Every Coin Has Two Sides: Reactive Oxygen Species during Rice⁻ Magnaporthe oryzae Interaction
Reactive oxygen species (ROS) are involved in many important processes, including the growth, development, and responses to the environments, in rice ( ) and . Although ROS are known to be critical components in rice⁻ interactions, their regulations and pathways have not yet been completely revealed...
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description | Reactive oxygen species (ROS) are involved in many important processes, including the growth, development, and responses to the environments, in rice (
) and
. Although ROS are known to be critical components in rice⁻
interactions, their regulations and pathways have not yet been completely revealed. Recent studies have provided fascinating insights into the intricate physiological redox balance in rice⁻
interactions. In
, ROS accumulation is required for the appressorium formation and penetration. However, once inside the rice cells,
must scavenge the host-derived ROS to spread invasive hyphae. On the other side, ROS play key roles in rice against
. It has been known that, upon perception of
, rice plants modulate their activities of ROS generating and scavenging enzymes, mainly on NADPH oxidase OsRbohB, by different signaling pathways to accumulate ROS against rice blast. By contrast, the
virulent strains are capable of suppressing ROS accumulation and attenuating rice blast resistance by the secretion of effectors, such as AvrPii and AvrPiz-t. These results suggest that ROS generation and scavenging of ROS are tightly controlled by different pathways in both
and rice during rice blast. In this review, the most recent advances in the understanding of the regulatory mechanisms of ROS accumulation and signaling during rice⁻
interaction are summarized. |
doi_str_mv | 10.3390/ijms20051191 |
format | Article |
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) and
. Although ROS are known to be critical components in rice⁻
interactions, their regulations and pathways have not yet been completely revealed. Recent studies have provided fascinating insights into the intricate physiological redox balance in rice⁻
interactions. In
, ROS accumulation is required for the appressorium formation and penetration. However, once inside the rice cells,
must scavenge the host-derived ROS to spread invasive hyphae. On the other side, ROS play key roles in rice against
. It has been known that, upon perception of
, rice plants modulate their activities of ROS generating and scavenging enzymes, mainly on NADPH oxidase OsRbohB, by different signaling pathways to accumulate ROS against rice blast. By contrast, the
virulent strains are capable of suppressing ROS accumulation and attenuating rice blast resistance by the secretion of effectors, such as AvrPii and AvrPiz-t. These results suggest that ROS generation and scavenging of ROS are tightly controlled by different pathways in both
and rice during rice blast. In this review, the most recent advances in the understanding of the regulatory mechanisms of ROS accumulation and signaling during rice⁻
interaction are summarized.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms20051191</identifier><identifier>PMID: 30857220</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Accumulation ; Actin ; Antioxidants ; Appressoria ; Binding sites ; Deletion mutant ; Disease Resistance ; Enzymes ; G protein-coupled receptors ; Genes ; Glutathione peroxidase ; Glutathione reductase ; Histone deacetylase ; Host-Pathogen Interactions ; Infections ; Kinases ; Magnaporthe - pathogenicity ; Magnaporthe - physiology ; Morphogenesis ; NAD(P)H oxidase ; NADPH ; Nicotinamide ; Oryza - metabolism ; Oryza - microbiology ; Oxidative stress ; Pathogenicity ; Peroxidase ; Plant Diseases - microbiology ; Polarity ; Proteins ; Reactive Oxygen Species - metabolism ; Reductases ; Review ; Scavenging ; Transcription factors</subject><ispartof>International journal of molecular sciences, 2019-03, Vol.20 (5), p.1191</ispartof><rights>2019. