Fight Hard or Die Trying: Current Status of Lipid Signaling during Plant–Pathogen Interaction

Plant diseases pose a substantial threat to food availability, accessibility, and security as they account for economic losses of nearly $300 billion on a global scale. Although various strategies exist to reduce the impact of diseases, they can introduce harmful chemicals to the food chain and have an impact on the environment. Therefore, it is necessary to understand and exploit the plants’ immune systems to control the spread of pathogens and enable sustainable agriculture. Recently, growing pieces of evidence suggest a functional myriad of lipids to be involved in providing structural integrity, intracellular and extracellular signal transduction mediators to substantial cross-kingdom cell signaling at the host–pathogen interface. Furthermore, some pathogens recognize or exchange plant lipid-derived signals to identify an appropriate host or development, whereas others activate defense-related gene expression. Typically, the membrane serves as a reservoir of lipids. The set of lipids involved in plant–pathogen interaction includes fatty acids, oxylipins, phospholipids, glycolipids, glycerolipids, sphingolipids, and sterols. Overall, lipid signals influence plant–pathogen interactions at various levels ranging from the communication of virulence factors to the activation and implementation of host plant immune defenses. The current review aims to summarize the progress made in recent years regarding the involvement of lipids in plant–pathogen interaction and their crucial role in signal transduction.


Introduction
Plants are continuously exposed to "stress conditions" throughout their life cycle, starting from seed germination to the seed setting stage [1][2][3]. To progress and complete their life cycle even during single or combinatorial non-biological and biological stresses, plants adapt to continue thriving by evolving sophisticated defense mechanisms [4][5][6][7]. With multiple reports highlighting an increase in the frequency and incidences of these stresses in the past few decades [8,9], the most severe challenge at present is understanding the responses as well as adjustments that occur during the aversion of stress-triggered alterations in detail [3,10,11]. Most importantly, amongst many stresses, phytopathogensincited biological stress affects the growth, development, and yield of various crop plant species such as wheat, maize, rice, barley, sugarcane, chickpea, pearl millet, cotton, lentil, faba bean, etc. Over time, upon being challenged by devastating phytopathogens, plants have evolved both constitutive and inducible mechanisms to defend themselves in the best Control of the signaling of phosphatidic acid; resistance against drought, salt, and cold stress; inhibiting spore penetration and providing fungal resistance; induction of effector-triggered immunity and PAMP-triggered immunity against pathogens; regulating the signaling of Jasmonic acid and salicylic acid; wounding response in plants [34,38] Phosphatidylinositol-4,5-biphosphate, Phosphatidylinositol-4-phosphate Phosphoinositidespecific phospholipase C Phosphatidic acid, Diacylglycerol, and Inositol phosphate Plant protein localization induces effector-triggered immunity and PAMP-triggered immunity during pathogen attack; resistance during drought, heat, and salt stress [39,40] Phosphorylcholine, Phosphorylethanolamine Non-specific phospholipase C

Phosphorylalcohol, Diacylglycerol
Root development; response during cold and salt stress [41] Diacylglycerol Diacylglycerol kinase Phosphatidic acid Effector-triggered response against pathogens; signaling of defense response during salt and cold stress; enhances plant growth and development [42] Phosphatidic acid Phosphatidic acid kinase Diacylglycerol pyrophosphate Induction of an ABA-mediated response to pathogen attack [43,44] Phosphorylated Phosphatidylinositol

Phosphatidylinositol kinase Phosphoinositides
Induction of a phosphatidylinositol-mediated stress response [45] Phosphatidyl ethanolamines Fatty acid amide hydrolase

Brassinosteroids
Resistance against bacterial blight disease and fungal pathogen [50] Linolenic acid Jasmonic acid carboxyl methyltransferase Jasmonates Induces defense-related genes; resistance to B. cinerea attack [51,52]  , and Phyto-oxylipins (fungi). At the back end, this mechanism of imparting resistance against phytopathogens is directly or indirectly controlled by ROS bursting, calcium signaling, mechano-sensory responses, lipid raft, and the surface perception of elicitors by interacting with other transcription factors, phospholipases, and kinases. Additionally, during pathogen infection, the "cuticle" (made up of certain cutin monomers or wax components) responds faster to the pathogen elicitors. Thus, it activates plant disease resistance through PTI and ETI.  Phyto-oxylipins (fungi). At the back end, this mechanism of imparting resistance against phytopathogens is directly or indirectly controlled by ROS bursting, calcium signaling, mechano-sensory responses, lipid raft, and the surface perception of elicitors by interacting with other transcription factors, phospholipases, and kinases. Additionally, during pathogen infection, the "cuticle" (made up of certain cutin monomers or wax components) responds faster to the pathogen elicitors. Thus, it activates plant disease resistance through PTI and ETI.

