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Progress and gaps in understanding mechanisms of ash tree resistance to emerald ash borer, a model for wood‐boring insects that kill angiosperms
63 I. 64 II. 64 III. 65 IV. 71 V. 72 75 References 75 SUMMARY: We review the literature on host resistance of ash to emerald ash borer (EAB, Agrilus planipennis), an invasive species that causes widespread mortality of ash. Manchurian ash (Fraxinus mandshurica), which coevolved with EAB, is more res...
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Published in: | The New phytologist 2016-01, Vol.209 (1), p.63-79 |
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description | 63 I. 64 II. 64 III. 65 IV. 71 V. 72 75 References 75 SUMMARY: We review the literature on host resistance of ash to emerald ash borer (EAB, Agrilus planipennis), an invasive species that causes widespread mortality of ash. Manchurian ash (Fraxinus mandshurica), which coevolved with EAB, is more resistant than evolutionarily naïve North American and European congeners. Manchurian ash was less preferred for adult feeding and oviposition than susceptible hosts, more resistant to larval feeding, had higher constitutive concentrations of bark lignans, coumarins, proline, tyramine and defensive proteins, and was characterized by faster oxidation of phenolics. Consistent with EAB being a secondary colonizer of coevolved hosts, drought stress decreased the resistance of Manchurian ash, but had no effect on constitutive bark phenolics, suggesting that they do not contribute to increased susceptibility in response to drought stress. The induced resistance of North American species to EAB in response to the exogenous application of methyl jasmonate was associated with increased bark concentrations of verbascoside, lignin and/or trypsin inhibitors, which decreased larval survival and/or growth in bioassays. This finding suggests that these inherently susceptible species possess latent defenses that are not induced naturally by larval colonization, perhaps because they fail to recognize larval cues or respond quickly enough. Finally, we propose future research directions that would address some critical knowledge gaps. |
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A ; Cipollini, Don ; Bonello, Pierluigi</creator><creatorcontrib>Villari, Caterina ; Herms, Daniel A ; Whitehill, Justin G. A ; Cipollini, Don ; Bonello, Pierluigi</creatorcontrib><description>63 I. 64 II. 64 III. 65 IV. 71 V. 72 75 References 75 SUMMARY: We review the literature on host resistance of ash to emerald ash borer (EAB, Agrilus planipennis), an invasive species that causes widespread mortality of ash. Manchurian ash (Fraxinus mandshurica), which coevolved with EAB, is more resistant than evolutionarily naïve North American and European congeners. Manchurian ash was less preferred for adult feeding and oviposition than susceptible hosts, more resistant to larval feeding, had higher constitutive concentrations of bark lignans, coumarins, proline, tyramine and defensive proteins, and was characterized by faster oxidation of phenolics. Consistent with EAB being a secondary colonizer of coevolved hosts, drought stress decreased the resistance of Manchurian ash, but had no effect on constitutive bark phenolics, suggesting that they do not contribute to increased susceptibility in response to drought stress. The induced resistance of North American species to EAB in response to the exogenous application of methyl jasmonate was associated with increased bark concentrations of verbascoside, lignin and/or trypsin inhibitors, which decreased larval survival and/or growth in bioassays. This finding suggests that these inherently susceptible species possess latent defenses that are not induced naturally by larval colonization, perhaps because they fail to recognize larval cues or respond quickly enough. Finally, we propose future research directions that would address some critical knowledge gaps.</description><identifier>ISSN: 0028-646X</identifier><identifier>EISSN: 1469-8137</identifier><identifier>DOI: 10.1111/nph.13604</identifier><identifier>PMID: 26268949</identifier><language>eng</language><publisher>England: Academic Press</publisher><subject>Acetates - pharmacology ; adults ; Agrilus ; Agrilus planipennis ; Animals ; Anti-Infective Agents - metabolism ; Antibiosis ; bark ; bioassays ; boring insects ; coevolution ; Coleoptera - physiology ; constitutive defense ; coumarins ; Cyclopentanes - pharmacology ; emerald ash borer ; Fraxinus ; Fraxinus - immunology ; Fraxinus - parasitology ; Fraxinus mandshurica ; Glucosides - metabolism ; host defense mechanisms ; hosts ; induced defense ; induced resistance ; invasive species ; Larva ; larvae ; lignans ; lignin ; Lignin - metabolism ; Magnoliopsida - immunology ; Magnoliopsida - parasitology ; methyl jasmonate ; Models, Biological ; mortality ; Oviposition ; oxidation ; Oxylipins - pharmacology ; Phenols - metabolism ; phylogeny ; Plant Growth Regulators - pharmacology ; plant–insect interactions ; proline ; proteins ; Species Specificity ; Tansley reviews ; trypsin inhibitors ; Trypsin Inhibitors - metabolism ; tyramine ; verbascoside ; water stress ; Wood ; wood‐borers</subject><ispartof>The New phytologist, 2016-01, Vol.209 (1), p.63-79</ispartof><rights>2015 New Phytologist Trust</rights><rights>2015 The Authors. New Phytologist © 2015 New Phytologist Trust</rights><rights>2015 The Authors. New Phytologist © 2015 New Phytologist Trust.</rights><rights>Copyright © 2015 New Phytologist Trust</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5524-4c3621627e0d00dfc0e315099e0a9b9b8ecc4077328fb5b8f2f7cd58e75184ef3</citedby><cites>FETCH-LOGICAL-c5524-4c3621627e0d00dfc0e315099e0a9b9b8ecc4077328fb5b8f2f7cd58e75184ef3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/newphytologist.209.1.63$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/newphytologist.209.1.63$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,58213,58446</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26268949$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Villari, Caterina</creatorcontrib><creatorcontrib>Herms, Daniel A</creatorcontrib><creatorcontrib>Whitehill, Justin G. A</creatorcontrib><creatorcontrib>Cipollini, Don</creatorcontrib><creatorcontrib>Bonello, Pierluigi</creatorcontrib><title>Progress and gaps in understanding mechanisms of ash tree resistance to emerald ash borer, a model for wood‐boring insects that kill angiosperms</title><title>The New phytologist</title><addtitle>New Phytol</addtitle><description>63 I. 64 II. 64 III. 65 IV. 71 V. 72 75 References 75 SUMMARY: We review the literature on host resistance of ash to emerald ash borer (EAB, Agrilus planipennis), an invasive species that causes widespread mortality of ash. Manchurian ash (Fraxinus mandshurica), which coevolved with EAB, is more resistant than evolutionarily naïve North American and European congeners. Manchurian ash was less preferred for adult feeding and oviposition than susceptible hosts, more resistant to larval feeding, had higher constitutive concentrations of bark lignans, coumarins, proline, tyramine and defensive proteins, and was characterized by faster oxidation of phenolics. Consistent with EAB being a secondary colonizer of coevolved hosts, drought stress decreased the resistance of Manchurian ash, but had no effect on constitutive bark phenolics, suggesting that they do not contribute to increased susceptibility in response to drought stress. The induced resistance of North American species to EAB in response to the exogenous application of methyl jasmonate was associated with increased bark concentrations of verbascoside, lignin and/or trypsin inhibitors, which decreased larval survival and/or growth in bioassays. This finding suggests that these inherently susceptible species possess latent defenses that are not induced naturally by larval colonization, perhaps because they fail to recognize larval cues or respond quickly enough. Finally, we propose future research directions that would address some critical knowledge gaps.</description><subject>Acetates - pharmacology</subject><subject>adults</subject><subject>Agrilus</subject><subject>Agrilus planipennis</subject><subject>Animals</subject><subject>Anti-Infective Agents - metabolism</subject><subject>Antibiosis</subject><subject>bark</subject><subject>bioassays</subject><subject>boring insects</subject><subject>coevolution</subject><subject>Coleoptera - physiology</subject><subject>constitutive defense</subject><subject>coumarins</subject><subject>Cyclopentanes - pharmacology</subject><subject>emerald ash borer</subject><subject>Fraxinus</subject><subject>Fraxinus - immunology</subject><subject>Fraxinus - parasitology</subject><subject>Fraxinus mandshurica</subject><subject>Glucosides - metabolism</subject><subject>host defense mechanisms</subject><subject>hosts</subject><subject>induced defense</subject><subject>induced resistance</subject><subject>invasive species</subject><subject>Larva</subject><subject>larvae</subject><subject>lignans</subject><subject>lignin</subject><subject>Lignin - metabolism</subject><subject>Magnoliopsida - immunology</subject><subject>Magnoliopsida - parasitology</subject><subject>methyl jasmonate</subject><subject>Models, Biological</subject><subject>mortality</subject><subject>Oviposition</subject><subject>oxidation</subject><subject>Oxylipins - pharmacology</subject><subject>Phenols - metabolism</subject><subject>phylogeny</subject><subject>Plant Growth Regulators - pharmacology</subject><subject>plant–insect interactions</subject><subject>proline</subject><subject>proteins</subject><subject>Species Specificity</subject><subject>Tansley reviews</subject><subject>trypsin inhibitors</subject><subject>Trypsin Inhibitors - metabolism</subject><subject>tyramine</subject><subject>verbascoside</subject><subject>water stress</subject><subject>Wood</subject><subject>wood‐borers</subject><issn>0028-646X</issn><issn>1469-8137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqF0lFr1TAUB_AiipvTB7-ABnxR2N1O0jZNHmWoE4YOdOBbSNPT3lzbpsvp5XLf_AjiR_STmLu77UEQ-xJofucfwj9Z9pzDCU_f6TgtT3guoXiQHfJC6oXiefUwOwQQaiEL-e0ge0K0AgBdSvE4OxBSSKULfZj9uoyhi0jE7Niwzk7E_MjWY4OR5vTLjx0b0C3t6GkgFlpmacnmiMjSlN8Zh2wODAeMtm9utusQMR4zy4bQYM_aENkmhOb3j59pZ5foR0I3E5uXdmbffd-n0zsfaMI40NPsUWt7wme361F29f7d17PzxcXnDx_P3l4sXFmKYlG4XAouRYXQADStA8x5CVojWF3rWqFzBVRVLlRbl7VqRVu5plRYlVwV2OZH2et97hTD9RppNoMnh31vRwxrMlzxsgJecv5_WuVKcaUkJPrqL7oK6zimi-xUpbXkukrqzV65GIgitmaKfrBxaziYXacmdWpuOk32xW3iuh6wuZd3JSZwugcb3-P230nm0-X5XeTxfmJFc4j3EyNupuV2Dn3oUrNGgDbcyDzxl3ve2mBsFz2Zqy8CuATg6Uml-_wBKbjGuA</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Villari, Caterina</creator><creator>Herms, Daniel A</creator><creator>Whitehill, Justin G. 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A</au><au>Cipollini, Don</au><au>Bonello, Pierluigi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Progress and gaps in understanding mechanisms of ash tree resistance to emerald ash borer, a model for wood‐boring insects that kill angiosperms</atitle><jtitle>The New phytologist</jtitle><addtitle>New Phytol</addtitle><date>2016-01</date><risdate>2016</risdate><volume>209</volume><issue>1</issue><spage>63</spage><epage>79</epage><pages>63-79</pages><issn>0028-646X</issn><eissn>1469-8137</eissn><abstract>63 I. 64 II. 64 III. 65 IV. 71 V. 72 75 References 75 SUMMARY: We review the literature on host resistance of ash to emerald ash borer (EAB, Agrilus planipennis), an invasive species that causes widespread mortality of ash. Manchurian ash (Fraxinus mandshurica), which coevolved with EAB, is more resistant than evolutionarily naïve North American and European congeners. Manchurian ash was less preferred for adult feeding and oviposition than susceptible hosts, more resistant to larval feeding, had higher constitutive concentrations of bark lignans, coumarins, proline, tyramine and defensive proteins, and was characterized by faster oxidation of phenolics. Consistent with EAB being a secondary colonizer of coevolved hosts, drought stress decreased the resistance of Manchurian ash, but had no effect on constitutive bark phenolics, suggesting that they do not contribute to increased susceptibility in response to drought stress. The induced resistance of North American species to EAB in response to the exogenous application of methyl jasmonate was associated with increased bark concentrations of verbascoside, lignin and/or trypsin inhibitors, which decreased larval survival and/or growth in bioassays. This finding suggests that these inherently susceptible species possess latent defenses that are not induced naturally by larval colonization, perhaps because they fail to recognize larval cues or respond quickly enough. Finally, we propose future research directions that would address some critical knowledge gaps.</abstract><cop>England</cop><pub>Academic Press</pub><pmid>26268949</pmid><doi>10.1111/nph.13604</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetates - pharmacology adults Agrilus Agrilus planipennis Animals Anti-Infective Agents - metabolism Antibiosis bark bioassays boring insects coevolution Coleoptera - physiology constitutive defense coumarins Cyclopentanes - pharmacology emerald ash borer Fraxinus Fraxinus - immunology Fraxinus - parasitology Fraxinus mandshurica Glucosides - metabolism host defense mechanisms hosts induced defense induced resistance invasive species Larva larvae lignans lignin Lignin - metabolism Magnoliopsida - immunology Magnoliopsida - parasitology methyl jasmonate Models, Biological mortality Oviposition oxidation Oxylipins - pharmacology Phenols - metabolism phylogeny Plant Growth Regulators - pharmacology plant–insect interactions proline proteins Species Specificity Tansley reviews trypsin inhibitors Trypsin Inhibitors - metabolism tyramine verbascoside water stress Wood wood‐borers |
title | Progress and gaps in understanding mechanisms of ash tree resistance to emerald ash borer, a model for wood‐boring insects that kill angiosperms |
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