ReviewHorticulture research2014
Elucidating the molecular responses of apple rootstock resistant to ARD pathogens: challenges and opportunities for development of genomics-assisted breeding tools.
Review in Horticulture research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.
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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.
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Who cites it
22 citing papers in PubMed, 62 citations in OpenAlex.
- Intercropping between persimmon and apple enriched the leaf endophytes and rhizosphere communities against apple root rot.BMC plant biology · 2025Article
- Engineering saline-alkali-tolerant apple rootstock by knocking down MdGH3 genes in M9-T337.Stress biology · 2025Article
- The MdERF61-mdm-miR397b-MdLAC7b module regulates apple resistance to Fusarium solani via lignin biosynthesis.Plant physiology · 2024Article
- Biphenyls and dibenzofurans of the rosaceous subtribe Malinae and their role as phytoalexins.Planta · 2023Review
- MdERF114 enhances the resistance of apple roots to Fusarium solani by regulating the transcription of MdPRX63.Plant physiology · 2023Article
- Deciphering the Mechanism of Tolerance to Apple Replant Disease Using a Genetic Mapping Approach in a Malling 9 ×International journal of molecular sciences · 2023Article
- Comprehensive transcriptome analysis of different potato cultivars provides insight into early blight disease caused by Alternaria solani.BMC plant biology · 2023Article
- Article
- Inter-row cropping and rootstock genotype selection in a UK cider orchard to combat apple replant disease.Phytopathology research · 2023Article
- Article
- Transcriptome changes associated with apple (Malus domestica) root defense response after Fusarium proliferatum f. sp. malus domestica infection.BMC genomics · 2022Article
- Identification of Candidate Genes Associated With Tolerance to Apple Replant Disease by Genome-Wide Transcriptome Analysis.Frontiers in microbiology · 2022Article
- Evolutions and Managements of Soil Microbial Community Structure Drove by Continuous Cropping.Frontiers in microbiology · 2022Review
- Comprehensive Analysis of the Influence of Fulvic Acid from Paper Mill Effluent on Soil Properties, Soil Microbiome, and Growth ofACS omega · 2021Article
- Production of Siderophores by an Apple Root-AssociatedMolecules (Basel, Switzerland) · 2021Article
- Laccase Directed Lignification Is One of the Major Processes Associated With the Defense Response AgainstFrontiers in plant science · 2021Article
- A systematic analysis of apple root resistance traits toHorticulture research · 2020Review
- Root system traits impact early fire blight susceptibility in apple (Malus × domestica).BMC plant biology · 2019Article
- Genes Involved in Stress Response and Especially in Phytoalexin Biosynthesis Are Upregulated in FourFrontiers in plant science · 2019Article
- Targeted Metabolic Profiling Indicates Apple Rootstock Genotype-Specific Differences in Primary and Secondary Metabolite Production and Validate Quantitative Contribution From Vegetative Growth.Frontiers in plant science · 2018Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Apple replant disease (ARD) is a major limitation to the establishment of economically viable orchards on replant sites due to the buildup and long-term survival of pathogen inoculum. Several soilborne necrotrophic fungi and oomycetes are primarily responsible for ARD, and symptoms range from serious inhibition of growth to the death of young trees. Chemical fumigation has been the primary method used for control of ARD, and manipulating soil microbial ecology to reduce pathogen density and aggressiveness is being investigated. To date, innate resistance of apple rootstocks as a means to control this disease has not been carefully explored, partly due to the complex etiology and the difficulty in phenotyping the disease resistance. Molecular defense responses of plant roots to soilborne necrotrophic pathogens are largely elusive, although considerable progress has been achieved using foliar disease systems. Plant defense responses to necrotrophic pathogens consist of several interacting modules and operate as a network. Upon pathogen detection by plants, cellular signals such as the oscillation of Ca(2+) concentration, reactive oxygen species (ROS) burst and protein kinase activity, lead to plant hormone biosynthesis and signaling. Jasmonic acid (JA) and ethylene (ET) are known to be fundamental to the induction and regulation of defense mechanisms toward invading necrotrophic pathogens. Complicated hormone crosstalk modulates the fine-tuning of transcriptional reprogramming and metabolic redirection, resulting in production of antimicrobial metabolites, enzyme inhibitors and cell wall refortification to restrict further pathogenesis. Transcriptome profiling of apple roots in response to inoculation with Pythium ultimum demonstrated that there is a high degree of conservation regarding the molecular framework of defense responses compared with those observed with foliar tissues. It is conceivable that the timing and intensity of genotype-specific defense responses may lead to different outcomes between rootstocks in response to invasion by necrotrophic pathogens. Elucidation of host defense mechanisms is critical in developing molecular tools for genomics-assisted breeding of resistant apple rootstocks. Due to their perennial nature, use of resistant rootstocks as a component for disease management might offer a durable and cost-effective benefit to tree performance than the standard practice of soil fumigation for control of ARD.
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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.