Primary Response of Host Plant against Microbial Infection
The cuticle can be regarded as a storehouse of signal translators when a pathogen finds a susceptible and ideal host to infect and colonize. Cuticular lipids are present on cell surfaces and act as messenger molecules during plant-pathogen interaction. The signal perception of such events depends upon the metabolism of lipid messengers such as oxylipins and phospholipases (Table 1). Several transcription factors regulate and initiate the lipid pathways involved in defense and eventually lead to the death of infected cells [53][54][55]; for example, MYB30 (a Myb-domain transcription factor), a transcription factor that exhibits rapid, specific, and transient transcriptional initiation in response to Xanthomonas campestris infection and acts as a positive regulator of hypersensitive cell death in Arabidopsis [56].
Similarly, the overexpression of MYB30 in tobacco and Arabidopsis has been shown to contribute to the highly resistant nature of transgenic Arabidopsis and tobacco to powerful fungal pathogens. It is worth noting that a total of 14 lipid-associated genes are activated at an early response during X. campestris-infection. However, the upregulation of cuticular genes, VLCFAs, and their derivatives, particularly through MYB30, might be responsible for lipid signaling related to hypersensitive cell death response [56].
In Arabidopsis att1 (aberrant induction of type III genes) mutant, the Pseudomonas syrinage infection resulted in 70% reduced cutin content [57]. ATT1 encodes for CYP86A2, a cytochrome P450 monooxygenase that catalyzes fatty acid oxidation and the biosynthesis of extracellular lipids such as cutin. In att1, CYP86A2 is not functional; therefore, a decrease in cutin content was observed. Eventually, this facilitates the expression of bacterial type III gene AvrPto and HrpL as well as enhances the severity of disease caused by P. syringae.
In another report, it was observed that cutin monomers promote appressorium formation and spore germination in two devastating pathogens: Magnaporthe grisea and Colletotrichum gloeosporioides. In contrast, cutin monomers stimulate the formation of an appressorial tube in Blumeria graminis [31]. Thus, CUT2, a cutinase encoding gene, is involved in the penetration peg formation of M. grisea fungus. CUT2 has a dual role as a barrier to pathogens and a signaling regulator during microbial pathogenicity and plant defense. In another study, cutinases were observed to be secreted from a powdery mildew-causing pathogen, Erysiphe graminis, and to induce appressorium formation on a host plant. However, removing such cuticular waxes altered cuticle thicknesses due to the symptoms of multiple avr genotypes 4 (sma4). The Arabidopsis mutants, lacs (Long-Chain Acyl-Coenzyme A Synthetase) and bre1 (E3 ubiquitin ligase), suppress spore germination and comparatively reduce the conidial growth of B. graminis on barley. Thus, the reduced permeability and thickness of the cuticle arrest the surface invasion and restrict the entry of pathogens [31,32,58]. In addition, cuticles also differentiate the significant germination processes of various fungi and regulate the plant-pathogen infection process. For example, in the Arabidopsis sma4 mutant, the avirulent strain of P. syringae pv. tomato can easily cause infection, and this mutant exerts normal susceptibility towards one of the most devastating biotrophic pathogens, Erysiphe cichoracearum, but not the necrotrophic fungus Botrytis cinerea. This is because of the LACS2-encoded cutin-based inhibition of spore germination and penetration [32,33,59].
