TY - JOUR
T1 - Functional dissection of protein domains involved in the immunomodulatory properties of PE_PGRS33 of Mycobacterium tuberculosis
AU - Zumbo, Antonella
AU - Palucci, Ivana
AU - Cascioferro, Alessandro
AU - Sali, Michela
AU - Ventura, Marcello
AU - D'Alfonso, Pamela
AU - Iantomasi, Raffaella
AU - Di Sante, Gabriele
AU - Ria, Francesco
AU - Sanguinetti, Maurizio
AU - Fadda, Giovanni
AU - Manganelli, Riccardo
AU - Delogu, Giovanni
PY - 2013
Y1 - 2013
N2 - PE_PGRSs are a large family of proteins identified in Mycobacterium tuberculosis complex and in few other pathogenic mycobacteria. The PE domain of PE_PGRS33 mediates localization of the protein on the mycobacterial cell surface, where the PGRS domain is available to interact with host components. In this study, PE_PGRS33 and its functional deletion mutants were expressed in M. smegmatis, and in vitro and in vivo assays were used to dissect the protein domains involved in the immunomodulatory properties of the protein. We demonstrate that PE_PGRS33-mediated secretion of TNF-α by macrophages occurs by extracellular interaction with TLR2. Our results also show that while the PGRS domain of the protein is required for triggering TNF-α secretion, mutation in the PE domain affects the pro-inflammatory properties of the protein. These results indicate that PE_PGRS33 is a protein with immunomodulatory activity and that protein stability and localization on the mycobacterial surface can affect these properties.
AB - PE_PGRSs are a large family of proteins identified in Mycobacterium tuberculosis complex and in few other pathogenic mycobacteria. The PE domain of PE_PGRS33 mediates localization of the protein on the mycobacterial cell surface, where the PGRS domain is available to interact with host components. In this study, PE_PGRS33 and its functional deletion mutants were expressed in M. smegmatis, and in vitro and in vivo assays were used to dissect the protein domains involved in the immunomodulatory properties of the protein. We demonstrate that PE_PGRS33-mediated secretion of TNF-α by macrophages occurs by extracellular interaction with TLR2. Our results also show that while the PGRS domain of the protein is required for triggering TNF-α secretion, mutation in the PE domain affects the pro-inflammatory properties of the protein. These results indicate that PE_PGRS33 is a protein with immunomodulatory activity and that protein stability and localization on the mycobacterial surface can affect these properties.
KW - Mycobacterium tuberculosis
KW - PE_PGRS
KW - TLR2
KW - Mycobacterium tuberculosis
KW - PE_PGRS
KW - TLR2
UR - http://hdl.handle.net/10807/48011
U2 - 10.1111/2049-632X.12096
DO - 10.1111/2049-632X.12096
M3 - Article
SN - 2049-632X
SP - 232
EP - 239
JO - Pathogens and Disease
JF - Pathogens and Disease
ER -