Pregled bibliografske jedinice broj: 431986
Title: Molecular characterization of the Dot/Icm-translocated AnkH and AnkJ eukaryotic-like effectors of Legionella pneumophila
Title: Molecular characterization of the Dot/Icm-translocated AnkH and AnkJ eukaryotic-like effectors of Legionella pneumophila // Legionella 2009
Pariz, Francuska, 2009. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 431986 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Title: Molecular characterization of the Dot/Icm-translocated AnkH and AnkJ eukaryotic-like effectors of Legionella pneumophila
Autori
Habyarimana, Fabien ; Al Khodor, Souhaila ; Šantić, Marina ; Price, Chris ; Abu Kwaik, Yousef
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
Legionella 2009
Mjesto i datum
Pariz, Francuska, 13.10.2009. - 17.10.2009
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
legionella; ANK repeat; Dot/Icm; effector
Sažetak
The eukaryotic-like Ankyrin H (AnkH) and AnkJ proteins of Legionella pneumophila are required for intracellular proliferation. In this report, we show that expression of ankH and ankJ is temporally triggered by a network of interacting regulatory cascades. Intracellular bacteria translocate AnkH and AnkJ and 5 other Ank proteins into the macrophage cytosol via the Dot/Icm type IV secretion system. The IcmSW chaperones are essential for translocation of AnkJ but not AnkH. The ankH and ankJ mutants are severely defective in intrapulmonary proliferation in mice. The 10 C-terminal residues and the ANK domains of AnkH and AnkJ are required for translocation. Expression of AnkH and AnkJ fusions within HEK293 cells show a punctuate distribution in the cytosol but no association with endocytic vesicles, the Golgi apparatus or the ER. Interestingly, the defect in intracellular proliferation of the ankH or ankJ mutants is rescued in HEK293 cells expressing the respective effector. W e conclude that AnkH and AnkJ are effectors translocated by the Dot/Icm system by distinct mechanisms and modulate distinct cytosolic processes in the host cell. This is the first demonstration of a trans-complementation of an effector mutant of L. pneumophila through expression of the respective effector in the host cell.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
062-0621273-1275 - Patogeneza eksperimentalne legioneloze (Dorić, Miljenko, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Marina Šantić
(autor)