DFG project G:(GEPRIS)233993717

Effector glycosyltransferases of the human pathogen Legionella pneumophila

CoordinatorProfessor Dr. Klaus Aktories
Grant period2013 - 2017
Funding bodyDeutsche Forschungsgemeinschaft
 DFG
IdentifierG:(GEPRIS)233993717

Note: Legionella pneumophila is a human pathogen, which causes severe pneumonia called Legionnaires disease. The bacterium invades and replicates inside alveolar macrophages. Therefore, Legionella injects effector proteins by type-IV-secretion into the host cytosol to arrange an intracellular Legionella-containing vacuole (LCV) where Legionella can replicate. The Legionella effectors SetA and Lpg1961 show high sequence similarities to glycosyltransferases and are toxic when introduced into eukaryotic cells. SetA was implicated in the subversion of eukaryotic vesicle trafficking. The function of Lpg1961 is unknown. Initial biochemical studies showed that SetA possesses an N-terminal glycosyltransferase domain and a C-terminal PtdIns(3)P-binding domain. Using yeast genetics, cell biology and protein biochemical methods, the host substrates of the glycosyltransferases should be identified and the molecular and functional consequences of their glycosylation elucidated. We aim to analyze the structure-function relationships of glycosyltransferases SetA and Lpg1961. The proposed studies should clarify the effects of the glycosyltransferases in the host cells and their roles during the Legionella infection process.
   

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 Record created 2023-01-31, last modified 2024-09-28