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The crucial role of Campylobacter jejuni genes in anti-ganglioside antibody induction in Guillain-Barré syndrome
Peggy C.R. Godschalk, Astrid P. Heikema, Michel Gilbert, Tomoko Komagamine, C. Wim Ang, Jobine Glerum, Denis Brochu, Jianjun Li, Nobuhiro Yuki, Bart C. Jacobs, Alex van Belkum, Hubert P. Endtz
Peggy C.R. Godschalk, Astrid P. Heikema, Michel Gilbert, Tomoko Komagamine, C. Wim Ang, Jobine Glerum, Denis Brochu, Jianjun Li, Nobuhiro Yuki, Bart C. Jacobs, Alex van Belkum, Hubert P. Endtz
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Article Microbiology

The crucial role of Campylobacter jejuni genes in anti-ganglioside antibody induction in Guillain-Barré syndrome

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Abstract

Molecular mimicry of Campylobacter jejuni lipo-oligosaccharides (LOS) with gangliosides in nervous tissue is considered to induce cross-reactive antibodies that lead to Guillain-Barré syndrome (GBS), an acute polyneuropathy. To determine whether specific bacterial genes are crucial for the biosynthesis of ganglioside-like structures and the induction of anti-ganglioside antibodies, we characterized the C. jejuni LOS biosynthesis gene locus in GBS-associated and control strains. We demonstrated that specific types of the LOS biosynthesis gene locus are associated with GBS and with the expression of ganglioside-mimicking structures. Campylobacter knockout mutants of 2 potential GBS marker genes, both involved in LOS sialylation, expressed truncated LOS structures without sialic acid, showed reduced reactivity with GBS patient serum, and failed to induce an anti-ganglioside antibody response in mice. We demonstrate, for the first time, to our knowledge, that specific bacterial genes are crucial for the induction of anti-ganglioside antibodies.

Authors

Peggy C.R. Godschalk, Astrid P. Heikema, Michel Gilbert, Tomoko Komagamine, C. Wim Ang, Jobine Glerum, Denis Brochu, Jianjun Li, Nobuhiro Yuki, Bart C. Jacobs, Alex van Belkum, Hubert P. Endtz

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Figure 4

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SDS-PAGE analysis of LOS from GB11 WT and mutants. The genome strain NCT...
SDS-PAGE analysis of LOS from GB11 WT and mutants. The genome strain NCTC 11168 was included as a control. Lane 1, WT GB11; lane 2, GB11 cst-II mutant; lane 3, GB11 orf10/orf11 mutant; lane 4, GB11 orf11 mutant; lane 5, NCTC 11168. (A) Silver staining of the LOS revealed faster-migrating LOS cores for the GB11 cst-II and orf10/orf11 mutants compared with the WT, indicating that these mutants have a truncated LOS. The orf11 mutant LOS showed migration patterns identical to those of WT LOS. (B) A Western blot incubated with GB11 patient serum showed a reduced reactivity for the cst-II and orf10/orf11 mutants but unchanged reactivity for the orf11 mutant when compared with the WTs. (C) For the cst-II and orf10/orf11 mutants, the reactivity with cholera toxin, a ligand for GM1-oligosaccharide structures, was almost completely lost. Reactivity with the orf11 mutant remained unchanged.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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