Research group Group Barragan

Our current research on the pathobiology of parasitic infections integrates molecular parasitology with immunology and cell biology to understand how obligate intracellular parasites interact with the host.
Bild Antonio B

Dendritic cell (green) infected by Toxoplasma gondii (red).

We work on the intracellular parasite Toxoplasma gondii, which is an important opportunistic pathogen in humans and animals, and a model for understanding the biology of intracellular parasitism. The research aims to define the molecular mechanisms utilized by Toxoplasma, and related apicomplexan parasites, to manipulate the host´s immune system to their own advantage and thereby promote colonization and transmission of infection.

Host cell manipulation and immunomodulation are important features of obligate intracellular parasites. Yet, the precise mechanisms leading to systemic dissemination of intracellular parasites (acute infection) and life-long persistence in the central nervous system (chronic infection) of the human or animal hosts remain enigmatic.

The processes of host-cell interaction, systemic dissemination and persistence are studied using molecular and cellular experimental approaches and various imaging modalities. Understanding the immune evasion strategies utilized by Toxoplasma and how it orchestrates the subversion of leukocytes may provide key elements of pathogenesis and on the rationale for designing future prophylaxis.

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Department of Molecular Biosciences, The Wenner-Gren Institute

Toxoplasma traps immune cells in blood vessels to rapidly colonize the brain

A recent study published in Nature Communications by the Barragan group reveals how Toxoplasma manipulates infected leukocytes, causing them to become sequestered in cerebral capillaries. After replicating, the parasites exit the leukocytes and swiftly reach neurons. These findings provide new insight into the parasite's journey from the bloodstream into the brain. Microbial translocation across the blood-brain barrier (BBB) is a prerequisite for colonization of the central nervous system. The obligate intracellular parasite Toxoplasma gondii chronically infects the brain parenchyma of humans and animals, in a remarkably stealthy fashion. We investigated the mechanisms of BBB traversal by T. gondii (genotypes I, II, III) and T. gondii-infected leukocytes, using intracarotid arterial delivery into the cerebral circulation of mice. Unexpectedly, parasitized dendritic cells (DCs) and other peripheral blood mononuclear cells were found to persistently sequester within cortical capillaries. Post-replicative egress of T. gondii from sequestered DCs was followed by rapid parasite localization within cortical neurons. Infection-induced microvascular inflammation dramatically elevated the sequestration of parasitized DCs, while treatments targeting the ICAM-1/CD18 leukocyte adhesion axis with blocking antibodies strongly reverted sequestration. The parasite effectors TgWIP and GRA15, known to promote leukocyte hypermigration and inflammatory activation, further increased both the capillary sequestration of infected DCs and cerebral parasite loads in a strain-dependent manner. These findings reveal that the sequestration of parasitized leukocytes in cortical capillaries, with subsequent BBB traversal following parasite egress, provides a novel mechanism for T. gondii's rapid access to cortical neurons during primary infection.  

Department of Molecular Biosciences, The Wenner-Gren Institute

Identity theft the secret of the cat parasite's success

The parasite Toxoplasma is carried by a large portion of the global human population. Now a study led by researchers at Stockholm University shows how this microscopic parasite so successfully spreads in the body, for example to the brain. The parasite infects immune cells and hijacks their identity. The study is published in the scientific journal Cell Host & Microbe.

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