ArticleBiotechnology letters2025
Oral administration of Bacillus subtilis spores expressing Staphylococcus aureus IsdB induces mucosal immune responses in mice.
Article in Biotechnology letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
purposeBacillus subtilis spores, known for their durability and well-developed genetic manipulation tools, show promise for oral vaccine delivery. Staphylococcus aureus is a major global health concern due to multidrug resistance and lack of a vaccine. This study explored the potential of B. subtilis spores engineered to express IsdB, a key S. aureus iron acquisition protein, on their surface and evaluated the immunogenic effect of recombinant spores through oral administration in mice.
methodB. subtilis spores were engineered to display a key S. aureus protein, IsdB, fused with spore coat protein, CotB, and confirmed by PCR. Western blotting, sporeELISA, and immunofluorescence microscopy verified the surface expression of IsdB. The engineered BsHT2377 spores were orally administered to Swiss mice at two different doses, and antibody levels in both serum and feces were measured using ELISA.
resultPCR confirmed the targeted integration of the isdB gene into B. subtilis, generating the strain BsHT2377. Western blotting, sporeELISA, and immunofluorescence microscopy validated IsdB surface display on BsHT2377 spores. Oral administration triggered a gut-localised immune response in mice, with significantly elevated fecal IgA but no substantial increase in serum IgG.
conclusionThis study engineered a novel B. subtilis strain, BsHT2377, that displays the S. aureus IsdB protein on its spore surface. Oral administration in mice significantly increased fecal IgA, indicating a mucosal immune response. These findings highlight the potential of B. subtilis spores as oral vaccine carriers and offer insights to support the optimization of future vaccine designs.
Indexed as
Identifiers
40660064What 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.