Evidence map›Paper›PMID 41128994›Full record

ArticleAntonie van Leeuwenhoek2025

Metabolite characterization of probiotic Enterococcus Faecium for targeting Salmonella Entrica gut bacteria causing gastroenteritis.

Kashef Choudhary, Muhammad Naveed, Tariq Aziz, Syeda Izma Makhdoom, Muhammad Waseem, Nada K Alharbi, Fatma Alshehri, Ashwag Shami, Maher S Alwethaynani, Fahad Al-Asmari and 2 more

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Article in Antonie van Leeuwenhoek, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Kashef ChoudharyDepartment of Biotechnology, Faculty of Science and Technology, University of Central Punjab, Lahore, 54590, Pakistan.
Muhammad NaveedDepartment of Biotechnology, Faculty of Science and Technology, University of Central Punjab, Lahore, 54590, Pakistan. naveed.quaidian@gmail.com.
Tariq AzizLaboratory of Animal Health, Hygiene and Food Quality, University of Ioannina, Arta, Greece. iwockd@gmail.com.
Syeda Izma MakhdoomDepartment of Biotechnology, Faculty of Science and Technology, University of Central Punjab, Lahore, 54590, Pakistan.
Muhammad WaseemDepartment of Biotechnology, Faculty of Science and Technology, University of Central Punjab, Lahore, 54590, Pakistan.
Nada K AlharbiDepartment of Biology, College of Science, Princess Nourah bint Abdulrahman University, P. O. Box 84428, 11671, Riyadh, Saudi Arabia.
Fatma AlshehriDepartment of Biology, College of Science, Princess Nourah bint Abdulrahman University, P. O. Box 84428, 11671, Riyadh, Saudi Arabia.
Ashwag ShamiDepartment of Biology, College of Science, Princess Nourah bint Abdulrahman University, P. O. Box 84428, 11671, Riyadh, Saudi Arabia.
Maher S AlwethaynaniDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, Shaqra University, Alquwayiyah, Riyadh, Saudi Arabia.
Fahad Al-AsmariDepartment of Food and Nutrition Sciences, College of Agricultural and Food Sciences, King Faisal University, Al Ahsa, Saudi Arabia.
Areej A AlhhazmiClinical Laboratory Sciences Department, Applied Medical Sciences, Taibah University, Medina, Saudi Arabia.
Fakhria A Al-JoufiDepartment of Pharmacology, College of Pharmacy, Jouf University, 72341, Aljouf, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastroenteritis is a prevalent digestive disorder that contributes to significant morbidity worldwide, often caused by pathogenic bacteria. Probiotics are increasingly recognized for their therapeutic potential in treating gastrointestinal diseases due to their beneficial effects on gut health. This study aimed to explore the antimicrobial, antioxidant, anti-diabetic, and anti-inflammatory properties of Enterococcus faecium metabolites, isolated from a milk sample, against Salmonella enterica. The bacterial strains were isolated using the streak plate method and molecularly characterized, with Enterococcus faecium showing 93.79% sequence similarity and Salmonella enterica showing 96.97% similarity in 16S rRNA sequencing. Metabolites of Enterococcus faecium were extracted using solvents such as ethanol, methanol, n-butanol, and ethyl acetate, resulting in 14 bioactive compounds, including lactic acid, acetic acid, and indole. Antimicrobial activity was evaluated via the disc diffusion method, revealing a dose-dependent increase in the zone of inhibition, reaching 20 mm at 100 µg/mL against Salmonella enterica. Antioxidant activity, assessed using the DPPH assay, exhibited a maximum scavenging rate of 99.8% at 550 µg/mL, while anti-diabetic activity showed 84.66% inhibition of alpha-amylase at 500 µg/mL. The anti-inflammatory activity demonstrated 99% inhibition of protein denaturation at the same concentration. No hemolytic activity was observed at lower concentrations, with the maximum hemolysis of 90% occurring at 250 µg/mL. In conclusion, Enterococcus faecium metabolites exhibited significant in vitro antimicrobial, antioxidant, anti-diabetic, and anti-inflammatory activities, indicating their promise as candidates for further investigation in the context of Salmonella enterica-induced gastroenteritis and related metabolic disorders. Future studies should focus on further clinical applications of these metabolites.

Indexed as

Enterococcus faeciumGastroenteritisGastrointestinal MicrobiomeProbioticsSalmonella entericaAnimalsAnti-Bacterial AgentsAntioxidantsHumansMicrobial Sensitivity TestsMilkRNA, Ribosomal, 16SAnti-Bacterial AgentsAntioxidantsRNA, Ribosomal, 16SAnti-inflammatory effectsAntimicrobial activityEnterococcus faeciumGastroenteritisSalmonella enterica

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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.