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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Plant Sci.</journal-id>
<journal-title>Frontiers in Plant Science</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Plant Sci.</abbrev-journal-title>
<issn pub-type="epub">1664-462X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fpls.2024.1520688</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Plant Science</subject>
<subj-group>
<subject>Mini Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Antioxidant-mediated suppression of ferroptosis in <italic>Pyricularia oryzae</italic>: a novel approach to rice blast management for sustainable rice production</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Santoni</surname>
<given-names>Mattia</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
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<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Molina-Hernandez</surname>
<given-names>Junior Bernardo</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2715115"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kunova</surname>
<given-names>Andrea</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/194058"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Cortesi</surname>
<given-names>Paolo</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/205402"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Brunetti</surname>
<given-names>Barbara</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rocculi</surname>
<given-names>Pietro</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/776024"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Christodoulou</surname>
<given-names>Michael S.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1837131"/>
<role content-type="https://credit.niso.org/contributor-roles/funding-acquisition/"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Danesi</surname>
<given-names>Francesca</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/149889"/>
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</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Department of Agricultural and Food Sciences (DISTAL), University of Bologna</institution>, <addr-line>Cesena</addr-line>, <country>Italy</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Department of Food, Environmental and Nutritional Sciences (DeFENS), University of Milan</institution>, <addr-line>Milan</addr-line>, <country>Italy</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Interdepartmental Centre for Industrial Agri-Food Research (CIRI), University of Bologna</institution>, <addr-line>Cesena</addr-line>, <country>Italy</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Bochra Amina Bahri, University of Georgia, United States</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Nicol&#xe1;s M. Cecchini, National University of Cordoba (CIQUIBIC), Argentina</p>
<p>Katarzyna Otulak-Kozie&#x142;, Warsaw University of Life Sciences, Poland</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Mattia Santoni, <email xlink:href="mailto:mattia.santoni@unibo.it">mattia.santoni@unibo.it</email>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>20</day>
<month>12</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>15</volume>
<elocation-id>1520688</elocation-id>
<history>
<date date-type="received">
<day>31</day>
<month>10</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>09</day>
<month>12</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2024 Santoni, Molina-Hernandez, Kunova, Cortesi, Brunetti, Rocculi, Christodoulou and Danesi</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Santoni, Molina-Hernandez, Kunova, Cortesi, Brunetti, Rocculi, Christodoulou and Danesi</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access 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.</p>
</license>
</permissions>
<abstract>
