Pereiro Iago, Bendali Amel, Tabnaoui Sanae, Alexandre Lucile, Srbova Jana, Bilkova Zuzana, Deegan Shane, Joshi Lokesh, Viovy Jean-Louis, Malaquin Laurent, Dupuy Bruno, Descroix Stéphanie
Laboratoire Physico Chimie Curie , Institut Curie , PSL Research University , CNRS UMR168 , 75005 Paris , France . Email:
Sorbonne Universités , UPMC Univ Paris 06 , 75005 Paris , France.
Chem Sci. 2017 Feb 1;8(2):1329-1336. doi: 10.1039/c6sc03880h. Epub 2016 Oct 10.
A microfluidic method to specifically capture and detect infectious bacteria based on immunorecognition and proliferative power is presented. It involves a microscale fluidized bed in which magnetic and drag forces are balanced to retain antibody-functionalized superparamagnetic beads in a chamber during sample perfusion. Captured cells are then cultivated by infusing nutritionally-rich medium. The system was validated by the direct one-step detection of Typhimurium in undiluted unskimmed milk, without pre-treatment. The growth of bacteria induces an expansion of the fluidized bed, mainly due to the volume occupied by the newly formed bacteria. This expansion can be observed with the naked eye, providing simple low-cost detection of only a few bacteria and in a few hours. The time to expansion can also be measured with a low-cost camera, allowing quantitative detection down to 4 cfu (colony forming unit), with a dynamic range of 100 to 10 cfu ml in 2 to 8 hours, depending on the initial concentration. This mode of operation is an equivalent of quantitative PCR, with which it shares a high dynamic range and outstanding sensitivity and specificity, operating at the live cell rather than DNA level. Specificity was demonstrated by controls performed in the presence of a 500× excess of non-pathogenic . The system's versatility was demonstrated by its successful application to the detection and quantitation of O157:H15 and . This new technology allows fast, low-cost, portable and automated bacteria detection for various applications in food, environment, security and clinics.
本文提出了一种基于免疫识别和增殖能力特异性捕获和检测感染性细菌的微流控方法。该方法涉及一个微尺度流化床,在样品灌注过程中,磁力和曳力相互平衡,使抗体功能化的超顺磁性珠粒保留在腔室内。然后通过注入营养丰富的培养基来培养捕获的细胞。该系统通过直接一步检测未稀释的全脂牛奶中的鼠伤寒沙门氏菌进行了验证,无需预处理。细菌的生长会导致流化床膨胀,主要是由于新形成的细菌所占的体积。这种膨胀肉眼可见,可在几小时内简单低成本地检测出仅少量细菌。膨胀时间也可用低成本相机测量,可实现低至4 cfu(菌落形成单位)的定量检测,根据初始浓度,在2至8小时内动态范围为100至10 cfu/ml。这种操作模式相当于定量PCR,与之具有高动态范围以及出色的灵敏度和特异性,且是在活细胞而非DNA水平上运行。通过在存在500倍过量非致病性细菌的情况下进行对照实验证明了其特异性。该系统通过成功应用于检测和定量O157:H15和其他细菌证明了其通用性。这项新技术允许在食品、环境、安全和临床等各种应用中进行快速、低成本、便携式和自动化的细菌检测。