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Exploring the role of host-parasite genotypes in the congenital transmission of Chagas disease: an emergent infectious disease in Europe

Project description

Genetic causes of Chagas disease

Chagas disease (CD) is a chronic disease caused by the protozoan Trypanosoma cruzi that affects millions of people worldwide. Although in endemic regions CD is a vector-borne disease, in non-endemic countries the disease is mainly spread by congenital transmission. Scientists of the EU-funded ChaConGen project plan to investigate the molecular and clinical aspects of this route of transmission. In particular, they will study the genetic components involved in the congenital transmission of Chagas disease. The results will shed light on the genetic causes of congenital CD, which could help to target the group of infected pregnant women at higher risk of transmission providing the basis for a better control of congenital transmission.

Objective

Chagas disease (CD) is a parasitic, systemic and chronic disease caused by the protozoan Trypanosoma cruzi. Approximately 30% of chronically infected people develop cardiac, digestive, neurological or mixed alterations. CD affects 7 million people worldwide, mainly in endemic areas of 21 continental Latin American countries, where T. cruzi is mainly a vector-borne disease. In non-endemic regions, a major role is played by congenital (mother-to-fetus) transmission, leading CD to become an emerging disease in Europe and other non-endemic regions. It is increasingly clear that more efforts are needed at the basic research level to improve our understanding of the molecular and clinical aspects of this route of transmission. Understanding the genetic bases of the interaction between the host and the parasite could shed light into the molecular mechanisms behind congenital transmission. In this project, we aim to use state-of-the-art genomic techniques to understand the relationship between T. cruzi genotype and the host genotype in congenital transmission of CD. Identifying the factors governing this matter will not only help to better understand the mechanisms behind the diseases, but it could also help to target the group of infected pregnant women at higher risk of transmission. We will examine the parasite and the host genotypes in blood samples from infected pregnant women transmitting and not transmitting the infection. We will assess parasite diversity by developing a new strategy for T. cruzi genetic typing based on the MinION, a portable long-read DNA sequencer. For the genotyping of the host, we will use genome-wide SNP arrays. We will use multivariate analysis for determining putative relationships between host and parasite genotypes and congenital transmission of CD. This project will provide the first attempt at determining genetic causes of congenital CD considering both, host and parasite genotypes by applying the state-of-the-art genomic techniques.

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MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)

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Call for proposal

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(opens in new window) H2020-MSCA-IF-2019

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Coordinator

FUNDACION PRIVADA INSTITUTO DE SALUD GLOBAL BARCELONA
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 224 496,96
Address
C ROSSELLO 132 PLANTA 05
08036 Barcelona
Spain

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Region
Este Cataluña Barcelona
Activity type
Research Organisations
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 224 496,96

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