ArticleMikrochimica acta2026
Phage tail fiber protein-based fluorescence immunochromatographic test strip for rapid and sensitive detection of shiga toxin-producing Escherichia coli O103.
Article in Mikrochimica acta, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
Shiga toxin-producing Escherichia coli (STEC) poses a severe threat to global public health and food safety, creating an urgent need for rapid and sensitive detection of STEC. Herein, a novel fluorescent immunochromatography test strip (FITS) is reported for the detection of STEC O103 using QDs-loaded dendritic silica spheres (named SQS) as a signal tag. The novel FITS employs a phage tail fiber protein as a superior antibody alternative, which was functionalized on the SQS and demonstrates excellent capability for bacterial recognition and binding. This assay successfully achieves the sensitive detection of STEC O103 (2.2 × 102 CFU/mL) within 12 min, achieving performance comparable to conventional PCR while significantly reducing assay time. More significantly, the results of the FITS in real samples were in good agreement with those from PCR, exhibiting comparable accuracy and reproducibility. Given its rapidity, simplicity, sensitivity, and visual detectability, the proposed FITS stands out as an ideal approach for STEC O103 detection and shows great promise for the early warning and diagnosis of bacterial infections.
Indexed as
Identifiers
41902963What OpenQuestion holds
Registered trials
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.