Additionally, Candidatus Liberibacter spp., causing Huanglongbing disease, shows virulence via the secretion of lipopolysaccharides (LPS) that help in the colonization of citrus fruits [60]. Moreover, bacterial pathogens activate non-specific phospholipase C (NPCs) and activate PI-PLC during their infection period. Upon infection with Ralstonia solanacearum (Strain 8107), the activity of both phospholipase D (PLD) and phospholipase C (PLC) get decreased due to the silencing of the NbSEC14 gene (the Sec14-protein superfamily codes for phosphatidylinositol/phosphatidylcholine transfer protein). Recently, in Arabidopsis, the expression of the NPC6 gene (Non-specific phospholipase C6) has been observed to be downregulated after treatment with Phytophthora parasitica and flg22 (Flagellin 22). However, NPC3 (Non-specific phospholipase C3) and NPC4 (Non-specific phospholipase C4) have been observed to be activated in response to Golovinomyces orotii, B. cinerea, P. parasitica, and P. syringae treatment. Furthermore, NPCQ (NPC Intracellular Cholesterol Transporter 1) and NPC4 expression were responsive to two other bacterial elicitors named HrpzZ and flg22 [61].

Lipids and Lipid-Derivatives Involved in Host Signaling Response
The plant oxylipins or Phyto-oxylipins (POs) are a class of oxidized lipids produced in a wide range of stressed conditions that further induce stress-activated signaling pathways. They are found as esterified glycerolipids or in a free form. The PO signatures are plant-specific and regulated by the kind of pathogens, affected plant organs, and the pathogen's lifestyle [73,74]. For example, tobacco plants have been observed to accumulate α-dioxygenase (α-DOX) and 9-lipoxygenase (LOX) products after infection with P. syringae. In contrast, potato and tomato plants accumulate 9(S)-and 13(S)-polyunsaturated fatty acid hydroperoxides upon infection by P. infestans and B. cinerea, respectively [75][76][77][78].
Within the huge variety of POs, jasmonic acid (JA) and its derivatives are wellknown LOX-derived molecules that are quickly accumulated in pathogen-damaged tissues/plants [52,79]. Within the class of JA-derivatives, the methyl-JAs are volatile compounds produced for signaling communication in an intra and interspecific manner. According to the reports related to pathogen response, (+)-7-iso-jasmonoyl-L-isoleucine (JA-Ile) has been observed to be accumulated within five minutes in the leaves of Arabidopsis thaliana distantly located from the wounding areas [68,80]. Furthermore, in this regard, the trio signaling process of Ca 2+ , reactive oxygen species (ROS), and electrical couplingmediated plasma membrane potential (Vm) regulate long-distance signaling for a quick response instead of direct hormonal movements [81,82]. Furthermore, JA induces signaling that encourages the pump or ion channel encoding genes and favors the release of long-distance Ca 2+ -signaling [83,84]. However, at present, complete knowledge of pattern-associated molecular patterning and damage-associated molecular patterns in PO-mediated signaling during pathogen attack is lacking. The PLs are the integral components of the membrane bilayer and provide the perceiving areas during plant-pathogen interaction. They have regulatory roles in plant immunity. PL-based signaling includes the activation of phospholipases (PLs) and protein kinases (PKs) to induce a variety of intracellular signaling molecules by phosphorylating or cleaving the bonds of PL to regulate diverse physiological processes of plants [85,86]. There are three categories of PLs based on their substrate specificities and enzymatic activities: Phospholipase A (PLA), PLC, and PLD.
Phosphatidic acid (PA) is known to be central player for lipid transport across membranes in addition to its defensive role, and it also acts as a precursor for PI, PC, and PE [92]. Furthermore, PAs play a crucial role in stomatal closure with the aid of ABA-mediated signaling by targeting the activities of the respiratory burst oxidase homologs (RBOHD and RBOHF) [43,93]. Phospholipase D α1 (PLDα1) generates PA, which binds with RBOHD and RBOHF and triggers ROS production. This ROS production stimulates stomatal closure. The role of PLDα1 and RBOH in stomatal closure is also supported by the observation that the mutants of PLDα1 and RBOH show insensitivity to ABA.
