The glyceraldehyde-3-phosphate dehydrogenase and the small GTPase Rab 2 are crucial for Brucella replication

The intracellular pathogen Brucella abortus survives and replicates inside host cells within an endoplasmic reticulum (ER)-derived replicative organelle named the "Brucella-containing vacuole" (BCV). Here, we developed a subcellular fractionation method to isolate BCVs and characterize for...

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Veröffentlicht in:PLoS pathogens 2009-06, Vol.5 (6), p.e1000487-e1000487
Hauptverfasser: Fugier, Emilie, Salcedo, Suzana P, de Chastellier, Chantal, Pophillat, Matthieu, Muller, Alexandre, Arce-Gorvel, Vilma, Fourquet, Patrick, Gorvel, Jean-Pierre
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container_issue 6
container_start_page e1000487
container_title PLoS pathogens
container_volume 5
creator Fugier, Emilie
Salcedo, Suzana P
de Chastellier, Chantal
Pophillat, Matthieu
Muller, Alexandre
Arce-Gorvel, Vilma
Fourquet, Patrick
Gorvel, Jean-Pierre
description The intracellular pathogen Brucella abortus survives and replicates inside host cells within an endoplasmic reticulum (ER)-derived replicative organelle named the "Brucella-containing vacuole" (BCV). Here, we developed a subcellular fractionation method to isolate BCVs and characterize for the first time the protein composition of its replicative niche. After identification of BCV membrane proteins by 2 dimensional (2D) gel electrophoresis and mass spectrometry, we focused on two eukaryotic proteins: the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the small GTPase Rab 2 recruited to the vacuolar membrane of Brucella. These proteins were previously described to localize on vesicular and tubular clusters (VTC) and to regulate the VTC membrane traffic between the endoplasmic reticulum (ER) and the Golgi. Inhibition of either GAPDH or Rab 2 expression by small interfering RNA strongly inhibited B. abortus replication. Consistent with this result, inhibition of other partners of GAPDH and Rab 2, such as COPI and PKC iota, reduced B. abortus replication. Furthermore, blockage of Rab 2 GTPase in a GDP-locked form also inhibited B. abortus replication. Bacteria did not fuse with the ER and instead remained in lysosomal-associated membrane vacuoles. These results reveal an essential role for GAPDH and the small GTPase Rab 2 in B. abortus virulence within host cells.
doi_str_mv 10.1371/journal.ppat.1000487
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subjects Animals
Bacteria
Bacteriology
Biochemistry
Brucella abortus
Brucella abortus - cytology
Brucella abortus - growth & development
Cell Biology/Membranes and Sorting
Cell division
Cell Line
Cell Membrane
Cell Membrane - chemistry
Cell Membrane - microbiology
Cell Survival
Endoplasmic Reticulum
Endoplasmic Reticulum - microbiology
Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)
Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - chemistry
Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - metabolism
Guanosine triphosphatase
Host-Pathogen Interactions
Host-Pathogen Interactions - physiology
Immunohistochemistry
Immunology
Infections
Life Sciences
Mass spectrometry
Membrane Proteins
Membrane Proteins - chemistry
Membrane Proteins - metabolism
Microbiology and Parasitology
Microbiology/Cellular Microbiology and Pathogenesis
Oxidoreductases
Physiological aspects
Proteins
rab2 GTP-Binding Protein
rab2 GTP-Binding Protein - chemistry
rab2 GTP-Binding Protein - metabolism
Secretory Pathway
Secretory Pathway - physiology
Vacuoles
Vacuoles - chemistry
Vacuoles - enzymology
Vacuoles - microbiology
title The glyceraldehyde-3-phosphate dehydrogenase and the small GTPase Rab 2 are crucial for Brucella replication
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