The response of resistant kiwifruit (Actinidia chinensis) to armoured scale insect (Diaspididae) feeding
The responses of five experimental genotypes and one commercial variety of kiwifruit ( Actinidia chinensis ) to attack by two polyphagous, congeneric armoured scale insect pests ( Hemiberlesia rapax and H. lataniae ) are described. H. lataniae feeding elicits a response in the bark and fruit of all...
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description | The responses of five experimental genotypes and one commercial variety of kiwifruit (
Actinidia chinensis
) to attack by two polyphagous, congeneric armoured scale insect pests (
Hemiberlesia rapax
and
H. lataniae
) are described.
H. lataniae
feeding elicits a response in the bark and fruit of all but one of the experimental genotypes, leading to the development of wound periderm over a 4–5 week period, and death of the insect. The response, which differs slightly between tissue types and genotypes, consists of wound periderm formation in a bowl shape beneath and around the insect, preventing its stylet from reaching normal unmodified parenchyma tissue. Wound periderm cell walls become suberised and cells beneath the insect become filled with phenolic compounds. In some cases, cells beneath the insect become hypertrophic or undergo lysis, exhibiting characteristics of a hypersensitive-like response. The remaining genotype showed no physical change in tissue structure in response to
H. lataniae
feeding, and the insects survived but were substantially reduced in size. These results suggest that both physical and chemical plant resistance responses are involved. In contrast,
H. rapax
elicited no observable histological response from any of the genotypes and the insects developed normally on bark and fruit. Both insect species developed normally on leaf petioles and these exhibit only slight cell wall thickening in response to their feeding. This unusual plant defensive response to a sucking insect has similarities to simple types of gall formation in response to insect and pathogen attack and has characteristics of resistance gene-mediated models of plant defence. |
doi_str_mv | 10.1007/s11829-011-9124-9 |
format | Article |
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Actinidia chinensis
) to attack by two polyphagous, congeneric armoured scale insect pests (
Hemiberlesia rapax
and
H. lataniae
) are described.
H. lataniae
feeding elicits a response in the bark and fruit of all but one of the experimental genotypes, leading to the development of wound periderm over a 4–5 week period, and death of the insect. The response, which differs slightly between tissue types and genotypes, consists of wound periderm formation in a bowl shape beneath and around the insect, preventing its stylet from reaching normal unmodified parenchyma tissue. Wound periderm cell walls become suberised and cells beneath the insect become filled with phenolic compounds. In some cases, cells beneath the insect become hypertrophic or undergo lysis, exhibiting characteristics of a hypersensitive-like response. The remaining genotype showed no physical change in tissue structure in response to
H. lataniae
feeding, and the insects survived but were substantially reduced in size. These results suggest that both physical and chemical plant resistance responses are involved. In contrast,
H. rapax
elicited no observable histological response from any of the genotypes and the insects developed normally on bark and fruit. Both insect species developed normally on leaf petioles and these exhibit only slight cell wall thickening in response to their feeding. This unusual plant defensive response to a sucking insect has similarities to simple types of gall formation in response to insect and pathogen attack and has characteristics of resistance gene-mediated models of plant defence.</description><identifier>ISSN: 1872-8855</identifier><identifier>EISSN: 1872-8847</identifier><identifier>DOI: 10.1007/s11829-011-9124-9</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Actinidia ; Actinidia chinensis ; Bark ; Behavioral Sciences ; Biomedical and Life Sciences ; Cell walls ; Chemical industry ; Chemical plants ; Defensive behavior ; Ecology ; Entomology ; Eutrophication ; Feeding ; Fruits ; Genotypes ; Hemiberlesia lataniae ; Herbivores ; Insects ; Invertebrates ; Kiwifruit ; Life Sciences ; Lysis ; Original Paper ; Parenchyma ; Pest resistance ; Pests ; Phenolic compounds ; Phenols ; Plant Pathology ; Plant resistance ; Plant Sciences ; Thickening ; Wounds</subject><ispartof>Arthropod-plant interactions, 2011-06, Vol.5 (2), p.149-161</ispartof><rights>Springer Science+Business Media B.V. 2011</rights><rights>Springer Science+Business Media B.V. 2011.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-3c23dfba853e47650caf73b57441da8c87b0989114b464eff0b78f307c44101e3</citedby><cites>FETCH-LOGICAL-c316t-3c23dfba853e47650caf73b57441da8c87b0989114b464eff0b78f307c44101e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11829-011-9124-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11829-011-9124-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,778,782,27907,27908,41471,42540,51302</link.rule.ids></links><search><creatorcontrib>Hill, M. G.</creatorcontrib><creatorcontrib>Mauchline, N. A.</creatorcontrib><creatorcontrib>Jones, M. K.</creatorcontrib><creatorcontrib>Sutherland, P. W.</creatorcontrib><title>The response of resistant kiwifruit (Actinidia chinensis) to armoured scale insect (Diaspididae) feeding</title><title>Arthropod-plant interactions</title><addtitle>Arthropod-Plant Interactions</addtitle><description>The responses of five experimental genotypes and one commercial variety of kiwifruit (
Actinidia chinensis
) to attack by two polyphagous, congeneric armoured scale insect pests (
Hemiberlesia rapax
and
H. lataniae
) are described.