On the other hand, PA also binds with the ABI protein phosphatase 2C (the negative regulator of ABA-mediated signaling) to inhibit phosphatase activity [94,95]. It has also been suggested that PA can act as a ubiquitous signaling component for diverse abiotic and biotic stress-induced signaling pathways. This is because of the differential binding of PA to target enzymes or proteins that alter their localization and activity. The mutation in AtPLDβ1 (Phospholipase D β1-encoding gene) shows compromised resistance against B. cinerea, elucidating the positive role of PA in the JA pathway. Lysophospholipids (LPL) and PI also have a role in plant defense ( Figure 1). PI is produced by phosphatases and lipid kinases (Figure 2), as described earlier. They serve as a precursor for stress-signaling lipids such as DAG and inositol phosphatases [96]. The signaling pathway of LPL is involved in an overlapped manner with PA-induced signaling [97,98]. The activity of PLAs induces LPL generation from the glycerophospholipids such as sphingosylphosphorylcholine and sphingosine-1-phosphate lysophosphatidylcholine. The specificity and the signaling activity are defined by the acyl chain position, length, saturation degree, and phosphate head group. LPL-specific lipid signaling is involved in pest attack, pathogen infection, and wounding [45,99].
In plants, sphingolipids are the major signaling structural components of plasma membranes as well as other endo-membranes and play crucial roles in the host-pathogen interactions and other stress responses [47,100]. Chemically, sphingolipids are ceramidecontaining fatty acid nonglycerol lipids connected to long-chain amino alcohol [101,102]. Because of their highly hydroxylated nature, sphingolipids improve membrane properties such as stability and permeability and even regulate protection against fungal pathogens and other environmental stresses [102]. This can be understood by the fact that sphingolipids are used to induce cell death in plants, which eventually limits the pathogen spread from damaged tissues. For example, a sphingosine analog is produced by Alternaria alternata f.sp. lycopersici, which serves as a virulence factor and causes programmed cell death both in plants and animals [103].
Additionally, the AAL toxin and fumonisin (toxins of Fusarium moniliforme) impede the biosynthesis of sphingolipids by targeting ceramide synthase, resulting in the accumulation of long-chain bases. Eventually, this increased level of long-chain bases or their ratio to ceramide signals causes pathogen-based programmed cell death [104,105]. The R protein ASC1 recognizes these toxins and confers resistance by mediating alternative ceramide synthesis and the transfer of GPI-anchored protein to the Golgi apparatus from the endoplasmic reticulum. Thus, the transfer of ceramides to the membrane eventually plays an essential role in modulating programmed cell death.

Phospholipase and Its Role in Defense Signaling
Phospholipase plays a versatile role in pathogen response and acts rapidly on the perception of stimuli [30]. The transcription of PLA, PLD, PLC, and diacylglycerol kinase (DGK)-encoding genes and their enzymatic activities have been reported to be enhanced upon elicitor treatment and pathogen infection in tomato (Solanum lycopersicum), rice (Oryza sativa), Arabidopsis (A. thaliana), and tobacco (Nicotiana tabacum) [106][107][108] (Table 2). Pathogen recognition initiates the cascade of phospholipase-dependent signaling pathways. PLAs hydrolyze membranous PL to produce LPL ( Figure 2) and free fatty acids (FFA). PLAs are categorized into DAD (defective in the anther dehiscence), patatin-like proteins (pPLAs), and secretory phospholipase A2 (PLA2s). However, SAG101 (senescence-associated carboxylesterase 101), PAD4 (phytoalexin deficient 4), and EDS1 (enhanced disease susceptibility1) are the main components that shuttle during signaling via the activities of PLAs [30]. In a study, perforin-like proteins (PLP) and patatin-related phospholipase 2A (pPLA 2α) are activated after the invasion of P. syringae pv. tomato or B. cinerea [30]. In Arabidopsis, the modified regulation of PLP2 alters plant susceptibility to P. syringae pv. tomato or B. cinerea, whereas the expression of PLP2 promotes the growth of necrotizing pathogens but enhances the resistance towards devastating viral pathogen CMV (Figure 3). PLP2 expression promotes oxylipin accumulation in advanced stages of Botrytis invasion via α-DOX pathways and restricts the spreading of hypersensitive response (HR) [30]. Conclusively, PLP2 activities may be driven by pathogens to accelerate colonization within the host. In Arabidopsis, PLD and PLA activities are supposed to be interlinked during the plant defense response. When P. syringae expressing AvrBst (an effector molecule) infects the Pi-0 ecotype of Arabidopsis (Figure 3), PA production occurs through PLD pathways, which is mandatory for HR responses. A loss of function mutation in SOBERI1 (SUPPRESSOR OF AVRBST-ELICITED RESISTANCE 1) (exhibiting PLA activities) displays the resistance phe-notype in the Pi-0 plant. In contrast, in the Col-0 a-susceptible Arabidopsis ecotype, SOBERI (PLA2) activity competes for the substrate with PLD, thus reducing the accumulation of PA to elicit an AvrBst response [109].
