Saved in:
Bibliographic Details
Main Authors: Martínez, Clara, Rodriguez, Sergio, Trueba, Alba, Rey-Varela, Diego, Toranzo, Alicia E, Dieguez, Ana L, Dubert, Javier
Format: Artículo científico
Language:en
Published: Journal of invertebrate pathology 2026
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/41580066/
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1868266095176056833
author Martínez, Clara
Rodriguez, Sergio
Trueba, Alba
Rey-Varela, Diego
Toranzo, Alicia E
Dieguez, Ana L
Dubert, Javier
author_facet Martínez, Clara
Rodriguez, Sergio
Trueba, Alba
Rey-Varela, Diego
Toranzo, Alicia E
Dieguez, Ana L
Dubert, Javier
Martínez, Clara
Rodriguez, Sergio
Trueba, Alba
Rey-Varela, Diego
Toranzo, Alicia E
Dieguez, Ana L
Dubert, Javier
collection PubMed - marine biology
contents Uncovering how major extracellular proteins drive virulence and functional compensation in the mollusk pathogen Vibrio europaeus. Martínez, Clara Rodriguez, Sergio Trueba, Alba Rey-Varela, Diego Toranzo, Alicia E Dieguez, Ana L Dubert, Javier Vibrio Animals Virulence Bacterial Proteins Bivalvia Bivalve aquaculture is a major component of global seafood production. However, its sustainability is severely threatened by recurrent outbreaks of vibriosis, caused by Vibrio europaeus that has emerged as a significant threat worldwide, affecting key aquaculture shellfish species. This study presents the first comprehensive characterization of the extracellular products (ECPs) and secretome of the mollusk pathogen Vibrio europaeus. A total of 108 different proteins were identified in the wild-type (WT) secretome, with the extracellular proteins VemA, VepA, and GbpA, accounting for nearly 70% of the total secreted protein content. A significant proportion of cytoplasmic proteins were also detected in the WT secretome, consistent with their secretion through outer membrane vesicles (OMVs) observed by electron microscopy. Functional assays confirmed that VemA is essential for virulence toward Manila clam juveniles (Ruditapes philippinarum), whereas VepA and GbpA appear to play complementary or modulatory roles. Surprisingly, simultaneous deletion of vemA, vepA, and gbpA genes induced extensive secretory reprogramming, with this mutant secreting 823 proteins, nearly eight times more than the WT, and exhibiting novel enzymatic activities. Approximately half of the secreted proteins in the triple mutant were cytoplasmic in origin, likely associated with a hypervesiculation phenotype observed by electron microscopy. Despite its expanded repertoire of virulence-associated proteins, the triple mutant displayed the lowest virulence in challenge assays, suggesting that the loss of the main ECPs triggers compensatory stress responses that remodel secretion but does not restore the virulence phenotype. Overall, these findings demonstrate that VemA, VepA, and GbpA are key determinants of virulence and secretory homeostasis in V. europaeus, revealing an adaptive mechanism linking OMV-mediated secretion, proteomic plasticity, and pathogenic potential in marine Vibrio species and provide better understanding how pathogens evolve to maintain or expand their virulence capacity.
format Artículo científico
id pubmed_41580066
institution PubMed
language en
publishDate 2026
publisher Journal of invertebrate pathology
record_format pubmed
spellingShingle Uncovering how major extracellular proteins drive virulence and functional compensation in the mollusk pathogen Vibrio europaeus.
Martínez, Clara
Rodriguez, Sergio
Trueba, Alba
Rey-Varela, Diego
Toranzo, Alicia E
Dieguez, Ana L
Dubert, Javier
Vibrio
Animals
Virulence
Bacterial Proteins
Bivalvia
Uncovering how major extracellular proteins drive virulence and functional compensation in the mollusk pathogen Vibrio europaeus. Martínez, Clara Rodriguez, Sergio Trueba, Alba Rey-Varela, Diego Toranzo, Alicia E Dieguez, Ana L Dubert, Javier Vibrio Animals Virulence Bacterial Proteins Bivalvia Bivalve aquaculture is a major component of global seafood production. However, its sustainability is severely threatened by recurrent outbreaks of vibriosis, caused by Vibrio europaeus that has emerged as a significant threat worldwide, affecting key aquaculture shellfish species. This study presents the first comprehensive characterization of the extracellular products (ECPs) and secretome of the mollusk pathogen Vibrio europaeus. A total of 108 different proteins were identified in the wild-type (WT) secretome, with the extracellular proteins VemA, VepA, and GbpA, accounting for nearly 70% of the total secreted protein content. A significant proportion of cytoplasmic proteins were also detected in the WT secretome, consistent with their secretion through outer membrane vesicles (OMVs) observed by electron microscopy. Functional assays confirmed that VemA is essential for virulence toward Manila clam juveniles (Ruditapes philippinarum), whereas VepA and GbpA appear to play complementary or modulatory roles. Surprisingly, simultaneous deletion of vemA, vepA, and gbpA genes induced extensive secretory reprogramming, with this mutant secreting 823 proteins, nearly eight times more than the WT, and exhibiting novel enzymatic activities. Approximately half of the secreted proteins in the triple mutant were cytoplasmic in origin, likely associated with a hypervesiculation phenotype observed by electron microscopy. Despite its expanded repertoire of virulence-associated proteins, the triple mutant displayed the lowest virulence in challenge assays, suggesting that the loss of the main ECPs triggers compensatory stress responses that remodel secretion but does not restore the virulence phenotype. Overall, these findings demonstrate that VemA, VepA, and GbpA are key determinants of virulence and secretory homeostasis in V. europaeus, revealing an adaptive mechanism linking OMV-mediated secretion, proteomic plasticity, and pathogenic potential in marine Vibrio species and provide better understanding how pathogens evolve to maintain or expand their virulence capacity.
title Uncovering how major extracellular proteins drive virulence and functional compensation in the mollusk pathogen Vibrio europaeus.
topic Vibrio
Animals
Virulence
Bacterial Proteins
Bivalvia
url https://pubmed.ncbi.nlm.nih.gov/41580066/