Evidence map›Paper›PMID 40693324›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2026

Bioengineered Bacterial Vesicles and Biomimetic Hybrids Eliminate Biofilms and Balance the Gut Microbiome.

Leila Pourtalebi Jahromi, Benedikt Kronast, Jennifer Munkert, Lorenzo Sana, Marcus Koch, Heike Danzer, Sirka Dormeyer, Shuhan Jiang, Fabian Herrmann, Matthias Weiler and 4 more

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
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

14 authors.

Leila Pourtalebi JahromiFriedrich-Alexander-Universität Erlangen-Nürnberg, Faculty of Science, Department of Biology, Pharmaceutical Biology, Staudtstr. 5, 91058, Erlangen, Germany.
Benedikt KronastFriedrich-Alexander-Universität Erlangen-Nürnberg, Faculty of Science, Department of Biology, Pharmaceutical Biology, Staudtstr. 5, 91058, Erlangen, Germany.
Jennifer MunkertFriedrich-Alexander-Universität Erlangen-Nürnberg, Faculty of Science, Department of Biology, Pharmaceutical Biology, Staudtstr. 5, 91058, Erlangen, Germany.
Lorenzo SanaFriedrich-Alexander-Universität Erlangen-Nürnberg, Faculty of Science, Department of Biology, Pharmaceutical Biology, Staudtstr. 5, 91058, Erlangen, Germany.
Marcus KochINM-Leibniz-Institute for New Materials, 66123, Saarbrücken, Germany.
Heike DanzerDepartment of Internal Medicine 3, Rheumatology and Immunology, Friedrich-Alexander-Universiät Erlangen-Nürnberg (FAU) and Universitätsklinikum Erlangen, 91054, Erlangen, Germany.
Sirka DormeyerDepartment of Internal Medicine 3, Rheumatology and Immunology, Friedrich-Alexander-Universiät Erlangen-Nürnberg (FAU) and Universitätsklinikum Erlangen, 91054, Erlangen, Germany.
Shuhan JiangMax Planck Institute for the Science of Light, 91058, Erlangen, Germany.
Fabian HerrmannInstitute of Pharmaceutical Biology and Phytochemistry, University of Münster, 48149, Münster, Germany.
Matthias WeilerDepartment of Physics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058, Erlangen, Germany.
Anna KashkanovaMax Planck Institute for the Science of Light, 91058, Erlangen, Germany.
Vahid SandoghdarMax Planck Institute for the Science of Light, 91058, Erlangen, Germany.
Mario M ZaissDepartment of Internal Medicine 3, Rheumatology and Immunology, Friedrich-Alexander-Universiät Erlangen-Nürnberg (FAU) and Universitätsklinikum Erlangen, 91054, Erlangen, Germany.
Gregor FuhrmannFriedrich-Alexander-Universität Erlangen-Nürnberg, Faculty of Science, Department of Biology, Pharmaceutical Biology, Staudtstr. 5, 91058, Erlangen, Germany.ORCID https://orcid.org/0000-0002-6688-5126

Funding

Bundesministerium für Bildung und Forschung 13XP5029AH2020 European Research Council 945602
6 · The paper itself

Abstract

Antibiotic-resistant pathogens are a global health challenge, necessitating innovative solutions beyond conventional antibiotics. This study introduces biomimetic nanocarriers - hybrids of bacteriomimetic liposomes and biocompatible Myxobacteria outer-membrane vesicles (OMVs) - as tunable platforms for targeted antibiotic delivery. Comparative analyses of their physicochemical properties and interactions with immune cells, intestinal epithelium, and biofilm-forming pathogens reveal distinct advantages. Hybrids excel at delivering antibiotics to intracellular targets, while Myxobacteria OMVs, particularly those of strain SBSr 073, evade immune clearance and prolong extracellular drug exposure. To support clinical translation, this study optimizes antibiotic encapsulation methods for SBSr 073 OMVs and evaluates the short- and long-term impact of Cystobacter ferrugineus 23 strain OMVs on the gut microbiome in mice. Summing up, this study highlights the promise of Myxobacteria OMVs and their biomimetic hybrids as versatile tools for treating Gram-negative biofilm-forming pathogens. These findings underscore the potential of bioengineered and biomimetic drug carriers for combating antimicrobial resistance and pave the way for their translation toward difficult-to-treat infections.

Indexed as

BioengineeringBiofilmsBiomimetic MaterialsBiomimeticsGastrointestinal MicrobiomeAnimalsAnti-Bacterial AgentsLiposomesMiceAnti-Bacterial AgentsLiposomesantibioticsbiofilmsgut microbiomehybridsliposomesmyxobacteriaouter‐membrane vesicle

Identifiers

PMID40693324
PMCPMC12994561

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.