Mason Rugen-Hankey, Priya Desikan, George Harpum, Chongjing Xia, Victor Hugo Moura de Souza, Unnati Sonawala, Lida Derevnina, Beth Molloy, Anika Damm, Sebastian Eves-van den Akker
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{"title":"Better Late than Never: The Impact of Hatching Time on <i>Heterodera schachtii</i> Parasitism.","authors":"Mason Rugen-Hankey, Priya Desikan, George Harpum, Chongjing Xia, Victor Hugo Moura de Souza, Unnati Sonawala, Lida Derevnina, Beth Molloy, Anika Damm, Sebastian Eves-van den Akker","doi":"10.1094/MPMI-06-26-0057-R","DOIUrl":null,"url":null,"abstract":"<p><p>Plant-parasitic nematodes are a diverse group collectively capable of infecting most major crops. Among the most damaging are the cyst nematodes, which can remain dormant in the soil for decades as infection-competent, developmentally arrested, second-stage juveniles in eggs. Hatching is stimulated by a variety of factors. However, the impact of hatching factor responsiveness on nematode morphology, physiology, gene expression, and infection biology has not been explored. We examined the impact of hatching time on the beet cyst nematode, <i>Heterodera schachtii</i>. We found that late hatchers invaded host roots and established feeding sites in greater numbers than early hatchers. We demonstrate variation in baseline parasitism gene expression and in responsiveness of genes to effectostimulins-small, plant-derived molecules that upregulate parasitism genes. Three quarters of effectostimulin-induced transcriptional changes were also modulated, either positively or negatively, by hatching time. Although there were no observable morphological differences between early- and late-hatching nematodes on their day of hatching, the late hatchers displayed signs of faster utilization of internal energy reserves after 7 days at 4°C, as evidenced by less body area attributed to fat, than early hatchers. Finally, we found no evidence of substantive genetic differences between early and late hatchers-they were representative of a single population, despite the observed differences in infection, gene expression, and physiology. Taken together, nongenetic differences likely drive late hatchers to more rapidly utilize their internal energy reserves, to be differentially responsive to host-derived signals, and to be ultimately more infective than their early-hatching counterparts. [Formula: see text] Copyright © 2026 The Author(s). This is an open access article distributed under the CC BY 4.0 International license.</p>","PeriodicalId":19009,"journal":{"name":"Molecular Plant-microbe Interactions","volume":" ","pages":"MPMI06260057R"},"PeriodicalIF":3.9000,"publicationDate":"2026-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Plant-microbe Interactions","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1094/MPMI-06-26-0057-R","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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Abstract
Plant-parasitic nematodes are a diverse group collectively capable of infecting most major crops. Among the most damaging are the cyst nematodes, which can remain dormant in the soil for decades as infection-competent, developmentally arrested, second-stage juveniles in eggs. Hatching is stimulated by a variety of factors. However, the impact of hatching factor responsiveness on nematode morphology, physiology, gene expression, and infection biology has not been explored. We examined the impact of hatching time on the beet cyst nematode, Heterodera schachtii . We found that late hatchers invaded host roots and established feeding sites in greater numbers than early hatchers. We demonstrate variation in baseline parasitism gene expression and in responsiveness of genes to effectostimulins-small, plant-derived molecules that upregulate parasitism genes. Three quarters of effectostimulin-induced transcriptional changes were also modulated, either positively or negatively, by hatching time. Although there were no observable morphological differences between early- and late-hatching nematodes on their day of hatching, the late hatchers displayed signs of faster utilization of internal energy reserves after 7 days at 4°C, as evidenced by less body area attributed to fat, than early hatchers. Finally, we found no evidence of substantive genetic differences between early and late hatchers-they were representative of a single population, despite the observed differences in infection, gene expression, and physiology. Taken together, nongenetic differences likely drive late hatchers to more rapidly utilize their internal energy reserves, to be differentially responsive to host-derived signals, and to be ultimately more infective than their early-hatching counterparts. [Formula: see text] Copyright © 2026 The Author(s). This is an open access article distributed under the CC BY 4.0 International license.