The Role of Arabinogalactan Type II Degradation in Plant-Microbe Interactions

Arabinogalactans (AGs) are structural polysaccharides of the plant cell wall. A small proportion of the AGs are associated with hemicellulose and pectin. Furthermore, AGs are associated with proteins forming the so-called arabinogalactan proteins (AGPs), which can be found in the plant cell wall or attached through a glycosylphosphatidylinositol (GPI) anchor to the plasma membrane. AGPs are a family of highly glycosylated proteins grouped with cell wall proteins rich in hydroxyproline. These glycoproteins have important and diverse functions in plants, such as growth, cellular differentiation, signaling, and microbe-plant interactions, and several reports suggest that carbohydrate components are crucial for AGP functions. In beneficial plant-microbe interactions, AGPs attract symbiotic species of fungi or bacteria, promote the development of infectious structures and the colonization of root tips, and furthermore, these interactions can activate plant defense mechanisms. On the other hand, plants secrete and accumulate AGPs at infection sites, creating cross-links with pectin. As part of the plant cell wall degradation machinery, beneficial and pathogenic fungi and bacteria can produce the enzymes necessary for the complete depolymerization of AGs including endo-β-(1,3), β-(1,4) and β-(1,6)-galactanases, β-(1,3/1,6) galactanases, α-L-arabinofuranosidases, β-L-arabinopyranosidases, and β-D-glucuronidases. These hydrolytic enzymes are secreted during plant-pathogen interactions and could have implications for the function of AGPs. It has been proposed that AGPs could prevent infection by pathogenic microorganisms because their degradation products generated by hydrolytic enzymes of pathogens function as damage-associated molecular patterns (DAMPs) eliciting the plant defense response. In this review, we describe the structure and function of AGs and AGPs as components of the plant cell wall. Additionally, we describe the set of enzymes secreted by microorganisms to degrade AGs from AGPs and its possible implication for plant-microbe interactions.


INTRODUCTION
Cell wall is an essential component of plant cells; they confer flexibility and mechanical support to the cell and perform important functions such as the maintenance of cell, preservation of osmotic pressure, movement of water and nutrients, management of intercellular communication between adjacent cells and prominent involvement in plant-microbe interactions, constituting the main barrier against potential pathogens (Burton et al., 2010;Keegstra, 2010).
Plant cell wall proteins (CWPs) constitute ∼5-10% of dry weight of the PCW mass. Analysis of the Arabidopsis thaliana proteome has provided important information regarding the diversity of these proteins. CWPs are classified into nine functional classes according to their predicted domains, and their possible partners have been proposed. The nine CWPs classes are proteins that act on carbohydrates; oxide reductases, proteases, proteins with interaction domains, proteins potentially involved in signaling, structural proteins, proteins related to lipid metabolism, miscellaneous proteins, and proteins with unknown function (Jamet et al., 2008;Albenne et al., 2013). An alternative classification of non-enzymatic proteins associated with the PCW into two groups has been proposed: hydroxyproline-rich glycoproteins (HRGPs), also known as the HRGP superfamily; glycine-rich proteins (GRPs) or the GRP superfamily. HRGPs are classified according to their hydroxyproline/proline proportion into different subfamilies such as extensins, proline-rich proteins (PRPs), arabinogalactan proteins (AGPs), solanaceous lectins, and subcellular PELPK proteins (Pro-Glu-Leu/Ile/Val-Pro-Lys). Alternately, GRPs have been classified into five classes based on their Gly-rich repeats (Class I to V) (Rashid, 2016).