<p>Ferroptosis, an iron-dependent form of regulated cell death, has recently emerged as a crucial process in the pathogenesis of <italic>Pyricularia oryzae</italic>, the causal agent of the devastating rice blast disease, which causes billions of dollars in annual losses. This mini review explores the potential of antioxidants in suppressing ferroptosis in <italic>P. oryzae</italic> to promote sustainable rice production, with significant implications for global food security and nutrition. We critically analyze the current literature on the mechanisms of ferroptosis in <italic>P. oryzae</italic>, including iron metabolism and lipid peroxidation, the role of different antioxidants in inhibiting this cell death pathway, and the potential applications of antioxidant-based strategies for the management of rice blast disease. Recent discoveries, such as the efficacy of the natural flavonoid tangeretin in inhibiting fungal ferroptosis by interfering with the accumulation of iron and reactive oxygen species, highlight the promise of natural and nature-inspired compounds for disease management. The use of antioxidants to modulate ferroptosis in <italic>P. oryzae</italic> offers several advantages over traditional fungicide-based approaches, including improved safety, sustainability, and potential nutritional benefits through antioxidant-enriched rice varieties. However, challenges such as optimizing delivery methods, managing potential resistance, and ensuring efficacy under different environmental conditions need to be addressed. To achieve these goals, future research should focus on identifying the most effective antioxidant compounds, exploring synergistic combinations, and developing sustainable application methods.</p>
</abstract>
<kwd-group>
<kwd>antioxidants</kwd>
<kwd>ferroptosis</kwd>
<kwd>
<italic>Magnaporthe oryzae</italic>
</kwd>
<kwd>peroxidation</kwd>
<kwd>plant-pathogen interactions</kwd>
<kwd>
<italic>Pyricularia oryzae</italic>
</kwd>
<kwd>reactive oxygen species</kwd>
<kwd>rice blast disease</kwd>
</kwd-group>
<contract-num rid="cn001">2022E7KW2W</contract-num>
<contract-sponsor id="cn001">Ministero dell'Universit&#xe0; e della Ricerca<named-content content-type="fundref-id">10.13039/501100021856</named-content>
</contract-sponsor>
<counts>
<fig-count count="2"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="59"/>
<page-count count="7"/>
<word-count count="2352"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Plant Pathogen Interactions</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1" sec-type="intro">
<label>1</label>
<title>Introduction</title>
<p>Rice, the most important staple food for over half of the global population, faces a major threat from blast disease caused by <italic>Pyricularia oryzae</italic> (teleomorph <italic>Magnaporthe oryzae</italic>). This ascomycete filamentous fungus significantly impacts global rice production and food security (<xref ref-type="bibr" rid="B24">Islam et&#xa0;al., 2023</xref>), leading to 10&#x2013;30% yield losses (<xref ref-type="bibr" rid="B10">Dean et&#xa0;al., 2012</xref>), with severe outbreaks causing up to 50% crop loss (<xref ref-type="bibr" rid="B45">Scheuermann et&#xa0;al., 2012</xref>; <xref ref-type="bibr" rid="B36">Nalley et&#xa0;al., 2016</xref>). <italic>P. oryzae</italic> infects various parts of rice plants (leaves, stems, nodes, and panicles), causing widespread damage. Different lineages are able to infect also other important cereal crops like millet, barley, and wheat (<xref ref-type="bibr" rid="B56">Wilson, 2021</xref>). Of particular global concern is the <italic>P. oryzae</italic> pathotype <italic>Triticum</italic>, which causes wheat blast&#x2014;a devastating disease that impacts wheat, another major staple crop (<xref ref-type="bibr" rid="B3">Castroagudin et&#xa0;al., 2016</xref>). Wheat blast has already led to significant crop losses in South America and South Asia, with the potential to spread further. This pathotype poses a serious threat to global food security due to its adaptability and resistance to common fungicides (<xref ref-type="bibr" rid="B8">Cruz and Valent, 2017</xref>; <xref ref-type="bibr" rid="B4">Ceresini et&#xa0;al., 2018</xref>). Ongoing research focuses on early detection methods, molecular markers for specific pathotype identification, and the development of resistant wheat varieties to mitigate the impact of this dangerous pathogen (<xref ref-type="bibr" rid="B23">Ikeda et&#xa0;al., 2024</xref>).</p>
<p>The economic impact of blast is substantial, with annual damage estimated at $70 billion (<xref ref-type="bibr" rid="B45">Scheuermann et&#xa0;al., 2012</xref>; <xref ref-type="bibr" rid="B55">Valent, 2021</xref>). Despite ongoing research, effective long-term solutions remain elusive, and climate change alongside with increasing pathogen resistance urge for innovative management approaches (<xref ref-type="bibr" rid="B53">Singh and Maurya, 2021</xref>; <xref ref-type="bibr" rid="B52">Singh et&#xa0;al., 2023</xref>).</p>
