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  • Differential carbohydrate recognition by Campylobacter jejuni strain 11168: influences of temperature and growth conditions

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    Author(s)
    Day, Christopher J
    Tiralongo, Joe
    Hartnell, Regan D
    Logue, Carie-Anne
    Wilson, Jennifer C
    von Itzstein, Mark
    Korolik, Victoria
    Griffith University Author(s)
    von Itzstein, Mark
    Korolik, Victoria
    Wilson, Jenny C.
    Day, Christopher J.
    Tiralongo, Joe
    Year published
    2009
    Metadata
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    Abstract
    The pathogenic clinical strain NCTC11168 was the first Campylobacter jejuni strain to be sequenced and has been a widely used laboratory model for studying C. jejuni pathogenesis. However, continuous passaging of C. jejuni NCTC11168 has been shown to dramatically affect its colonisation potential. Glycan array analysis was performed on C. jejuni NCTC11168 using the frequently passaged, non-colonising, genome sequenced (11168-GS) and the infrequently passaged, original, virulent (11168-O) isolates grown or maintained under various conditions. Glycan structures recognised and bound by C. jejuni included terminal mannose, ...
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    The pathogenic clinical strain NCTC11168 was the first Campylobacter jejuni strain to be sequenced and has been a widely used laboratory model for studying C. jejuni pathogenesis. However, continuous passaging of C. jejuni NCTC11168 has been shown to dramatically affect its colonisation potential. Glycan array analysis was performed on C. jejuni NCTC11168 using the frequently passaged, non-colonising, genome sequenced (11168-GS) and the infrequently passaged, original, virulent (11168-O) isolates grown or maintained under various conditions. Glycan structures recognised and bound by C. jejuni included terminal mannose, N-acetylneuraminic acid, galactose and fucose. Significantly, it was found that only when challenged with normal oxygen at room temperature did 11168-O consistently bind to sialic acid or terminal mannose structures, while 11168-GS bound these structures regardless of growth/maintenance conditions. Further, binding of un-capped galactose and fucosylated structures was significantly reduced when C. jejuni was maintained at 25 degrees C under atmospheric oxygen conditions. These binding differences identified through glycan array analysis were confirmed by the ability of specific lectins to competitively inhibit the adherence of C. jejuni to a Caco-2 intestinal cell line. Our data suggests that the binding of mannose and/or N-acetylneuraminic acid may provide the initial interactions important for colonisation following environmental exposure.
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    Journal Title
    PLoS One
    Volume
    4
    Issue
    3
    Publisher URI
    http://www.plosone.org
    DOI
    https://doi.org/10.1371/journal.pone.0004927
    Copyright Statement
    © 2009 Day, Christopher et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution License CCAL. (http://www.plos.org/journals/license.html)
    Subject
    Microbiology not elsewhere classified
    Publication URI
    http://hdl.handle.net/10072/28547
    Collection
    • Journal articles

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