Identification of a novel antigen of pathogenic Leptospira spp. that reacted with convalescent mice sera

Nobuo Koizumi1, Haruo Watanabe1

  • 1Department of Bacteriology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan.

Insights

Severe leptospirosis can be modeled in C3H/HeJ mice. Researchers identified a novel virulence antigen, LAg42, in pathogenic Leptospira species, suggesting its role in disease severity.

Area of Science:

  • Infectious Diseases
  • Microbiology
  • Immunology
  • Animal Models

Background:

  • Leptospirosis is a significant zoonotic disease caused by pathogenic Leptospira bacteria.
  • Understanding the virulence factors of Leptospira is crucial for developing effective diagnostics and treatments.
  • C3H/HeJ mice are often used in infectious disease research, but their suitability as a model for severe leptospirosis required investigation.

Purpose of the Study:

  • To evaluate the virulence of human-isolated Leptospira strains in C3H/HeJ mice.
  • To establish an acute lethal mouse model for severe leptospirosis.
  • To identify novel antigens of pathogenic Leptospira spp. involved in virulence.

Main Methods:

  • Infection of C3H/HeJ mice with clinical isolates of Leptospira from severe human leptospirosis cases.
  • Observation of survival rates and disease progression in infected mice.
  • Screening of Leptospira antigens using convalescent mouse sera to identify immunogenic proteins.

Main Results:

  • Infection with clinical Leptospira isolates proved lethal to C3H/HeJ mice, validating the model for severe leptospirosis.
  • A novel 42 kDa inner-membrane protein, designated LAg42, was identified as reactive with convalescent sera.
  • The gene encoding LAg42 is conserved in pathogenic Leptospira but absent in non-pathogenic strains, indicating its potential role in virulence.

Conclusions:

  • C3H/HeJ mice serve as an effective acute lethal model for studying severe leptospirosis.
  • LAg42 is a potential virulence factor of pathogenic Leptospira, with its immunogenic region located in the C-terminal domain.
  • The identification of LAg42 provides a new target for understanding and potentially combating Leptospira infections.

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