cAMP and EPAC are key players in the regulation of the signal transduction pathway involved Ą-hemolysin autophagic response. Plos Pathogens.

MESTRE, M.B.; COLOMBO, M. I.

PLOS PATHOGENS

PUBLIC LIBRARY SCIENCE

Lugar: San Francisco; Año: 2012 vol. 8

1553-7366

Staphylococcus aureus is a microorganism which causes serious diseases in the human being. This microorganism is able to escape the phagolysosomal pathway increasing the intracellular bacterial survival and killing the eukaryotic host cell to spread the infection. One of the key features of S. aureus infection is the production of a series of virulence factors, including secreted enzymes and toxins. We have shown that the pore-forming toxin a-hemolysin (Hla) is the S. aureus secreted factor responsible for the activation of the autophagic pathway and that this response occurs through a PI3K/Beclin1-independent form. In the present report we demonstrate that cAMP has a key role in the regulation of this autophagic response. Our results indicate that cAMP is able to inhibit the autophagy induced by Hla and that PKA, the classical cAMP effector, does not participate in this regulation. We presented evidence that EPAC and Rap2b, through calpain activation, are the proteins involved in the regulation of Hla-induced autophagy. Similar results were obtained in cells infected with different S. aureus strains. Interestingly, in this report we show for the first time that both EPAC and Rap2b are recruited to the S. aureus-containing phagosome, likely to benefit bacterial replication and survival. We believe that our findings have important implications in understanding innate immune processes involved in intracellular pathogen invasion of the host cell.