The study reveals that a conserved clade of pentatricopeptide repeat (PPR) genes in Arabidopsis thaliana generates secondary siRNAs that contribute to plant immunity, with these PPR loci undergoing extensive duplication and diversification to create a varied siRNA pool for pathogen defense. This PPR‑siRNA system is proposed as a novel family of defense genes with potential for engineering broad‑spectrum disease resistance.

The study visualizes subcellular dynamics following activation of the NRC4 resistosome, showing that NRC4 enrichment at the plasma membrane triggers calcium influx, followed by sequential disruption of mitochondria, plastids, endoplasmic reticulum, and cytoskeleton, culminating in plasma membrane rupture and cell death. These observations define a temporally ordered cascade of organelle and membrane events that execute plant immune cell death.

The study used proximity labeling, co‑immunoprecipitation, and fluorescence microscopy to dissect the protein components and pathways governing distinct extracellular vesicle (EV) subpopulations in Arabidopsis, identifying roles for EXO70 exocyst subunits, RIN4, and VAP27. Mutant analyses revealed that disruptions in exo70 family genes, rin4, rabA2a, scd1, and vap27 reduce EV secretion and increase susceptibility to the fungal pathogen Colletotrichum higginsianum, highlighting EV secretion as a key facet of plant immunity.

The study combined spatial transcriptomics and single-nuclei RNA sequencing to map soybean (Glycine max) responses to Asian soybean rust caused by Phakopsora pachyrhizi, revealing two distinct host cell states: pathogen‑occupied regions and adjacent non‑infected regions that show heightened defense gene expression. Gene co‑expression network analysis identified a key immune‑related module active in the stressed cells, highlighting a cell‑non‑autonomous defense mechanism.

The study investigates the conserved EDVID motif in the coiled‑coil domain of plant CC‑NLR immune receptors, revealing its role as a predictor of canonical CC‑NLR function and oligomeric assembly. It identifies a preceding acidic “preEDVID” motif in certain Arabidopsis‑related CC‑NLRs and shows that loss of the EDVID motif defines a distinct NLR subgroup, while acidic residues in the helper NLR NRG1.1 are crucial for cell‑death activity.

The study identifies the RNA‑binding protein AtG3BP1 as a phosphorylation target of MAPKs MPK3, MPK4, and MPK6 at Ser257 in Arabidopsis thaliana and shows that this modification promotes susceptibility to bacterial pathogens, suppresses ROS accumulation and salicylic acid biosynthesis, and maintains stomatal opening. Phospho‑mimic and phospho‑dead mutants reveal that phosphorylation stabilizes AtG3BP1 by preventing proteasomal degradation, highlighting a novel post‑translational control layer in plant immunity.

The study reveals that Arabidopsis actin depolymerization factors (ADF2/3/4) have a nuclear moonlighting role, directly interacting with WRKY transcription factors to regulate immune‑related gene expression. Nuclear, rather than cytosolic, ADFs are essential for defense against both virulent and avirulent Pseudomonas syringae, highlighting a non‑canonical mechanism linking actin dynamics to transcriptional control in plant immunity.

The study shows that the SnRK1 catalytic subunit KIN10 directs tissue-specific growth‑defense programs in Arabidopsis thaliana by reshaping transcriptomes. kin10 knockout mutants exhibit altered root transcription, reduced root growth, and weakened defense against Pseudomonas syringae, whereas KIN10 overexpression activates shoot defense pathways, increasing ROS and salicylic acid signaling at the cost of growth.

The study examines how the SnRK1 catalytic subunit KIN10 integrates carbon availability with root growth regulation in Arabidopsis thaliana. Loss of KIN10 reduces glucose‑induced inhibition of root elongation and triggers widespread transcriptional reprogramming of metabolic and hormonal pathways, notably affecting auxin and jasmonate signaling under sucrose supplementation. These findings highlight KIN10 as a central hub linking energy status to developmental and environmental cues in roots.

The study shows that the ERF transcription factor PTI5, previously identified as a susceptibility factor, is strongly induced during Bacillus subtilis biofilm establishment on potato roots and modulates ethylene‑dependent immune signaling. Silencing PTI5 enhances bacterial abundance and increases colonization by the arbuscular mycorrhizal fungus Rhizophagus irregularis, indicating PTI5 restricts both pathogenic and beneficial microbial interactions. These findings provide mechanistic insight for managing beneficial plant‑microbe relationships in crops.