How does the oxidative burst of macrophages kill bacteria? Still an open question.

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 Microbiol

journal_title

Molecular microbiology

authors

Slauch JM

doi

10.1111/j.1365-2958.2011.07612.x

subject

Has Abstract

pub_date

2011-05-01 00:00:00

pages

580-3

issue

3

eissn

0950-382X

issn

1365-2958

journal_volume

80

pub_type

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