Due to its composition, the PCW represents a recalcitrant and complex structure that must be overcome during plant-microbe interactions. Microorganisms, mainly bacteria and fungi, are capable of producing and secreting a plethora of cell walldegrading enzymes (CWDEs), which carry out a coordinated and synergistic deconstruction of the main structural polysaccharides of the PCW, producing soluble sugars that constitute an abundant source of organic carbon to guarantee their nutrition and survival (Gibson et al., 2011;Kubicek et al., 2014). The set of CWDEs includes cellulases, hemicellulases, pectinases, ligninases and accessory enzymes such as monooxygenases, which significantly increase the action of other polysaccharidases. These CWDEs have been described in several species of fungi and bacteria because they have great biotechnological potential (Malgas et al., 2017;Matias de Oliveira et al., 2018). Although it has not been precisely established whether all polysaccharidases constitute virulence factors, at least some such as endo-β-(1,4)-xylanases (Brito et al., 2006), pectin methyl esterases (Sella et al., 2016), arabinofuranosidases (Wu et al., 2016), and polygalacturonases, among others (Nakajima and Akutsu, 2013;Villa-Rivera et al., 2017a), are known to be essential for the establishment of the infection. Several studies have shown that plant pathogenic bacteria and fungi secrete a set of enzymes that degrade arabinogalactans from AGPs, however, little attention has been paid to their role in infection processes. Although there is evidence that AGPs play important functions in plant-microbe interactions, most studies on this topic have focused on the responses of plants to beneficial or pathogenic microorganisms. In this review, we describe the structure and function of AGs and AGPs as components of the PCW. Additionally, we describe the set of enzymes secreted by microorganisms to degrade AGs from AGPs and what is known regarding its role in plantmicrobe interactions.

AGs AND AGPs STRUCTURE
AGs are structural components of the PCW; they are mainly composed of galactose and arabinose and are ubiquitously distributed in the plant kingdom (Seifert and Roberts, 2007;Tan et al., 2012). Depending on their structure, AGs are grouped into three main types.
Nuclear magnetic resonance (NMR) spectroscopy analyzes performed in different models have demonstrated substantial variability in the structure of AG type II; however, three common characteristics have been observed: first, a main backbone composed of two blocks of three galactopyranose residues linked by β-(1,3) bonds, with the junction between the three galactosyl blocks being a β-(1,6) bond; second, bifurcated branches of arabinose, rhamnose, glucuronic acid, and galactose anchored in the main chain at residues one and two of galactopyranoses; third, a common branch consisting of six residues of α-L-(1,5)arabinofuranose and two α-L-(1,3)-arabinofuranoses grouped into one unit, with α-L-(1,4)-rhamnose, β-D-(1-6)-glucuronic acid forming a second unit. Both units are anchored to the main chain of β-(1,3)-galactopyranoses (Tan et al., 2010(Tan et al., , 2012. A third structure of AGs has been described, which is mainly associated with pectic polysaccharides in several plant species, consisting of a main backbone of D-galactopyranose residues linked by β-(1,6) bonds with side chains at position O-3 composed of L-arabinoses, arabinans, or individual Dgalactopyranose units ( Figure 1C; Raju and Davidson, 1994;Dong and Fang, 2001;Capek et al., 2009;de Oliveira et al., 2013).
AG type II are commonly anchored to a protein core, and these glycoproteins are denominated arabinogalactan proteins (AGPs). The protein core of AGPs (10% of AGPs) is a short backbone composed of 10 to 20 amino acids. The peptide undergoes posttranslational modifications: conversions of proline residues to hydroxyproline (forming the hydroxyproline domain) and the O-glycosylation of hydroxyproline and possibly serine and threonine residues with AG type II (90% of AGPs). In some cases, the protein core of AGPs contains within its structure a small sequence consisting of basic amino acids, and has a hydrophobic transmembrane domain located at the C-terminal end (Figures 1D,E; Gaspar et al., 2001;Showalter, 2001;Schultz et al., 2002;Showalter and Basu, 2016b). AGPs are found in the PCW, the apoplastic space, and some secretions such as exudates, and some adhere to the plasma membrane through a glycosylphosphatidylinositol (GPI) anchor in the hydrophobic domain. GPI binds to AGPs through a phosphoethanolamine linked to an oligosaccharide composed of D-mannose-(1-2)-α-D-mannose-(1,6)-α-D-mannose (1-4)-α-D-N-acetylglucosamine bound to a lipid residue of inositylphosphoceramide (Oxley and Bacic, 1999;Seifert and Roberts, 2007;Ellis et al., 2010). A consensus cleavage site has been identified in the classic AGP-deduced amino acid sequences, which constitutes a GPI-anchored recognition signal and is located before the transmembrane domain (Schultz et al., 2002).
