immune system
• as expected, PMA-stimulated peritoneal exudate neutrophils from homozygotes fail to generate hypochlorous acid (HOCl) from hydrogen peroxide, due to absence of peroxidase activity
• also, peritoneal exudate neutrophils from homozygotes show a slightly higher level of O2- generation than those of wild-type mice
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• homozygotes are viable, fertile and developmentally normal with normal clearance of intraperitoneal S. aureus by 48 hrs post-infection
• however, homozygotes show increased susceptibility to intratracheal infection with C. albicans, with severe alveolar and peribronchiolar pneumonia resulting in death of two-thirds of mutants by 5 days post-infection even at a relatively low dose (4 106 fungi/mouse)
• when challenged intraperitoneally at a similar dose (4 106 fungi/mouse), both wild-type and mutant mice show no obvious signs of severe infection at 7 days after challenge, despite significant fungal dissemination in various mutant organs, with lungs and kidneys being most severely affected
• at a higher i.p. dose (108 fungi/mouse), all homozygotes die by 2 days, whereas all wild-type mice survive for 7 days without many signs of distress
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homeostasis/metabolism
• as expected, PMA-stimulated peritoneal exudate neutrophils from homozygotes fail to generate hypochlorous acid (HOCl) from hydrogen peroxide, due to absence of peroxidase activity
• also, peritoneal exudate neutrophils from homozygotes show a slightly higher level of O2- generation than those of wild-type mice
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hematopoietic system
• as expected, PMA-stimulated peritoneal exudate neutrophils from homozygotes fail to generate hypochlorous acid (HOCl) from hydrogen peroxide, due to absence of peroxidase activity
• also, peritoneal exudate neutrophils from homozygotes show a slightly higher level of O2- generation than those of wild-type mice
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