<p>Recent advances in understanding the pathogenesis of <italic>P. oryzae</italic> have revealed the role of ferroptosis, an iron-dependent regulated cell death, in the infection process (<xref ref-type="bibr" rid="B47">Shen et&#xa0;al., 2020</xref>). Characterized by lipid peroxide and iron-dependent reactive oxygen species (ROS) accumulation, ferroptosis is crucial for the development of infection structures and disease progression (<xref ref-type="bibr" rid="B27">Kou et&#xa0;al., 2019</xref>; <xref ref-type="bibr" rid="B47">Shen et&#xa0;al., 2020</xref>, <xref ref-type="bibr" rid="B50">2023</xref>). Evidence suggests that iron and lipid peroxidation are necessary for ferroptosis spread, and involve a signal that propagates upstream of cell rupture (<xref ref-type="bibr" rid="B41">Riegman et&#xa0;al., 2020</xref>). This discovery has prompted research into antioxidants as a novel disease control strategy. Antioxidants have demonstrated the ability to suppress ferroptosis in various biological systems (<xref ref-type="bibr" rid="B17">Ge et&#xa0;al., 2021</xref>; <xref ref-type="bibr" rid="B59">Zhang et&#xa0;al., 2021</xref>; <xref ref-type="bibr" rid="B42">Rizzardi et&#xa0;al., 2022</xref>; <xref ref-type="bibr" rid="B58">Zhang et&#xa0;al., 2024</xref>), sparking interest in their potential to interrupt the infection cycle of <italic>P. oryzae</italic> and enhance rice plant resistance (<xref ref-type="bibr" rid="B30">Liu and Zhang, 2022</xref>).</p>
<p>This mini review summarizes current knowledge of ferroptosis in pathogenesis of <italic>P. oryzae</italic> and the potential of antioxidants in suppressing this process. Our focus is specifically on antioxidant-based approaches to suppress ferroptosis in <italic>P. oryzae</italic>, rather than strategies such as biological control, breeding for resistant cultivars, or genetic engineering. We examine recent advances, discuss antioxidant interventions, and explore implications for sustainable management of rice blast. We also highlight controversies, identify research gaps, and propose future directions, aiming to provide a concise overview of how targeting ferroptosis through antioxidant strategies could contribute to more effective and environmentally friendly approaches to manage rice blast disease, supporting global food security and sustainable agriculture.</p>
</sec>
<sec id="s2">
<label>2</label>
<title>Ferroptosis: mechanisms and significance in <italic>Pyricularia oryzae</italic>
</title>
<p>The hallmarks of ferroptosis in <italic>P. oryzae</italic> are the accumulation of lipid peroxides, elevated levels of intracellular ferric iron (Fe <sup>3+</sup>), and the consequent generation of ROS (<xref ref-type="bibr" rid="B29">Liu et&#xa0;al., 2024</xref>). Researchers have identified key players in this process, highlighting the critical role of iron metabolism regulated by the transcription factor Fep1 (<xref ref-type="bibr" rid="B27">Kou et&#xa0;al., 2019</xref>; <xref ref-type="bibr" rid="B30">Liu and Zhang, 2022</xref>). <xref ref-type="bibr" rid="B1">Abdul et&#xa0;al. (2018)</xref> showed that cell death is characterized by membrane damage caused by the accumulation of lipid peroxides to lethal concentrations due to the oxidation of polyunsaturated fatty acids in membrane phospholipids, which is essential for ferroptotic cell death, underlining the importance of membrane integrity. Recent research has also highlighted the role of calcium signaling with high Ca<sup>2+</sup> levels in ROS-dependent cell death due to an imbalance in cellular redox status, such as in ferroptosis (<xref ref-type="bibr" rid="B34">Molina-Hernandez et&#xa0;al., 2022</xref>).</p>
<p>In <italic>P. oryzae</italic>, ROS regulation plays important roles in both development and virulence. ROS generation has been linked to the NADPH oxidase (NOX) complex. A pioneering work by <xref ref-type="bibr" rid="B13">Egan et&#xa0;al. (2007)</xref> showed that NOX1 and NOX2 are important sources of ROS during appressorium development and ferroptosis, thus representing potential targets for possible control strategies.</p>
