Chlamydial variants differ in ability to ascend the genital tract in the guinea pig model of chlamydial genital infection

Infect Immun. 2015 Aug;83(8):3176-83. doi: 10.1128/IAI.00532-15. Epub 2015 May 26.

Abstract

An important question in the study of chlamydial genital tract disease is why some women develop severe upper tract disease while others have mild or even "silent" infections with or without pathology. Animal studies suggest that the pathological outcome of an infection is dependent upon both the composition of the infecting chlamydial population and the genotype of the host, along with host physiological effects, such as the cyclical production of reproductive hormones and even the size of the infecting inoculum or the number of repeated infections. In this study, we compared two variants of Chlamydia caviae, contrasting in virulence, with respect to their abilities to ascend the guinea pig genital tract. We then determined the effect of combining the two variants on the course of infection and on the bacterial loads of the two variants in the genital tract. Although the variants individually had similar infection kinetics in the cervix, SP6, the virulent variant, could be isolated from the oviducts more often and in greater numbers than the attenuated variant, AZ2. SP6 also elicited higher levels of interleukin 8 (IL-8) in the lower genital tract and increased leukocyte infiltration in the cervix and uterus compared to AZ2. When the two variants were combined in a mixed infection, SP6 outcompeted AZ2 in the lower genital tract; however, AZ2 was able to ascend the genital tract as readily as SP6. These data suggest that the ability of SP6 to elicit an inflammatory response in the lower genital tract facilitates the spread of both variants to the oviducts.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chlamydia / classification
  • Chlamydia / physiology*
  • Chlamydia Infections / immunology
  • Chlamydia Infections / microbiology*
  • Disease Models, Animal
  • Female
  • Guinea Pigs
  • Humans
  • Interleukin-8 / immunology
  • Reproductive Tract Infections / immunology
  • Reproductive Tract Infections / microbiology*

Substances

  • Interleukin-8