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Biology subjects

Pulido, H.

Publications and source records attributed to Pulido, H..

2 recordsLinked to original sources

Ecological context unmasks cryptic effects of glyphosate tolerance on soybean metabolism and performance of the virus vector Epilachna varivestis

O_LIGlyphosate-tolerant Roundup Ready (RR) soybean, engineered with the CP4 EPSPS gene, is one of the worlds most widely cultivated GM crops, yet its ecological consequences under realistic multi-species biotic conditions remain poorly understood. We investigated how RR soybean and its near-isogenic non-GM counterpart respond to concurrent colonization by two rhizobacteria, Bradyrhizobium japonicum and Delftia acidovorans, infection by Bean pod mottle virus (BPMV), and feeding by the virus vector Epilachna varivestis. C_LIO_LIUsing a fully factorial multi-species design, we combined LC-MS/GC-MS metabolomics, weighted co-expression network analysis (WGCNA), and herbivore performance bioassays to assess genotype-dependent shifts in soybean metabolism and their consequences for herbivore performance. C_LIO_LIUnder baseline conditions, RR and non-GM plants were metabolically indistinguishable. Under concurrent microbial and viral stress, RR plants diverged markedly, prioritizing selective isoflavonoid accumulation and lipid remodeling over broad-spectrum defenses, and showing attenuated rhizobacteria-mediated benefits for herbivore survival. These genotype-specific effects were entirely absent in single-species treatments. C_LIO_LITransgene effects on soybean metabolism and tritrophic interactions are cryptic under simplified experimental conditions but emerge clearly under ecologically realistic multi-species stress, with direct implications for how GM crops are evaluated in agricultural and regulatory contexts. C_LI

ecology↗

Beneficial rhizobacteria and virus infection modulate the soybean metabolome and influence the feeding preferences of the virus vector Epilachna varivestis.

There is growing evidence that microbial plant symbionts shape interactions between plants and other organisms by modulating gene expression and metabolism. However, the detailed mechanisms mediating such effects are not well understood, particularly in systems where plants interact simultaneously with multiple symbionts and antagonists. In this study, we employed a multi-factorial design to explore the individual and combined effects of two plant-beneficial rhizobacteria (Delftia acidovorans and Bradyrhizobium japonicum) and a pathogen (Bean pod mottle virus: BPMV) on gene expression and metabolite production by soybean plants, as well as downstream effects on plant interactions with a beetle vector of BPMV Epilachna varivestis. Our results document microbial effects on basic metabolism and defense pathways, resulting in increased levels of primary metabolites and depletion of secondary metabolites. These changes are consistent with the observed feeding preferences of beetles for rhizobia-inoculated and virus-infected plants. Together, our results indicate that BPMV infection and rhizobacteria colonization cause dramatic changes in plant metabolites related to nutrition and defense, with significant consequences for an agriculturally important pathosystem.

ecology↗