Summary
Signaling functions of metabolites have been gathering interest in the context of infection, cancer, and metabolic disorders. However, how metabolic communication networks shape the pathology of infection remains poorly understood. Our group has recently reported that chronic infection with lymphocytic choriomeningitis (LCMV) in mice leads to reprogramming of the hepatic urea cycle with a concomitant increase with blood ammonia levels. Despite being typically considered as a waste product with neurotoxic effect, ammonia is involved in relevant pathways for energy production, cell proliferation, and survival. Additionally, ammonia is a small, gaseous molecule that might modulate cellular functions in distant tissues, as described for other gasotransmitters. Therefore, I hypothesize that infection-induced hyperammonemia has poorly recognized signaling functions that might influence immune responses, tissue damage, or sickness behavior. To test this hypothesis, I will combine state-of-the-art metabolic analyses, pharmacological and genetic tools. I expect to establish whether hyperammonemia is broadly associated with viral infections in mice, and/or whether it is a direct consequence of virus-induced liver damage. Additionally, I will analyze tissue-specific and organismal effects of hyperammonemia and determine whether this impacts on sickness behavior or infection outcomes. This interdisciplinary approach combining immunology, metabolism and neuroscience will allow me to characterize mechanisms of host response to viral infections, which pose outstanding challenges to current biology and medicine. Additionally, I expect to unveil inter-organ communication networks that link metabolically active tissues and the brain. These may have strong implications not only for infection but also for a wide range of metabolic disorders.
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More information & hyperlinks
Web resources: | https://cordis.europa.eu/project/id/101028971 |
Start date: | 01-04-2021 |
End date: | 31-03-2023 |
Total budget - Public funding: | 174 167,04 Euro - 174 167,00 Euro |
Cordis data
Original description
Signaling functions of metabolites have been gathering interest in the context of infection, cancer, and metabolic disorders. However, how metabolic communication networks shape the pathology of infection remains poorly understood. Our group has recently reported that chronic infection with lymphocytic choriomeningitis (LCMV) in mice leads to reprogramming of the hepatic urea cycle with a concomitant increase with blood ammonia levels. Despite being typically considered as a waste product with neurotoxic effect, ammonia is involved in relevant pathways for energy production, cell proliferation, and survival. Additionally, ammonia is a small, gaseous molecule that might modulate cellular functions in distant tissues, as described for other gasotransmitters. Therefore, I hypothesize that infection-induced hyperammonemia has poorly recognized signaling functions that might influence immune responses, tissue damage, or sickness behavior. To test this hypothesis, I will combine state-of-the-art metabolic analyses, pharmacological and genetic tools. I expect to establish whether hyperammonemia is broadly associated with viral infections in mice, and/or whether it is a direct consequence of virus-induced liver damage. Additionally, I will analyze tissue-specific and organismal effects of hyperammonemia and determine whether this impacts on sickness behavior or infection outcomes. This interdisciplinary approach combining immunology, metabolism and neuroscience will allow me to characterize mechanisms of host response to viral infections, which pose outstanding challenges to current biology and medicine. Additionally, I expect to unveil inter-organ communication networks that link metabolically active tissues and the brain. These may have strong implications not only for infection but also for a wide range of metabolic disorders.Status
CLOSEDCall topic
MSCA-IF-2020Update Date
28-04-2024
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EU-Programme-Call
Horizon 2020
H2020-EU.1. EXCELLENT SCIENCE
H2020-EU.1.3. EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions (MSCA)
H2020-EU.1.3.2. Nurturing excellence by means of cross-border and cross-sector mobility
H2020-MSCA-IF-2020
MSCA-IF-2020 Individual Fellowships