, a plant root-colonizing basidiomycete fungus, exhibits strong growth-promoting activity in symbiosis with a broad range of plants. Here, we report the potential of to improve growth, yield, and disease resistance in wheat in the field. In the present study, successfully colonized wheat through chlamydospores and formed dense mycelial networks that covered roots. Plants subjected to the seed soaking (SS) treatment with chlamydospore suspensions enhanced tillering 2.28-fold compared to the non-inoculated wheat in the tillering stage. In addition, colonization promoted vegetative growth significantly during the three-leaf, tillering, and jointing stages. Moreover, the -SS-treatment enhanced wheat yield by 16.37 ± 1.63%, by increasing grains per ear and panicle weight and decreased damage to wheat shoot and root architecture markedly, with high field control effects against (81.59 ± 1.32%), (82.19 ± 1.59%), and (75.98 ± 1.36%). Most of the primary metabolites, such as amino acids, nucleotides, and lipids, involved in vegetative reproduction were increased in -SS-treatment plants, whereas secondary metabolites, such as terpenoids, polyketides, and alkaloids, decreased following inoculation. The up-regulated processes of protein, carbohydrate, and lipid metabolism indicated that colonization increased growth, yield, and disease resistance via the acceleration of plant primary metabolism. In conclusion, improved morphological, physiological, and metabolic substance levels, and further promoted its growth, yield, and disease resistance in wheat.
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http://dx.doi.org/10.1080/15592324.2023.2213934 | DOI Listing |
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S Dehm, Masonic Cancer Center, University of Minnesota, Minneapolis, United States.
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Christian Medical College, Vellore, Tamil Nadu, India.
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January 2025
ICAR-National Institute for Plant Biotechnology, New Delhi, 110012, Delhi, India.
Small RNA sequencing analysis in two chickpea genotypes, JG 62 (Fusarium wilt-susceptible) and WR 315 (Fusarium wilt-resistant), under Fusarium wilt stress led to identification of 544 miRNAs which included 406 known and 138 novel miRNAs. A total of 115 miRNAs showed differential expression in both the genotypes across different combinations. A miRNA, Car-miR398 targeted copper chaperone for superoxide dismutase (CCS) that, in turn, regulated superoxide dismutase (SOD) activity during chickpea-Foc interaction.
View Article and Find Full Text PDFClin Rev Allergy Immunol
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Division of Allergy and Clinical Immunology, The Johns Hopkins Asthma & Allergy Center, Johns Hopkins University School of Medicine, 5501 Hopkins Bayview Circle, Room 3B.71, Baltimore, MD, 21224, USA.
Asthma is a chronic airway inflammatory disease that affects millions globally. Although glucocorticoids are a mainstay of asthma treatment, a subset of patients show resistance to these therapies, resulting in poor disease control and increased morbidity. The complex mechanisms underlying steroid-resistant asthma (SRA) involve Th1 and Th17 lymphocyte activity, neutrophil recruitment, and NLRP3 inflammasome activation.
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