Target intelligence / Profile preview

Campylobacter jejuni lipooligosaccharide (LOS)

Target
LOS
Molecular classification
Bacterial surface polysaccharide, Endotoxin, Glycolipid, Virulence factor
01

Overview

Campylobacter jejuni lipooligosaccharide (LOS) is a critical glycolipid component of the outer membrane of Campylobacter jejuni, a leading cause of bacterial gastroenteritis worldwide (Frontiers in Microbiology, 2020). Unlike typical lipopolysaccharides, LOS lacks an O-antigen but contains a lipid A moiety and a core oligosaccharide that often mimics human gangliosides, such as GM1 and GD1a (PNAS, 2004). This molecular mimicry is the primary driver of post-infectious autoimmune disorders, most notably Guillain-Barré syndrome (GBS), where host antibodies against LOS cross-react with peripheral nerves (European Journal of Microbiology and Immunology, 2012). LOS also functions as a potent endotoxin, activating Toll-like receptor 4 (TLR4) to trigger pro-inflammatory cytokine production and contributing to the severity of enteritis (Journal of Biological Chemistry, 2013). Beyond its role in pathogenesis, LOS provides a permeability barrier against hydrophobic antibiotics and protects the bacterium from host innate immune factors like cationic antimicrobial peptides (Journal of Antimicrobial Chemotherapy, 2009). Consequently, LOS is a significant target for vaccine development and a focal point for understanding antibiotic resistance and autoimmune triggers in campylobacteriosis (MDPI, 2021).

Other names
Lipo-oligosaccharideCampylobacter jejuni endotoxinC. jejuni LOSLipooligosaccharide
02

Mechanism of action

Binding to the lipid A moiety to disrupt bacterial membrane integrity; acting as a permeability barrier for hydrophobic antibiotics; and induction of protective antibodies via glycoconjugate vaccination.

03

Biological functions

Immune response modulationCell adhesionBacterial survivalAntibiotic resistanceMolecular mimicry
04

Disease associations

InfectionInflammationGuillain-Barré syndromeMiller Fisher syndromeReactive arthritis
05

Safety considerations

Risk of inducing autoimmune Guillain-Barré syndrome through molecular mimicryHigh structural variability due to phase variationPotential for enhancing bacterial resistance if membrane permeability is altered
06

Interacting drugs

Polymyxin B

2 more in the full profile.

07

Biomarkers

Anti-ganglioside antibodies (e.g., anti-GM1 IgG)LOS sialylation statusLOS biosynthesis gene cluster (e.g., cstII, cgtB)Heat-stable (HS) serotypes

Beyond the preview

Go deeper on Campylobacter jejuni lipooligosaccharide (LOS).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Campylobacter jejuni lipooligosaccharide (LOS).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call