Bioengineered 3D microvessels and complementary animal models reveal mechanisms of Trypanosoma congolense sequestration

In the mammalian host, Trypanosoma congolense cytoadheres, or sequesters, to the vascular endothelium. Although sequestration influences clinical outcome, disease severity and organ pathology, its determinants and mediators remain unknown. Challenges such as the variability of animal models, the only-recently developed tools to genetically manipulate the parasite, and the lack of physiologically-relevant in vitro models have hindered progress. Here, we engineered brain and cardiac 3D bovine endothelial microvessel models that mimic the bovine brain microvasculature and the bovine aorta, respectively. By perfusing these models with two T. congolense strains, we investigated the roles of flow for parasite sequestration and tropism for different endothelial beds. We discovered that sequestration is dependent on cyclic adenosine monophosphate (cAMP) signalling, closely linked to parasite proliferation, but not associated with parasite transmission to the tsetse fly vector. Finally, by comparing the expression profiles of sequestered and non-sequestered parasites collected from a rodent model, we showed gene expression changes in sequestered parasites, including of surface variant antigens. This work presents a physiologically-relevant platform to study trypanosome interactions with the vasculature and provides a deeper understanding of the molecular and biophysical mechanisms underlying T. congolense sequestration.

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Publication Details

Journal
Communications Biology
Published
2025-02-26
DOI
https://doi.org/10.1038/s42003-025-07739-z
Citations
4
Primary Topic
Trypanosoma species research and implications
Type
article
Field-Weighted Citation Impact
5.42
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article

Bioengineered 3D microvessels and complementary animal models reveal mechanisms of Trypanosoma congolense sequestration

Sílvia Sanz, Sara Silva Pereira, Viola Introini, Luísa M. Figueiredo et al.
4 citations
Communications Biology
Trypanosoma species research and implications
5.42
article

Bioengineered 3D microvessels and complementary animal models reveal mechanisms of Trypanosoma congolense sequestration

Sílvia Sanz, Sara Silva Pereira, Viola Introini, Luísa M. Figueiredo, Maria Bernabeu, Mariana De Niz, Aitor Casas-Sánchez, Teresa Porqueddu, Diana Carrasqueira, Maria Zorrinho-Almeida
article en
4 citations

Abstract

In the mammalian host, Trypanosoma congolense cytoadheres, or sequesters, to the vascular endothelium. Although sequestration influences clinical outcome, disease severity and organ pathology, its determinants and mediators remain unknown. Challenges such as the variability of animal models, the only-recently developed tools to genetically manipulate the parasite, and the lack of physiologically-relevant in vitro models have hindered progress. Here, we engineered brain and cardiac 3D bovine endothelial microvessel models that mimic the bovine brain microvasculature and the bovine aorta, respectively. By perfusing these models with two T. congolense strains, we investigated the roles of flow for parasite sequestration and tropism for different endothelial beds. We discovered that sequestration is dependent on cyclic adenosine monophosphate (cAMP) signalling, closely linked to parasite proliferation, but not associated with parasite transmission to the tsetse fly vector. Finally, by comparing the expression profiles of sequestered and non-sequestered parasites collected from a rodent model, we showed gene expression changes in sequestered parasites, including of surface variant antigens. This work presents a physiologically-relevant platform to study trypanosome interactions with the vasculature and provides a deeper understanding of the molecular and biophysical mechanisms underlying T. congolense sequestration.

Communications BiologyVol. 8(1)
Northwestern University (US), University of Lisbon (PT), Liverpool School of Tropical Medicine (GB), Universidade Politécnica de Lisboa (PT), Universidade Católica Portuguesa (PT), European Molecular Biology Laboratory (ES), Instituto Gulbenkian de Ciência (PT)
Life below water
Openalex Percentile: Top 5%
Trypanosoma species research and implications
5.42
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