cellular
• change in actin cytoskeleton remodeling causing significant increase in percentage of Salmonella-infected cells and cells harbouring more than one bacterium per cell when bone marrow derived macrophages (BMDMs) were subjected to opsonized S. Typhimurium infection
• normal percentage of Salmonella-infected cells and cells harbouring more than one bacterium per cell when cytochalasin D pre-treated BMDMs were subjected to opsonized S. Typhimurium infection
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hematopoietic system
• increased mobility in collagen matrix in vitro
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immune system
• increased mobility in collagen matrix in vitro
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• increased levels of CXCL2, CXCL10, CCL3, CCL4 and CCL5 after intravenous infection with Salmonella Typhimurium
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• increased levels of CXCL10 after intravenous infection with Salmonella Typhimurium
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• after intravenous infection with Salmonella Typhimurium
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• after intravenous infection with Salmonella Typhimurium
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• increased levels of TNFA after intravenous infection with Salmonella Typhimurium
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• progressive increase in bacterial load, overall and in spleen and liver after intravenous or oral infection with Salmonella Typhimurium
• decreased survival rates after intravenous or oral infection with Salmonella Typhimurium
• higher bacterial load in lungs after infection with M. tuberculosis
• increased parenchymal infiltration by granulomatous reaction and lympho-histiocytic inflammatory cells in lungs after infection with M. tuberculosis
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homeostasis/metabolism
• increased levels of CXCL2, CXCL10, CCL3, CCL4 and CCL5 after intravenous infection with Salmonella Typhimurium
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• increased levels of CXCL10 after intravenous infection with Salmonella Typhimurium
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• after intravenous infection with Salmonella Typhimurium
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• after intravenous infection with Salmonella Typhimurium
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• increased levels of TNFA after intravenous infection with Salmonella Typhimurium
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mortality/aging
• progressive increase in bacterial load, overall and in spleen and liver after intravenous or oral infection with Salmonella Typhimurium
• decreased survival rates after intravenous or oral infection with Salmonella Typhimurium
• higher bacterial load in lungs after infection with M. tuberculosis
• increased parenchymal infiltration by granulomatous reaction and lympho-histiocytic inflammatory cells in lungs after infection with M. tuberculosis
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respiratory system
• large parenchymal consolidation in lungs after infection with M. tuberculosis
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