A mouse model for Chlamydia suis genital infection

Manuela Donati1, Maria Di Paolo2, Alison Favaroni2

  • 1Section of Microbiology, DIMES, University of Bologna, 40138 Bologna, Italy manuela.donati@unibo.it.

Pathogens and Disease
|April 9, 2015
PubMed

Insights

A new mouse model effectively simulates Chlamydia suis genital infections. This model reveals C. suis infection resolves faster than Chlamydia trachomatis infection in mice.

Area of Science:

  • Reproductive infectious diseases
  • Microbiology
  • Immunology

Background:

  • Chlamydia suis and Chlamydia trachomatis are significant causes of genital infections.
  • Understanding the pathogenesis and host response is crucial for developing effective treatments.
  • A robust animal model is needed for comparative studies of these Chlamydia species.

Purpose of the Study:

  • To develop and characterize a mouse model for Chlamydia suis genital infection.
  • To compare the course and resolution of C. suis infection with C. trachomatis infection in mice.
  • To evaluate the utility of this model for comparative Chlamydia research.

Main Methods:

  • Ninety-nine mice were intravaginally inoculated with C. suis, C. trachomatis (genotype E or F) elementary bodies (EBs), or a control.
  • Infection was monitored by isolating Chlamydia from vaginal swabs at various time points (3, 5, 7, 12 days post-infection).
  • Presence of viable organisms in the uterus and tubes was assessed up to 28 days post-infection.

Main Results:

  • Secretory anti-C. suis IgA was detected in all inoculated mice by 7 days post-infection.
  • C. suis was isolated from vaginal swabs up to 12 days post-infection, with a more rapid decline than C. trachomatis.
  • Viable C. suis and C. trachomatis were recovered from reproductive tracts for extended periods, indicating persistent infection.

Conclusions:

  • Mice are susceptible to intravaginal inoculation with C. suis, establishing a viable infection model.
  • C. suis infection exhibits a more rapid course and resolution compared to C. trachomatis infection in this mouse model.
  • This developed mouse model is suitable for comparative investigations of C. suis and C. trachomatis pathogenesis and immune responses.

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