Perception of unrelated microbe-associated molecular patterns triggers conserved yet variable physiological and transcriptional changes in Brassica rapa ssp. pekinensis
Pattern-triggered immunity (PTI) includes the different transcriptional and physiological responses that enable plants to ward off microbial invasion. Surface-localized pattern-recognition receptors (PRRs) recognize conserved microbe-associated molecular patterns (MAMPs) and initiate a branched sign...
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creator | Kim, Wanhui Prokchorchik, Maxim Tian, Yonghua Kim, Seulgi Jeon, Hyelim Segonzac, Cécile |
description | Pattern-triggered immunity (PTI) includes the different transcriptional and physiological responses that enable plants to ward off microbial invasion. Surface-localized pattern-recognition receptors (PRRs) recognize conserved microbe-associated molecular patterns (MAMPs) and initiate a branched signaling cascade that culminate in an effective restriction of pathogen growth. In the model species
Arabidopsis thaliana
, early PTI events triggered by different PRRs are broadly conserved although their nature or intensity is dependent on the origin and features of the detected MAMP. In order to provide a functional basis for disease resistance in leafy vegetable crops, we surveyed the conservation of PTI events in
Brassica rapa
ssp.
pekinensis
. We identified the PRR homologs present in
B. rapa
genome and found that only one of the two copies of the bacterial Elongation factor-Tu receptor (EFR) might function. We also characterized the extent and unexpected specificity of the transcriptional changes occurring when
B. rapa
seedlings are treated with two unrelated MAMPs, the bacterial flagellin flg22 peptide and the fungal cell wall component chitin. Finally, using a MAMP-induced protection assay, we could show that bacterial and fungal MAMPs elicit a robust immunity in
B. rapa
, despite significant differences in the kinetic and amplitude of the early signaling events. Our data support the relevance of PTI for crop protection and highlight specific functional target for disease resistance breeding in Brassica crops. |
doi_str_mv | 10.1038/s41438-020-00410-0 |
format | Article |
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Arabidopsis thaliana
, early PTI events triggered by different PRRs are broadly conserved although their nature or intensity is dependent on the origin and features of the detected MAMP. In order to provide a functional basis for disease resistance in leafy vegetable crops, we surveyed the conservation of PTI events in
Brassica rapa
ssp.
pekinensis
. We identified the PRR homologs present in
B. rapa
genome and found that only one of the two copies of the bacterial Elongation factor-Tu receptor (EFR) might function. We also characterized the extent and unexpected specificity of the transcriptional changes occurring when
B. rapa
seedlings are treated with two unrelated MAMPs, the bacterial flagellin flg22 peptide and the fungal cell wall component chitin. Finally, using a MAMP-induced protection assay, we could show that bacterial and fungal MAMPs elicit a robust immunity in
B. rapa
, despite significant differences in the kinetic and amplitude of the early signaling events. Our data support the relevance of PTI for crop protection and highlight specific functional target for disease resistance breeding in Brassica crops.</description><identifier>ISSN: 2662-6810</identifier><identifier>EISSN: 2052-7276</identifier><identifier>DOI: 10.1038/s41438-020-00410-0</identifier><identifier>PMID: 33328480</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/449/2169/2107 ; 631/449/2661/2666 ; Agriculture ; Bacteria ; Biomedical and Life Sciences ; Brassica ; Brassica rapa ; Cell walls ; Chitin ; Crops ; Disease resistance ; Ecology ; Elongation ; Flagellin ; Fungi ; Genomes ; Homology ; Immunity ; Life Sciences ; Microorganisms ; Pattern recognition ; Physiological responses ; Physiology ; Plant breeding ; Plant Breeding/Biotechnology ; Plant Genetics and Genomics ; Plant protection ; Plant Sciences ; Receptors ; Seedlings ; Signaling ; Transcription</subject><ispartof>Horticulture research, 2020-11, Vol.7 (1), p.186, Article 186</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is published under http://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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-5f9c3cd6fedf8d9c22545a982a4440f1778be9b6d888429fc83ade0769c31d8f3</citedby><cites>FETCH-LOGICAL-c474t-5f9c3cd6fedf8d9c22545a982a4440f1778be9b6d888429fc83ade0769c31d8f3</cites><orcidid>0000-0002-5537-7556</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/PMC7603518/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603518/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,41099,42168,51554,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33328480$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Wanhui</creatorcontrib><creatorcontrib>Prokchorchik, Maxim</creatorcontrib><creatorcontrib>Tian, Yonghua</creatorcontrib><creatorcontrib>Kim, Seulgi</creatorcontrib><creatorcontrib>Jeon, Hyelim</creatorcontrib><creatorcontrib>Segonzac, Cécile</creatorcontrib><title>Perception of unrelated microbe-associated molecular patterns triggers conserved yet variable physiological and transcriptional changes in Brassica rapa ssp. pekinensis</title><title>Horticulture research</title><addtitle>Hortic Res</addtitle><addtitle>Hortic Res</addtitle><description>Pattern-triggered immunity (PTI) includes the different transcriptional and physiological responses that enable plants to ward off microbial invasion. Surface-localized pattern-recognition receptors (PRRs) recognize conserved microbe-associated molecular patterns (MAMPs) and initiate a branched signaling cascade that culminate in an effective restriction of pathogen growth. In the model species
Arabidopsis thaliana
, early PTI events triggered by different PRRs are broadly conserved although their nature or intensity is dependent on the origin and features of the detected MAMP. In order to provide a functional basis for disease resistance in leafy vegetable crops, we surveyed the conservation of PTI events in
Brassica rapa
ssp.
