Evidence map›Paper›PMID 42125966›Full record

ArticleBiotechnology journal2026

Establishment and Comparison of High-Throughput Immunoassays for Quantifying Clostridioides difficile Infection Biomarkers.

Hanool Yun, Na-Hyeon Kwon, Minhee Kang, Tae Yeul Kim, Hee-Jin Jeong

Abstract readComparative Study
In one paragraph

Article in Biotechnology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Hanool YunDepartment of Biological and Chemical Engineering, Hongik University, Sejong, Republic of Korea.
Na-Hyeon KwonDepartment of Biological and Chemical Engineering, Hongik University, Sejong, Republic of Korea.
Minhee KangBiomedical Engineering Research Center, Smart Healthcare Research Institute, Samsung Medical Center, Seoul, Republic of Korea.
Tae Yeul KimDepartment of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Hee-Jin JeongDepartment of Biological and Chemical Engineering, Hongik University, Sejong, Republic of Korea.

Funding

2026 Hongik University Innovation Support Program Fund2026 Hongik University Research FundSamsung Medical Center #SMO1250691
6 · The paper itself

Abstract

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.

Indexed as

Bacterial ProteinsBacterial ToxinsClostridioides difficileClostridium InfectionsEnterotoxinsHigh-Throughput Screening AssaysAntibodies, BacterialBiomarkersEnzyme-Linked Immunosorbent AssayHumansImmunoassaySensitivity and SpecificityAntibodies, BacterialBacterial ProteinsBacterial ToxinsBiomarkersEnterotoxinstcdA protein, Clostridium difficiletoxB protein, Clostridium difficileantibodyClostridioides difficile infectionELISAFLISAimmunoassay

Identifiers

PMID42125966
PMCPMC13383591

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.