作者: Liljana Petrovska , Richard J. Aspinall , Li Barber , Simon Clare , Cameron P. Simmons
DOI: 10.1111/J.1462-5822.2004.00419.X
关键词:
摘要: Summary Salmonella enterica serovar Typhimurium (S. Typhimurium) and several mutant derivatives were able to enter efficiently murine bone marrow-derived dendritic cells using mechanisms predominantly independent of the Salmonella pathogenicity island 1 type III secretion system. The levels intracellular bacteria did not increase significantly over many hours after invasion. Using fluid endocytic tracers other markers, S. Typhimurium-containing vacuoles (SCVs) physically distinguishable from early compartments. Fifty eighty per cent SCVs harbouring wild-type or aroA, invH ssaV associated with late endosome markers. In contrast, sifA was shown escape into cytosol infected cells. aroC more efficient than in delivering a eukaryotic promoter-driven green fluorescent protein reporter gene for expression detectably efficiency MHC class I presentation model antigen ovalbumin T compared similar derivative. Mice expressing develop enhanced cytotoxic cell interferon-γ production derivatives.