# A safe and efficacious inactivated vaccine aids prevent reproductive failure associated with congenital toxoplasmosis in ovine

**Authors:** Javier Regidor-Cerrillo, Andrea Largo-de la Torre, Roberto Sánchez-Sánchez, Ignacio Ferre, Javier Moreno-Gonzalo, Luis Miguel Ortega-Mora

PMC · DOI: 10.1186/s13567-026-01720-2 · 2026-03-19

## TL;DR

A new inactivated vaccine helps prevent reproductive failure in sheep caused by congenital toxoplasmosis, showing promising results in trials.

## Contribution

Development of an inactivated vaccine based on a T. gondii Type III isolate to prevent congenital toxoplasmosis in sheep.

## Key findings

- The vaccine achieved 100% viable gestations in vaccinated sheep in one trial and 78% in another.
- Vaccinated sheep showed a significant decrease in early fetal losses and improved lamb viability.
- The vaccine effectively controlled T. gondii multiplication in the cotyledons.

## Abstract

Toxoplasma gondii is an apicomplexan parasite causing reproductive failure in small ruminants. In this study, we evaluated the capacity of an inactivated vaccine to prevent reproductive failure caused by congenital toxoplasmosis in sheep. The vaccine is based on an antigen extract obtained from a low passage T. gondii Type III isolate (TgPigSp1) preserving the ability to spontaneously produce cysts in vitro and following a procedure involving parasite inactivation via hyperosmotic shock and membrane proteins solubilisation. The vaccine prototype, consisting of 40 µg of parasite extract adjuvanted with QuilA®, was evaluated in two different trials using a pregnant ovine model of T. gondii infection based on orally challenging sheep at 90 days of gestation with 10 sporulated oocysts of the heterologous Type II isolate TgShSp1. Two subcutaneous immunizations at days 55 and 76 of pregnancy caused mild and transient local reactions and had no discernible impact on gestation. Vaccination triggered both specific cellular and humoral immune responses. The proportion of viable gestations resulted in 100% (vaccine trial 1) and 78% (vaccine trial 2) in vaccinated/challenged ewes versus 50% in unvaccinated/challenged sheep. This increase in viable gestations was associated with a significant increase of lambs born viable for vaccine trial 1 (62.5%) and a decrease of early foetal losses (i.e. abortion) for vaccine trial 2 (70%), associated with control of T. gondii multiplication in the cotyledons. This inactivated vaccine could be a suitable and practical tool to mitigate economic losses in sheep caused by T. gondii outbreaks.

The online version contains supplementary material available at 10.1186/s13567-026-01720-2.

## Linked entities

- **Chemicals:** QuilA® (PubChem CID 56841866)
- **Diseases:** toxoplasmosis (MONDO:0005989)
- **Species:** Toxoplasma gondii (taxon 5811)

## Full-text entities

- **Genes:** Protease [NCBI Gene 114115257]
- **Diseases:** thrombosis (MESH:D013927), inflammatory (MESH:D007249), late reproductive failure (MESH:D051437), swelling (MESH:D004487), stillbirths (MESH:D050497), necrosis (MESH:D009336), foetal malformations (MESH:C564254), calcification (MESH:D002114), hyperthermia (MESH:D005334), gliosis (MESH:D005911), foetal losses (MESH:D016388), RIPC (MESH:D000080822), overdose (MESH:D062787), febrile (MESH:D000071072), leukomalacia (MESH:D007969), Abortions (MESH:D000026), Congenital toxoplasmosis (MESH:D014125), necrotic placentitis (MESH:D010922), pain (MESH:D010146), dystocia (MESH:D004420), placental infarcts (MESH:D007238), death (MESH:D003643), cyst (MESH:D003560), Infection (MESH:D007239), haemorrhage (MESH:D006470), T. gondii infection (MESH:D014123), oedema (MESH:C536897), lesion (MESH:D009059)
- **Chemicals:** Glycine (MESH:D005998), polyacrylamide (MESH:C016679), water (MESH:D014867), dithiothreitol (MESH:D004229), Tween 20 (MESH:D011136), CO2 (MESH:D002245), sucrose (MESH:D013395), HCl (MESH:D006851), bisacrylamide (MESH:C021221), mebezonium iodide (MESH:C059325), PBS (MESH:D007854), penicillin (MESH:D010406), TBS (MESH:D013725), methanol (MESH:D000432), paraffin (MESH:D010232), xylazine (MESH:D014991), embutramide (MESH:C059324), formalin (MESH:D005557), H2SO4 (MESH:C033158), bis (MESH:D001729), amphotericin B (MESH:D000666), glycerol (MESH:D005990), FITC (MESH:D016650), acetic (MESH:D019342), heparin (MESH:D006493), SDS (MESH:D012967), bromophenol blue (MESH:D001978), QuilA (MESH:C046386), acrylamide (MESH:D020106), ethanol (MESH:D000431), Triton X-100 (MESH:D017830), Igepal  Ca-630 (MESH:C010615), Coomassie (-), streptomycin (MESH:D013307)
- **Species:** Sus scrofa (pig, species) [taxon 9823], Border disease virus (no rank) [taxon 358764], Capra hircus (domestic goat, species) [taxon 9925], Schmallenberg virus (no rank) [taxon 1133363], Ovis aries (domestic sheep, species) [taxon 9940], Neospora caninum (species) [taxon 29176], Homo sapiens (human, species) [taxon 9606], Chlamydia abortus (species) [taxon 83555], Toxoplasma gondii (species) [taxon 5811], Mus musculus (house mouse, species) [taxon 10090], Felis catus (cat, species) [taxon 9685], Coxiella burnetii (species) [taxon 777]
- **Cell lines:** Vero — Chlorocebus sabaeus (Green monkey), Spontaneously immortalized cell line (CVCL_0059)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13003711/full.md

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Source: https://tomesphere.com/paper/PMC13003711