<p>Shen and colleagues (<xref ref-type="bibr" rid="B47">Shen et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B48">Shen and Naqvi, 2021</xref>; <xref ref-type="bibr" rid="B50">Shen et&#xa0;al., 2023</xref>; <xref ref-type="bibr" rid="B49">Shen and Naqvi, 2024</xref>) have shown that ferroptosis is essential for appressorium maturation, successful rice cell penetration, and rice tissue colonization. Modulating ferroptosis can significantly affect the virulence of <italic>P. oryzae</italic>, suggesting potential disease control avenues.</p>
<p>Despite these advances, controversy remains. <xref ref-type="bibr" rid="B54">Stockwell et&#xa0;al. (2017)</xref> highlighted the need for precise molecular markers to differentiate ferroptosis from other cell death forms. The role of ferroptosis in <italic>P. oryzae</italic> strains infecting non-rice hosts is still largely unexplored (<xref ref-type="bibr" rid="B49">Shen and Naqvi, 2024</xref>).</p>
<p>Environmental influences on ferroptosis represent another area of uncertainty. Studies have questioned how temperature (<xref ref-type="bibr" rid="B37">Onaga et&#xa0;al., 2017</xref>), humidity (<xref ref-type="bibr" rid="B39">Qiu et&#xa0;al., 2022</xref>), and drought stress (<xref ref-type="bibr" rid="B2">Bidzinski et&#xa0;al., 2016</xref>) might influence the pathogenic process and virulence under changing climatic conditions. However, the direct effects of these factors on ferroptosis in <italic>P. oryzae</italic> are not yet fully understood.</p>
</sec>
<sec id="s3">
<label>3</label>
<title>Natural and synthetic compounds and their role in suppressing ferroptosis in <italic>Pyricularia oryzae</italic>
</title>
<p>Natural and synthetic compounds have shown effectiveness in&#xa0;modulating ferroptosis, offering promising possibilities for controlling <italic>P. oryzae</italic> infections (<xref ref-type="bibr" rid="B51">Sies et&#xa0;al., 2017</xref>). While the role&#xa0;of ferroptosis in <italic>P. oryzae</italic> pathogenicity has been established (<xref ref-type="bibr" rid="B47">Shen et&#xa0;al., 2020</xref>), the specific effects of inhibitory compounds&#x2014;whether natural, nature-inspired, or synthetic&#x2014;on this cell death pathway remain under investigation. <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1</bold>
</xref> illustrates the key molecular components involved and highlights potential intervention targets. Natural antioxidants, particularly glutathione and (poly)phenolics (PCs), along with nature-inspired and synthetic inhibitors, have emerged as promising agents for suppressing this pathogenic process in <italic>P. oryzae</italic>.</p>
<fig id="f1" position="float">
<label>Figure&#xa0;1</label>
<caption>
<p>Schematic representation of the ferroptosis pathway in <italic>Pyricularia oryzae</italic> and potential antioxidant intervention points. The figure shows key cellular components involved in ferroptosis, including iron sources, NADPH oxidase, reactive oxygen species (ROS), lipid peroxides, and the glutathione (GSH)/glutathione disulfide (GSSG), part of glutathione peroxidase 4 (GPX4) system. Created with <uri xlink:href="https://BioRender.com">BioRender.com</uri>.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpls-15-1520688-g001.tif"/>
</fig>
<sec id="s3_1">
<label>3.1</label>
<title>Glutathione and related systems</title>
<p>Glutathione (GSH), a crucial cellular antioxidant (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>), plays a vital role in regulating ferroptosis. Stockwell and colleagues (2017) established that GSH is essential for maintaining cellular redox balance and detoxifying lipid hydroperoxides through glutathione peroxidase 4. <xref ref-type="bibr" rid="B14">Fernandez and Wilson (2014)</xref> demonstrated the importance of glutathione-related systems for <italic>P. oryzae</italic> virulence in rice blast disease. <xref ref-type="bibr" rid="B22">Huang et&#xa0;al. (2011)</xref> identified the MoHYR1 gene in <italic>P. oryzae</italic>, encoding a protein with a GPX domain that utilizes GSH to detoxify ROS. Deletion of MoHYR1 increased sensitivity to H<sub>2</sub>O<sub>2</sub> and reduced virulence, linking GSH-dependent mechanisms to the pathogen&#x2019;s ability to overcome host defenses.</p>
<fig id="f2" position="float">
<label>Figure&#xa0;2</label>
<caption>