H. lataniae
feeding elicits a response in the bark and fruit of all but one of the experimental genotypes, leading to the development of wound periderm over a 4–5 week period, and death of the insect. The response, which differs slightly between tissue types and genotypes, consists of wound periderm formation in a bowl shape beneath and around the insect, preventing its stylet from reaching normal unmodified parenchyma tissue. Wound periderm cell walls become suberised and cells beneath the insect become filled with phenolic compounds. In some cases, cells beneath the insect become hypertrophic or undergo lysis, exhibiting characteristics of a hypersensitive-like response. The remaining genotype showed no physical change in tissue structure in response to
H. lataniae
feeding, and the insects survived but were substantially reduced in size. These results suggest that both physical and chemical plant resistance responses are involved. In contrast,
H. rapax
elicited no observable histological response from any of the genotypes and the insects developed normally on bark and fruit. Both insect species developed normally on leaf petioles and these exhibit only slight cell wall thickening in response to their feeding. This unusual plant defensive response to a sucking insect has similarities to simple types of gall formation in response to insect and pathogen attack and has characteristics of resistance gene-mediated models of plant defence.</description><subject>Actinidia</subject><subject>Actinidia chinensis</subject><subject>Bark</subject><subject>Behavioral Sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Cell walls</subject><subject>Chemical industry</subject><subject>Chemical plants</subject><subject>Defensive behavior</subject><subject>Ecology</subject><subject>Entomology</subject><subject>Eutrophication</subject><subject>Feeding</subject><subject>Fruits</subject><subject>Genotypes</subject><subject>Hemiberlesia lataniae</subject><subject>Herbivores</subject><subject>Insects</subject><subject>Invertebrates</subject><subject>Kiwifruit</subject><subject>Life Sciences</subject><subject>Lysis</subject><subject>Original Paper</subject><subject>Parenchyma</subject><subject>Pest resistance</subject><subject>Pests</subject><subject>Phenolic compounds</subject><subject>Phenols</subject><subject>Plant Pathology</subject><subject>Plant resistance</subject><subject>Plant Sciences</subject><subject>Thickening</subject><subject>Wounds</subject><issn>1872-8855</issn><issn>1872-8847</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kD1PwzAQhi0EEqXwA9gsscAQ8FdiZ6zKp1SJpcyW45xbl9YpdirEv8dREExMd8Pzvnd6ELqk5JYSIu8SpYrVBaG0qCkTRX2EJlRJVigl5PHvXpan6CylDSEVZ0JO0Hq5Bhwh7buQAHdu2H3qTejxu__0Lh58j69ntvfBt95gu_YBQkZucN9hE3fdIUKLkzVbwD532Izfe5P2GW8N3GAH0PqwOkcnzmwTXPzMKXp7fFjOn4vF69PLfLYoLKdVX3DLeOsao0oOQlYlscZJ3pRSCNoaZZVsSK1qSkUjKgHOkUYqx4m0GSAU-BRdjb372H0cIPV6k18M-aRmgjAmKkrqTNGRsrFLKYLT--h3Jn5pSvQgVI9CdRaqB6F6yLAxkzIbVhD_mv8PfQOKlnio</recordid><startdate>20110601</startdate><enddate>20110601</enddate><creator>Hill, M. G.</creator><creator>Mauchline, N. A.</creator><creator>Jones, M. K.</creator><creator>Sutherland, P. W.</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X2</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</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>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M0K</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>20110601</creationdate><title>The response of resistant kiwifruit (Actinidia chinensis) to armoured scale insect (Diaspididae) feeding</title><author>Hill, M. G. ; Mauchline, N. A. ; Jones, M. K. ; Sutherland, P. W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-3c23dfba853e47650caf73b57441da8c87b0989114b464eff0b78f307c44101e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Actinidia</topic><topic>Actinidia chinensis</topic><topic>Bark</topic><topic>Behavioral Sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Cell walls</topic><topic>Chemical industry</topic><topic>Chemical plants</topic><topic>Defensive