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Guevarra, P.

Publications and source records attributed to Guevarra, P..

2 recordsLinked to original sources

A constitutively active cortical nitrate-uptake cell state underlies nitrogen-use efficiency in perennial ryegrass

Perennial ryegrass (Lolium perenne) is the most widely sown forage grass of temperate agriculture and a major sink for fertiliser nitrogen, yet the cellular basis of its nitrogen-use efficiency (NUE) is unknown. We built a single-nucleus atlas of 76,684 root nuclei from a high- and a low-NUE genotype under matched nitrogen resupply. High-affinity nitrate uptake is concentrated in one cortical cell state that co-expresses nine NRT2 transporters and all three NAR2 partner proteins, a state that whole-root RNA-seq of the same tissue cannot resolve. Under reduced nitrogen the low-NUE genotype induces this state, whereas the high-NUE genotype does not; it expresses NRT2.3 at a higher baseline and uses different NRT2 paralogs, with one array member nearly silent. Across 44 annual and perennial Pooideae genomes, the same gene families show no life-history difference in copy number, evolutionary rate or selection intensity. Their regulation, however, varies in the same direction as between the two genotypes: the perennial Brachypodium sylvaticum expresses the NRT2.3 ortholog at the level that the annual B. distachyon reaches only under nitrogen deprivation, and an N-efficient barley genotype does not induce the transporters that an N-sensitive genotype induces. NUE differences are therefore associated with constitutive versus inducible deployment of a conserved toolkit, and the expression and presence/absence variants we identify are candidate breeding markers. The atlas, the first for a forage grass, is released as an open web resource.

plant biology↗

An experimentally tractable Arabidopsis-Swede Midge model to explore host reprogramming by gall-inducing insects

Insect-induced galls are striking examples of host developmental reprogramming, yet their causal mechanisms remain poorly understood because few insect gall systems combine experimental tractability with precise control of insect and host developmental state. Here, we establish Arabidopsis thaliana and the gall-inducing Swede Midge (Contarinia nasturtii) as an experimental system for insect gall research. We show that the Swede Midge, a major pest of Brassica crops, completes its full life cycle on Arabidopsis, and induces characteristic inflorescence galls. To define and quantify galling while accounting for changes in developmental stage in both partners, we developed three complementary approaches. On the insect side, a larval phenotyping pipeline monitors how many larvae are present and how far they have developed, and a larval droplet assay delivers defined numbers of stage-selected larvae directly to host inflorescences, fixing the insect input and establishing a precise time zero for the interaction. We found that early-stage larvae can induce galls, whereas late-stage larvae (L3) cannot, defining the developmental window for gall induction. On the host side, we established a phyllotactic dissection and staging framework that enables galled and non-galled floral tissues to be compared at defined developmental positions. We found that galling enlarged floral buds, floral primordia and the inflorescence meristem while delaying floral developmental progression, with accompanying changes in cell size, shape and tissue organisation. Together, these tools combine Arabidopsis genetics with controlled insect manipulation, opening the way to mechanistic dissection of how insects reprogram plant pathways.

plant biology↗