Perforin-2 Breaches the Envelope of Phagocytosed Bacteria Allowing Antimicrobial Effectors Access to Intracellular Targets.
Fangfang BaiRyan M McCormackSuzanne HowerGregory V PlanoMathias G LichtenheldGeorge P MunsonPublished in: Journal of immunology (Baltimore, Md. : 1950) (2018)
Perforin-2, the product of the MPEG1 gene, limits the spread and dissemination of bacterial pathogens in vivo. It is highly expressed in murine and human phagocytes, and macrophages lacking Perforin-2 are compromised in their ability to kill phagocytosed bacteria. In this study, we used Salmonella enterica serovar Typhimurium as a model intracellular pathogen to elucidate the mechanism of Perforin-2's bactericidal activity. In vitro Perforin-2 was found to facilitate the degradation of Ags contained within the envelope of phagocytosed bacteria. In contrast, degradation of a representative surface Ag was found to be independent of Perforin-2. Consistent with our in vitro results, a protease-sensitive, periplasmic superoxide dismutase (SodCII) contributed to the virulence of S. Typhimurium in Perforin-2 knockout but not wild-type mice. In aggregate, our studies indicate that Perforin-2 breaches the envelope of phagocytosed bacteria, facilitating the delivery of proteases and other antimicrobial effectors to sites within the bacterial cell.
Keyphrases
- wild type
- staphylococcus aureus
- escherichia coli
- endothelial cells
- pseudomonas aeruginosa
- cell therapy
- magnetic resonance
- listeria monocytogenes
- stem cells
- magnetic resonance imaging
- genome wide
- antimicrobial resistance
- cystic fibrosis
- reactive oxygen species
- gene expression
- adipose tissue
- dna methylation
- quantum dots
- type diabetes
- candida albicans
- biofilm formation
- transcription factor
- hydrogen peroxide
- highly efficient