Evidence map›Paper›PMID 41039273›Full record

ArticleBMC microbiology2025

Prophylactic efficacy of probiotics and their metabolites against Staphylococcus epidermidis.

Anna Phan, Kanchan Thapa, Muhammad Abrar Hashmi, Aditi Mohapatra, Gwendolyn Ho, Grisham Narayan Tholan, Debabrata Biswas

Abstract read
In one paragraph

Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Anna PhanBiological Sciences Program-Molecular and Cellular Biology, University of Maryland, College Park, State Maryland, MD 20742, USA.
Kanchan ThapaDepartment of Animal and Avian Sciences, University of Maryland, College Park, State Maryland, MD 20742, USA.
Muhammad Abrar HashmiDepartment of Animal and Avian Sciences, University of Maryland, College Park, State Maryland, MD 20742, USA.
Aditi MohapatraDepartment of Biology, University of Maryland, College Park, MD, USA.
Gwendolyn HoDepartment of Biology, University of Maryland, College Park, MD, USA.
Grisham Narayan TholanDepartment of Biology, University of Maryland, College Park, MD, USA.
Debabrata BiswasDepartment of Animal and Avian Sciences, University of Maryland, College Park, State Maryland, MD 20742, USA. dbiswas@umd.edu.

Funding

USDA-National Institute of Food and Agriculture 2018-5110628809
6 · The paper itself

Abstract

backgroundStaphylococcus epidermidis is a prevalent common microorganism found on the skin of most mammals, including humans. However, S. epidermidis is also known as an opportunistic pathogen that can cause diseases if the skin microbiome becomes skewed to favor its overgrowth. This situation can be worsened if the causative strains are antibiotic-resistant. To explore potential alternatives to replace conventional antibiotics, we aim to use probiotics, specifically Lacticaseibacillus rhamnosus and Lactiplantibacillus plantarum, in controlling the growth, colonization, and biofilm formation of a multidrug-resistant S. epidermidis.

resultsMultidrug-resistant S. epidermidis was co-cultured with either L. rhamnosus or L. plantarum, and antimicrobial activity was assessed by counting S. epidermidis colonies at various timepoints. Under co-culture conditions, growth of S. epidermidis was decreased over time in the presence of either probiotic, specifically, a significant reduction was observed after 48 hours (p=0.0062). Additionally, S. epidermidis was treated with cell-free culture supernatant (CFCS) collected from probiotics to investigate the mechanism of inhibition. CFCS from 72-hour Lactobacilli cultures significantly inhibited S. epidermidis growth within 4 hours (p<0.05), and no S. epidermidis was detected after 72 hours (p=0.0003) when treated with 50% CFCS. Both CFCSs also reduced biofilm formation and bacterial counts after 24 hours, with complete inhibition by 48 h. Gene expression analysis revealed that exposure to CFCS led to downregulation of S. epidermidis genes associated with metabolism and cell division (arcC, gts, mutS, mur1, and ftsZ). Fluorescence microscopy indicated compromised cell wall integrity, evidenced by reduced HADA fluorescence and increased propidium iodide staining.

conclusionL. plantarum and L. rhamnosus possess strong antimicrobial activity against multidrug-resistantS. epidermidis, supporting their potential as alternative strategies to control S. epidermidis colonization.

Indexed as

Lacticaseibacillus rhamnosusLactiplantibacillus plantarumProbioticsStaphylococcal InfectionsStaphylococcus epidermidisAnti-Bacterial AgentsBiofilmsCoculture TechniquesDrug Resistance, Multiple, BacterialHumansAnti-Bacterial AgentsAntibiotic resistanceBiofilmLactobacillusProbioticsStaphylococcus epidermidis

Identifiers

PMID41039273
PMCPMC12492936

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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.