Editorial: Plant cell wall in pathogenesis, parasitism and symbiosis, Volume II

COPYRIGHT © 2023 Vicré and Lionetti. This is an openaccess article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. TYPE Editorial PUBLISHED 20 June 2023 DOI 10.3389/fpls.2023.1230438

A wide range of organisms that interact with plants must interface with the plant cell wall (CW) (Lionetti and Metraux, 2014). The view of the CW as only a static cellular barrier in these interactions is outdated. Cell wall polysaccharides, phenolic compounds, and proteins, in addition to regulating important growth and development processes, are also sources of elicitors that activate cell signaling pathways (Nguema-Ona et al., 2013). Surveillance mechanisms detect CW contacts with other organisms, and specific signaling pathways and responses are activated (Swaminathan et al., 2022) (Figure 1). During biotic interactions and abiotic stresses, the structure and composition of plant CW can be regulated at the biosynthetic level and through precise, continuous post-synthetic remodeling. As a consequence, the CW must be understood as a strategic space between organisms where intelligent and dynamic molecular strategies are implemented to overwhelm a fight or cooperate for specific physiological processes (Bacete et al., 2018;Castilleux et al., 2018;De Lorenzo et al., 2019).
Cell wall enzymes and their inhibitors play key roles in apoplastic metabolism (Rui and Dinneny, 2020). Invertases (INVs) and pectin methylesterases (PMEs) play essential roles in carbohydrate metabolism, stress responses, and sugar signaling (Bellincampi et al., 2014;Tauzin and Giardina, 2014;Del Corpo et al., 2020). In this collection, Coculo and Lionetti reviewed the roles of invertase inhibitors (INVI) and pectin methylesterase inhibitors (PMEI) belonging to the "Plant Invertase/Pectin Methylesterase Inhibitor Superfamily" (Lionetti et al., 2017). An updated overview of the specific activity of the characterized isoforms, their specific functions in plant physiology, and their applications in biotechnology is provided. After the pioneering work in 2007 (Lionetti et al., 2007), several piece of evidence supported the role of PMEIs in plant resistance to stresses (An et al., 2008;Liu et al., 2018). With a genome-wide analysis and transcriptomics of the PMEI genes in Brassica napus, Wang et al. identified several BnPMEIs as resistance gene candidates in response to Sclerotinia sclerotiorum, suggesting them as possible tools to breed new and improved genotypes more resistant to Sclerotinia stem rot. Specific CW changes can occur in the vicinity of plasmodesmata during viral infection (Lionetti et al., 2015;Stavolone and Lionetti, 2017). Viruses can modify pectin, callose, and structural proteins near plasmodesmata by increasing their size exclusion limit (Kozieł et al., 2021). Loṕez-Gonzaĺez et al. addressed the little-explored impact of virus infections on secondary CW and plant development. The authors found a correlation between the developmental alterations induced in Arabidopsis by specific strains of turnip mosaic virus and specific changes in xylan and lignin biosynthesis. Although callose deposition is a response to both elicitors and pathogens, the mechanisms involved in its biosynthesis and degradation remain to be unraveled (German et al., 2023). Li et al. summarized the research progress on plant callose and its synthesizing enzymes in plant physiology.
Microfungi are also important etiological agents for plants (Doehlemann et al., 2017). The fungal pathogen Sphaerulina musiva causes stem canker with the consequent mortality of Populus trees. Populus deltoides can induce a lignified periderm to contain the pathogen, but the precise characterization of lignin changes in response to S. musiva infection is unknown. Bryant et al.identified a higher syringyl:guaiacil ratio, a higher Klason lignin content and lower p-hydroxybenzoate content in Septoria-infected P. deltoides trees compared to the healthy plant. This knowledge can favor biotechnological approaches aimed at improving the resilience and increasing the biomass yield of Populus for biofuel production.
Interesting contributions in this collection concern plant-parasite interactions. A fine-tuned re-arrangement of host CW is induced in response to infection by both plant-parasitic cyst nematodes and root-knot nematodes (Zhang et al., 2017;Bozbuga et al., 2018;Meidani et al., 2019). Veronico et al. found that drought stress affects CW metabolism in tomato roots, limiting feeding site development and reproduction of the nematode Meloidogyne incognita. Parasitic plants, such as Cuscuta species, severely damage economically important crops (Jhu and Sinha, 2022). These green parasites absorb resources through an invasive organ called the haustorium, which differentiates into vascular hyphae that establish a connection with the host plant's vasculature. The degradation and modification of host CWs allow haustorium to effectively invade host tissues. Yokoyama et al. propose that Cuscuta campestris APETALA2/ETHYLENE RESPONSE FACTORS (ERFs) can activate the transcription of the CW enzymatic genes in haustorium to favor its invasion of tobacco and Arabidopsis plants.
Plant CW is a field of molecular dialogues and agreements with symbiotic microbes to establish intimate interfaces for developmental coordination and nutrient exchange (Balestrini and Bonfante, 2014). Plants can establish mutualistic symbiosis with arbuscular mycorrhizal fungi, and phosphorus transfer across the CW specialized interfacial compartment is an important process in the mycorrhizal pathway (Begum et al., 2019). Exploiting the Rhizophagus irregularis-Lotus japonicus interaction, Nguyen and Saito showed that polyphosphate in fungal CWs and apoplastic phosphatases play an important role in phosphorus transfer at the symbiotic interface in arbuscules. Mycorrhizal fungi can be involved in mutualistic interactions during orchid seed germination (Põlme et al., 2018). Chen et al. identified several genes codifying CW structural proteins such as epidermisspecific secreted glycoprotein, proline-rich receptor-like protein, and leucine-rich repeat (LRR) extensin-like protein, which are particularly involved in the symbiosis of Tulasnella and Serendipita fungi with Dendrobium officinale.
Bioinoculants represent an environmentally-friendly agricultural practice to alleviate drought stress in crops (Kour et al., 2022). The work presented by Wilmowitz et al. indicates that the inoculation of maize seeds with Glomus sp. and Bacillus sp. can help to cope with drought stress, preventing inhibition of photosynthesis and disruption of redox balance. Glomus sp. and Bacillus sp. can modify pectin methylesterification and hemicellulose content of maize leaves, possibly leading to alleviation of the negative effects of drought. These important contributions advance our understanding of the relationships between plants and the environment at the CW interface, which will be helpful to engineer biotechnological strategies for agriculture and bioenergy fields. As a closing remark, we are grateful to the authors and reviewers for their invaluable contributions to this Research Topic.

Author contributions
VL draft the editorial text. MV revised and approved the final version of the editorial. All authors approved the submitted version.

Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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