2005
DOI: 10.1016/j.clim.2004.07.010
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Cellular bioterrorism: how Brucella corrupts macrophage physiology to promote invasion and proliferation

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Cited by 64 publications
(27 citation statements)
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“…In fact, ROS and nitric oxide production have been shown to be important for microbicidal activity against Brucella in macrophages (126). SodC, a Cu/Zn superoxide dismutase that counteracts ROS production, is required by B. abortus for survival within macrophages and virulence in a mouse model of infection (127).…”
Section: Brucellamentioning
confidence: 99%
“…In fact, ROS and nitric oxide production have been shown to be important for microbicidal activity against Brucella in macrophages (126). SodC, a Cu/Zn superoxide dismutase that counteracts ROS production, is required by B. abortus for survival within macrophages and virulence in a mouse model of infection (127).…”
Section: Brucellamentioning
confidence: 99%
“…As pathogens evolve they acquire the necessary virulence factors to invade and propagate within their hosts. Brucella has virulence factors that are important in the hostepathogen interaction and modifying phagocytosis, phagolysosome fusion, cytokine secretion and apoptosis [2]. Once intracellular, Brucella localizes in early phagosomes avoiding fusion with late endosomes and lysosomes [3].…”
Section: Introductionmentioning
confidence: 99%
“…After entering the host, Brucella is taken up by macrophage and dendritic cells. Brucella can survive and replicate in this immune cells and evad adaptive immune system (21,23). Macrophages are key elements in the cellular immune response against intracellular bacteria like Brucella (17).…”
Section: 12cell-mediated Immunitymentioning
confidence: 99%