| Autor: |
Sidak-Loftis LC; Program in Vector-borne Disease, Department of Veterinary Microbiology and Pathology, Washington State Universitygrid.30064.31, Pullman, Washington, USA., Rosche KL; Program in Vector-borne Disease, Department of Veterinary Microbiology and Pathology, Washington State Universitygrid.30064.31, Pullman, Washington, USA., Pence N; Institute of Biological Chemistry, Washington State Universitygrid.30064.31, Pullman, Washington, USA., Ujczo JK; United States Department of Agriculture, Agricultural Research Service, Animal Disease Research Unit, Pullman, Washington, USA., Hurtado J; Program in Vector-borne Disease, Department of Veterinary Microbiology and Pathology, Washington State Universitygrid.30064.31, Pullman, Washington, USA.; School of Molecular Biosciences, Washington State Universitygrid.30064.31, Pullman, Washington, USA., Fisk EA; Program in Vector-borne Disease, Department of Veterinary Microbiology and Pathology, Washington State Universitygrid.30064.31, Pullman, Washington, USA., Goodman AG; School of Molecular Biosciences, Washington State Universitygrid.30064.31, Pullman, Washington, USA., Noh SM; Program in Vector-borne Disease, Department of Veterinary Microbiology and Pathology, Washington State Universitygrid.30064.31, Pullman, Washington, USA.; United States Department of Agriculture, Agricultural Research Service, Animal Disease Research Unit, Pullman, Washington, USA., Peters JW; Institute of Biological Chemistry, Washington State Universitygrid.30064.31, Pullman, Washington, USA., Shaw DK; Program in Vector-borne Disease, Department of Veterinary Microbiology and Pathology, Washington State Universitygrid.30064.31, Pullman, Washington, USA.; School of Molecular Biosciences, Washington State Universitygrid.30064.31, Pullman, Washington, USA. |
| Abstrakt: |
The insect immune deficiency (IMD) pathway is a defense mechanism that senses and responds to Gram-negative bacteria. Ticks lack genes encoding upstream components that initiate the IMD pathway. Despite this deficiency, core signaling molecules are present and functionally restrict tick-borne pathogens. The molecular events preceding activation remain undefined. Here, we show that the unfolded-protein response (UPR) initiates the IMD network. The endoplasmic reticulum (ER) stress receptor IRE1α is phosphorylated in response to tick-borne bacteria but does not splice the mRNA encoding XBP1. Instead, through protein modeling and reciprocal pulldowns, we show that Ixodes IRE1α complexes with TRAF2. Disrupting IRE1α-TRAF2 signaling blocks IMD pathway activation and diminishes the production of reactive oxygen species. Through in vitro , in vivo , and ex vivo techniques, we demonstrate that the UPR-IMD pathway circuitry limits the Lyme disease-causing spirochete Borrelia burgdorferi and the rickettsial agents Anaplasma phagocytophilum and A. marginale (anaplasmosis). Altogether, our study uncovers a novel linkage between the UPR and the IMD pathway in arthropods. IMPORTANCE The ability of an arthropod to harbor and transmit pathogens is termed "vector competency." Many factors influence vector competency, including how arthropod immune processes respond to the microbe. Divergences in innate immunity between arthropods are increasingly being reported. For instance, although ticks lack genes encoding key upstream molecules of the immune deficiency (IMD) pathway, it is still functional and restricts causative agents of Lyme disease (Borrelia burgdorferi) and anaplasmosis (Anaplasma phagocytophilum). How the IMD pathway is activated in ticks without classically defined pathway initiators is not known. Here, we found that a cellular stress response network, the unfolded-protein response (UPR), functions upstream to induce the IMD pathway and restrict transmissible pathogens. Collectively, this explains how the IMD pathway can be activated in the absence of canonical pathway initiators. Given that the UPR is highly conserved, UPR-initiated immunity may be a fundamental principle impacting vector competency across arthropods. |
