| Issue |
BIO Web Conf.
Volume 237, 2026
2026 8th International Conference on Biotechnology and Biomedicine (ICBB 2026)
|
|
|---|---|---|
| Article Number | 02017 | |
| Number of page(s) | 6 | |
| Section | Pharmacology, Natural Products and Drug Delivery | |
| DOI | https://doi.org/10.1051/bioconf/202623702017 | |
| Published online | 10 June 2026 | |
Antigen-Displaying Outer Membrane Vesicles from Engineered Probiotics for Combating Pseudomonas aeruginosa Infection
School of Engineering Medicine, Beihang University, Beijing, China
* Corresponding author: This email address is being protected from spambots. You need JavaScript enabled to view it.
Abstract
The clinical use of broad-spectrum antibiotics often disrupts the host microbiota, increasing the risk and severity of Pseudomonas aeruginosa infections. To address this, we developed a novel probiotic-based immunization strategy using an antibiotic-induced susceptible mouse model. Specifically, we first selected the probiotic Escherichia coli Nissle 1917 (EcN) —the only non-pathogenic E. coli strain with well-documented biosafety and the ability to enhance host immune function to produce outer membrane vesicles (OMVs) displaying either the OprI or PpyR antigen from P. aeruginosa, which possess inherent immunostimulatory activity suitable for vaccine development and self-assembling surface display capability. Upon comparing these OMVs through intranasal immunization, OMVs displaying OprI, an antigen that elicits a robust mucosal immune response associated with Th17 cell polarization, demonstrated superior protective efficacy. Building on this result, we then constructed an orally engineered probiotic strain, EcN- OMV-OprI, designed for gut colonization and the sustained secretion of antigen-displaying OMVs. In antibiotic-pretreated mice, the oral administration of EcN-OMV-OprI significantly increased the 7-day survival rate from 0% to 80% following P. aeruginosa infection and effectively suppressed bacterial burden in the lungs. Together, these findings present a safe and promising strategy for preventing secondary P. aeruginosa infections following clinical antibiotic exposure.
© The Authors, published by EDP Sciences, 2026
This is an Open Access article distributed under the terms of the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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