<p>Molecular structures of antioxidants (glutathione, tangeretin and curcumin), synthetic inhibitors of ferroptosis (ferrostatin-1 and liproxstatin-1), and iron chelators (deferoxamine) involved in modulating iron-dependent cell death in <italic>P. oryzae</italic>.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpls-15-1520688-g002.tif"/>
</fig>
<p>
<xref ref-type="bibr" rid="B43">Samalova et&#xa0;al. (2014)</xref> showed that <italic>P. oryzae</italic> maintains a highly reduced cytoplasmic glutathione pool during infection, with only slight shifts in oxidation during development. This tight regulation of GSH redox state, coupled with the fungus&#x2019;s extreme resistance to external H<sub>2</sub>O<sub>2</sub> exposure, underscores robust antioxidant defenses of <italic>P. oryzae</italic>. In fact, more recent studies with <italic>P. oryzae</italic> have demonstrated that rice produces H<sub>2</sub>O<sub>2</sub> shortly after inoculation with a virulent strain of <italic>P. oryzae</italic> (<xref ref-type="bibr" rid="B5">Chi et&#xa0;al., 2009</xref>; <xref ref-type="bibr" rid="B26">Kato et&#xa0;al., 2009</xref>). <xref ref-type="bibr" rid="B9">Dangol et&#xa0;al. (2019)</xref> showed that glutathione depletion, induced by erastin, a small antitumor agent, leads to iron- and ROS-dependent ferroptotic cell death in rice cells during <italic>P. oryzae</italic> infection, highlighting the interplay among glutathione, iron, and ROS in plant-pathogen interactions.</p>
</sec>
<sec id="s3_2">
<label>3.2</label>
<title>Tangeretin and other (poly)phenolics</title>
<p>PCs have shown promise as antioxidants and potential suppressors of oxidative stress in various biological systems (<xref ref-type="bibr" rid="B40">Quideau et&#xa0;al., 2011</xref>). Curcumin (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>), for instance, demonstrated antifungal properties against plant pathogens (<xref ref-type="bibr" rid="B21">Hu et&#xa0;al., 2017</xref>), suggesting potential for further investigation in <italic>P. oryzae</italic> ferroptosis through suppression of iron accumulation.</p>
<p>Recent research has expanded our understanding of PCs&#x2019; role in plant-fungal interactions. <xref ref-type="bibr" rid="B33">Moin et&#xa0;al. (2024)</xref> conducted an <italic>in silico</italic> study suggesting that certain flavonoids may influence pathogenicity of <italic>P. oryzae</italic>. These results support the potential of PCs in plant-fungal interactions (<xref ref-type="bibr" rid="B46">Shalaby and Horwitz, 2015</xref>). In 2021, <xref ref-type="bibr" rid="B28">Liang et&#xa0;al. (2021)</xref> highlighted the potential of PCs in suppressing ferroptosis in <italic>P. oryzae</italic>. Notably, tangeretin, a flavonoid from citrus peels (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>), effectively inhibits fungal ferroptosis and suppresses rice blast disease by impairing iron and ROS accumulation and suppressing lipid peroxidation in <italic>P. oryzae</italic> conidia, which are crucial for appressorium formation and subsequent pathogenesis.</p>
<p>These findings on natural antioxidants, particularly flavonoids like tangeretin and other PCs, not only demonstrate their direct potential in suppressing ferroptosis in <italic>P. oryzae</italic>, but also provide valuable structural and functional insights that could serve as templates for the design and synthesis of novel, nature-inspired molecules with enhanced efficacy and specificity against rice blast disease. Additionally, other PCs in rice, such as hydroxybenzoic and hydroxycinnamic acids, play a vital role in plant defense by enhancing structural integrity, acting as direct antimicrobial agents, and regulating hypersensitive responses during biotic stress (see <xref ref-type="supplementary-material" rid="SM1">
<bold>Supplementary Table&#xa0;1</bold>
</xref>).</p>
</sec>
<sec id="s3_3">
<label>3.3</label>
<title>Other ferroptosis inhibitors and iron chelators</title>