AGPs are members of the HRGP superfamily, and based on their polypeptide core and the presence/absence of particular motifs/domains, they are classified into classic and non-classic AGPs (Showalter, 2001;Showalter et al., 2010). Classical AGPs are characterized by an N-terminal signal peptide, a central domain of variable length enriched in proline, alanine, serine, and threonine (PAST) (Figure 1D), and the C-terminal GPI anchor. Other classic AGPs are AG peptides, the structure of which contains 10-13 amino acids (Schultz et al., 2000). Conversely, non-classic AGPs have a low content of hydroxyproline and are enriched in cysteine and asparagine. Analyses of different plant tissues have revealed a high heterogeneity in the structure and composition of AGPs (both core proteins and carbohydrate moieties) (Gaspar et al., 2001;Showalter, 2001). Non-classical or chimeric AGPs have different conserved domains by which they are classified into subfamilies: lysine-rich AGPs with PAST domains separated by Lys-rich regions (Yang and Showalter, 2007), fasciclin-like arabinogalactan proteins (FLAs), with a fasciclin domain possibly involved in cell adhesion (Johnson et al., 2003), phytocyanin-like AGPs (PAGs) (Mashiguchi et al., 2009;Ma et al., 2017), and xylogen-like AGPs (XYLPs) with nonspecific lipid transfer protein (nsLTP) domains (Kobayashi et al., 2011). AGPs-extensin hybrids (HAEs) have also been identified (Showalter et al., 2010).
Regarding how AGPs work, it has also been proposed that soluble AGPs could be involved in cell-cell signaling (Schultz et al., 1998;Motose et al., 2004;Pereira et al., 2014), and GPI-AGPs in lipid rafts/nanodomains in eudicots could be involved in cell-cell communication, signal transduction, immune response, and transport (Borner et al., 2005;Grennan, 2007;Johnson et al., 2017). In support of these hypotheses, some studies have shown that classic AGPs bind reversibly to Ca 2+ in a pH-dependent manner, suggesting that AGP-Ca 2+ oscillators might integrate most signaling pathways downstream of the initial Ca 2+ signal, which would explain the participation of AGPs in many biological process (Lamport and Varnai, 2013;Lamport et al., 2014). On the other hand, there is evidence in Arabidopsis that the mechanism responsible for clathrinmediated endocytosis of extracellular lanthanum cargoes, requires extracellular AGPs anchored to the plasma membrane , and classic lysine-rich AtAGP18 could function as a coreceptor that binds to signaling molecules and interacts with transmembrane proteins, possibly receptor-likekinases (RLKs) (Zhang et al., 2011). Specifically, it has been proposed that FLA AGPs are involved in cell-to-cell adhesion and cell signaling (Shi et al., 2003;Showalter and Basu, 2016a).
Currently, despite many studies on AGPs, it remains unclear whether their function resides in the protein backbones, in the glycan epitopes or both. However, given that the mass of AGPs constitutes more than 90% of sugars and that the oligosaccharides play a role in signal transduction in plants, it seems logical to consider these sugars as representatives of the interactive molecular surface defining their function in multiple plant processes. In this sense, heterologous expression studies, in vitro enzyme assay and analyses of knockout mutants of genes encoding Hyp-galactosyltransferases (GALTs and HPGTs) that specifically add galactose to AGPs in A. thaliana, have shown that glycosylation is essential for plant growth and development (Showalter and Basu, 2016b). On the other hand, enzymatic degradation of the AG type II of AGPs is a strategy that it utilized by microorganisms during their interactions with plants.

DEGRADATION OF AGs BY ENZYMES OF MICROORGANISMS
Fungi and bacteria are capable of synthesizing and secreting the enzymes necessary for complete hydrolysis of AG type II, and these enzymes are listed in Table 1 and schematized in Figure 2.