of PA to target enzymes or proteins that alter their localization and activity. The mutation in AtPLDβ1 (Phospholipase D β1-encoding gene) shows compromised resistance against B. cinerea, elucidating the positive role of PA in the JA pathway.
Lysophospholipids (LPL) and PI also have a role in plant defense (Figure 1). PI is produced by phosphatases and lipid kinases (Figure 2), as described earlier. They serve as a precursor for stress-signaling lipids such as DAG and inositol phosphatases [96]. The signaling pathway of LPL is involved in an overlapped manner with PA-induced signaling [97,98]. The activity of PLAs induces LPL generation from the glycerophospholipids such as sphingosylphosphorylcholine and sphingosine-1-phosphate lysophosphatidylcholine. The specificity and the signaling activity are defined by the acyl chain position, length, saturation degree, and phosphate head group. LPL-specific lipid signaling is involved in pest attack, pathogen infection, and wounding [45,99]. transcriptional level than the secreted protein level, as depicted by a study on a mutant (B. glumae AU6208 tof1). The virulence assessment of mutant and LipA regulation by the tof1/R system suggested the significance of lipase during infection that positively mediates bacterial populations. The above findings summarize the activity of B. glumae lipase and its interaction with the host lipid that may trigger plant responses [115,116]. Moreover, the plant develops several molecular regulation and response strategies associated with lipase activities after the successful infection of pathogens (Table 2).

Figure 3.
Surface signaling responses of hosts after the primary invasion of pathogenic species. During an immune response, the fundamental tenet is the ability to detect the presence of devastating agents (such as phytopathogens) followed by activating the defense responses. In plants, immunity is governed by transmembrane pattern recognition receptors (PRRs) and other downstream cellular components. These downstream immunity-related components include key enzymes-phospholipases-which draw much of our attention. PLAs are a superfamily of functionally diverse enzymes that actually govern membrane dynamics. The large superfamily of Phospholipases is divided into three sub-families: Phospholipase A (PLA), Phospholipase C (PLC), and Phospholipase D (PLD). These Phospholipases often hydrolyze various plasma membrane and intracellular membranes-derived phospholipids, phosphatidylinositol, and related-derivatives to generate signaling molecules such as phosphatidic acid, oxylipins, free fatty acids, and lysophospholipids as well as other molecules (inositol trisphosphate, diacylglycerol) Figure 3. Surface signaling responses of hosts after the primary invasion of pathogenic species. During an immune response, the fundamental tenet is the ability to detect the presence of devastating agents (such as phytopathogens) followed by activating the defense responses. In plants, immunity is governed by transmembrane pattern recognition receptors (PRRs) and other downstream cellular components. These downstream immunity-related components include key enzymesphospholipases-which draw much of our attention. PLAs are a superfamily of functionally diverse enzymes that actually govern membrane dynamics. The large superfamily of Phospholipases is divided into three sub-families: Phospholipase A (PLA), Phospholipase C (PLC), and Phospholipase D (PLD). These Phospholipases often hydrolyze various plasma membrane and intracellular membranes-derived phospholipids, phosphatidylinositol, and related-derivatives to generate signaling molecules such as phosphatidic acid, oxylipins, free fatty acids, and lysophospholipids as well as other molecules (inositol trisphosphate, diacylglycerol) that ultimately impart resistance against bacteria (Pseudomonas syringae) as well as fungi (Botrytis cinerea and Magnaporthe grisea).
