in milk. To this end, an on-site colorimetric-based sustainable assay has been developed and optimized using an L (5) Taguchi design to obtain results in hours without PCR amplification. To determine the level of () contamination, after induction with 150 µL of breast milk, the B-Per bacterial protein extraction kit was added to a solution containing an alginate-based microcapsule assay. Within this 3 mm spherical novel sensor design, X-Gal (5-Bromo-4-Chloro-3-Indolyl β-d-Galactopyranoside) was entrapped at a concentration of 2 mg/mL. The outward diffusing X-Gal was cleaved by β-galactosidase from and dimerized in the solution to yield a blue color after incubation at 40 °C. Color intensity was correlated with the level of contamination using a categorical scale. After an 8 h incubation period, a continuous imaging scale based on intensity normalization was used to determine a binary lower limit of detection (LOD), which corresponded to 10 colony forming unit per mL (CFU/mL) and above. The cost of the overall assay was estimated to be $0.81 per sample, well under the $3 benchmark for state-of-the-art immune-based test kits for pathogen detection in biofluids. Considering the reported binary LOD cutoff of 10 CFU/mL and above, this proposed hydrogel-based assay is suited to meet global requirements for screening breast milk or milk for pathogenic organisms of 10 CFU/mL, with a percentage of false positives to be determined in future efforts.
目前尚无经济实惠的诊断方法能够在牛奶中实现对病原体的敏感、快速和现场检测。为此,本研究采用 L(5)田口设计对基于比色的现场可持续测定法进行了开发和优化,该方法无需 PCR 扩增即可在数小时内获得结果。为了确定污染水平,将含有基于藻酸盐的微胶囊测定法的溶液加入到含有 150 µL 母乳的溶液中,然后加入 B-Per 细菌蛋白提取试剂盒。在这个 3 毫米的球形新型传感器设计中,将 X-Gal(5-溴-4-氯-3-吲哚基-β-d-半乳糖吡喃糖苷)以 2 mg/mL 的浓度包埋。向外扩散的 X-Gal 被β-半乳糖苷酶从细菌中裂解,并在溶液中二聚化,在 40°C 孵育后产生蓝色。颜色强度与污染水平使用分类量表相关联。经过 8 小时孵育期后,使用基于强度归一化的连续成像量表来确定二进制检测下限(LOD),该下限对应于 10 个菌落形成单位每毫升(CFU/mL)及以上。总体测定法的成本估计为每个样品 0.81 美元,远低于用于生物体液中病原体检测的最先进免疫测试试剂盒的 3 美元基准。考虑到报告的二进制 LOD 截止值为 10 CFU/mL 及以上,这种基于水凝胶的测定法适合满足筛选母乳或牛奶中致病性生物 10 CFU/mL 的全球要求,未来的工作将确定假阳性率。