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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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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