Abstract:
:Reactive oxygen species (ROS) are critical components of the antimicrobial repertoire of macrophages, yet the mechanisms by which ROS damage bacteria in the phagosome are unclear. The NADH-dependent phagocytic oxidase produces superoxide, which dismutes to form H(2)O(2). The Barras and Méresse labs use a GFP fusion to an OxyR regulated gene to show that phagocyte-derived H(2)O(2) is gaining access to the Salmonella cytoplasm. However, they have also shown previously that Salmonella has redundant systems to detoxify this H(2)O(2). Although Salmonella propagate in a unique vacuole, their data suggest that ROS are not diminished in this modified phagosome. These recent results are put into the context of our overall understanding of potential oxidative bacterial damage occurring in macrophages.
journal_name
Mol Microbioljournal_title
Molecular microbiologyauthors
Slauch JMdoi
10.1111/j.1365-2958.2011.07612.xsubject
Has Abstractpub_date
2011-05-01 00:00:00pages
580-3issue
3eissn
0950-382Xissn
1365-2958journal_volume
80pub_type
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