ReviewCrop health2025
Cellular plasticity and transcriptional reprogramming in plant-nematode interactions: insights into feeding site formation and plant defense.
Review in Crop health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Plant-parasitic nematodes, especially sedentary endoparasites, threaten global agriculture by inducing cellular plasticity in host plants to form specialized feeding structures. Sedentary nematodes such as root-knot and cyst nematodes establish feeding sites, including giant cells and syncytia, to extract nutrients from the host. Feeding site formation involves complex biological processes, including cell cycle activation, metabolic reprogramming, cytoskeleton rearrangement, and hormonal signaling. This review explores the underlying molecular mechanism driving plant cellular plasticity, focusing on the role of the transcription factors that regulate gene expression during organogenesis, peculiar to giant cells and syncytia, essential for the nematode's sustenance during the sedentary life stage. Key transcription factors, including members of the MYB, WRKY, ARF, ERF, and LBD families, are modulated by nematode effectors during compatible interactions to reprogram plant gene expression to facilitate the development of the nematode feeding site. Despite the roles of transcription factors in establishing feeding sites, they present other roles in regulating plant defense responses, thereby balancing growth reprogramming with the activation of plant immune signaling pathways. The review also highlights the allowance limit of plant physiological processes during cellular reprogramming and defense response, providing insights into how certain plants can resist nematode infection. Furthermore, emerging biotechnological strategies, including molecular breeding and gene editing, are discussed as potential approaches to disrupt nematode-induced reprogramming, highlighting novel avenues for enhancing crop resistance. Understanding the molecular mechanism and physiological dynamics between cellular plasticity and transcriptional regulation in plant-nematode interactions is essential for developing sustainable solutions to mitigate the impact of plant-parasitic nematodes on agricultural production.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.