Mapping host-microbe transcriptional interactions by dual perturb-seq

Intracellular pathogens and other endosymbionts reprogram host cell transcription to suppress immune responses and recalibrate biosynthetic pathways. This reprogramming is critical in determining the outcome of infection or colonisation. Here, we combine pooled CRISPR knockout screening with dual host–microbe single–cell RNA–sequencing to identify the molecular mediators of these transcriptional interactions, a method we term dual perturb–seq. Applying dual perturb–seq to the intracellular pathogen Toxoplasma gondii , we are able to identify previously uncharacterised effector proteins and directly infer their function from the transcriptomic data. We show that Tg GRA59 contributes to the export of other effector proteins from the parasite into the host cell and identify a novel effector, Tg SOS1, that is necessary for sustained host STAT6 signalling and thereby contributes to parasite immune evasion and persistence. Together, this work demonstrates a novel tool that can be broadly adapted to interrogate host–microbe transcriptional interactions and reveal mechanisms of infection and immune evasion. ### Competing Interest Statement The authors have declared no competing interest.