IHEM   20887
INSTITUTO DE HISTOLOGIA Y EMBRIOLOGIA DE MENDOZA DR. MARIO H. BURGOS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
ROLE OF HOST CELL DYNEIN/DYNACTIN IN THE BIOGENESIS OF THE PARASITOPHOROUS VACUOLE WHERE COXIELLA BURNETII RESIDES AND MULTIPLIES.
Autor/es:
ORTIZ, RM; DISTEL, JS; AGUILERA MO; BERÓN W
Lugar:
Puerto Natales
Reunión:
Workshop; Current advances in membrane trafficking: Implications for polarity and diseases; 2014
Institución organizadora:
EMBO
Resumen:
Dynein/dynactin motor complex plays an important role in membrane trafficking in mammaliancells. This is a multisubunit molecular motor that drives centripetal transport of membranouscargoes along microtubules (Mts). Dynactin consists of distinct subunits such as p150Glued anddynamitinp50. Small GTPases of Rab family interact with motor proteins. Rab7, through itseffector RILP, associates dynein/dynactin motor to late endosomal compartments which aretransported to perinuclear region. Coxiella burnetii (Cb) is an intracellular obligate pathogen, causal agent of fever Q, which transits through the phagocytic pathway of host cell to form a compartment with autophagolysosomal features called parasitophorous vacuole (PV). Rab7 is recruited to PV and regulates PV formation. Little evidence exists about the interrelation of intracellular trafficking of Cb with the microtubule-motor system. To determine the role of Mts/dynein/dynactin and Rab7/RILP in the PV biogenesis, HeLa cells were transfected with pEGFP-p150Glued, pEGFP-Dynamitina-p50, pEGFP-RILP, pEGFP-Rab7 or negative mutants (pRFP-p150Glued CC1, pRFP-RILPΔN, pEGFP-Rab7T22N) and then infected with Cb. After  48 h, cells were processed for Indirect Immunofluorescence and analyzed by confocal  microscopy.The following parameters were determined: number of infected cells, Cb intracellular multiplication(FFU assay), number and size of PVs, and recruitment of the studied proteins on PVs. The resultsshowed that wild type forms of overexpressed proteins were recruited on the PV membranewithout significantly affecting its size and number compared with the EGFP. The size of VPsdecreased and their number increased when the mutated proteins were overexpressed. Interestingly these mutants were recruited onto PV membrane. The Cb intracellular multiplication was diminished in cell overexpressing the mutated proteins regarding to those overexpressing the wild type proteins. In conclusion, our results suggest the transport of early C. burnetii-containing phagosomes would use the Mts/dynein/dynactin system to be transported from the cell periphery to the perinuclear region to promote PV formation.