Evidence map›Paper›PMID 41491928›Full record

ArticleBMC genomics2026

Regulatory RNA Ern0160 controls Enterococcus faecium virulence through direct modulation of expression of LysM domain-containing proteins.

Loren Dejoies, Valérie Bordeau, Killian Le Neindre, Sophie Reissier, Kevin Arnould, Brice Felden, Svetlana Chabelskaya, François Guérin, Charlotte Michaux, Vincent Cattoir

Abstract read
In one paragraph

Article in BMC genomics, 2026. 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

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2 · The registry

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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

10 authors.

Loren DejoiesDepartment of Clinical Microbiology, Rennes University Hospital, Rennes, France.
Valérie BordeauUniversity of Rennes, Inserm UMR_S 1230, Bacterial RNAs and Medicine, Rennes, France.
Killian Le NeindreDepartment of Clinical Microbiology, Rennes University Hospital, Rennes, France.
Sophie ReissierDepartment of Clinical Microbiology, Rennes University Hospital, Rennes, France.
Kevin ArnouldUniversity of Rennes, Inserm UMR_S 1230, Bacterial RNAs and Medicine, Rennes, France.
Brice FeldenUniversity of Rennes, Inserm UMR_S 1230, Bacterial RNAs and Medicine, Rennes, France.
Svetlana ChabelskayaUniversity of Rennes, Inserm UMR_S 1230, Bacterial RNAs and Medicine, Rennes, France.
François GuérinDepartment of Clinical Microbiology, Rennes University Hospital, Rennes, France.
Charlotte MichauxUniversity of Rennes, Inserm UMR_S 1230, Bacterial RNAs and Medicine, Rennes, France. charlotte.michaux@univ-rennes.fr.
Vincent CattoirDepartment of Clinical Microbiology, Rennes University Hospital, Rennes, France. vincent.cattoir@chu-rennes.fr.

Funding

Agence Nationale de la Recherche ANR-15-CE12-0003-01Agence Nationale de la Recherche ANR-22-PAMR-0002Fondation pour la Recherche Médicale FDM 20170637920
6 · The paper itself

Abstract

backgroundEnterococcus faecium is a commensal of the human gut microbiota that can become an opportunistic pathogen, particularly in immunocompromised individuals. Small RNAs (sRNA) are thought to contribute to this shift by enabling rapid bacterial adaptation to environmental changes. Despite this, knowledge of sRNA in E. faecium remains limited. Ern0160, in particular, has attracted interest for its involvement in antibiotic and biocide responses, as well as its role in intestinal colonization in a murine model.

resultsIn this study, we investigated the functions of Ern0160 in E. faecium Aus0004 reference strain and sought to identify its mRNA targets. Transcriptomic and in silico analyses revealed potential regulatory targets, including two homologous genes encoding LysM-containing domain proteins (EFAU004_01059 and EFAU004_01150), both associated with enterococcal pathogenicity. Experimental validation confirmed that increased expression of Ern0160 led to repression of these genes. We further demonstrated direct and specific interactions between Ern0160 and the two homologous target mRNAs. Functional assays in the Galleria mellonella larvae infection model showed that deletion of Ern0160 resulted in increased host mortality, whereas deletion of its targets genes resulted in decreased mortality. These results are consistent with previous findings linking these genes to E. faecium virulence in murine model of systemic and urinary tract infections.

conclusionsOur findings suggest that Ern0160 contributes to a regulatory network that modulates E. faecium colonization and infection by targeting genes involved in antimicrobial response and virulence. This study highlights the potential of regulatory RNAs such as Ern0160 to shape the pathogenic behavior of a multi-drug resistant and clinically significant bacterium.

Indexed as

Bacterial ProteinsEnterococcus faeciumGene Expression Regulation, BacterialRNA, BacterialRNA, Small UntranslatedAnimalsGram-Positive Bacterial InfectionsHumansMiceMothsVirulenceBacterial ProteinsRNA, BacterialRNA, Small UntranslatedE. faeciumRegulationsRNAVirulence

Identifiers

PMID41491928
PMCPMC12870237

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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.