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Updated: May 14, 2026

A Protein Microarray Assay for Serological Determination of Antigen-specific Antibody Responses Following Clostridium difficile Infection
Published on: June 15, 2018
Establishment and Comparison of High-Throughput Immunoassays for Quantifying Clostridioides difficile Infection
Hanool Yun1, Na-Hyeon Kwon1, Minhee Kang2
1Department of Biological and Chemical Engineering, Hongik University, Sejong, Republic of Korea.
None:
Clostridioides difficile infection (CDI) is the leading cause of healthcare-associated diarrhea, most often occurring after antibiotic exposure. In this study, we established three immunoassays: indirect enzyme-linked immunosorbent assay (ELISA), sandwich ELISA, and fluorescence-linked immunosorbent assay (FLISA), using antibodies specific to the major virulence factors, toxin A (TcdA) and toxin B (TcdB). Indirect ELISA demonstrated high specificity with an overall assay time within 21 h, achieving sensitive detection of both toxins. Although more time- and resource-intensive (22 h), sandwich ELISA is advantageous for applications where pre-coated plates or ready-to-use membranes can reduce assay time. FLISA, using optimized fluorescent dye-conjugated antibodies, offered the most rapid workflow and simplest preparation, with potential for multiplex detection, though its sensitivity was lower than that of ELISA. All three assays were implemented in a 96-well plate format, which supported parallel sample processing, reduced turnaround times, and offered scalability for high-throughput applications. Depending on assay requirements, such as analytical sensitivity, turnaround time, and cost-effectiveness, these methods provide complementary approaches for the detection of TcdA and TcdB.
