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Kelley, B. R.

Publications and source records attributed to Kelley, B. R..

2 recordsLinked to original sources

A beneficial bacteria influences myo-inositol homeostasis to protect plants during drought

Exposure to abiotic stress is one of the primary factors limiting crop productivity with drought stress is the most prevalent. Under drought, plants can produce osmolytes that increase water retention and prevent severe drought symptoms. Plant responses by extension also impact their associated root microbiomes through altered root metabolite concentrations and exudation. For example, myo-inositol (MI) serves as a precursor to osmolytes and also serves as a mediator for plant-microbe interactions in Arabidopsis thaliana (Arabidopsis). Here, we inoculated plants with Pantoea sp. R4 (R4), an isolate that can catabolize MI, and subjected them to drought. We observed that R4 colonized plants experiencing drought maintained their leaf relative water content while uninoculated planted did not, and that this colonization coincided with enrichment of MI in the shoots and depletion of MI in the roots. Interestingly, exogenous MI alone rescued water retention in wild-type Col-0, but not in int1 mutants, which lack the tonoplast MI transporter. Together, our results show that R4 colonization under drought conditions increases MI in the shoots, that this accumulation is associated with increased leaf water retention, and that INT1-mediated MI transport is required for this protection. Our results suggest that microbial colonization can alter how MI is localized in plants, which can inform future development of treatments to protect plants from drought.

microbiology↗

Plant inositol transport influences bacterial colonization phenotypes

Plant microbiomes are assembled and modified through a complex milieu of biotic and abiotic factors. Despite dynamic and fluctuating contributing variables, specific host metabolites are consistently identified as important mediators of microbial interactions. We combine information from a large-scale metatranscriptomic dataset from natural poplar trees and experimental genetic manipulation assays in model Arabidopsis seedlings to converge on a conserved role for transport of the plant metabolite myo-inositol in mediating host-microbe interactions. While microbial catabolism of this compound is often linked to increased host colonization, we identify motility phenotypes that occur independently of catabolism, suggesting that inositol may additionally serve as a eukaryotic-derived signaling molecule to modulate microbial activities. Our data suggests host control of this compound and resulting microbial behavior are important mechanisms at play surrounding the host metabolite inositol.

microbiology↗