Evidence map›Paper›PMID 41162498›Full record

ArticleScientific reports2025

Isolation, functional characterization and antibiofilm properties of a lytic Enterococcus phage RG1 against multidrug resistant E. faecium.

Rakesh Kumar Singh, Riya Anand, Ajeet Singh, Zinnu Rain, Pradyot Prakash, Ganesh Kumar Maurya

Abstract read
In one paragraph

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

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rakesh Kumar Singh *Zoology Section, Mahila Mahavidyalaya, Banaras Hindu University, Varanasi, 221005, India.
Riya Anand *Zoology Section, Mahila Mahavidyalaya, Banaras Hindu University, Varanasi, 221005, India.
Ajeet SinghZoology Section, Mahila Mahavidyalaya, Banaras Hindu University, Varanasi, 221005, India.
Zinnu RainDepartment of Microbiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221005, India.
Pradyot PrakashDepartment of Microbiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221005, India.
Ganesh Kumar MauryaZoology Section, Mahila Mahavidyalaya, Banaras Hindu University, Varanasi, 221005, India. gkmaurya@bhu.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enterococcus faecium, a multidrug-resistant (MDR), commensal human pathogen, frequently causes nosocomial infections and imposes serious threat to public health, which demanded more research for the development of alternative therapeutics against them. Bacteriophage therapy as an alternative to antibiotics has reappeared as therapeutics against MDR bacterial infections. Here, we isolated and characterized a novel lytic phage, RG1, from the Ganga River against E. faecium ATCC 35667 and checked their efficacy against several clinical isolates of E. faecium. Whole genome sequencing revealed that the RG1 belongs to genus Efemquintavirus, and has a dsDNA genome of 41,364 base pairs with 35.54% GC content, which encodes 65 putative open reading frames without any virulence, antibiotic resistance or lysogeny genes. Bacteriophage RG1 displayed high stability across different pH, temperatures and chloroform concentrations. The phage RG1 exhibited antibacterial and antibiofilm activity over both ATCC and clinical isolates of E. faecium likely due to its wider host range, which paves the way inside the precision phage therapy. Interestingly, the presence of ribose, maltose and trehalose sugars showed more suppression of bacterial growth of MDR E. faecium isolate in presence of the phage RG1, while sugar alcohols synergistically supported host lysis by this phage. These findings highlight the therapeutic potential of the phage RG1 against the MDR E. faecium under clinical setup.

Indexed as

BacteriophagesBiofilmsDrug Resistance, Multiple, BacterialEnterococcus faeciumGenome, ViralHumansPhage TherapyAntibiotic resistanceBiofilmEnterococciPhage therapySugar molecules

Identifiers

PMID41162498
PMCPMC12572221

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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.