Department of Biomedical Engineering, National Cheng Kung University, Tainan, Taiwan.
Department of Urology, Chimei Medical Center, Tainan, Taiwan.
Sci Rep. 2017 Apr 12;7:46336. doi: 10.1038/srep46336.
Successful treatments against bacterial infections depend on antimicrobial susceptibility testing (AST). However, conventional AST requires more than 24 h to obtain an outcome, thereby contributing to high patient mortality. An antibiotic therapy based on experiences is therefore necessary for saving lives and escalating the emergence of multidrug-resistant pathogens. Accordingly, a fast and effective drug screen is necessary for the appropriate administration of antibiotics. The mixed pathogenic nature of infectious diseases emphasizes the need to develop an assay system for polymicrobial infections. On this basis, we present a novel technique for simultaneous and quantitative monitoring of co-cultured microorganisms by coupling optical diffusometry with bead-based immunoassays. This simple integration simultaneously achieves a rapid AST analysis for two pathogens. Triple color particles were simultaneously recorded and subsequently analyzed by functionalizing different fluorescent color particles with dissimilar pathogen-specific antibodies. Results suggested that the effect of the antibiotic, gentamicin, on co-cultured Pseudomonas aeruginosa and Staphylococcus aureus was effectively distinguished by the proposed technique. This study revealed a multiplexed and time-saving (within 2 h) platform with a small sample volume (~0.5 μL) and a low initial bacterial count (50 CFU per droplet, ~10 CFU/mL) for continuously monitoring the growth of co-cultured microorganisms. This technique provides insights into timely therapies against polymicrobial diseases in the near future.
成功治疗细菌感染依赖于抗菌药物敏感性测试 (AST)。然而,常规 AST 需要超过 24 小时才能得出结果,从而导致患者死亡率高。因此,基于经验的抗生素治疗对于挽救生命和提高多药耐药病原体的出现是必要的。相应地,需要快速有效的药物筛选来适当使用抗生素。传染病的混合发病性质强调需要开发针对混合感染的检测系统。在此基础上,我们提出了一种新的技术,通过将光学漫射测量法与基于珠粒的免疫测定法相结合,对共培养微生物进行同时和定量监测。这种简单的集成同时实现了两种病原体的快速 AST 分析。通过用不同的病原体特异性抗体对不同荧光颜色的珠子进行功能化,同时记录三颜色颗粒并随后进行分析。结果表明,所提出的技术可有效区分抗生素庆大霉素对共培养铜绿假单胞菌和金黄色葡萄球菌的作用。本研究揭示了一种多重且节省时间(2 小时内)的平台,该平台具有小样本量(0.5 μL)和低初始细菌计数(每个液滴 50 CFU,10 CFU/mL),可连续监测共培养微生物的生长。这项技术为未来及时治疗多微生物疾病提供了思路。