Secondly, PLC (Ca 2+ -dependent membrane protein) responds to pathogen elicitors after the invasion at the membrane region and triggers the PLC pathway through PAMP recognition [30]. In rice, OsPLC1 (Phospholipase C1) gene expression was induced during the incompatibility between M. grisea-O. sativa interaction, which confirmed the role of OsPLC1 in signaling during pathogen infection [30]. In the S. lycopersicum cell suspension culture, the upregulation of Cf-4 (a membrane-anchored protein that provides resistance to Cladosporium fulvum) resistance gene via the activity of Avr4 (a cognate pathogen effector) induced a rapid accumulation of PA through the DGK-PLC pathways [110]. Further, Slplc4 gene silencing impaired Avr4/Cf4-stimulated HR and facilitated the susceptibility of Cf-4 plants to Cladosporium fulvum [62]. However, SlPLC6 silencing in tomato did not influence Avr4/Cf-4 induced HR but compensated resistance induced by R-genes such as Prf/Pto (resistance to Phytophthora infestans/Pseudomonas syringae pv. tomato), Ve1 (an encoding protein for resistance to Verticillium wilt disease), and Cf-4 [111]. Additionally, the abrogation of PA through n-butanol compensates for cell wall-based resistance in Arabidopsis to sensitive powdery mildew pathogen and AvrRpm1/RPM1 triggered immunity. This disease-resistant protein, RPM1, is recognized as the AvrRpm1 type III effector avirulence protein from Pseudomonas syringae [111]. The molecular dissection of Arabidopsis defense response revealed that AtPLDδ contributes to invasion resistance toward sensitive mildew pathogens.
Interestingly, several lipid-signaling genes have also been observed to induce resistance; for example, AtPLDβ1 (which enhances the concentration of oxidative species, salicylic acid, and increments the resistance to P. syringae), OsPLDβ1 (elevates the resistance level to diverse pathogens in rice), and SlPLD β1 (enhances resistance in host species) [108,112]. Indeed, EDS1 or PAMP-dependent host response tightly controls negative regulators such as PUB13 (an E3-ubiquitin ligase containing a U-box domain), MAPKKK (mitogen-activated protein kinase kinase kinase), EDR1 (enhanced disease resistance 1), and Ca 2+ /SR1 (calmodulin-binding transcription factor). Interestingly, PI4KIIIβ1 and PI4KIII2β regulate FLS2 (encodes for LRR receptor-like serine/threonine-protein kinase) homeostasis, and flagellin recognized PRR, and negatively regulate salicylic acid (SA) signaling to suggest a supposed braking mechanism for pattern-triggered immunity (PTI) [108,113].
Fungal pathogens may alter their growth activities and morphology in response to the surface signals of a host. When Ustilago maydis infects maize plants, it converts the nonfilamentous pathogenic form into a filamentous form to enhance invasion and colonization. The lipase activities of the fungus U. maydis are solely responsible for the consequential liberation of lipids on a surface that helps to change its pathogenic nature [114].
Additionally, some lipases play a primary role in pathogenicity in the panicle blast disease of rice caused by Burkholderia glumae. The pathogenic strain of B. glumae (AU6208) shows the secretion of Lipase A (LipA) on rice that is regulated by tof1/R (a quorum-sensing system) [115]. The tof1/R in B. glumae is a specific signaling system that depends upon the cell density produced by the tof1 (topoisomerase I-interacting factor) gene, whereas tof1 regulators attach with signals at a threshold amount and mediate the desired gene expression. However, the B. glumae AU6208 strain with the tof1 mutant shows a slight concentration of lipase but does not release any N acyl-homoserine lactone (AHL) compounds. It is more likely that tof1/R-mediated LipA regulation is more common at the transcriptional level than the secreted protein level, as depicted by a study on a mutant (B. glumae AU6208 tof1). The virulence assessment of mutant and LipA regulation by the tof1/R system suggested the significance of lipase during infection that positively mediates bacterial populations. The above findings summarize the activity of B. glumae lipase and its interaction with the host lipid that may trigger plant responses [115,116]. Moreover, the plant develops several molecular regulation and response strategies associated with lipase activities after the successful infection of pathogens (Table 2).

