Evidence map›Paper›PMID 41520010›Full record

ArticleScientific reports2026

Synergistic antipersister, efflux inhibitory & antibiofilm activities of vaginal Lactobacillus-derived postbiotics against UPEC: toward a novel therapeutic for utis.

Veena G Nair, David Raj Chellappan, Ramya Devi Durai, Rajesh Y B R D, Dhiviya Narbhavi, Anupriya A, Prabhusaran N, Saisubramanian Nagarajan

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Vaginal Microbiome and Preterm Birth in Pregnant Women From India.The journal of obstetrics and gynaecology research · 2026
    Article
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

8 authors.

Veena G NairAntimicrobial Resistance Lab, Centre for Research in Infectious Diseases, School of Chemical and Biotechnology, SASTRA Deemed to be University, Thanjavur, 613401, Tamil Nadu, India.
David Raj ChellappanCentral Animal House Facility, SASTRA Deemed to be University, Thanjavur, 613401, India.
Ramya Devi DuraiPharmaceutical Technology Laboratory, School of Chemical and Biotechnology, SASTRA Deemed to be University, Thanjavur, 613401, India.
Rajesh Y B R DDepartment of Chemistry, School of Chemical and Biotechnology, SASTRA Deemed University, Thanjavur, 613 401, Tamil Nadu, India.
Dhiviya NarbhaviDepartment of Obstetrics and Gynaecology, TSRMMCH&RC, Tiruchirappalli, Tamil Nadu, India.
Anupriya ADepartment of Microbiology, TSRMMCH&RC, Tiruchirappalli, Tamil Nadu, India.
Prabhusaran NResearch Faculty, Institutional Research Board TSRMMCH&RC, Tiruchirappalli, Tamil Nadu, India.
Saisubramanian NagarajanAntimicrobial Resistance Lab, Centre for Research in Infectious Diseases, School of Chemical and Biotechnology, SASTRA Deemed to be University, Thanjavur, 613401, Tamil Nadu, India. sai@scbt.sastra.edu.

Funding

Department of Science and Technology, Ministry of Science and Technology, India DST/WOS-B/HN-32/2021Indian Council of Medical Research EMDR/SG/14/2024/01-04170
6 · The paper itself

Abstract

Bacterial persisters, phenotypic variants that can survive high doses of antibiotics, pose a significant challenge in treating chronic infections and contribute to post-treatment relapses. In this study, we investigated the impact of cell-free supernatant (CFS) from human vaginal Lactobacillus spp. on the formation of E. coli UTI89 persister cells. Among various antibiotics tested, colistin exposure resulted in the highest percentage of persister cells, followed by meropenem, with ampicillin showing the least effect. Fractionation of the CFS via column chromatography yielded seven fractions, with fractions C4 and C7 demonstrating a synergistic inhibition of E. coli persisters. Gas chromatography-mass spectrometry (GC-MS) identified itaconic anhydride and (-)-terpinen-4-ol as the key metabolites responsible for this effect. When combined with colistin and meropenem, these compounds (8 µg/ml and 5 µg/ml, respectively) significantly reduced persister cell formation. The bactericidal action was found to be ROS-dependent, as evidenced by the reduced efficacy in the presence of thiourea, a hydroxyl radical scavenger. Additionally, these metabolites increased membrane permeability and inhibited efflux pumps, further enhancing antibiotic efficacy. Building on these findings, we developed a novel postbiotic-based vaginal wash formulation incorporating (-)-terpinen-4-ol, itaconic anhydride, and tryptamine, another metabolite with antibiofilm properties. These bioactive compounds, isolated from indigenous human vaginal Lactobacillus spp., were incorporated into a poloxamer 407-based formulation designed to prevent urinary tract infections (UTIs) and combat antimicrobial resistance. Preclinical studies conducted on BALB/c mice models validated the formulation's efficacy and safety, highlighting its potential for clinical translation. This approach of combining the antipersister, efflux inhibitory, and antibiofilm activities of these postbiotics within a practical therapeutic formulation offers a promising strategy for improving UTI management and combating the growing challenge of antibiotic tolerance.

Indexed as

Anti-Bacterial AgentsBiofilmsEscherichia coli InfectionsLactobacillusProbioticsUrinary Tract InfectionsUropathogenic Escherichia coliVaginaAnimalsFemaleHumansMiceMicrobial Sensitivity TestsAnti-Bacterial AgentsAnti-persister potentialCell-free supernatantCustomised vaginal washPostbioticsPreclinical validationUropathogenic E coli persistersVaginal probiotics

Identifiers

PMID41520010
PMCPMC12876057

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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.