Abnormally high digestive enzyme activity and gene expression explain the contemporary evolution of a Diabrotica biotype able to feed on soybeans
Western corn rootworm (Diabrotica virgifera) (WCR) depends on the continuous availability of corn. Broad adoption of annual crop rotation between corn (Zea mays) and nonhost soybean (Glycine max) exploited WCR biology to provide excellent WCR control, but this practice dramatically reduced landscape...
Gespeichert in:
Veröffentlicht in: | Ecology and evolution 2012-08, Vol.2 (8), p.2005-2017 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2017 |
---|---|
container_issue | 8 |
container_start_page | 2005 |
container_title | Ecology and evolution |
container_volume | 2 |
creator | Curzi, Matías J. Zavala, Jorge A. Spencer, Joseph L. Seufferheld, Manfredo J. |
description | Western corn rootworm (Diabrotica virgifera) (WCR) depends on the continuous availability of corn. Broad adoption of annual crop rotation between corn (Zea mays) and nonhost soybean (Glycine max) exploited WCR biology to provide excellent WCR control, but this practice dramatically reduced landscape heterogeneity in East‐central Illinois and imposed intense selection pressure. This selection resulted in behavioral changes and “rotation‐resistant” (RR) WCR adults. Although soybeans are well defended against Coleopteran insects by cysteine protease inhibitors, RR‐WCR feed on soybean foliage and remain long enough to deposit eggs that will hatch the following spring and larvae will feed on roots of planted corn. Other than documenting changes in insect mobility and egg laying behavior, 15 years of research have failed to identify any diagnostic differences between wild‐type (WT)‐ and RR‐WCR or a mechanism that allows for prolonged RR‐WCR feeding and survival in soybean fields. We documented differences in behavior, physiology, digestive protease activity (threefold to fourfold increases), and protease gene expression in the gut of RR‐WCR adults. Our data suggest that higher constitutive activity levels of cathepsin L are part of the mechanism that enables populations of WCR to circumvent soybean defenses, and thus, crop rotation. These new insights into the mechanism of WCR tolerance of soybean herbivory transcend the issue of RR‐WCR diagnostics and management to link changes in insect gut proteolytic activity and behavior with landscape heterogeneity. The RR‐WCR illustrates how agro‐ecological factors can affect the evolution of insects in human‐altered ecosystems.
Western corn rootworm (Diabrotica virgifera) (WCR) depends on the continuous availability of corn. Broad adoption of annual crop rotation between corn (Zea mays) and nonhost soybean (Glycine max) exploited WCR biology to provide excellent WCR control, but this practice dramatically reduced landscape heterogeneity in East‐central Illinois and imposed intense selection pressure. This selection resulted in behavioral changes and ‘rotation‐resistant’ (RR) WCR adults. Our data strongly suggest that higher constitutive activity of cathepsin L and differential gene expression are components of the mechanism that enables U.S. Corn Belt populations of WCR that enter soybean fields to circumvent soybean defenses, and thus, crop rotation. These new insights into the mechanism of WCR tolerance of soybean herb |
