| Literature DB >> 33425777 |
Darya Slonova1,2, Alexandra Posvyatenko2, Alexey Kibardin2, Elena Sysolyatina3, Elena Lyssuk2, Svetlana Ermolaeva3, Sergei Obydennyi4,5, Nikolay Gnuchev6, Georgii Georgiev6, Konstantin Severinov1, Sergey Larin2.
Abstract
PGLYRP1/Tag-7/PGRP-S is one of mammalian peptidoglycan recognition proteins (PGRPs). Here, we demonstrate that human recombinant PGLYRP1/Tag-7/PGRP-S potentiates the response of murine macrophage-like ANA-1 cells and human macrophages to facultative intracellular pathogen Listeria monocytogenes. PGLYRP1/Tag-7/PGRP-S binds to the surface of L. monocytogenes and other bacterial cells but has no effect on their growth in culture. While PGLYRP1/Tag-7/PGRP-S treatment modestly enhanced phagocytosis of bacteria by ANA-1 cells, the intracellular survival of PGLYRP1/Tag-7/PGRP-S treated L. monocytogenes was strongly inhibited 2 h after internalization. PGLYRP1/Tag-7/PGRP-S treatment of bacteria boosted oxidative burst induction and increased the level of proinflammatory cytokine IL-6 produced by ANA-1, however, these effects happened too late to be responsible for decreased intracellular survival of bacteria. Our results thus suggest that PGLYRP1/Tag-7/PGRP-S acts as a molecular sensor for detection of L. monocytogenes infection of mammalian cells that leads to increased killing through a mechanism(s) that remains to be defined.Entities:
Keywords: Listeria monocytogenes; PGLYRP1 protein; Tag-7; innate immunity; peptidoglycan recognition protein; peptidoglycan recognition protein-S; phagocytosis
Year: 2020 PMID: 33425777 PMCID: PMC7785527 DOI: 10.3389/fcimb.2020.582803
Source DB: PubMed Journal: Front Cell Infect Microbiol ISSN: 2235-2988 Impact factor: 5.293