Journal of Bacteriology · 2018 · 13 citations · 44 references
Life SciencesMicrobiologyMolecular BiologyHost-pathogen InteractionsInflammationStructural BiologyBacterial PathogenesisBacterial ToxinsEnzyme InhibitionPathogen DiscoveryToxin-mediated PathogenesisBacterial Toxin BiologyEnzymatic Toxin ActivityEnzymesHost Cell Death ModulationMicrobial Extracellular EnzymesPhospholipase A2 ToxinsUbiquitin SystemUbiquitin-mediated Proteolysis
Bacterial phospholipases act as intracellular and extracellular enzymes promoting the destruction of phospholipid barriers and inflammation during infections. Identifying enzymes with a common mechanism of activation is an initial step in understanding structural and functional properties. These properties serve as critical information for the design of specific inhibitors to reduce enzymatic activity and ameliorate host cell death. In this study, we identify and verify cytotoxic PLA 2 enzymes from several bacterial pathogens. Similar to the founding member of the group, ExoU, these enzymes share the property of ubiquitin-mediated activation. The identification and validation of potential toxins from multiple bacterial species provide additional proteins from which to derive structural insights that could lead to paninhibitors useful for treating a variety of infections.
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