Fucose dependent rotavirus and norovirus require fucosidase activity for optimal replication

Rotavirus (RV) and norovirus (NoV) are enteric viruses responsible for acute gastroenteritis that require fucosylated histo-blood group antigens for infection in humans. How the interaction of these viruses with fucosylated glycans modulates infection is not well understood. Treatment of target cells with a bacterial α1,2 fucosidase enzyme reduced RV and NoV infection in vitro, but increased replication in vivo. Conversely, the fucosidase inhibitor 1-deoxyfuconojirimycin impaired viral replication in both models, highlighting the role of fucosidase activity in fucose-dependent enteric virus infection. This underscores the complexity of fucose interactions for these viruses and implicates fucosidase activity as a potential antiviral target for RV and NoV.

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Publication Details

Journal
npj Viruses
Published
2025-11-29
DOI
https://doi.org/10.1038/s44298-025-00164-3
Primary Topic
Viral gastroenteritis research and epidemiology
Type
article
Field-Weighted Citation Impact
0.00

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Fucose dependent rotavirus and norovirus require fucosidase activity for optimal replication

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npj Viruses
Viral gastroenteritis research and epidemiology
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Fucose dependent rotavirus and norovirus require fucosidase activity for optimal replication

Nazaret Peña-Gil, Joana Rocha‐Pereira, Roberto Cárcamo‐Calvo, Ana Melero, Roberto Gozalbo‐Rovira, Jesús Rodríguez‐Díaz, Cristina Santiso-Bellón, Marı́a J. Yebra, Nânci Santos-Ferreira, Javier Buesa, Vicente Monedero, Sergi López-Navarro, Sonia Llanos-Villatoro
article en

Abstract

Rotavirus (RV) and norovirus (NoV) are enteric viruses responsible for acute gastroenteritis that require fucosylated histo-blood group antigens for infection in humans. How the interaction of these viruses with fucosylated glycans modulates infection is not well understood. Treatment of target cells with a bacterial α1,2 fucosidase enzyme reduced RV and NoV infection in vitro, but increased replication in vivo. Conversely, the fucosidase inhibitor 1-deoxyfuconojirimycin impaired viral replication in both models, highlighting the role of fucosidase activity in fucose-dependent enteric virus infection. This underscores the complexity of fucose interactions for these viruses and implicates fucosidase activity as a potential antiviral target for RV and NoV.

npj VirusesVol. 3(1)
Universitat de València (ES), Rega Institute for Medical Research (BE), Instituto de Agroquímica y Tecnología de Alimentos (ES), INCLIVA Health Research Institute (ES), KU Leuven (BE)
Fonds Wetenschappelijk Onderzoek, KU Leuven, Ministerio de Ciencia e Innovación, Agencia Estatal de Investigación
Openalex Percentile: Top 56%
Viral gastroenteritis research and epidemiology
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