Hemagglutinin Protease HapA Associated With <i>Vibrio cholerae</i> Outer Membrane Vesicles (OMVs) Disrupts Tight and Adherens Junctions

This study explores the virulence mechanisms of Vibrio cholerae, with a particular emphasis on HapA, a zinc metalloprotease delivered via outer membrane vesicles (OMVs). The findings reveal that OMV-associated HapA disrupts the integrity of tight and adherens junctions in intestinal epithelial cell models more effectively than its purified counterpart, suggesting that association with OMVs substantially potentiates the pathogenic effects of HapA. The study further details the uptake of V. cholerae OMVs by epithelial cells, as well as their targeted degradation of key junctional proteins, including claudin, ZO-1, and β-catenin. These results highlight the critical role of OMV-associated HapA in compromising epithelial barrier function. Additionally, the use of spheroids and intestinal organoids in our experiments provides deeper insight into bacterial pathogenesis, offering valuable information for the development of targeted therapeutic strategies.

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Publication Details

Journal
Journal of Extracellular Vesicles
Published
2025-05-01
DOI
https://doi.org/10.1002/jev2.70092
Citations
3
Primary Topic
Vibrio bacteria research studies
Type
article
Field-Weighted Citation Impact
5.39

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article

Hemagglutinin Protease HapA Associated With Vibrio cholerae Outer Membrane Vesicles (OMVs) Disrupts Tight and Adherens Junctions

Aftab Nadeem, Madeleine Ramstedt, Palwasha Baryalai, Eric Toh et al.
3 citations
Journal of Extracellular Vesicles
Vibrio bacteria research studies
5.39
article

Hemagglutinin Protease HapA Associated With Vibrio cholerae Outer Membrane Vesicles (OMVs) Disrupts Tight and Adherens Junctions

Aftab Nadeem, Madeleine Ramstedt, Palwasha Baryalai, Eric Toh, Bernt Eric Uhlin, Sun Nyunt Wai, David Irenaeus
article en
3 citations

Abstract

This study explores the virulence mechanisms of Vibrio cholerae, with a particular emphasis on HapA, a zinc metalloprotease delivered via outer membrane vesicles (OMVs). The findings reveal that OMV-associated HapA disrupts the integrity of tight and adherens junctions in intestinal epithelial cell models more effectively than its purified counterpart, suggesting that association with OMVs substantially potentiates the pathogenic effects of HapA. The study further details the uptake of V. cholerae OMVs by epithelial cells, as well as their targeted degradation of key junctional proteins, including claudin, ZO-1, and β-catenin. These results highlight the critical role of OMV-associated HapA in compromising epithelial barrier function. Additionally, the use of spheroids and intestinal organoids in our experiments provides deeper insight into bacterial pathogenesis, offering valuable information for the development of targeted therapeutic strategies.

Journal of Extracellular VesiclesVol. 14(5)
Umeå University (SE)
Kempe Foundation, Cancerfonden, Vetenskapsrådet, Umeå Universitet, Kempestiftelserna
Openalex Percentile: Top 5%
Vibrio bacteria research studies
5.39
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Hemagglutinin Protease HapA Associated With <i>Vibrio cholerae</i> Outer Membrane Vesicles (OMVs) Disrupts Tight and Adherens Junctions — Aftab Nadeem, Madeleine Ramstedt, et al. · Journal of Extracellular Vesicles (2025) | TGRS Research Map | TGRS