doi_str_mv | 10.1002/ece3.331 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3434003</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2290305954</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4711-a78ab449ae15f110068ae6dab086425a1c5ea86d78c04b8c4ed4a97f15840ba73</originalsourceid><addsrcrecordid>eNqFks-K1TAUh4sozjAO-AQScOOmY9IkTbsRhuv1Dwy40XU4SU_vzdAm16S9Wt_CNzZ1xnEUxGyScD4-ck5-RfGU0QtGafUSLfILztmD4rSiQpZKyebhvfNJcZ7SNc2rppWg6nFxUlWtVBVlp8X3S-NDHGEYFrJ3uz3p3A7T5I5I0H9bRiRg881NCwHfkR36XPh6iJiSC349DuA8mfZIbPATjocQIS4Ej2GYpxUJPQHy2oGJYXIWiHFhWg7ZawYkUyA9Ykcyl8JiEHx6UjzqYUh4frufFZ_ebD9u3pVXH96-31xelVYoxkpQDRghWkAme5YHUTeAdQeGNrWoJDArEZq6U42lwjRWYCegVT2TjaAGFD8rXt14D7MZsbPopwiDPkQ35gZ0AKf_rHi317tw1FxwQSnPghe3ghg-z3loenTJ4jCAxzAnzRSrpGKtrP6PUt7Itm5_Wp__hV6HOfo8CZ1_jXIqWyl-C20MKUXs797NqF5ToddU6JyKjD673-cd-CsDGShvgC9uwOWfIr3dbPkq_AE14MMb</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2290305954</pqid></control><display><type>article</type><title>Abnormally high digestive enzyme activity and gene expression explain the contemporary evolution of a Diabrotica biotype able to feed on soybeans</title><source>Wiley Online Library Open Access</source><source>DOAJ Directory of Open Access Journals</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Curzi, Matías J. ; Zavala, Jorge A. ; Spencer, Joseph L. ; Seufferheld, Manfredo J.</creator><creatorcontrib>Curzi, Matías J. ; Zavala, Jorge A. ; Spencer, Joseph L. ; Seufferheld, Manfredo J.</creatorcontrib><description>Western corn rootworm (Diabrotica virgifera) (WCR) depends on the continuous availability of corn. Broad adoption of annual crop rotation between corn (Zea mays) and nonhost soybean (Glycine max) exploited WCR biology to provide excellent WCR control, but this practice dramatically reduced landscape heterogeneity in East‐central Illinois and imposed intense selection pressure. This selection resulted in behavioral changes and “rotation‐resistant” (RR) WCR adults. Although soybeans are well defended against Coleopteran insects by cysteine protease inhibitors, RR‐WCR feed on soybean foliage and remain long enough to deposit eggs that will hatch the following spring and larvae will feed on roots of planted corn. Other than documenting changes in insect mobility and egg laying behavior, 15 years of research have failed to identify any diagnostic differences between wild‐type (WT)‐ and RR‐WCR or a mechanism that allows for prolonged RR‐WCR feeding and survival in soybean fields. We documented differences in behavior, physiology, digestive protease activity (threefold to fourfold increases), and protease gene expression in the gut of RR‐WCR adults. Our data suggest that higher constitutive activity levels of cathepsin L are part of the mechanism that enables populations of WCR to circumvent soybean defenses, and thus, crop rotation. These new insights into the mechanism of WCR tolerance of soybean herbivory transcend the issue of RR‐WCR diagnostics and management to link changes in insect gut proteolytic activity and behavior with landscape heterogeneity. The RR‐WCR illustrates how agro‐ecological factors can affect the evolution of insects in human‐altered ecosystems.