pekinensis
. We identified the PRR homologs present in
B. rapa
genome and found that only one of the two copies of the bacterial Elongation factor-Tu receptor (EFR) might function. We also characterized the extent and unexpected specificity of the transcriptional changes occurring when
B. rapa
seedlings are treated with two unrelated MAMPs, the bacterial flagellin flg22 peptide and the fungal cell wall component chitin. Finally, using a MAMP-induced protection assay, we could show that bacterial and fungal MAMPs elicit a robust immunity in
B. rapa
, despite significant differences in the kinetic and amplitude of the early signaling events. Our data support the relevance of PTI for crop protection and highlight specific functional target for disease resistance breeding in Brassica crops.</description><subject>631/449/2169/2107</subject><subject>631/449/2661/2666</subject><subject>Agriculture</subject><subject>Bacteria</subject><subject>Biomedical and Life Sciences</subject><subject>Brassica</subject><subject>Brassica rapa</subject><subject>Cell walls</subject><subject>Chitin</subject><subject>Crops</subject><subject>Disease resistance</subject><subject>Ecology</subject><subject>Elongation</subject><subject>Flagellin</subject><subject>Fungi</subject><subject>Genomes</subject><subject>Homology</subject><subject>Immunity</subject><subject>Life Sciences</subject><subject>Microorganisms</subject><subject>Pattern recognition</subject><subject>Physiological responses</subject><subject>Physiology</subject><subject>Plant breeding</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant Genetics and Genomics</subject><subject>Plant protection</subject><subject>Plant Sciences</subject><subject>Receptors</subject><subject>Seedlings</subject><subject>Signaling</subject><subject>Transcription</subject><issn>2662-6810</issn><issn>2052-7276</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9Uctu1TAQjRCIVqU_wAJZYp3Wr8TOBgkqHpUqwQLWluOMc11y7eBJrnT_iM_EbUqBDRvbmjmP8ZyqesnoBaNCX6JkUuiaclpTKlk5n1SnnDa8Vly1T8u7bXndakZPqnPEW0opayQXjXpenQghuJaanlY_v0B2MC8hRZI8WWOGyS4wkH1wOfVQW8TkwlZKE7h1spnMdlkgRyRLDuMIGYlLESEfCuoICznYHGw_AZl3RwxpSmNwdiI2DoVhI7oc7i1Lze1sHAFJiORdLmYFSLKdLUGcL8gM30OEiAFfVM-8nRDOH-6z6tuH91-vPtU3nz9eX729qZ1Ucqkb3znhhtbD4PXQOc4b2dhOcyulpJ4ppXvo-nbQWkveeaeFHYCqttDYoL04q95suvPa72FwEMvEk5lz2Nt8NMkG828nhp0Z08GoloqG6SLw-kEgpx8r4GJu05rLV9FwqVjDO6HvUHxDlS0jZvCPDoyau4DNFrApAZv7gA0tpFd_z_ZI-R1nAYgNgKVV1pr_eP9H9hcGG7dK</recordid><startdate>20201101</startdate><enddate>20201101</enddate><creator>Kim, Wanhui</creator><creator>Prokchorchik, Maxim</creator><creator>Tian, Yonghua</creator><creator>Kim, Seulgi</creator><creator>Jeon, Hyelim</creator><creator>Segonzac, Cécile</creator><general>Nature Publishing Group UK</general><general>Oxford University Press</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5537-7556</orcidid></search><sort><creationdate>20201101</creationdate><title>Perception of unrelated microbe-associated molecular patterns triggers conserved yet variable physiological and transcriptional changes in Brassica rapa ssp. pekinensis</title><author>Kim, Wanhui ; Prokchorchik, Maxim ; Tian, Yonghua ; Kim, Seulgi ; Jeon, Hyelim ; Segonzac, Cécile</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-5f9c3cd6fedf8d9c22545a982a4440f1778be9b6d888429fc83ade0769c31d8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>631/449/2169/2107</topic><topic>631/449/2661/2666</topic><topic>Agriculture</topic><topic>Bacteria</topic><topic>Biomedical and Life Sciences</topic><topic>Brassica</topic><topic>Brassica rapa</topic><topic>Cell walls</topic><topic>Chitin</topic><topic>Crops</topic><topic>Disease resistance</topic><topic>Ecology</topic><topic>Elongation</topic><topic>Flagellin</topic><topic>Fungi</topic><topic>Genomes</topic><topic>Homology</topic><topic>Immunity</topic><topic>Life Sciences</topic><topic>Microorganisms</topic><topic>Pattern