Phage-encoded sRNA counteracts xenogeneic silencing in pathogenic E. coli

Horizontal gene transfer introduces foreign DNA that can disrupt cellular processes and is therefore subject to xenogeneic silencing by nucleoid-associated proteins such as H-NS and Hha. In Enterohaemorrhagic Escherichia coli (EHEC), prophages make up a large fraction of the accessory genome and encode many virulence factors, yet their expression must overcome this silencing. We identify a prophage-encoded small RNA (sRNA), HnrS, that functions as an anti-silencing factor by targeting the H-NS paralogue Hha. HnrS is a short (66-nt) sRNA that is enriched in the locus of enterocyte effacement (LEE⁺) E. coli strains and present in up to nine copies in EHEC and Enteropathogenic Escherichia coli (EPEC) genomes. HnrS base-pairs with the hha ribosome-binding site to inhibit translation, thereby modulating Hha–H-NS repression of virulence loci including the LEE type III secretion system. Loss of HnrS alters motility, T3SS expression, and a subset of Hha-regulated genes. These findings reveal an RNA-based counter-silencing strategy encoded by prophage to relieve xenogenic silencing.

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Publication Details

Journal
PLoS Pathogens
Published
2026-08-18
DOI
https://doi.org/10.1371/journal.ppat.1014486
Primary Topic
Escherichia coli research studies
Type
article
Field-Weighted Citation Impact
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article

Phage-encoded sRNA counteracts xenogeneic silencing in pathogenic E. coli

Daniel G. Mediati, Ruiting Lan, Pietro Ridone, Saleh F. Alquethamy et al.
PLoS Pathogens
Escherichia coli research studies
article

Phage-encoded sRNA counteracts xenogeneic silencing in pathogenic E. coli

Daniel G. Mediati, Ruiting Lan, Pietro Ridone, Saleh F. Alquethamy, Pranita Poudyal, Asim Ullah, Jai Justin Tree, Vibhuti Nandel, Serena Li, Sean McAteer, Lawrence Menz, Shafagh Waters, Timothy J. Dallman, Michael Payne, Jacob Scadden, David Gally, Brandon Sy, Mathew Baker, Dougall Norris
article en

Abstract

Horizontal gene transfer introduces foreign DNA that can disrupt cellular processes and is therefore subject to xenogeneic silencing by nucleoid-associated proteins such as H-NS and Hha. In Enterohaemorrhagic Escherichia coli (EHEC), prophages make up a large fraction of the accessory genome and encode many virulence factors, yet their expression must overcome this silencing. We identify a prophage-encoded small RNA (sRNA), HnrS, that functions as an anti-silencing factor by targeting the H-NS paralogue Hha. HnrS is a short (66-nt) sRNA that is enriched in the locus of enterocyte effacement (LEE⁺) E. coli strains and present in up to nine copies in EHEC and Enteropathogenic Escherichia coli (EPEC) genomes. HnrS base-pairs with the hha ribosome-binding site to inhibit translation, thereby modulating Hha–H-NS repression of virulence loci including the LEE type III secretion system. Loss of HnrS alters motility, T3SS expression, and a subset of Hha-regulated genes. These findings reveal an RNA-based counter-silencing strategy encoded by prophage to relieve xenogenic silencing.

PLoS PathogensVol. 22(8)
Openalex Percentile: Top 11%
Escherichia coli research studies
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