Transcriptional modification of host cells harboring Toxoplasma gondii bradyzoites prevents IFN gamma-mediated cell death
Details
Publication Year 2021-12-16,Volume 30,Issue #2,Page 232-247e6
Journal Title
Cell Host & Microbe
Abstract
Toxoplasma gondii develops a latent infection in the muscle and central nervous system that acts as a reservoir for acute-stage reactivation in vulnerable patients. Little is understood about how parasites manipulate host cells during latent infection and the impact this has on survival. We show that bradyzoites impart a unique transcriptional signature on infected host cells. Many of these transcriptional changes rely on protein export and result in the suppression of type I interferon (IFN) and IFNγ signaling more so than in acute stages. Loss of the protein export component, MYR1, abrogates transcriptional remodeling and prevents suppression of IFN signaling. Among the exported proteins, the inhibitor of STAT1 transcription (IST) plays a key role in limiting IFNγ signaling in bradyzoites. Furthermore, bradyzoite protein export protects host cells from IFNγ-mediated cell death, even when export is restricted to latent stages. These findings highlight the functional importance of host manipulation in Toxoplasma's bradyzoite stages.
Publisher
Cell Press
Keywords
Apicomplexa; Myc-regulation 1 (MYR1); Toxoplasma gondii; bradyzoites; cell death; interferon; latent infection; pathogen effector proteins; protein export
Research Division(s)
Bioinformatics; Advanced Technology And Biology; Infectious Diseases And Immune Defence
PubMed ID
34921775
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2022-03-04 01:43:21
Last Modified: 2022-03-04 02:01:22
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