Brugnera Michelle Fernanda, Bundalian Reynaldo, Laube Tamara, Julián Esther, Luquin Marina, Zanoni Maria Valnice Boldrin, Pividori Maria Isabel
Grup de Sensors i Biosensors, Departament de Química, Universitat Autònoma de Barcelona, Bellaterra, Spain; Department of Analytical Chemistry, Institute of Chemistry, UNESP-Univ Estadual Paulista, Araraquara, SP, Brazil.
Grup de Sensors i Biosensors, Departament de Química, Universitat Autònoma de Barcelona, Bellaterra, Spain; Department of Chemistry, College of Arts and Sciences, Angeles University Foundation, Angeles City, Philippines.
Talanta. 2016 Jun 1;153:38-44. doi: 10.1016/j.talanta.2016.02.041. Epub 2016 Feb 18.
This paper addresses a sensitive method for the detection of mycobacteria in hemodialysis water samples based on a magneto-actuated immunoassay with optical readout. In this approach, micro (2.8μm) sized magnetic particles were modified with an antibody against the lipoarabinomannan (LAM) located in the mycobacterial cell wall. The system relies on the immunocapturing of the mycobacteria with the tailored antiLAM magnetic particles to pre-concentrate the bacteria from the hemodialysis samples throughout an immunological reaction. The performance of the immunomagnetic separation on the magnetic carrier was evaluated using confocal microscopy to study the binding pattern, as well as a magneto-actuated immunoassay with optical readout for the rapid detection of the bacteria in spiked hemodialysis samples. In this approach, the antiLAM polyclonal antibody was labeled with fluorescein isothiocyanate. The optical readout was achieved by the incubation with a secondary anti-fluorescein antibody labeled with peroxidase as optical reporter. The magneto-actuated immunoassay was able to detect mycobacteria contamination in hemodialysis water at a limit of detection of 13CFUmL(-1) in a total assay time of 3h without any previous culturing pre-enrichment step.
本文介绍了一种基于磁驱动免疫分析和光学读数的灵敏方法,用于检测血液透析水样中的分枝杆菌。在这种方法中,用针对位于分枝杆菌细胞壁中的脂阿拉伯甘露聚糖(LAM)的抗体修饰微米级(2.8μm)磁性颗粒。该系统依靠用定制的抗LAM磁性颗粒对分枝杆菌进行免疫捕获,通过免疫反应从血液透析样本中预富集细菌。使用共聚焦显微镜研究结合模式,评估磁性载体上免疫磁分离的性能,并采用磁驱动免疫分析和光学读数对加标的血液透析样本中的细菌进行快速检测。在这种方法中,抗LAM多克隆抗体用异硫氰酸荧光素标记。通过与用过氧化物酶标记的抗荧光素二抗作为光学报告分子孵育来实现光学读数。磁驱动免疫分析能够在无需任何先前培养预富集步骤的情况下,在3小时的总检测时间内检测出血液透析水中的分枝杆菌污染,检测限为13CFUmL(-1)。