Staphylococcus aureus, phagocyte NADPH oxidase and chronic granulomatous disease.

Abstract:

:Dysfunction of phagocytes is a relevant risk factor for staphylococcal infection. The most common hereditary phagocyte dysfunction is chronic granulomatous disease (CGD), characterized by impaired generation of reactive oxygen species (ROS) due to loss of function mutations within the phagocyte NADPH oxidase NOX2. Phagocytes ROS generation is fundamental to eliminate pathogens and to regulate the inflammatory response to infection. CGD is characterized by recurrent and severe bacterial and fungal infections, with Staphylococcus aureus as the most frequent pathogen, and skin and lung abscesses as the most common clinical entities. Staphylococcus aureus infection may occur in virtually any human host, presumably because of the many virulence factors of the bacterium. However, in the presence of functional NOX2, staphylococcal infections remain rare and are mainly linked to breaches of the skin barrier. In contrast, in patients with CGD, S. aureus readily survives and frequently causes clinically apparent disease. Astonishingly, little is known why S. aureus, which possesses a wide range of antioxidant enzymes (e.g. catalase, SOD), is particularly sensitive to control through NOX2. In this review, we will evaluate the discovery of CGD and our present knowledge of the role of NOX2 in S. aureus infection.

journal_name

FEMS Microbiol Rev

authors

Buvelot H,Posfay-Barbe KM,Linder P,Schrenzel J,Krause KH

doi

10.1093/femsre/fuw042

subject

Has Abstract

pub_date

2017-03-01 00:00:00

pages

139-157

issue

2

eissn

0168-6445

issn

1574-6976

pii

fuw042

journal_volume

41

pub_type

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