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-a3c9798132b0d165fbeb984f3ac8125ed0f4ada24cb6ae1f8d5f93b1e799ed3e3</citedby><cites>FETCH-LOGICAL-c412t-a3c9798132b0d165fbeb984f3ac8125ed0f4ada24cb6ae1f8d5f93b1e799ed3e3</cites><orcidid>0000-0003-3981-6675</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429160/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429160/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30857220$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kou, Yanjun</creatorcontrib><creatorcontrib>Qiu, Jiehua</creatorcontrib><creatorcontrib>Tao, Zeng</creatorcontrib><title>Every Coin Has Two Sides: Reactive Oxygen Species during Rice⁻ Magnaporthe oryzae Interaction</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Reactive oxygen species (ROS) are involved in many important processes, including the growth, development, and responses to the environments, in rice (
) and
. Although ROS are known to be critical components in rice⁻
interactions, their regulations and pathways have not yet been completely revealed. Recent studies have provided fascinating insights into the intricate physiological redox balance in rice⁻
interactions. In
, ROS accumulation is required for the appressorium formation and penetration. However, once inside the rice cells,
must scavenge the host-derived ROS to spread invasive hyphae. On the other side, ROS play key roles in rice against
. It has been known that, upon perception of
, rice plants modulate their activities of ROS generating and scavenging enzymes, mainly on NADPH oxidase OsRbohB, by different signaling pathways to accumulate ROS against rice blast. By contrast, the
virulent strains are capable of suppressing ROS accumulation and attenuating rice blast resistance by the secretion of effectors, such as AvrPii and AvrPiz-t. These results suggest that ROS generation and scavenging of ROS are tightly controlled by different pathways in both
and rice during rice blast. In this review, the most recent advances in the understanding of the regulatory mechanisms of ROS accumulation and signaling during rice⁻
interaction are summarized.</description><subject>Accumulation</subject><subject>Actin</subject><subject>Antioxidants</subject><subject>Appressoria</subject><subject>Binding sites</subject><subject>Deletion mutant</subject><subject>Disease Resistance</subject><subject>Enzymes</subject><subject>G protein-coupled receptors</subject><subject>Genes</subject><subject>Glutathione peroxidase</subject><subject>Glutathione reductase</subject><subject>Histone deacetylase</subject><subject>Host-Pathogen Interactions</subject><subject>Infections</subject><subject>Kinases</subject><subject>Magnaporthe - pathogenicity</subject><subject>Magnaporthe - physiology</subject><subject>Morphogenesis</subject><subject>NAD(P)H oxidase</subject><subject>NADPH</subject><subject>Nicotinamide</subject><subject>Oryza - metabolism</subject><subject>Oryza - microbiology</subject><subject>Oxidative stress</subject><subject>Pathogenicity</subject><subject>Peroxidase</subject><subject>Plant Diseases - microbiology</subject><subject>Polarity</subject><subject>Proteins</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Reductases</subject><subject>Review</subject><subject>Scavenging</subject><subject>Transcription factors</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkc1KAzEUhYMo_u9cS8CNC6vJzcx04kKQUrWgCP6sQyZzp6a0SU1mqnXnc_k2PoktVqmu7oX7ncM9HEL2ODsWQrITOxhFYCzlXPIVsskTgBZjWXt1ad8gWzEOGAMBqVwnG4LlaRuAbRLVnWCY0o63jl7pSB9ePL23JcZTeofa1HaC9PZ12kdH78doLEZaNsG6Pr2zBj_fP-iN7js99qF-QurD9E0j7bkaw1zs3Q5Zq_Qw4u5ibpPHi-5D56p1fXvZ65xft0zCoW5pYWRb5lxAwUqepVWBhcyTSmiTc0ixZFWiSw2JKTKNvMrLtJKi4NiWEkuBYpucffuOm2KEpUFXBz1U42BHOkyV11b9vTj7pPp-orIEJM_YzOBwYRD8c4OxViMbDQ6H2qFvogIuWSI5JOkMPfiHDnwT3CyeAiEAQEqYU0fflAk-xoDV7zOcqXlzarm5Gb6_HOAX_qlKfAFca5au</recordid><startdate>20190308</startdate><enddate>20190308</enddate><creator>Kou, Yanjun</creator><creator>Qiu, Jiehua</creator><creator>Tao, Zeng</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3981-6675</orcidid></search><sort><creationdate>20190308</creationdate><title>Every Coin Has Two Sides: Reactive Oxygen Species during Rice⁻ Magnaporthe oryzae Interaction</title><author>Kou, Yanjun ; Qiu, Jiehua ; Tao, Zeng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-a3c9798132b0d165fbeb984f3ac8125ed0f4ada24cb6ae1f8d5f93b1e799ed3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Accumulation</topic><topic>Actin</topic><topic>Antioxidants</topic><topic>Appressoria</topic><topic>Binding sites</topic><topic>Deletion mutant</topic><topic>Disease Resistance</topic><topic>Enzymes</topic><topic>G protein-coupled receptors</topic><topic>Genes</topic><topic>Glutathione peroxidase</topic><topic>Glutathione reductase</topic><topic>Histone deacetylase</topic><topic>Host-Pathogen Interactions</topic><topic>Infections</topic><topic>Kinases</topic><topic>Magnaporthe - pathogenicity</topic><topic>Magnaporthe - physiology</topic><topic>Morphogenesis</topic><topic>NAD(P)H oxidase</topic><topic>NADPH</topic><topic>Nicotinamide</topic><topic>Oryza - metabolism</topic><topic>Oryza - microbiology</topic><topic>Oxidative stress</topic><topic>Pathogenicity</topic><topic>Peroxidase</topic><topic>Plant Diseases - microbiology</topic><topic>Polarity</topic><topic>Proteins</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Reductases</topic><topic>Review</topic><topic>Scavenging</topic><topic>Transcription factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kou, Yanjun</creatorcontrib><creatorcontrib>Qiu, Jiehua</creatorcontrib><creatorcontrib>Tao, Zeng</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kou, Yanjun</au><au>Qiu, Jiehua</au><au>Tao, Zeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Every Coin Has Two Sides: Reactive Oxygen Species during Rice⁻ Magnaporthe oryzae Interaction</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2019-03-08</date><risdate>2019</risdate><volume>20</volume><issue>5</issue><spage>1191</spage><pages>1191-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Reactive oxygen species (ROS) are involved in many important processes, including the growth, development, and responses to the environments, in rice (
) and
. Although ROS are known to be critical components in rice⁻
interactions, their regulations and pathways have not yet been completely revealed. Recent studies have provided fascinating insights into the intricate physiological redox balance in rice⁻
interactions. In
, ROS accumulation is required for the appressorium formation and penetration. However, once inside the rice cells,
must scavenge the host-derived ROS to spread invasive hyphae. On the other side, ROS play key roles in rice against
. It has been known that, upon perception of
, rice plants modulate their activities of ROS generating and scavenging enzymes, mainly on NADPH oxidase OsRbohB, by different signaling pathways to accumulate ROS against rice blast. By contrast, the
virulent strains are capable of suppressing ROS accumulation and attenuating rice blast resistance by the secretion of effectors, such as AvrPii and AvrPiz-t. These results suggest that ROS generation and scavenging of ROS are tightly controlled by different pathways in both
and rice during rice blast. In this review, the most recent advances in the understanding of the regulatory mechanisms of ROS accumulation and signaling during rice⁻
interaction are summarized.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>30857220</pmid><doi>10.3390/ijms20051191</doi><orcidid>https://orcid.org/0000-0003-3981-6675</orcidid><oa>free_for_read</oa></addata></record> |
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source | MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Accumulation Actin Antioxidants Appressoria Binding sites Deletion mutant Disease Resistance Enzymes G protein-coupled receptors Genes Glutathione peroxidase Glutathione reductase Histone deacetylase Host-Pathogen Interactions Infections Kinases Magnaporthe - pathogenicity Magnaporthe - physiology Morphogenesis NAD(P)H oxidase NADPH Nicotinamide Oryza - metabolism Oryza - microbiology Oxidative stress Pathogenicity Peroxidase Plant Diseases - microbiology Polarity Proteins Reactive Oxygen Species - metabolism Reductases Review Scavenging Transcription factors |
title | Every Coin Has Two Sides: Reactive Oxygen Species during Rice⁻ Magnaporthe oryzae Interaction |
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