In addition, a C-terminal carbohydrate binding module (CBM) has been described as part of the three-dimensional structure of exo1,3GAL, classified as CBM13 in Clostridium thermocellum (symmetric β-trefoil fold topology) (Jiang et al., 2012) and CBM35 in Phanerochaete chrysosporium (β-jellyroll fold with a single calcium ion-binding site) ( Figure 2E; Matsuyama et al., 2020). Interestingly, several studies have shown that typical side chains of AG type II do not interfere with the exo1,3Gal activity, and the enzyme structure contains a space capable of accommodating the β-(1,6)-galactose residues, which allows the protein to surpass the branches of the AG structure (Matsuyama et al., 2020). Nevertheless, the activity of exo1,3GAL has been shown to increase significantly in response to the action of β-(1,6)-D-galactanase, β-L-arabinopyranosidase and α-L-arabinofuranosidase (Okawa et al., 2013).
There are no crystallized structures of endo1,6GAL and 1,6GAL; however, a prediction of the three-dimensional structure of Colletotrichum lindemuthianum endo1,6GAL has been reported. The endo1,6GAL model adopts a (β/α)8 TIM barrel fold topology (eight-stranded parallel β-strand, forming a central barrel surrounded by eight α-helices) with a putative active site located at the C-terminus, which is consistent with the characteristic structure of GH30 family enzymes ( Figure 2C; Villa-Rivera et al., 2017b). These enzymes have been characterized from fungi and bacteria and have also been expressed in heterologous models ( Table 1).
Based on the specificity of the substrate, ABFs are classified into three types: arabinofuranosidase A is capable of hydrolyzing α-(1,5)-L-arabinofuranosyl bonds of arabinoxylooligosaccharides but does not act on polysaccharides; arabinofuranosidase B acts on linear and branched arabinooligosaccharides and polymers; and the third type of arabinofuranosidase shows a high specificity for complex natural substrates and is known generically as an arabinofuranohydrolase (Numan and Bhosle, 2006;Lagaert et al., 2014;Poria et al., 2020). The regional selectivity of ABFs has also been evaluated. Accordingly, ABFs belonging to GH51 and GH54 are capable of removing arabinosyl residues from the internal and terminal non-reducing ends of xylopyranosyl residues with monoand disubstitutions. However, the ABFs of the GH54 family show weak activity on internal di-substitutions compared with GH51, which are more versatile in terms of substrate specificity (Koutaniemi and Tenkanen, 2016;Dos Santos et al., 2018). On the other hand, ABFs of the GH62 family show selectivity toward α-(1,2) and α-(1,3) anchors in arabinoxylans mono-substituted with arabinofuranosyl residues (Sarch et al., 2019). Interestingly, bifunctional enzymes with α-Larabinofuranosidase/xylobiohydrolase (Ravanal et al., 2010) or α-L-arabinofuranosidase/β-xylosidase activities have also been described (Huy et al., 2013).
Several crystallized and characterized ABFs, which present a diversity of structures generally consisting of two domains: the catalytic domain and the arabinose binding module (ABD). The structure of the Streptomyces avermitilis ABF belonging to the GH43 family, presents a core catalytic domain composed of a five blanched β-propeller with an ABD similar to CBM42 located at the C-terminus adopting a β-trefoil fold (three similar subdomains assembled against one another around a pseudo3-fold axis) topology (Fujimoto et al., 2010). With respect to ABFs of the GH51 family, the enzymes from Geobacillus stearethermophilus (Hovel et al., 2003), Clostridium thermocellum (Taylor et al., 2006), and Thermobacillus xylanilyticus (Paes et al., 2008) have been crystallized. The catalytic domain of the GH51 family ABFs has a (β/α)8 TIM-barrel fold topology and a C-terminal ABD domain with a jellyroll topology (Figure 2B; Hovel et al., 2003;Paes et al., 2008). The structure of Aspergillus luchuensis ABFs (formerly known as A. kawachii), belonging to the GH54 family, is composed of a catalytic domain (β-sandwich fold topology) similar to clan B of GH54 and an arabinose binding 1 http://www.cazy.org/ module (β-trefoil fold topology) similar to CBM13 (Figure 2D; Miyanaga et al., 2004).
