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Salicylic acid (SA) is an important phytohormone, well‐known for its regulatory role in shaping plant immune responses. In recent years, significant progress has been made in unravelling the molecular mechanisms underlying SA biosynthesis, perception, and downstream signalling cascades. Through the concerted efforts employing genetic, biochemical, and omics approaches, our understanding of SA‐mediated defence responses has undergone remarkable expansion. In general, following SA biosynthesis through Avr effectors of the pathogens, newly synthesized SA undergoes various biochemical changes to achieve its active/inactive forms (e.g. methyl salicylate). The activated SA subsequently triggers signalling pathways associated with the perception of pathogen‐derived signals, expression of defence genes, and induction of systemic acquired resistance (SAR) to tailor the intricate regulatory networks that coordinate plant immune responses. Nonetheless, the mechanistic understanding of SA‐mediated plant immune regulation is currently limited because of its crosstalk with other signalling networks, which makes understanding this hormone signalling more challenging. This comprehensive review aims to provide an integrated overview of SA‐mediated plant immunity, deriving current knowledge from diverse research outcomes. Through the integration of case studies, experimental evidence, and emerging trends, this review offers insights into the regulatory mechanisms governing SA‐mediated immunity and signalling. Additionally, this review discusses the potential applications of SA‐mediated defence strategies in crop improvement, disease management, and sustainable agricultural practices. [ABSTRACT FROM AUTHOR]

Plants constantly perceive and process environmental signals and balance between the energetic demands of growth and defense. Growth arrest upon pathogen attack was previously suggested to result from a redirection of the plants' metabolic resources towards the activation of plant defense. The energy sensor Target of Rapamycin (TOR) kinase is a conserved master coordinator of growth and development in all eukaryotes. Although TOR is positioned at the interface between development and defense, little is known about the mechanisms by which TOR may potentially regulate the relationship between these two modalities. The plant hormones cytokinin (CK) and gibberellin (GA) execute various aspects of plant development and defense. The ratio between CK and GA was reported to determine the outcome of developmental programmes. Here, investigating the interplay between TOR‐mediated development and TOR‐mediated defense in tomato, we found that TOR silencing resulted in rescue of several different aberrant developmental phenotypes, demonstrating that TOR is required for the execution of developmental cues. In parallel, TOR inhibition enhanced immunity in genotypes with a low CK/GA ratio but not in genotypes with a high CK/GA ratio. TOR‐inhibition mediated disease resistance was found to depend on developmental status, and was abolished in strongly morphogenetic leaves, while being strongest in mature, differentiated leaves. CK repressed TOR activity, suggesting that CK‐mediated immunity may rely on TOR downregulation. At the same time, TOR activity was promoted by GA, and TOR silencing reduced GA sensitivity, indicating that GA signalling requires normal TOR activity. Our results demonstrate that TOR likely acts in concert with CK and GA signalling, executing signalling cues in both defense and development. Thus, differential regulation of TOR or TOR‐mediated processes could regulate the required outcome of development‐defense prioritisation. Summary Statement: Target of Rapamycin (TOR) is positioned at the interface between development and defense, but little is known about the mechanisms by which TOR may regulate shifts between them. Here, we demonstrate that TOR likely acts in concert with cytokinin and gibberellin to execute signalling cues in both defense and development. [ABSTRACT FROM AUTHOR]

Developmental phytohormones regulate many physiological responses in plants, including growth and immunity in response to pathogens. Disease resistance mediated by developmental phytohormones such as cytokinin (CK), gibberellin (GA), and auxin (Aux), is the result of complex interactions between these phytohormones with the salicylic acid (SA)-jasmonate (JA)-ethylene (ET) backbone of immune signaling circuitry. Based on the available findings concerning phytohormone mediated plant resistance, this review attempts to develop the understanding of the defense roles of CKs, GAs, and Auxs, and their interplay with pathogen targeted defense hormones such as SA, JA and ET in plants, during biotic stress. Several phytohormone pathway genes and proteins have been reported to influence biotic stress resistance. In our analysis, we relate to specific roles uncovered for the Aux pathway TRANSPORT INHIBITOR RESISTANT 1 (TIR)/AUXIN SIGNALING F-BOX (AFB) and Gretchen Hagen 3 (GH3) proteins, the CK pathway isopentenyl transferase (IPT), CK oxidase (CKX), and Arabidopsis histidine kinase (AHK) proteins, and the GA pathway DELLA and GA20 oxidase proteins, in plant immunity and disease resistance. Additionally, we discuss microbial phytohormones that can enhance plant growth and resistance against pathogens, and the effect of phytohormones on modulation of the plant microbiome. Finally, we provide a concise overview of the possible approaches for modulating hormonal cross talk to improve plant health and resistance. [ABSTRACT FROM AUTHOR]