Western corn rootworm (Diabrotica virgifera) (WCR) depends on the continuous availability of corn. Broad adoption of annual crop rotation between corn (Zea mays) and nonhost soybean (Glycine max) exploited WCR biology to provide excellent WCR control, but this practice dramatically reduced landscape heterogeneity in East‐central Illinois and imposed intense selection pressure. This selection resulted in behavioral changes and ‘rotation‐resistant’ (RR) WCR adults. Our data strongly suggest that higher constitutive activity of cathepsin L and differential gene expression are components of the mechanism that enables U.S. Corn Belt populations of WCR that enter soybean fields to circumvent soybean defenses, and thus, crop rotation. These new insights into the mechanism of WCR tolerance of soybean herbivory transcend the issue of RR WCR diagnostics and management to link changes in insect gut proteolytic activity and behavior with landscape heterogeneity. The RR WCR illustrates how agro‐ecological factors can affect the evolution of insects in human‐altered ecosystems.</description><identifier>ISSN: 2045-7758</identifier><identifier>EISSN: 2045-7758</identifier><identifier>DOI: 10.1002/ece3.331</identifier><identifier>PMID: 22957201</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Adults ; Agricultural practices ; Behavior ; Cathepsin L ; Cereal crops ; contemporary evolution ; Corn ; Crop rotation ; Cysteine proteinase ; Diabrotica ; Diabrotica virgifera ; Diagnostic systems ; Diet ; Digestive system ; Egg laying ; Eggs ; Enzymatic activity ; Enzyme activity ; Evolution ; Foliage ; Gastrointestinal tract ; Gene expression ; Glycine max ; Herbivory ; Heterogeneity ; Insects ; Land area ; Landscape ; landscape heterogeneity ; Larvae ; Leaves ; Motility ; Original Research ; Pest resistance ; plant defenses ; plant–insect interactions ; Protease ; Protease inhibitors ; Proteinase inhibitors ; Proteolysis ; Soybeans ; Vegetables ; Zea mays</subject><ispartof>Ecology and evolution, 2012-08, Vol.2 (8), p.2005-2017</ispartof><rights>2012 The Authors. published by Blackwell Publishing Ltd.</rights><rights>2012. This work is published under http://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2012 Published by Blackwell Publishing Ltd. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4711-a78ab449ae15f110068ae6dab086425a1c5ea86d78c04b8c4ed4a97f15840ba73</citedby><cites>FETCH-LOGICAL-c4711-a78ab449ae15f110068ae6dab086425a1c5ea86d78c04b8c4ed4a97f15840ba73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434003/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434003/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1411,11541,27901,27902,45550,45551,46027,46451,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22957201$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Curzi, Matías J.</creatorcontrib><creatorcontrib>Zavala, Jorge A.</creatorcontrib><creatorcontrib>Spencer, Joseph L.</creatorcontrib><creatorcontrib>Seufferheld, Manfredo J.</creatorcontrib><title>Abnormally high digestive enzyme activity and gene expression explain the contemporary evolution of a Diabrotica biotype able to feed on soybeans</title><title>Ecology and evolution</title><addtitle>Ecol Evol</addtitle><description>Western corn rootworm (Diabrotica virgifera) (WCR) depends on the continuous availability of corn. Broad adoption of annual crop rotation between corn (Zea mays) and nonhost soybean (Glycine max) exploited WCR biology to provide excellent WCR control, but this practice dramatically reduced landscape heterogeneity in East‐central Illinois and imposed intense selection pressure. This selection resulted in behavioral changes and “rotation‐resistant” (RR) WCR adults. Although soybeans are well defended against Coleopteran insects by cysteine protease inhibitors, RR‐WCR feed on soybean foliage and remain long enough to deposit eggs that will hatch the following spring and larvae will feed on roots of planted corn. Other than documenting changes in insect mobility and egg laying behavior, 15 years of research have failed to identify any diagnostic differences between wild‐type (WT)‐ and RR‐WCR or a mechanism that allows for prolonged RR‐WCR feeding and survival in soybean fields. We documented differences in behavior, physiology, digestive protease activity (threefold to fourfold increases), and protease gene expression in the gut of RR‐WCR adults. Our data suggest that higher constitutive activity levels of cathepsin L are part of the mechanism that enables populations of WCR to circumvent soybean defenses, and thus, crop rotation. These new insights into the mechanism of WCR tolerance of soybean herbivory transcend the issue of RR‐WCR diagnostics and management to link changes in insect gut proteolytic activity and behavior with landscape heterogeneity. The RR‐WCR illustrates how agro‐ecological factors can affect the evolution of insects in human‐altered ecosystems.