recognition</topic><topic>Physiological responses</topic><topic>Physiology</topic><topic>Plant breeding</topic><topic>Plant Breeding/Biotechnology</topic><topic>Plant Genetics and Genomics</topic><topic>Plant protection</topic><topic>Plant Sciences</topic><topic>Receptors</topic><topic>Seedlings</topic><topic>Signaling</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Wanhui</creatorcontrib><creatorcontrib>Prokchorchik, Maxim</creatorcontrib><creatorcontrib>Tian, Yonghua</creatorcontrib><creatorcontrib>Kim, Seulgi</creatorcontrib><creatorcontrib>Jeon, Hyelim</creatorcontrib><creatorcontrib>Segonzac, Cécile</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</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>PubMed Central (Full Participant titles)</collection><jtitle>Horticulture research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Wanhui</au><au>Prokchorchik, Maxim</au><au>Tian, Yonghua</au><au>Kim, Seulgi</au><au>Jeon, Hyelim</au><au>Segonzac, Cécile</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Perception of unrelated microbe-associated molecular patterns triggers conserved yet variable physiological and transcriptional changes in Brassica rapa ssp. pekinensis</atitle><jtitle>Horticulture research</jtitle><stitle>Hortic Res</stitle><addtitle>Hortic Res</addtitle><date>2020-11-01</date><risdate>2020</risdate><volume>7</volume><issue>1</issue><spage>186</spage><pages>186-</pages><artnum>186</artnum><issn>2662-6810</issn><eissn>2052-7276</eissn><abstract>Pattern-triggered immunity (PTI) includes the different transcriptional and physiological responses that enable plants to ward off microbial invasion. Surface-localized pattern-recognition receptors (PRRs) recognize conserved microbe-associated molecular patterns (MAMPs) and initiate a branched signaling cascade that culminate in an effective restriction of pathogen growth. In the model species
Arabidopsis thaliana
, early PTI events triggered by different PRRs are broadly conserved although their nature or intensity is dependent on the origin and features of the detected MAMP. In order to provide a functional basis for disease resistance in leafy vegetable crops, we surveyed the conservation of PTI events in
Brassica rapa
ssp.
pekinensis
. We identified the PRR homologs present in
B. rapa
genome and found that only one of the two copies of the bacterial Elongation factor-Tu receptor (EFR) might function. We also characterized the extent and unexpected specificity of the transcriptional changes occurring when
B. rapa
seedlings are treated with two unrelated MAMPs, the bacterial flagellin flg22 peptide and the fungal cell wall component chitin. Finally, using a MAMP-induced protection assay, we could show that bacterial and fungal MAMPs elicit a robust immunity in
B. rapa
, despite significant differences in the kinetic and amplitude of the early signaling events. Our data support the relevance of PTI for crop protection and highlight specific functional target for disease resistance breeding in Brassica crops.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33328480</pmid><doi>10.1038/s41438-020-00410-0</doi><orcidid>https://orcid.org/0000-0002-5537-7556</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/449/2169/2107 631/449/2661/2666 Agriculture Bacteria Biomedical and Life Sciences Brassica Brassica rapa Cell walls Chitin Crops Disease resistance Ecology Elongation Flagellin Fungi Genomes Homology Immunity Life Sciences Microorganisms Pattern recognition Physiological responses Physiology Plant breeding Plant Breeding/Biotechnology Plant Genetics and Genomics Plant protection Plant Sciences Receptors Seedlings Signaling Transcription |
title | Perception of unrelated microbe-associated molecular patterns triggers conserved yet variable physiological and transcriptional changes in Brassica rapa ssp. pekinensis |
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