Background: The interaction of plants with the complex microbial networks that inhabit them is important for plant health. While the reliance of plants on their microbial inhabitants for defense against invading pathogens is well documented, the acquisition of data concerning the relationships between plant developmental stage or aging, and microbiome assembly, is still underway. The plant hormone cytokinin (CK) regulates various plant growth and developmental processes. Here, examining the relationships between plant development and microbiome assembly, we observed developmental-age dependent changes in the phyllopshere microbiome. We show that age-related shifts in microbiome content vary based on content of, or sensitivity to, CK. Results: We found a developmental age associated decline in microbial richness and diversity, accompanied by a decline in the presence of growth promoting and resistance inducing Bacilli in the phyllosphere. This decline was absent from CK-rich or CK-hypersensitive genotypes. Bacillus isolates we obtained from CK rich genotypes were found to alter the expression of developmental genes to support morphogenesis and alter the leaf developmental program when applied to seedlings, and enhance yield and agricultural productivity when applied to mature plants. Conclusions: Our results support the notion that CK supports developmental functions in part via the bacterial community. [ABSTRACT FROM AUTHOR]

Plant immunity is often defined by the immunity hormones: salicylic acid (SA), jasmonic acid (JA), and ethylene (ET). These hormones are well known for differentially regulating defence responses against pathogens. In recent years, the involvement of other plant growth hormones such as auxin, gibberellic acid, abscisic acid, and cytokinins (CKs) in biotic stresses has been recognized. Previous reports have indicated that endogenous and exogenous CK treatment can result in pathogen resistance. We show here that CK induces systemic immunity in tomato (Solanum lycopersicum), modulating cellular trafficking of the pattern recognition receptor (PRR) LeEIX2, which mediates immune responses to Xyn11 family xylanases, and promoting resistance to Botrytis cinerea and Oidium neolycopersici in an SA‐ and ET‐dependent mechanism. CK perception within the host underlies its protective effect. Our results support the notion that CK promotes pathogen resistance by inducing immunity in the host. [ABSTRACT FROM AUTHOR]

Plant hormones act as chemical messengers, transducing cellular and organ-level cues, executing plant growth, development, reproduction, metabolism, and response to environmental stress. In addition to the production of hormones by plants, fungi can also produce compounds that are similar to phytohormones, and may modulate growth, physiology, and immunity in both plants and fungi. The "classical" plant growth hormone, cytokinin (CK) is known to have roles in plant-fungi interactions. In plants, CKs are involved in various processes including plant growth and development, seed germination, apical dominance, balance between shoot and root tissue, leaf senescence, and plant-pathogen-interactions. We recently reported that CK can also affect fungal development. CK is not produced solely by plants, as can be synthesized by plant-associated microorganisms such as bacteria and fungi. Fungal phytopathogens may also activate plant CK signalling/sensing via secretion of effector molecules. Fungal CKs secreted by (hemi)biotrophic pathogens can serve as virulence factors, however, most necrotrophic fungal plant pathogens have not been reported to secrete CKs during plant infection. Though a lifestyle-dependent role for CK signalling/perception was suggested for fungal plant pathogens, little is known about CK perception, sensing, and signalling in fungal organisms. In this review, we focus on the production of fungal CKs and their role in development and virulence, as well as the possibilities for CK perception and signalling in the fungal kingdom, where CHASE-domain containing proteins are largely absent. [ABSTRACT FROM AUTHOR]

The plant hormone cytokinin (CK) plays central roles in plant development and throughout plant life. The perception of CKs initiating their signaling cascade is mediated by histidine kinase receptors (AHKs). Traditionally thought to be perceived mostly at the endoplasmic reticulum (ER) due to receptor localization, CK was recently reported to be perceived at the plasma membrane (PM), with CK and its AHK receptors being trafficked between the PM and the ER. Some of the downstream mechanisms CK employs to regulate developmental processes are unknown. A seminal report in this field demonstrated that CK regulates auxin-mediated lateral root organogenesis by regulating the endocytic recycling of the auxin carrier PIN1, but since then, few works have addressed this issue. Modulation of the cellular cytoskeleton and trafficking could potentially be a mechanism executing responses downstream of CK signaling. We recently reported that CK affects the trafficking of the pattern recognition receptor LeEIX2, influencing the resultant defense output. We have also recently found that CK affects cellular trafficking and the actin cytoskeleton in fungi. In this work, we take an in-depth look at the effects of CK on cellular trafficking and on the actin cytoskeleton in plant cells. We find that CK influences the actin cytoskeleton and endomembrane compartments, both in the context of defense signaling—where CK acts to amplify the signal—as well as in steady state. We show that CK affects the distribution of FLS2, increasing its presence in the plasma membrane. Furthermore, CK enhances the cellular response to flg22, and flg22 sensing activates the CK response. Our results are in agreement with what we previously reported for fungi, suggesting a fundamental role for CK in regulating cellular integrity and trafficking as a mechanism for controlling and executing CK-mediated processes. [ABSTRACT FROM AUTHOR]