# Early upregulation of immune suppressors dominates the macrophage response to Toxoplasma gondii

## TL;DR

This study reveals how macrophages and Toxoplasma gondii interact at the start of infection, showing early immune suppression and parasite strategy.

## Contribution

The study identifies early transcriptional responses in macrophages and T. gondii during initial infection using time-resolved transcriptomics.

## Key findings

- Macrophages rapidly upregulate suppressors of cytokine signaling in response to live T. gondii infection.
- Toxoplasma gondii shows a delayed activation of secreted proteins after an initial increase in transcription and growth capacity.
- The interaction involves a transcriptional tug-of-war between host immune responses and parasite strategies.

## Abstract

The apicomplexan parasite Toxoplasma gondii is a master manipulator, subverting its host through secreted proteins, hormone disruption, and even behavioural changes. Macrophages, the immune system’s first responders, play a pivotal role in determining infection outcomes, yet the initial triggers shaping these complex responses remain elusive. This study unveils the earliest transcriptional shifts in a mouse macrophage-like cell line RAW264.7-T. gondii infection model. Using time-resolved transcriptomic profiling, we captured host and parasite gene expression dynamics within the critical 15–120 minute window — when the host mounts its first line of defence and the parasite secures its foothold. By leveraging inactivated parasites, we disentangled responses to active invasion from general immune activation. By 60 minutes, macrophages exhibited a trend of increased suppressor of cytokine signalling expression — uniquely tied to live infection — while stress and pro-growth genes became dysregulated. Meanwhile, T. gondii responded with a slow but strategic transcriptional shift: an early increase in transcription and growth capacity, followed by a delayed activation of secreted proteins. These findings reveal a tug-of-war at the transcriptional level, where macrophages show rapid upregulation, while T. gondii employs a measured, delayed strategy to carve out its replicative niche.