Structural heterogeneity of terminal glycans in Campylobacter jejuni lipooligosaccharides.

Lipooligosaccharides of the gastrointestinal pathogen Campylobacter jejuni are regarded as a major virulence factor and are implicated in the production of cross-reactive antibodies against host gangliosides, which leads to the development of autoimmune neuropathies such as Guillain-Barré and Fisher...

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Main Authors: Evgeny A Semchenko, Christopher J Day, Marc Moutin, Jennifer C Wilson, Joe Tiralongo, Victoria Korolik
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3397941?pdf=render
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author Evgeny A Semchenko
Christopher J Day
Marc Moutin
Jennifer C Wilson
Joe Tiralongo
Victoria Korolik
author_facet Evgeny A Semchenko
Christopher J Day
Marc Moutin
Jennifer C Wilson
Joe Tiralongo
Victoria Korolik
author_sort Evgeny A Semchenko
collection DOAJ
description Lipooligosaccharides of the gastrointestinal pathogen Campylobacter jejuni are regarded as a major virulence factor and are implicated in the production of cross-reactive antibodies against host gangliosides, which leads to the development of autoimmune neuropathies such as Guillain-Barré and Fisher Syndromes. C. jejuni strains are known to produce diverse LOS structures encoded by more than 19 types of LOS biosynthesis clusters. This study demonstrates that the final C. jejuni LOS structure cannot always be predicted from the genetic composition of the LOS biosynthesis cluster, as determined by novel lectin array analysis of the terminal LOS glycans. The differences were shown to be partially facilitated by the differential on/off status of three genes wlaN, cst and cj1144-45. The on/off status of these genes was also analysed in C. jejuni strains grown in vitro and in vivo, isolated directly from the host animal without passaging, using immunoseparation. Importantly, C. jejuni strains 331, 421 and 520 encoding cluster type C were shown to produce different LOS, mimicking asialo GM(1), asialo GM(2) and a heterogeneous mix of gangliosides and other glycoconjugates respectively. In addition, individual C. jejuni colonies were shown to consistently produce heterogeneous LOS structures, irrespective of the cluster type and the status of phase variable genes. Furthermore we describe C. jejuni strains (351 and 375) with LOS clusters that do not match any of the previously described LOS clusters, yet are able to produce LOS with asialo GM(2)-like mimicries. The LOS biosynthesis clusters of these strains are likely to contain genes that code for LOS biosynthesis machinery previously not identified, yet capable of synthesising LOS mimicking gangliosides.
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spelling doaj.art-e60d32f164a0468b95c46101462bfd6d2022-12-21T23:47:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0177e4092010.1371/journal.pone.0040920Structural heterogeneity of terminal glycans in Campylobacter jejuni lipooligosaccharides.Evgeny A SemchenkoChristopher J DayMarc MoutinJennifer C WilsonJoe TiralongoVictoria KorolikLipooligosaccharides of the gastrointestinal pathogen Campylobacter jejuni are regarded as a major virulence factor and are implicated in the production of cross-reactive antibodies against host gangliosides, which leads to the development of autoimmune neuropathies such as Guillain-Barré and Fisher Syndromes. C. jejuni strains are known to produce diverse LOS structures encoded by more than 19 types of LOS biosynthesis clusters. This study demonstrates that the final C. jejuni LOS structure cannot always be predicted from the genetic composition of the LOS biosynthesis cluster, as determined by novel lectin array analysis of the terminal LOS glycans. The differences were shown to be partially facilitated by the differential on/off status of three genes wlaN, cst and cj1144-45. The on/off status of these genes was also analysed in C. jejuni strains grown in vitro and in vivo, isolated directly from the host animal without passaging, using immunoseparation. Importantly, C. jejuni strains 331, 421 and 520 encoding cluster type C were shown to produce different LOS, mimicking asialo GM(1), asialo GM(2) and a heterogeneous mix of gangliosides and other glycoconjugates respectively. In addition, individual C. jejuni colonies were shown to consistently produce heterogeneous LOS structures, irrespective of the cluster type and the status of phase variable genes. Furthermore we describe C. jejuni strains (351 and 375) with LOS clusters that do not match any of the previously described LOS clusters, yet are able to produce LOS with asialo GM(2)-like mimicries. The LOS biosynthesis clusters of these strains are likely to contain genes that code for LOS biosynthesis machinery previously not identified, yet capable of synthesising LOS mimicking gangliosides.http://europepmc.org/articles/PMC3397941?pdf=render
spellingShingle Evgeny A Semchenko
Christopher J Day
Marc Moutin
Jennifer C Wilson
Joe Tiralongo
Victoria Korolik
Structural heterogeneity of terminal glycans in Campylobacter jejuni lipooligosaccharides.
PLoS ONE
title Structural heterogeneity of terminal glycans in Campylobacter jejuni lipooligosaccharides.
title_full Structural heterogeneity of terminal glycans in Campylobacter jejuni lipooligosaccharides.
title_fullStr Structural heterogeneity of terminal glycans in Campylobacter jejuni lipooligosaccharides.
title_full_unstemmed Structural heterogeneity of terminal glycans in Campylobacter jejuni lipooligosaccharides.
title_short Structural heterogeneity of terminal glycans in Campylobacter jejuni lipooligosaccharides.
title_sort structural heterogeneity of terminal glycans in campylobacter jejuni lipooligosaccharides
url http://europepmc.org/articles/PMC3397941?pdf=render
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