Joshi Rutwik, Ahmadi Hesaneh, Hasan Kashem Md Nayeem, Afnan Fariha, Parameswaran Siva, Chen Chau-Chyun, Levent Gizem, Li Wei
Department of Chemical Engineering, Texas Tech University, Lubbock, TX, USA.
Department of Mechanical Engineering, Texas Tech University, Lubbock, TX, USA.
Mater Today Bio. 2025 Jan 10;31:101472. doi: 10.1016/j.mtbio.2025.101472. eCollection 2025 Apr.
Timely isolation, recovery, and identification of from food samples is essential for prevention and control of foodborne outbreaks. Traditional culture-based isolation and serotyping techniques are time consuming and labor intensive. Despite the progress of innovative microfluidic or immunomagnetic isolation techniques, sophisticated lab equipment and microfabrication are often needed. Here, we present a novel, rapid yet simple method for isolation and recovery of from mixed bacterial populations in food matrices and blood. This method utilizes self-floating hollow glass microspheres (HGMS) coated with biodegradable layer-by-layer (LbL) films and specific antibodies. The isolation and recovery process can be completed in less than 2 h, without any sophisticated laboratory equipment or external force. In this study, we demonstrate that can be captured due to antigen-antibody interactions on the surface of HGMS, allowing them to float to the top. The HGMS can then be washed and subjected to enzymatic degradation of the LbL film to recover the captured bacteria. The recovered can subsequently be grown on selective agar plates for further analysis. Recovery efficiency of up to 22 % and detection limit of 100 CFU/mL were achieved. This method is expected to provide a viable alternative to traditional isolation techniques, especially in resource limited areas.
及时从食品样本中分离、复苏和鉴定[病原体名称未给出]对于预防和控制食源性疾病暴发至关重要。传统的基于培养的分离和血清分型技术既耗时又费力。尽管创新的微流控或免疫磁珠分离技术取得了进展,但通常仍需要精密的实验室设备和微加工技术。在此,我们提出了一种新颖、快速且简单的方法,用于从食品基质和血液中的混合细菌群体中分离和复苏[病原体名称未给出]。该方法利用涂有可生物降解层层(LbL)膜和特异性抗体的自浮空心玻璃微球(HGMS)。分离和复苏过程可在不到2小时内完成,无需任何精密实验室设备或外力。在本研究中,我们证明[病原体名称未给出]可因HGMS表面的抗原 - 抗体相互作用而被捕获,使其漂浮至顶部。然后可对HGMS进行洗涤,并对LbL膜进行酶降解以复苏捕获的细菌。复苏的[病原体名称未给出]随后可在选择性琼脂平板上培养以进行进一步分析。实现了高达22%的复苏效率和100 CFU/mL的检测限。该方法有望为传统分离技术提供可行的替代方案,尤其是在资源有限的地区。