Sialylation of campylobacter jejuni lipo-oligosaccharides: impact on phagocytosis and cytokine production in mice
<p style="text-align:justify;"> <b>Background:</b> Guillain-Barré syndrome (GBS) is a post-infectious polyradiculoneuropathy, frequently associated with antecedent Campylobacter jejuni (C. jejuni) infection. The presence of sialic acid on C. jejuni lipo-oligosaccharide (...
প্রধান লেখক: | , , , , , , , , , , |
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বিন্যাস: | Journal article |
ভাষা: | English |
প্রকাশিত: |
Public Library of Science
2012
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author | Huizinga, R Easton, A Donachie, A Guthrie, J Van Rijs, W Heikema, A Boon, L Samsom, J Jacobs, B Willison, H Goodyear, C |
author_facet | Huizinga, R Easton, A Donachie, A Guthrie, J Van Rijs, W Heikema, A Boon, L Samsom, J Jacobs, B Willison, H Goodyear, C |
author_sort | Huizinga, R |
collection | OXFORD |
description | <p style="text-align:justify;"> <b>Background:</b> Guillain-Barré syndrome (GBS) is a post-infectious polyradiculoneuropathy, frequently associated with antecedent Campylobacter jejuni (C. jejuni) infection. The presence of sialic acid on C. jejuni lipo-oligosaccharide (LOS) is considered a risk factor for development of GBS as it crucially determines the structural homology between LOS and gangliosides, explaining the induction of cross-reactive neurotoxic antibodies. Sialylated C. jejuni are recognised by TLR4 and sialoadhesin; however, the functional implications of these interactions in vivo are unknown.<br/><br/> <b>Methodology/Principal Findings:</b> In this study we investigated the effects of bacterial sialylation on phagocytosis and cytokine secretion by mouse myeloid cells in vitro and in vivo. Using fluorescently labelled GM1a/GD1a ganglioside-mimicking C. jejuni strains and corresponding (Cst-II-mutant) control strains lacking sialic acid, we show that sialylated C. jejuni was more efficiently phagocytosed in vitro by BM-MΦ, but not by BM-DC. In addition, LOS sialylation increased the production of IL-10, IL-6 and IFN-β by both BM-MΦ and BM-DC. Subsequent in vivo experiments revealed that sialylation augmented the deposition of fluorescent bacteria in splenic DC, but not macrophages. In addition, sialylation significantly amplified the production of type I interferons, which was independent of pDC.<br/><br/> <b>Conclusions/Significance:</b> These results identify novel immune stimulatory effects of C. jejuni sialylation, which may be important in inducing cross-reactive humoral responses that cause GBS. </p> |
first_indexed | 2024-03-06T22:50:33Z |
format | Journal article |
id | oxford-uuid:5ea2cd6d-efe8-4fe1-90a2-ff759255398d |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-06T22:50:33Z |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | dspace |
spelling | oxford-uuid:5ea2cd6d-efe8-4fe1-90a2-ff759255398d2022-03-26T17:41:56ZSialylation of campylobacter jejuni lipo-oligosaccharides: impact on phagocytosis and cytokine production in miceJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:5ea2cd6d-efe8-4fe1-90a2-ff759255398dEnglishSymplectic Elements at OxfordPublic Library of Science2012Huizinga, REaston, ADonachie, AGuthrie, JVan Rijs, WHeikema, ABoon, LSamsom, JJacobs, BWillison, HGoodyear, C <p style="text-align:justify;"> <b>Background:</b> Guillain-Barré syndrome (GBS) is a post-infectious polyradiculoneuropathy, frequently associated with antecedent Campylobacter jejuni (C. jejuni) infection. The presence of sialic acid on C. jejuni lipo-oligosaccharide (LOS) is considered a risk factor for development of GBS as it crucially determines the structural homology between LOS and gangliosides, explaining the induction of cross-reactive neurotoxic antibodies. Sialylated C. jejuni are recognised by TLR4 and sialoadhesin; however, the functional implications of these interactions in vivo are unknown.<br/><br/> <b>Methodology/Principal Findings:</b> In this study we investigated the effects of bacterial sialylation on phagocytosis and cytokine secretion by mouse myeloid cells in vitro and in vivo. Using fluorescently labelled GM1a/GD1a ganglioside-mimicking C. jejuni strains and corresponding (Cst-II-mutant) control strains lacking sialic acid, we show that sialylated C. jejuni was more efficiently phagocytosed in vitro by BM-MΦ, but not by BM-DC. In addition, LOS sialylation increased the production of IL-10, IL-6 and IFN-β by both BM-MΦ and BM-DC. Subsequent in vivo experiments revealed that sialylation augmented the deposition of fluorescent bacteria in splenic DC, but not macrophages. In addition, sialylation significantly amplified the production of type I interferons, which was independent of pDC.<br/><br/> <b>Conclusions/Significance:</b> These results identify novel immune stimulatory effects of C. jejuni sialylation, which may be important in inducing cross-reactive humoral responses that cause GBS. </p> |
spellingShingle | Huizinga, R Easton, A Donachie, A Guthrie, J Van Rijs, W Heikema, A Boon, L Samsom, J Jacobs, B Willison, H Goodyear, C Sialylation of campylobacter jejuni lipo-oligosaccharides: impact on phagocytosis and cytokine production in mice |
title | Sialylation of campylobacter jejuni lipo-oligosaccharides: impact on phagocytosis and cytokine production in mice |
title_full | Sialylation of campylobacter jejuni lipo-oligosaccharides: impact on phagocytosis and cytokine production in mice |
title_fullStr | Sialylation of campylobacter jejuni lipo-oligosaccharides: impact on phagocytosis and cytokine production in mice |
title_full_unstemmed | Sialylation of campylobacter jejuni lipo-oligosaccharides: impact on phagocytosis and cytokine production in mice |
title_short | Sialylation of campylobacter jejuni lipo-oligosaccharides: impact on phagocytosis and cytokine production in mice |
title_sort | sialylation of campylobacter jejuni lipo oligosaccharides impact on phagocytosis and cytokine production in mice |
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