Loading...
Polyketide synthase (PKS) reduces fusion of Legionella pneumophila-containing vacuoles with lysosomes and contributes to bacterial competitiveness during infection.
Shevchuk, Olga ; Pägelow, Dennis ; Rasch, Janine ; Döhrmann, Simon ; Günther, Gabriele ; Hoppe, Julia ; Ünal, Can Murat ; Bronietzki, Marc ; Gutierrez, Maximiliano Gabriel ; Steinert, Michael
Shevchuk, Olga
Pägelow, Dennis
Rasch, Janine
Döhrmann, Simon
Günther, Gabriele
Hoppe, Julia
Ünal, Can Murat
Bronietzki, Marc
Gutierrez, Maximiliano Gabriel
Steinert, Michael
Citations
Altmetric:
Advisors
Editors
Other Contributors
Issue Date
2014-11
Submitted date
Files
Loading...
original manuscript
Adobe PDF, 326.41 KB
Other Titles
Abstract
L. pneumophila-containing vacuoles (LCVs) exclude endocytic and lysosomal markers in human macrophages and protozoa. We screened a L. pneumophila mini-Tn10 transposon library for mutants, which fail to inhibit the fusion of LCVs with lysosomes by loading of the lysosomal compartment with colloidal iron dextran, mechanical lysis of infected host cells, and magnetic isolation of LCVs that have fused with lysosomes. In silico analysis of the mutated genes, D. discoideum plaque assays and infection assays in protozoa and U937 macrophage-like cells identified well established as well as novel putative L. pneumophila virulence factors. Promising candidates were further analyzed for their co-localization with lysosomes in host cells using fluorescence microscopy. This approach corroborated that the O-methyltransferase, PilY1, TPR-containing protein and polyketide synthase (PKS) of L. pneumophila interfere with lysosomal degradation. Competitive infections in protozoa and macrophages revealed that the identified PKS contributes to the biological fitness of pneumophila strains and may explain their prevalence in the epidemiology of Legionnaires' disease.
Citation
Polyketide synthase (PKS) reduces fusion of Legionella pneumophila-containing vacuoles with lysosomes and contributes to bacterial competitiveness during infection. 2014, 304 (8):1169-81 Int. J. Med. Microbiol.
Publisher
PubMed ID
PubMed Central ID
Additional Links
Embedded video
Type
Article
Language
en
Description
Series/Report no.
ISSN
1618-0607
