IcmF and DotU are required for optimal effector translocation and trafficking of the Legionella pneumophila vacuole

Infection and Immunity

Volumn 72, Issue 10, 2004, Pages 5972-5982

  VanRheenen, Susan M ^a   Duménil, Guillaume ^a,b   Isberg, Ralph R ^a  

^a TUFTS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; CELL PROTEIN; DOTU PROTEIN; GENE PRODUCT; ICMF PROTEIN; LYSOSOME ASSOCIATED MEMBRANE PROTEIN 1; MEMBRANE PROTEIN; REAGENT; SIDC PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BACTERIAL GENE; BACTERIAL GROWTH; BACTERIAL TRANSLOCATION; CELL COMPARTMENTALIZATION; CELL VACUOLE; CONTROLLED STUDY; DELETION MUTANT; DOTU GENE; FEMALE; GENE CLUSTER; GENE LOCATION; GENE MUTATION; GRAM NEGATIVE BACTERIUM; ICMF GENE; LEGIONELLA PNEUMOPHILA; LEGIONNAIRE DISEASE; LUNG ALVEOLUS MACROPHAGE; LYSOSOME; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN DOMAIN; SECRETION; WILD TYPE;

ANIMALS; BACTERIAL PROTEINS; BONE MARROW CELLS; CELL FUSION; ENDOCYTOSIS; ENDOSOMES; FEMALE; FEMUR; GENES, BACTERIAL; LEGIONELLA PNEUMOPHILA; MACROPHAGES, ALVEOLAR; MICE; MUTATION; PROTEIN TRANSPORT; VACUOLES;

EID: 4644244888     PISSN: 00199567     EISSN: None     Source Type: Journal    
DOI: 10.1128/IAI.72.10.5972-5982.2004     Document Type: Article

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