tetano
Editor, Senior Moderator
J Infect Dis. 2012 Jul 26. [Epub ahead of print]
The Combined Action of Influenza Virus and Staphylococcus aureus Panton-Valentine Leukocidin Provokes Severe Lung Epithelium Damage.
Niemann S, Ehrhardt C, Medina E, Warnking K, Tuchscherr L, Heitmann V, Ludwig S, Peters G, L?ffler B.
Source
Institute of Medical Microbiology, Braunschweig, Germany.
Abstract
S. aureus necrotizing pneumonia is a life-threatening disease that is frequently preceded by an influenza infection. The S. aureus toxin Panton-Valentine leukocidin (PVL) is most likely causative for necrotizing diseases, but the precise pathogenic mechanisms of PVL and a possible contribution of influenza virus remain to be elucidated. In this study, we present a model that explains how influenza virus and PVL act together to cause necrotizing pneumonia: An influenza infection activates the lung epithelium to produce chemoattractants for neutrophils. Upon superinfection with PVL-expressing S. aureus, the recruited neutrophils are rapidly killed by PVL, resulting in uncontrolled release of neutrophil proteases that damage the airway epithelium. The host counteracts this pathogen strategy by generating PVL-neutralizing antibodies and by neutralizing the released proteases via protease-inhibitors present in the serum. These findings can explain that necrotizing infections mainly develop in serum-free spaces (e.g., pulmonary alveoli) and open options for new therapeutic approaches.
PMID:
22837490
[PubMed - as supplied by publisher]
http://www.ncbi.nlm.nih.gov/pubmed/22837490
The Combined Action of Influenza Virus and Staphylococcus aureus Panton-Valentine Leukocidin Provokes Severe Lung Epithelium Damage.
Niemann S, Ehrhardt C, Medina E, Warnking K, Tuchscherr L, Heitmann V, Ludwig S, Peters G, L?ffler B.
Source
Institute of Medical Microbiology, Braunschweig, Germany.
Abstract
S. aureus necrotizing pneumonia is a life-threatening disease that is frequently preceded by an influenza infection. The S. aureus toxin Panton-Valentine leukocidin (PVL) is most likely causative for necrotizing diseases, but the precise pathogenic mechanisms of PVL and a possible contribution of influenza virus remain to be elucidated. In this study, we present a model that explains how influenza virus and PVL act together to cause necrotizing pneumonia: An influenza infection activates the lung epithelium to produce chemoattractants for neutrophils. Upon superinfection with PVL-expressing S. aureus, the recruited neutrophils are rapidly killed by PVL, resulting in uncontrolled release of neutrophil proteases that damage the airway epithelium. The host counteracts this pathogen strategy by generating PVL-neutralizing antibodies and by neutralizing the released proteases via protease-inhibitors present in the serum. These findings can explain that necrotizing infections mainly develop in serum-free spaces (e.g., pulmonary alveoli) and open options for new therapeutic approaches.
PMID:
22837490
[PubMed - as supplied by publisher]
http://www.ncbi.nlm.nih.gov/pubmed/22837490