<p>While ferroptosis inhibitors like ferrostatin-1 and liproxstatin-1, whose structures are shown in <xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>, have shown efficacy in mammalian systems (<xref ref-type="bibr" rid="B11">Dixon et&#xa0;al., 2012</xref>; <xref ref-type="bibr" rid="B16">Friedmann Angeli et&#xa0;al., 2014</xref>; <xref ref-type="bibr" rid="B32">Miotto et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B44">Scarpellini et&#xa0;al., 2023</xref>), their effects on <italic>P. oryzae</italic> are only now being explored. In recent years, research has begun to investigate the potential of other ferroptosis inhibitors (<italic>e.g.</italic>, ferrostatin-1 and deferoxamine (DFO) - structures shown in <xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>) in plant-pathogen interactions (<xref ref-type="bibr" rid="B9">Dangol et&#xa0;al., 2019</xref>), opening new possibilities for chemical control strategies of <italic>P. oryzae</italic>. For example, <xref ref-type="bibr" rid="B6">Christodoulou et&#xa0;al. (2024)</xref> demonstrated that DFO inhibits appressorium formation, likely through its chelating ability. The authors speculate that fungal cells might uptake DFO via specific transport systems such as proton symporters, actively transporting the compound based on extracellular iron concentrations. This targeted mechanism could significantly disrupt early conidial development, thereby reducing the virulence of the rice blast fungus.</p>
</sec>
</sec>
<sec id="s4">
<label>4</label>
<title>Implications of antioxidant-based strategies in rice blast control for human nutrition</title>
<p>The use of antioxidants to manage rice blast disease has a significant impact on global nutrition and food security. Rice provides essential nutrients for billions of people, especially in developing countries (<xref ref-type="bibr" rid="B35">Muthayya et&#xa0;al., 2014</xref>). Ensuring sustainable rice production and minimizing yield losses due to diseases such as rice blast are critical to preventing hunger and malnutrition worldwide (<xref ref-type="bibr" rid="B36">Nalley et&#xa0;al., 2016</xref>).</p>
<p>Agronomical approaches to enhance endogenous antioxidant levels in rice could provide dual benefits for both disease resistance and nutritional value. For GSH content, studies have shown that appropriate timing of nitrogen fertilization and water management practices can optimize GSH biosynthesis pathways and maintain cellular redox homeostasis through regulation of the GSH/GSSG ratio (<xref ref-type="bibr" rid="B19">Hasanuzzaman et&#xa0;al., 2017</xref>; <xref ref-type="bibr" rid="B7">Cimini et&#xa0;al., 2022</xref>). For PCs, several agronomical practices have been shown to modulate their accumulation in rice. For example, targeted stress conditions during grain development can enhance phenylpropanoid pathway activity and the resulting PC content (<xref ref-type="bibr" rid="B57">Yang et&#xa0;al., 2024</xref>). These agronomic interventions could be integrated with new approaches based on natural antioxidants, such as flavonoids like tangeretin which effectively inhibits fungal ferroptosis (<xref ref-type="bibr" rid="B28">Liang et&#xa0;al., 2021</xref>), into existing rice cultivation systems to enhance both disease resistance and nutritional value of rice crops (<xref ref-type="bibr" rid="B38">Pang et&#xa0;al., 2018</xref>).</p>
<p>Recent clinical studies have demonstrated that consumption of pigmented rice, particularly rich in PCs, mainly ferulic acid and anthocyanins, can improve antioxidant status (<xref ref-type="bibr" rid="B31">Mendoza-Sarmiento et&#xa0;al., 2023</xref>), while dietary supplements like curcumin can enhance plasma GSH levels, leading to improved cardiometabolic health through reduced oxidative stress and inflammation (<xref ref-type="bibr" rid="B12">Dludla et&#xa0;al., 2023</xref>).</p>
</sec>
<sec id="s5">
<label>5</label>
<title>Challenges and future directions</title>
<p>While antioxidants show great promise in suppressing ferroptosis in <italic>P. oryzae</italic>, several challenges remain. The specificity of antifungal action, potential off-target effects, and the development of fungal resistance are concerns that need to be addressed (<xref ref-type="bibr" rid="B15">Fisher et&#xa0;al., 2018</xref>). Moreover, the translation of laboratory findings to field applications presents logistical and regulatory hurdles (<xref ref-type="bibr" rid="B20">Hollomon, 2015</xref>). Future research should focus on identifying natural antioxidants that can effectively suppress ferroptosis in <italic>P. oryzae</italic> while being safe and bioavailable for human consumption (<xref ref-type="bibr" rid="B18">Goufo and Trindade, 