A rare PRIMER cell state in plant immunity

成果类型:
Article
署名作者:
Nobori, Tatsuya; Monell, Alexander; Lee, Travis A.; Sakata, Yuka; Shirahama, Shoma; Zhou, Jingtian; Nery, Joseph R.; Mine, Akira; Ecker, Joseph R.
署名单位:
Salk Institute; Salk Institute; Howard Hughes Medical Institute; Salk Institute; University of California System; University of California San Diego; Kyoto University; University of East Anglia; UK Research & Innovation (UKRI); Biotechnology and Biological Sciences Research Council (BBSRC); John Innes Center
刊物名称:
Nature
ISSN/ISSBN:
0028-3251
DOI:
10.1038/s41586-024-08383-z
发表日期:
2025-02-01
页码:
197-+
关键词:
chromatin accessibility arabidopsis resistance identification avirulence receptors pathogen surface death
摘要:
Plants lack specialized and mobile immune cells. Consequently, any cell type that encounters pathogens must mount immune responses and communicate with surrounding cells for successful defence. However, the diversity, spatial organization and function of cellular immune states in pathogen-infected plants are poorly understood(1). Here we infect Arabidopsis thaliana leaves with bacterial pathogens that trigger or supress immune responses and integrate time-resolved single-cell transcriptomic, epigenomic and spatial transcriptomic data to identify cell states. We describe cell-state-specific gene-regulatory logic that involves transcription factors, putative cis-regulatory elements and target genes associated with disease and immunity. We show that a rare cell population emerges at the nexus of immune-active hotspots, which we designate as primary immune responder (PRIMER) cells. PRIMER cells have non-canonical immune signatures, exemplified by the expression and genome accessibility of a previously uncharacterized transcription factor, GT-3A, which contributes to plant immunity against bacterial pathogens. PRIMER cells are surrounded by another cell state (bystander) that activates genes for long-distance cell-to-cell immune signalling. Together, our findings suggest that interactions between these cell states propagate immune responses across the leaf. Our molecularly defined single-cell spatiotemporal atlas provides functional and regulatory insights into immune cell states in plants.