Regarding other accessory enzymes for the deconstruction of AG type II, β-L-arabinopyranosidases (ABPs) (EC3.2.1.88) have also been reported. ABP hydrolyzes β-arabinopyranose from the non-reducing end of AG side chains . Two bifunctional proteins (Fo/AP1 and Fo/AP2) with β-Larabinopiranosidase/α-D-galactopyranosidase activity have been purified from Fusarium oxysporum, both of which are active toward larch wood arabinogalactan (LWAG), releasing only arabinopyranose (Sakamoto et al., 2010). ABPs have been purified and characterized from bacteria and fungi, and they have also been expressed in heterologous systems ( Table 1). The threedimensional structure of ABP consists in a catalytic domain (antiparallel β-domain) characteristic of the GH27 family and a CMB13 (antiparallel β-domain adopting a jellyroll structure) at the C-terminal end Lansky et al., 2014; Figure 2A).
It is important to mention that the combined action of exo1,3GAL, 1,6GAL, ABF, and ABP is more efficient than the sum of the independent activities in the depolymerization of AG type II (Okawa et al., 2013). Efficient hydrolysis of this polymer depends of the removal of β-(1,6)-galactose branches (Sakamoto and Ishimaru, 2013).

AGs HYDROLYSIS AND PLANT-MICROBE INTERACTIONS
AGPs play an interesting role in the response pathways of plants to abiotic stress (caused by low and high temperatures, drought, high salinity, excessive light, and floods) and biotic stress (caused by bacteria, fungi, nematodes, and viruses) (Mareri et al., 2018). Particularly, they are important for plant-microbe interactions, whether beneficial or pathogenic.
During beneficial plant-microbe interactions, plant roots produce a complex mucilage that constitutes an important carbon source for rhizosphere microorganisms. Root mucilage from pea, cowpea, wheat, maize, and rice has been reported to contain high levels of galactose and arabinose, the main components of AGs (Knee et al., 2001). Moreover, root tips and border-like cells (BLC) of A. thaliana can secrete pectic polysaccharides and AGPs to the rhizosphere (Vicre et al., 2005). Additionally, AGPs have been located in several root structures: epidermal, cortical, and endodermal cells, pericycle, apical meristem, and root infection structures (Nguema-Ona et al., 2013). In this sense, AGPs can act as attractants for symbiotic species of fungi and bacteria, promoting the development of infection structures and, therefore, root tip colonization. It has been observed that the induced alterations in the structure of AGPs trigger an inhibition in the attachment of Rhizobium to BLC and the root tip of A. thaliana (Vicre et al., 2005;Cannesan et al., 2012;Xie et al., 2012).
Furthermore, AGPs are found at the physical interface between root cells and the infecting structures of microorganisms, allowing for the root-symbiont nutrient exchange necessary for microbe survival. For this purpose, soil microbes such as Trichoderma viride and S. avermitilis, among other, produce polysaccharidases ( Table 1) that allow them to access and obtain monosaccharides or disaccharides derived from the hydrolysis of AGs, useful as a carbon source (Knee et al., 2001). On the other hand, it has been suggested that AGPs can prevent infection by pathogenic microorganisms or inhibit their development because the degradation products (oligosaccharides or glycopeptides) generated by hydrolytic enzymes of pathogens can act as damage-associated molecular patterns (DAMPs) and promote the plant defense response. Moreover, the colonization of the rhizosphere by beneficial microbes supported by AGPs, would also activate plant defense mechanisms such as induced systemic resistance (ISR), protecting the plant against pathogen attack, while symbiotic microorganisms could act as antagonists of pathogens and avoid infections. Finally, AGPs have been proposed to be modulators of the plant immune system, favoring the colonization of beneficial microbes (Nguema-Ona et al., 2013).
