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Variation in Bordetella bronchiseptica lipopolysaccharide during human infection

P Gueirard1, K Le Blay, A Le Coustumier

  • 1Laboratoire des Bordetella, Institut Pasteur, Paris, France.

Insights

Chronic Bordetella bronchiseptica respiratory infections in humans can involve lipopolysaccharide (LPS) changes. During infection, LPS O-chain loss increases bacterial susceptibility to serum, suggesting an intracellular niche selects for specific LPS types.

Area of Science:

  • Microbiology
  • Immunology
  • Infectious Diseases

Background:

  • Bordetella bronchiseptica can cause chronic respiratory infections in humans, potentially acquired from animals like rabbits.
  • Lipopolysaccharides (LPS) are key surface molecules of Gram-negative bacteria, influencing host-pathogen interactions and immune responses.
  • Previous work identified a human chronic B. bronchiseptica infection linked to rabbit contact.

Purpose of the Study:

  • To analyze the lipopolysaccharide (LPS) characteristics of human and animal Bordetella bronchiseptica isolates.
  • To investigate the changes in LPS during chronic infection and their impact on bacterial serum susceptibility.
  • To explore the potential role of an intracellular niche in selecting for specific LPS types.

Main Methods:

  • Lipopolysaccharide (LPS) analysis of human, rabbit, and other B. bronchiseptica isolates using sera from infected mice, rabbits, and humans.
  • Assessment of LPS antigenicity and molecular length.
  • Evaluation of bacterial susceptibility to the bactericidal effects of normal serum.

Main Results:

  • Lipopolysaccharide (LPS) antigenicity and length varied significantly among different B. bronchiseptica isolates.
  • A progressive loss of the O-chain component of LPS was observed during chronic infection.
  • Isolates with reduced O-chain exhibited increased susceptibility to the bactericidal activity of normal serum.

Conclusions:

  • Lipopolysaccharide (LPS) heterogeneity exists in Bordetella bronchiseptica isolates from various sources.
  • The loss of LPS O-chain during chronic infection is associated with altered serum resistance.
  • These findings suggest that an intracellular bacterial niche may select for B. bronchiseptica strains with specific LPS structures, potentially impacting virulence and immune evasion.

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