Infection of Hysterectomized Mice with Chlamydia muridarum and Chlamydia trachomatis

Infect Immun. 2017 Jun 20;85(7):e00197-17. doi: 10.1128/IAI.00197-17. Print 2017 Jul.

Abstract

We studied infection and immunity of hysterectomized mice infected with Chlamydia muridarum and Chlamydia trachomatis to determine if there were differences between these species in their ability to infect vaginal squamous epithelial cells in vivo independently of proximal upper genital tract tissues. We found that C. muridarum readily colonized and infected vaginal squamous epithelial cells, whereas C. trachomatis did not. Primary infection of the vaginal epithelium with C. muridarum produced infections of a duration longer than that reported for normal mice. Infection resulted in an inflammatory response in the vagina characterized by neutrophils and infiltrating submucosal plasma cells consisting primarily of T cells. Despite the delayed clearance, rechallenged C. muridarum-infected mice were highly immune. Mice vaginally infected with C. muridarum produced serum and vaginal wash antibodies and an antigen-specific gamma interferon-dominated Th1-biased T cell response. By comparison, mice vaginally infected with C. trachomatis exhibited transient low-burden infections, produced no detectable tissue inflammatory response, and failed to seroconvert. We discuss how these marked differences in the biology of vaginal infection between these otherwise genetically similar species are possibly linked to pathogen-specific virulence genes and how they may influence pathology and immunity in the upper genital tract.

Keywords: Chlamydia muridarum; Chlamydia trachomatis; hysterectomized mice; immunity; infection; pathology.

MeSH terms

  • Animals
  • Antibodies, Bacterial / analysis
  • Antibodies, Bacterial / blood
  • Chlamydia Infections / immunology
  • Chlamydia Infections / microbiology*
  • Chlamydia Infections / pathology*
  • Chlamydia muridarum / growth & development*
  • Chlamydia muridarum / immunology*
  • Chlamydia trachomatis / growth & development*
  • Female
  • Hysterectomy*
  • Interferon-gamma / metabolism
  • Mice, Inbred C57BL
  • T-Lymphocytes / immunology
  • Vagina / microbiology*

Substances

  • Antibodies, Bacterial
  • Interferon-gamma