Antibody Microarray for E. coli O157:H7 and Shiga Toxin in Microtiter Plates

• Main Authors: Andrew G. Gehring, Jeffrey D. Brewster, Yiping He, Peter L. Irwin, George C. Paoli, Tawana Simons, Shu-I Tu, Joseph Uknalis
• Format: Article
• Language: English
• Published: MDPI AG 2015-12-01
• Series: Sensors
• Subjects: antibody microarray; bacteria; centrifugation; fluorescence; immunoassay; multiwell; microtiter plate; multiplex; toxin
• Online Access: http://www.mdpi.com/1424-8220/15/12/29807

Antibody microarray is a powerful analytical technique because of its inherent ability to simultaneously discriminate and measure numerous analytes, therefore making the technique conducive to both the multiplexed detection and identification of bacterial analytes (i.e., whole cells, as well as associated metabolites and/or toxins). We developed a sandwich fluorescent immunoassay combined with a high-throughput, multiwell plate microarray detection format. Inexpensive polystyrene plates were employed containing passively adsorbed, array-printed capture antibodies. During sample reaction, centrifugation was the only strategy found to significantly improve capture, and hence detection, of bacteria (pathogenic Escherichia coli O157:H7) to planar capture surfaces containing printed antibodies. Whereas several other sample incubation techniques (e.g., static vs. agitation) had minimal effect. Immobilized bacteria were labeled with a red-orange-fluorescent dye (Alexa Fluor 555) conjugated antibody to allow for quantitative detection of the captured bacteria with a laser scanner. Shiga toxin 1 (Stx1) could be simultaneously detected along with the cells, but none of the agitation techniques employed during incubation improved detection of the relatively small biomolecule. Under optimal conditions, the assay had demonstrated limits of detection of ~5.8 × 105 cells/mL and 110 ng/mL for E. coli O157:H7 and Stx1, respectively, in a ~75 min total assay time.