2017</xref>), including optimizing delivery methods and exploring synergistic combinations with other antifungals. Investigating the potential of enhancing endogenous antioxidant systems in rice plants represents an exciting avenue for increasing resistance to <italic>P. oryzae</italic> infection (<xref ref-type="bibr" rid="B57">Yang et&#xa0;al., 2024</xref>). Additionally, research should explore how chitin-derived signals from fungal cell walls, which act as defense elicitors in rice (<xref ref-type="bibr" rid="B25">Kaku et&#xa0;al., 2006</xref>), might interact with iron and ROS-dependent pathways during <italic>P. oryzae</italic> infection. This multifaceted approach requires interdisciplinary collaboration among plant pathologists, nutritionists, agronomists, and food scientists to fully realize the potential of antioxidant-based strategies in both rice blast control and nutrition enhancement.</p>
</sec>
<sec id="s6" sec-type="conclusions">
<label>6</label>
<title>Conclusion</title>
<p>The rice blast disease, caused by <italic>P. oryzae</italic>, remains a significant threat to global rice production and food security. This mini review has explored the promising strategy of using antioxidants to suppress ferroptosis in <italic>P. oryzae</italic> for controlling this devastating disease. Recent discoveries, such as the efficacy of tangeretin in inhibiting fungal ferroptosis, highlight the potential of natural and nature-inspired compounds in rice blast management. These findings offer alternatives to traditional fungicides and opportunities to enhance rice&#x2019;s nutritional value through antioxidant enrichment.</p>
<p>Antioxidant-based approaches present several advantages, including improved safety and environmental friendliness compared to synthetic fungicides. However, challenges remain in optimizing delivery methods, addressing potential resistance, and ensuring efficacy in diverse conditions. Future research should focus on identifying effective antioxidant compounds, exploring synergistic combinations, and developing sustainable application methods. From a nutritional perspective, this approach offers possibilities for enhancing both rice resilience and its nutritional quality.</p>
</sec>
</body>
<back>
<sec id="s7" sec-type="author-contributions">
<title>Author contributions</title>
<p>MS: Conceptualization, Writing &#x2013; original draft, Writing &#x2013; review &amp; editing. JM-H: Writing &#x2013; original draft, Writing &#x2013; review &amp; editing. AK: Writing &#x2013; original draft, Writing &#x2013; review &amp; editing. PC: Writing &#x2013; review &amp; editing. BB: Writing &#x2013; review &amp; editing. PR: Writing &#x2013; review &amp; editing. MC: Funding acquisition, Writing &#x2013; original draft, Writing &#x2013; review &amp; editing. FD: Conceptualization, Funding acquisition, Writing &#x2013; original draft, Writing &#x2013; review &amp; editing.</p>
</sec>
<sec id="s8" sec-type="funding-information">
<title>Funding</title>
<p>The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was funded by the European Union - NextGenerationEU under the National Recovery and Resilience Plan (PNRR) - Mission 4 Education and research - Component 2 From research to business - Investment 1.1 Notice PRIN 2022 - DD N. 104 del 2/2/2022, from title &#x201c;Targeting ferroptosis in <italic>Pyricularia Oryzae</italic> to suppress rice blast (INFIRE)&#x201d;, proposal code 2022E7KW2W &#x2013; CUP J53D23009870006.</p>
</sec>
<sec id="s9" sec-type="COI-statement">
<title>Conflict of interest</title>
<p>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.</p>
</sec>
<sec id="s10" sec-type="ai-statement">
<title>Generative AI statement</title>
<p>The author(s) declare that no Generative AI was used in the creation of this manuscript.</p>
</sec>
<sec id="s11" sec-type="disclaimer">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<sec id="s12" sec-type="supplementary-material">
<title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fpls.2024.1520688/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fpls.2024.1520688/full#supplementary-material</ext-link>
</p>
<supplementary-material xlink:href="Table1.docx" id="SM1" mimetype="application/vnd.openxmlformats-officedocument.wordprocessingml.document"/>
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