behavior</topic><topic>Ecology</topic><topic>Entomology</topic><topic>Eutrophication</topic><topic>Feeding</topic><topic>Fruits</topic><topic>Genotypes</topic><topic>Hemiberlesia lataniae</topic><topic>Herbivores</topic><topic>Insects</topic><topic>Invertebrates</topic><topic>Kiwifruit</topic><topic>Life Sciences</topic><topic>Lysis</topic><topic>Original Paper</topic><topic>Parenchyma</topic><topic>Pest resistance</topic><topic>Pests</topic><topic>Phenolic compounds</topic><topic>Phenols</topic><topic>Plant Pathology</topic><topic>Plant resistance</topic><topic>Plant Sciences</topic><topic>Thickening</topic><topic>Wounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hill, M. G.</creatorcontrib><creatorcontrib>Mauchline, N. A.</creatorcontrib><creatorcontrib>Jones, M. K.</creatorcontrib><creatorcontrib>Sutherland, P. W.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</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>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Arthropod-plant interactions</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hill, M. G.</au><au>Mauchline, N. A.</au><au>Jones, M. K.</au><au>Sutherland, P. W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The response of resistant kiwifruit (Actinidia chinensis) to armoured scale insect (Diaspididae) feeding</atitle><jtitle>Arthropod-plant interactions</jtitle><stitle>Arthropod-Plant Interactions</stitle><date>2011-06-01</date><risdate>2011</risdate><volume>5</volume><issue>2</issue><spage>149</spage><epage>161</epage><pages>149-161</pages><issn>1872-8855</issn><eissn>1872-8847</eissn><abstract>The responses of five experimental genotypes and one commercial variety of kiwifruit (
Actinidia chinensis
) to attack by two polyphagous, congeneric armoured scale insect pests (
Hemiberlesia rapax
and
H. lataniae
) are described.
H. lataniae
feeding elicits a response in the bark and fruit of all but one of the experimental genotypes, leading to the development of wound periderm over a 4–5 week period, and death of the insect. The response, which differs slightly between tissue types and genotypes, consists of wound periderm formation in a bowl shape beneath and around the insect, preventing its stylet from reaching normal unmodified parenchyma tissue. Wound periderm cell walls become suberised and cells beneath the insect become filled with phenolic compounds. In some cases, cells beneath the insect become hypertrophic or undergo lysis, exhibiting characteristics of a hypersensitive-like response. The remaining genotype showed no physical change in tissue structure in response to
H. lataniae
feeding, and the insects survived but were substantially reduced in size. These results suggest that both physical and chemical plant resistance responses are involved. In contrast,
H. rapax
elicited no observable histological response from any of the genotypes and the insects developed normally on bark and fruit. Both insect species developed normally on leaf petioles and these exhibit only slight cell wall thickening in response to their feeding. This unusual plant defensive response to a sucking insect has similarities to simple types of gall formation in response to insect and pathogen attack and has characteristics of resistance gene-mediated models of plant defence.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s11829-011-9124-9</doi><tpages>13</tpages></addata></record> |
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subjects | Actinidia Actinidia chinensis Bark Behavioral Sciences Biomedical and Life Sciences Cell walls Chemical industry Chemical plants Defensive behavior Ecology Entomology Eutrophication Feeding Fruits Genotypes Hemiberlesia lataniae Herbivores Insects Invertebrates Kiwifruit Life Sciences Lysis Original Paper Parenchyma Pest resistance Pests Phenolic compounds Phenols Plant Pathology Plant resistance Plant Sciences Thickening Wounds |
title | The response of resistant kiwifruit (Actinidia chinensis) to armoured scale insect (Diaspididae) feeding |
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