| Literature DB >> 31291567 |
Iara Rocchi1, Charles F Ericson2, Kyle E Malter3, Sahar Zargar4, Fabian Eisenstein5, Martin Pilhofer5, Sinem Beyhan6, Nicholas J Shikuma7.
Abstract
Many bacteria interact with target organisms using syringe-like structures called contractile injection systems (CISs). CISs structurally resemble headless bacteriophages and share evolutionarily related proteins such as the tail tube, sheath, and baseplate complex. In many cases, CISs mediate trans-kingdom interactions between bacteria and eukaryotes by delivering effectors to target cells. However, the specific effectors and their modes of action are often unknown. Here, we establish an ex vivo model to study an extracellular CIS (eCIS) called metamorphosis-associated contractile structures (MACs) that target eukaryotic cells. MACs kill two eukaryotic cell lines, fall armyworm Sf9 cells and J774A.1 murine macrophage cells, by translocating an effector termed Pne1. Before the identification of Pne1, no CIS effector exhibiting nuclease activity against eukaryotic cells had been described. Our results define a new mechanism of CIS-mediated bacteria-eukaryote interaction and are a step toward developing CISs as novel delivery systems for eukaryotic hosts.Entities:
Keywords: CIS; MACs; T6SS; cell line; effector; phage; secretion system
Year: 2019 PMID: 31291567 DOI: 10.1016/j.celrep.2019.06.019
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423