Regarding the pathogen microbe-plant interaction, an accumulation of HRGPs has been detected as a result of the contact between the pathogen and PCW. For instance, during the infection of tomato roots with F. oxysporum, late accumulation of HRGPs has been observed in susceptible plants (Benhamou, 1990). Along the same lines, in response to F. oxysporum a consistent increase in the abundance of AGPs was observed, particularly in the roots of resistant cultivars of wax gourd (Benicasa hispida Cong.) but not in susceptible ones (Xie et al., 2011). Furthermore, immunohistochemical analysis of Sesbania exaltata tissues infected by Colletotrichum gloeosporioides has revealed a rapid accumulation of AGPs at the border between the vascular tissue and the necrotic lesion (Bowling et al., 2010). This evidence suggests that HRGP enhancement is a prerequisite for an efficient and localized plant defense response (Benhamou, 1990;Nguema-Ona et al., 2013). At the transcriptomic level, seven extensin genes and 23 genes encoding AGPs were differentially expressed in banana cultivars before and after infection with F. oxysporum. These data revealed that extensins and AGPs were dynamic components of the plant cell wall . In addition, 38 NbFLAs from Nicotiana benthamiana were significantly downregulated by infection with turnip mosaic virus (TuMV) or by infection with Pseudomonas syringae pv tomato strain DC3000 (Pst DC3000), suggesting a relationship between FLAs and immunity .
The accumulation of HRGPs at the infection sites can be explained because the PCW is not just a physical and passive barrier against pathogens; recently, this complex structure has emerged as a dynamic defense structure involved in sensing and monitoring stressing conditions that result in compensatory responses essential for the maintenance of cell integrity and stability. Abiotic and biotic factors, such as the disruption of the PCW during infection by pathogens, trigger molecular mechanisms of the signaling pathways that sense and maintain cell wall integrity, including sensors that detect changes in the cell surface and signals originating from the wall that transduce downstream signals (Bacete et al., 2018;Rui and Dinneny, 2020). Additionally, CWPs have an important role in defense against pathogens; this proteins carry out (a) a reinforcement of the plant cell wall through insolubilization and oxidative crosslinking of extensins and sensors resident in the plasma membrane (PRPs) through H 2 O 2 and peroxidases, (b) AGP secretion and accumulation at sites of infection by pathogens (Figure 3A), (c) binding of GRPs to pathogenic RNA to degrade its genetic material and, (d) transcription of genes that encode pathogenrelated proteins (PRs) using AGPs as a soluble molecular signal (Figure 3B; Rashid, 2016;Bacete et al., 2018).
Thus, the role of AGPs in the defense responses of plants against pathogens comprises the secretion and clumping of AGPs at the infection sites and the creation of cross-links with cell wall polysaccharides such as pectin. Covalent bonds have been described between the AGP At3g4530 from A. thaliana, arabinoxylan and rhamnogalacturonan I/homogalacturonan, which form an APAP1 structure (Tan et al., 2013); therefore, the action of enzymes that degrade AGs is necessary to allow the pathogen to surpass the PCW and penetrate the protoplast.
On the other hand, AGPs and other proteins attached to the plasma membrane by GPI anchoring, are involved in connecting the intracellular and extracellular space, and are good candidates for transducing signals from the extracellular space to the cytoplasm. In this sense, the receptor like kinase (RLK) family, AGPs, the mitogen-activated protein kinase (MAPK) pathway, and the target of rapamycin (TOR) pathway could be potential components of perceptual mechanisms of cell wall integrity (Pogorelko et al., 2013). It has been reported that some AGPs contain a domain of six cysteine residues designated the proline-AGP-cysteine domain (PAC) (like that identified in Cys-rich LAT52); this domain can interact with RLK receptors (Tang et al., 2002). In this way, it has been suggested that PAC domain might mediate the binding between some AGPs and RLKs (Figure 3B; Seifert and Roberts, 2007). Moreover, the fasciclin-like AGP SOS 5, has been reported as a GPI anchored protein that acts in a pathway involving two cell wall RLKs (FEI1 and FEI2) (Showalter and Basu, 2016a).
Evidence for the role of AGPs in cell signaling during plantmicrobe interactions shows that AGP17 from A. thaliana is necessary for the activation of systemic acquired resistance (SAR). This glycoprotein seems to be involved in the transduction pathway of intracellular changes in salicylic acid levels and genetic expression of the gene encoding PR1 (Gaspar et al., 2004). Furthermore, binding of β-GlcYariv to plant surface AGPs, triggers wound-like defense responses that include PCW reinforcement and callose synthesis (Guan and Nothnagel, 2004). In addition, treatment with β-Glc Yariv suppresses the expression of genes involved in gibberellin signaling, an effect similar to that caused by elicitors such as chitin (Mashiguchi et al., 2008).
