Toxoplasma gondii infection reduces serum progesterone levels and adverse effects at the maternal-foetal interface

Parasite Immunol. 2020 Feb;42(2):e12690. doi: 10.1111/pim.12690. Epub 2019 Dec 18.

Abstract

Aims: Pregnant BALB/c mice infected with a Toxoplasma gondii type II strain were used to determine how pregnancy interferes with the development of maternal immunity to T gondii and how infection disrupts pregnancy and foetal development.

Methods: Maternal and foetal parasite loads were assessed by amplification of T gondii SAG1 using qPCR. Adverse effects of infection were evaluated on foetal-placental development by quantification of implantation units undergoing resorption and by histopathological analyses. Serum progesterone levels were quantified by immunoassay. The effect of T gondii infection on maternal immunity was determined by assessing the cellular composition of spleens by flow cytometry.

Results: Infected pregnant mice exhibited clinical signs of infection, inflammation and necrosis at the maternal-foetal interface and decreased serum progesterone levels. In infected mice, there was a clear effect of pregnancy and infection on macrophage cell numbers. However, no differences in the parasite load were detected between non-pregnant and pregnant mice.

Conclusions: Maternal T gondii infection induced adverse effects at the maternal-foetal interface. Alterations were found in immune spleen cells, dependent on the day of pregnancy, relative to nonpregnant animals. The results obtained suggest a pregnancy-dependent mechanism during T gondii infection able to interfere with macrophage numbers.

Keywords: Toxoplasma gondii; congenital infection; immunology; pathology; pregnancy; progesterone; zoonosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Female
  • Genes, MHC Class II
  • Inflammation / immunology
  • Mice
  • Mice, Inbred BALB C
  • Parasite Load
  • Placenta / immunology
  • Pregnancy / immunology*
  • Progesterone / blood
  • Spleen / immunology
  • Toxoplasma / immunology*
  • Toxoplasmosis, Animal / immunology*
  • Toxoplasmosis, Animal / parasitology

Substances

  • Progesterone