Abstract

Although it is known that gestation could influence the clinical course of ovine toxoplasmosis, the precise effect of the term of gestation when sheep are infected are yet mostly unknown. The aim of this study was to evaluate the peripheral and placental immune responses developed in pregnant sheep after experimental infection with Toxoplasma gondii at different times of gestation. Thirty-six pregnant sheep were allocated in different groups, orally inoculated with sporulated oocysts of T. gondii at early, mid and late gestation and culled within 30 days post-infection. The peripheral humoral and cytokine responses were evaluated, as well as the transcription of cytokines at the placenta. Serological analysis revealed that, regardless the term of gestation when infected, specific IgG against T. gondii were detected from day 8 post-infection and there was an early peripheral release of IFN-γ at the first week post-infection followed by a short peak of IL10 and TNF-α at the second week post-infection. There were no significant differences in this response between infected groups. At the placenta, a similar increase in transcription of IFN-γ, and TNF-α was found at the three terms of gestation, while IL-4 increased mainly at the first and second terms and IL-10 transcription was higher at the last term. While these findings show that both Th1 and Th2 cytokines play a key role in the pathogenesis of ovine toxoplasmosis and that placental and peripheral immune responses do not closely correlate, there seems to be no clear modulation of these responses along the gestation.

Highlights

  • Ovine toxoplasmosis is an important infectious disease, caused by the protozoan Toxoplasma gondii, that results in heavy economic losses in the sheep industry worldwide as it is related to reproductive failure, principally abortions and weak newborn lambs [1]

  • While the pattern of serological antibodies was very similar among the three groups, those ewes infected at mid gestation (G2) showed significantly higher optical index (OI) than those animals infected at early gestation, on days 1, 5, 8 and 12 pi, and those infected at late gestation, on days 8, 12, 19 and 22

  • Regarding IL10, there were no statistically significant differences between infected groups at day 12 pi, when all of them showed higher level than control animals, G1 levels were higher than G2 at day 22 pi

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Summary

Introduction

Ovine toxoplasmosis is an important infectious disease, caused by the protozoan Toxoplasma gondii, that results in heavy economic losses in the sheep industry worldwide as it is related to reproductive failure, principally abortions and weak newborn lambs [1]. The paradigm that maternal immune response at the placenta level shifts from a Th1 phenotype, characterized by IFN-γ and TNF-α production, towards a Th2 phenotype, mainly represented by IL4 and IL10 production, from mid gestation is mostly based on murine experimental models [5]. These evidence cannot be extrapolated to Castaño et al Vet Res (2019) 50:66 sheep as there are several differences between mice and sheep in the histological structure of placenta, immune response and duration of pregnancy [6]. The few studies carried out to investigate this paradigm in sheep have not found differences at the peripheral immune response between pregnant and non-pregnant ewes [7, 8]

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