Jasmonate-Derived Oxylipins as the Critical Mediator in Plant-Pathogen Interaction
Oxylipins are a diverse class of oxidized lipids that are abundant in both plants and phytopathogens [117]. These are distributed as free forms, esterified with glycolipids/PL, or attached with other compounds, including isoleucine and methyl groups. Oxylipins can be derived from the free radical-catalyzed oxidation of polyunsaturated fatty acids (PUFA) via enzymatic and non-enzymatic pathways. Among these, an increased concentration of phytoprostane is observed in plants after successful exposure to pathogens that cause oxidative stress [118]. The application of phytoprostane to Arabidopsis cells restricts the cell death elicited by toxins and detoxifying enzymes (glycosyltransferase and glutathione S-transferases), the activation of mitogen-activated protein kinases (MAPK), and the biosynthesis of phytoalexins [118]. LOXs gene expression is induced in diseased plants and associated with resistance [117]. The expression level of two LOX-9-LOXs and 13-LOXs-is significantly enhanced during pathogen attack, and they induce signaling cascades of the defense response [119].

Successful Chase of Jasmonate: Elucidates Defense Clues during Pathogen Attack
Classically, jasmonate is a typical oxylipin that has an important role in the defense response during a pathogenic attack and it induces antimicrobial activities [117,120]. Mostly, pathogens such as X. campestris pv. phormiicola, Streptomyces scabies, and Pseudomonas cannabina pv. alisalensis show an enhanced production of 2,4-diamino-1,5-diphenyl-3hydroxypentane (COR) compounds [121,122]. Oomycetes and fungal pathogens secrete protein-rich effectors that activate JA signaling in Arabidopsis, along with susceptibility to the effector protein SECRETED IN XYLEM (SIX). The F0 causes the expression of LOB DOMAIN CONTAINING PROTEIN 20 (LBD20), which regulates the downstream function of MYC2 (encodes an MYC-related transcriptional activator that binds to an extended G-Box promoter motif and interacts with Jasmonate ZIM-domain proteins) and COI1 (encoding coronatine-insensitive protein 1, which plays a role in JA-regulated defense processes and coronatine-like elicitors perception) and increases pathogenesis [123].
LBD20 plays a crucial role in the JA-mediated defense response, and its expression causes the inhibition of JA signaling marked by VSP2 (Vegetative storage protein 2) and THI2.1 expression. Nevertheless, no effect of LBD20 has been observed on the PDF1.2 function. This indicates that LBD20 may promote pathogenesis. Interestingly, this THIONIN 2.1 protein functions as a defense factor that exerts its toxic effect at the cell membrane level [123].
Additionally, the HARxL44 effector protein in Hyaloperonospora arabidopsis induces ET/JA signaling, suppresses the SA response, and increases host infection susceptibility through the interference of MED19a (mediator of RNA polymerase II transcription subunit 19a) [124]. HaRxL44 induces the proteasome-mediated degradation of MED19a and causes enhanced infection in host species.
The pathogens enhance their activities from the surface level to the nucleus using different lipases and cause pathogenesis (Table 3). For example, during the invasion of the P. syringae pv. tomato (Pst) strain, DC3000 releases phytoalexins such as coronatine that bind to COI1 (JA-receptor COR insensitive 1) and mimic the structure of JA-IIe, leading to the activation of a JA-mediated response. COR or JA-IIe mediates the activation of JA2-like transcription factors that initiate SAMT1 and SAMT2 (S-Adenosylmethionine transporter 1/2) expression, which further regulates SA deactivation via methylation [128]. In Arabidopsis, activating the JA pathways that are regulated through E-2-hexenal enhances susceptibility to the Pst strain [129]. The characterization of OPR3 (Oxophytodienoate-Reductase 3) mutant shows that 12-oxo-phytodienoic acid (OPDA) (a precursor for JA biosynthesis) upregulates both COI1-dependent and COI1-independent genes that do not respond to JA. In tomato, P. syringae (Pst strain) can overcome host defenses and colonize onto plant apoplastic regions and their adjoining cells. The secretion of coronamic acid (CMA) and coronafacic acid (CFA) from COR (coronatine) activities modify the CFA operon and promote the binding of CFA ligase attachment with CMA and CFA with an amide linkage [130]. The toxic compounds released by the bacteria bind to COI receptors that regulate JA-derived responses. The significant role of COR helps in stomatal opening and promotes the entry of bacteria into the leaf. Instead of COR synthesis, the ability of Pst depends upon the entry of effector proteins into the host through T3SS (type III secretion system). T3SS encoded by hrc (Hypersensitive response and pathogenicity) and hrp (Hypersensitive response conserved) genes and is used by bacteria to insert type III effector in a target host to suppress ETI and PTI. Primarily, Pst secretes approximately 35 effectors, such as mono-ADP-ribosyltransferases (hopu1 and hopf2), an E3 ligase (Avrptob), phosphothreonine lyase (hopai1), cysteine proteases (AvrPphb and AvrRpt2), etc. [131].

