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

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. G...

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Main Authors: Christopher J Day, Joe Tiralongo, Regan D Hartnell, Carie-Anne Logue, Jennifer C Wilson, Mark von Itzstein, Victoria Korolik
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2654152?pdf=render
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spelling doaj-8116d4cc19f540a39d854df03cd8551f2020-11-25T02:22:01ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-01-0143e492710.1371/journal.pone.0004927Differential carbohydrate recognition by Campylobacter jejuni strain 11168: influences of temperature and growth conditions.Christopher J DayJoe TiralongoRegan D HartnellCarie-Anne LogueJennifer C WilsonMark von ItzsteinVictoria KorolikThe 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.http://europepmc.org/articles/PMC2654152?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Christopher J Day
Joe Tiralongo
Regan D Hartnell
Carie-Anne Logue
Jennifer C Wilson
Mark von Itzstein
Victoria Korolik
spellingShingle Christopher J Day
Joe Tiralongo
Regan D Hartnell
Carie-Anne Logue
Jennifer C Wilson
Mark von Itzstein
Victoria Korolik
Differential carbohydrate recognition by Campylobacter jejuni strain 11168: influences of temperature and growth conditions.
PLoS ONE
author_facet Christopher J Day
Joe Tiralongo
Regan D Hartnell
Carie-Anne Logue
Jennifer C Wilson
Mark von Itzstein
Victoria Korolik
author_sort Christopher J Day
title Differential carbohydrate recognition by Campylobacter jejuni strain 11168: influences of temperature and growth conditions.
title_short Differential carbohydrate recognition by Campylobacter jejuni strain 11168: influences of temperature and growth conditions.
title_full Differential carbohydrate recognition by Campylobacter jejuni strain 11168: influences of temperature and growth conditions.
title_fullStr Differential carbohydrate recognition by Campylobacter jejuni strain 11168: influences of temperature and growth conditions.
title_full_unstemmed Differential carbohydrate recognition by Campylobacter jejuni strain 11168: influences of temperature and growth conditions.
title_sort differential carbohydrate recognition by campylobacter jejuni strain 11168: influences of temperature and growth conditions.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-01-01
description 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.
url http://europepmc.org/articles/PMC2654152?pdf=render
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