As mentioned above, AG type II are essential components for the function of AGPs. In vitro assays using exo1,3GAL have shown that complete hydrolysis of arabinogalactan terminated its reactivity with β-Glc Yariv reagent, confirming that the AGP side chains are responsible for its activity (Kiyohara et al., 1997). On the other hand, the expression of a fungal exo1,3GAL in A. thaliana leads to a decrease in AGPs reactive to β-Glc Yariv and a severe tissue disorganization in hypocotyl and cotyledons. Furthermore, oligosaccharides released from AG type II were detected in the soluble fraction of transgenic plants (Yoshimi et al., 2020). Thus, hydrolysis of the carbohydrate component of AGPs by hydrolytic enzymes secreted by fungi and bacteria during penetration of the PCW would have consequences for the mechanisms of detection and monitoring of the integrity of the cell wall, favoring infection by pathogens. Damage to the PCW caused by the combination of cellulase and pectinase activities is responsible for the accumulation of jasmonic and salicylic acids in plants, and RLK (FEI2), and mechanosensitive Ca +2 channels localized in the plasma membrane (MCA1) are responsible for the activation of responses to damage (osmosensitive responses) (Engelsdorf et al., 2018).
Therefore, the secretion of AG type II-degrading enzymes by phytopathogens appears to be crucial for the establishment of host infection. Deletion of the MoAbfB gene encoding an α-Narabinofuranosidase B from Magnaporthe oryzae resulted in a reduction in disease severity in rice (Wu et al., 2016). Likewise, comparison of the genetic expression of an endo1,6GAL between pathogenic and non-pathogenic strains of C. lindemuthianum, showed that compared with most of the evaluated conditions, the levels of genetic expression were higher in pathogenic than non-pathogenic strains, supporting a role for this enzyme in the PCW degradation during the establishment of the infection (Villa-Rivera et al., 2017b). Finally, the inactivation of Malus domestica AGPs with β-Glc Yariv reagent, which exhibit an effect similar to that of degradation by enzymes, causes a more rapid progress of Penicillium spinulosum infection, thus reinforcing the notion that the inactivation of AG type II has an impact on the PCW integrity and the activation of plant defense responses (Leszczuk et al., 2019).

CONCLUSION AND PERSPECTIVES
Several lines of evidence support the proposal that AGPs play different and crucial roles in plant-microorganism interactions.
In general, most studies on the role of AGPs in plantmicroorganism interactions have focused on the response of plants. Evidence shown that in plant root tips AGPs are attractants of symbiotic species of fungi or bacteria and promoters of the development of infectious structures and colonization, as well, these interactions can activate plant defense mechanisms such as ISR. Furthermore, plants secrete and accumulate AGPs at infection sites, creating cross-links with pectin and probably other PCW polymers. In this sense, it is proposed that AGPs could prevent infection by pathogenic microorganisms because oligosaccharides or glycopeptides generated by hydrolytic enzymes of pathogens act as DAMPs and elicits the plant defense response. But then the question arises why the degradation of AGPs by successful pathogens is crucial for the establishment of the host infection. Moreover, the binding of β-Glc Yariv to AGPs on the plant surface elicits wound-like defense responses, yet, in contrast it can also promote a more rapid progress of fungal infections, similar to the action of the polysaccharidases. On the other hand, although it is well established that phytopathogenic and beneficial fungi and bacteria secrete a set of glycosyl hydrolases that degrade AG type II of AGPs, most of the reports available on these enzymes have focused on their biotechnological applications. Clearly, it is necessary to develop studies on the expression and secretion of AG type II-degrading enzymes, and on their degradation products and their role during the establishment of host infection.

AUTHOR CONTRIBUTIONS
MV-R and MZ-P wrote the first version of the manuscript and figures. MZ-P, HC-C, and EL-R corrected and improved the manuscript. All authors read and approved the submitted version of the manuscript.