Intracellular lipase
Increases stored lipid degradation [138] OPR3-silenced tomato (SlOPR3) mutants exhibit an elevated susceptibility toward necrotrophic pathogen B. cinerea due to a decline in JA-IIe and OPDA levels [131]. Further, it has also been shown that only OPDA treatment could restrict B. cinerea resistance in SlOPR3 transgenic plants by callose deposition. The inoculation of JA-deficient opr7-opr8-2 and GLV-deficient mutant (green leaf volatile) indicates the role of JA and Lipoxygenase 10 (LOX10) during bacterial/fungal infection [119,131].

Conclusions and Future Perspectives
The plant-pathogen interaction is a highly complex phenomenon. It includes a breadth of interrelated networks of signaling components and results either in a state of resistance or susceptibility. In this regard, lipid and lipid-derivatives act as pivotal modulators of interkingdom communication that include resistance, invasion, and pathogenesis mechanisms in plants. During recent years, which have seen significant strides forward in research, several studies have increased our understanding of lipid-derived interactions, lipid enzyme modifications, and the crucial role of lipid enzymes in defense response. First and foremost, plant cuticular waxes provide primary resistance to restrict the physical outgrowth of phytopathogens. Due to the continuous acceleration in broad-spectrum "omics" research efforts and the refinements in supportive instrumentation, we have recently acquired knowledge about the mechanism by which host plants use complex orchestrated membrane systems to utilize pathogen-derived lipids, elicitor molecules, and sphingolipids for activating signaling cascades. As a result, it is now known that plant lipids play central roles in the biosynthesis of cutin (Figure 2), the stimulation of signaling pathways that trigger different immune responses, and the reprogramming of defense-related genes.
Interestingly, in the past two decades, the identification of oxylipin's (including JA) role in defense and other biological mechanisms has increased the knowledge pool regarding oxylipins (including JA). Most importantly, studies in model plants have helped to uncover the role of lipids and associated derivatives in regulating resistance against pathogenic microbes. Overall, in the current context of available data, it has been determined that lipids play essential roles in growth, development, and the completion of the life cycle, as well as in pathogen (or elicitor) recognition and in inciting host defense responses. Despite these significant findings, knowledge has only been gathered for the model species and prominent pathogenic microbes; however, with the advent of new pathogenic races and strains appearing in new geographical areas, part of the focus has to be primarily shifted towards new plant species and new, emerging pathogenic races. This unexplored area points towards the missing pieces in the puzzle of lipid-mediated signaling.
Moreover, the mechanism behind the interaction at surface level, lipid concentration, and lipid specificity between plants and microbes at the nano-scale is yet to be considered. Pan-transcriptome and pan-proteome analysis will help in monitoring the signaling cues and activities of interaction-related compounds from the surface level. Furthermore, considering the recent discovery of RNAi and small RNA exchange between hosts and pathogens, there is a possibility of bidirectional cross-kingdom trafficking for small lipids.
Therefore, in the future, a detailed framework can be built to elucidate the sophisticated balance between the behaviors of both pathogen and host species. These continuous efforts will allow a critical understanding of gene regulation in both pathogens and hosts and the development of fine-tuned defense strategies. Furthermore, it will establish the possibility of "inducing resistance" in crops by spraying lipid and associated molecules as biocontrol agents. Additionally, the physiological roles of lipids (other than oxylipins) and phospholipases in plant-pathogen interaction can be elucidated. This could provide novel targets for the control of the progression of plant disease. Additionally, future research can focus on whether esterified forms of PO act as a reservoir for the rapid biosynthesis/release of other oxylipins. Considering all these avenues of research, there are still multiple neglected questions in lipid signaling that can be explored in near future.