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Zahid, N.

Publications and source records attributed to Zahid, N..

2 recordsLinked to original sources

H+ drives ultra-fast root-to-root responses to wounding

The plant-to-plant communication of damage is vital for plants to mount pre-emptive defensive responses in the face of threats. A variety of threats to the well-being of plants are found below ground; yet how plant roots activate inter-plant communication is largely unclear. Here we demonstrate that a wounded root rapidly releases protons (H+), that travel faster than any other "known" soluble biochemical signal due to a specialised diffusion mechanism. Within seconds after damage, cells in neighbouring unwounded roots sense the acidification and activate tissue-specific Ca2+ damage signalling. In turn, this triggers a differential growth response allowing the unwounded root to avoid the site of a potential threat. Our results reveal a non-canonical rapid response mechanism for inter-plant communication based on ultrafast proton diffusion.

plant biology↗

The genome and lifestage-specific transcriptomes of a plant-parasitic nematode and its host reveal susceptibility genes involved in trans-kingdom synthesis of vitamin B.

Plant-parasitic nematodes are a major, and in some cases a dominant, threat to crop production in all agricultural systems. The relative scarcity of classical resistance genes highlights a pressing need to identify new ways to develop nematode-resistant germplasm. Here, we sequence and assemble a high-quality genome of the model cyst nematode Heterodera schachtii to provide a platform for the first system-wide dual analysis of host and parasite gene expression over time, covering all major stages of the interaction. This novel approach enabled the analysis of the hologenome of the infection site, to identify metabolic pathways that were incomplete in the parasite but complemented by the host. Using a combination of bioinformatic, genetic, and biochemical approaches, we show that the highly atypical completion of vitamin B5 biosynthesis by the parasitic animal, putatively enabled by a horizontal gene transfer from a bacterium, is critically important for parasitism. Knockout of either the plant-encoded or the now nematode-encoded steps in the pathway blocks parasitism. Our experiments establish a reference for cyst nematodes, use this platform to further our fundamental understanding of the evolution of plant-parasitism by nematodes, and show that understanding congruent differential expression of metabolic pathways represents a new way to find nematode susceptibility genes, and thereby, targets for future genome editing-mediated generation of nematode-resistant crops.

genetics↗