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Hearn, C. T.

Publications and source records attributed to Hearn, C. T..

2 recordsLinked to original sources

Thiol depletion and disruption of proteostasis contribute to the phytotoxicity of juglone

O_LIJuglone is the phytotoxic 1,4-naphthoquinone responsible for the allelopathic effects of black walnut (Juglans nigra), yet how plants perceive and respond to juglone remain poorly understood. C_LIO_LIWe conducted transcriptome profiling of rosettes and roots of Arabidopsis thaliana exposed to juglone from 30 min to 5 d, along with targeted metabolic profiling, biochemical assays, and untargeted proteomics to gain a systems-level understanding of how plants respond to juglone and to test hypotheses underlying its phytotoxicity. C_LIO_LIJuglone exposure induced expression of genes involved in glutathione, cysteine, and sulfur metabolism pathways, and in protein homeostasis. We found that juglone depletes the pool of reduced glutathione (GSH) in roots, in part, through conjugation. We demonstrate that via upregulation of transcription factors (NAC53 and NAC78), the response to juglone activates components of the proteasome stress regulon and triggers extensive proteome remodeling with engagement of the autophagy pathway when proteasome capacity is limited. C_LIO_LIOur findings (i) indicate that thiol depletion and disruption of proteostasis through juglones dual redox cycling and alkylation activities are central to its phytotoxicity, (ii) cast doubt on previous reports that juglone targets a specific enzyme in plants or other organisms, and (iii) provide insight into how the chemical properties of allelopathic quinones shape their ecological roles. C_LI

plant biology↗

Microbial partners drive legume trait plasticity and tripartite interaction outcomes under combined stress environments

Plants often form partnerships with symbiotic microbes that improve plant performance. Increasing environmental stress is changing interaction dynamics between plants and their below-ground symbiotic partners, which can have cascading effects on above-ground trophic interactions. However, little work has examined how microbes protect plants against multiple stressors acting in concert, or the extent to which microbial genetic variation shapes context-dependent outcomes of tripartite interactions between microbes, plants, and herbivores. We experimentally manipulated the genetics of symbiotic microbial partners by individually inoculating a single legume species (Glycine max) with twenty-four genetically distinct strains of rhizobial bacteria. We quantified insect herbivore feeding and growth rates, as well as plant ecophysiological and performance traits under different combinations of drought and herbivore exposure. Rhizobial strains differentially influenced the effect of drought on legume ecophysiological traits. Certain strains increased photosynthesis and enhanced photoprotection under drought. Moreover, legumes under drought and herbivore exposure also exhibited increased photoprotection. Some strains were observed to limit herbivore growth rates under drought more effectively than others. A multivariate trait analysis revealed that strains differentially influenced legume trait syndromes and plasticity in response to stress in certain environments. Rhizobial strain variation was a key driver of tripartite interactions through changes in plant trait expression and plasticity under simultaneous abiotic and biotic stress, which had cascading effects on insect herbivore growth. A community approach incorporating multiple beneficial microbial strains may be effective for managing legume-rhizobia symbioses and introducing functional trait diversity and resistance traits into ecosystems.

ecology↗