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Secretory IgAN-glycans contribute to the protection againstE. coliO55 infection of germ-free piglets

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F21%3A00550089" target="_blank" >RIV/61388971:_____/21:00550089 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15110/21:73602947

  • Result on the web

    <a href="https://www.nature.com/articles/s41385-020-00345-8" target="_blank" >https://www.nature.com/articles/s41385-020-00345-8</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/s41385-020-00345-8" target="_blank" >10.1038/s41385-020-00345-8</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Secretory IgAN-glycans contribute to the protection againstE. coliO55 infection of germ-free piglets

  • Original language description

    Mucosal surfaces are colonized by highly diverse commensal microbiota. Coating with secretory IgA (SIgA) promotes the survival of commensal bacteria while it inhibits the invasion by pathogens. Bacterial coating could be mediated by antigen-specific SIgA recognition, polyreactivity, and/or by the SIgA-associated glycans. In contrast to many in vitro studies, only a few reported the effect of SIgA glycans in vivo. Here, we used a germ-free antibody-free newborn piglets model to compare the protective effect of SIgA, SIgA with enzymatically removedN-glycans, Fab, and Fc containing the secretory component (Fc-SC) during oral necrotoxigenicE. coliO55 challenge. SIgA, Fab, and Fc-SC were protective, whereas removal ofN-glycans from SIgA reduced SIgA-mediated protection as demonstrated by piglets' intestinal histology, clinical status, and survival. In vitro analyses indicated that deglycosylation of SIgA did not reduce agglutination ofE. coliO55. These findings highlight the role of SIgA-associatedN-glycans in protection. Further structural studies of SIgA-associated glycans would lead to the identification of those involved in the species-specific inhibition of attachment to corresponding epithelial cells.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10606 - Microbiology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Mucosal Immunology

  • ISSN

    1933-0219

  • e-ISSN

    1935-3456

  • Volume of the periodical

    14

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    511-522

  • UT code for WoS article

    000572598900001

  • EID of the result in the Scopus database

    2-s2.0-85091687047