Western corn rootworm (Diabrotica virgifera) (WCR) depends on the continuous availability of corn. Broad adoption of annual crop rotation between corn (Zea mays) and nonhost soybean (Glycine max) exploited WCR biology to provide excellent WCR control, but this practice dramatically reduced landscape heterogeneity in East‐central Illinois and imposed intense selection pressure. This selection resulted in behavioral changes and ‘rotation‐resistant’ (RR) WCR adults. Our data strongly suggest that higher constitutive activity of cathepsin L and differential gene expression are components of the mechanism that enables U.S. Corn Belt populations of WCR that enter soybean fields to circumvent soybean defenses, and thus, crop rotation. These new insights into the mechanism of WCR tolerance of soybean herbivory transcend the issue of RR WCR diagnostics and management to link changes in insect gut proteolytic activity and behavior with landscape heterogeneity. The RR WCR illustrates how agro‐ecological factors can affect the evolution of insects in human‐altered ecosystems.</description><subject>Adults</subject><subject>Agricultural practices</subject><subject>Behavior</subject><subject>Cathepsin L</subject><subject>Cereal crops</subject><subject>contemporary evolution</subject><subject>Corn</subject><subject>Crop rotation</subject><subject>Cysteine proteinase</subject><subject>Diabrotica</subject><subject>Diabrotica virgifera</subject><subject>Diagnostic systems</subject><subject>Diet</subject><subject>Digestive system</subject><subject>Egg laying</subject><subject>Eggs</subject><subject>Enzymatic activity</subject><subject>Enzyme activity</subject><subject>Evolution</subject><subject>Foliage</subject><subject>Gastrointestinal tract</subject><subject>Gene expression</subject><subject>Glycine max</subject><subject>Herbivory</subject><subject>Heterogeneity</subject><subject>Insects</subject><subject>Land area</subject><subject>Landscape</subject><subject>landscape heterogeneity</subject><subject>Larvae</subject><subject>Leaves</subject><subject>Motility</subject><subject>Original Research</subject><subject>Pest resistance</subject><subject>plant defenses</subject><subject>plant–insect interactions</subject><subject>Protease</subject><subject>Protease inhibitors</subject><subject>Proteinase inhibitors</subject><subject>Proteolysis</subject><subject>Soybeans</subject><subject>Vegetables</subject><subject>Zea mays</subject><issn>2045-7758</issn><issn>2045-7758</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>BENPR</sourceid><recordid>eNqFks-K1TAUh4sozjAO-AQScOOmY9IkTbsRhuv1Dwy40XU4SU_vzdAm16S9Wt_CNzZ1xnEUxGyScD4-ck5-RfGU0QtGafUSLfILztmD4rSiQpZKyebhvfNJcZ7SNc2rppWg6nFxUlWtVBVlp8X3S-NDHGEYFrJ3uz3p3A7T5I5I0H9bRiRg881NCwHfkR36XPh6iJiSC349DuA8mfZIbPATjocQIS4Ej2GYpxUJPQHy2oGJYXIWiHFhWg7ZawYkUyA9Ykcyl8JiEHx6UjzqYUh4frufFZ_ebD9u3pVXH96-31xelVYoxkpQDRghWkAme5YHUTeAdQeGNrWoJDArEZq6U42lwjRWYCegVT2TjaAGFD8rXt14D7MZsbPopwiDPkQ35gZ0AKf_rHi317tw1FxwQSnPghe3ghg-z3loenTJ4jCAxzAnzRSrpGKtrP6PUt7Itm5_Wp__hV6HOfo8CZ1_jXIqWyl-C20MKUXs797NqF5ToddU6JyKjD673-cd-CsDGShvgC9uwOWfIr3dbPkq_AE14MMb</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>Curzi, Matías J.</creator><creator>Zavala, Jorge A.</creator><creator>Spencer, Joseph L.</creator><creator>Seufferheld, Manfredo J.</creator><general>John Wiley & Sons, Inc</general><general>Blackwell Publishing Ltd</general><scope>24P</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7X2</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</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>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M0K</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>7U6</scope><scope>5PM</scope></search><sort><creationdate>201208</creationdate><title>Abnormally high digestive enzyme activity and gene expression explain the contemporary evolution of a Diabrotica biotype able to feed on soybeans</title><author>Curzi, Matías J. ; Zavala, Jorge A. ; Spencer, Joseph L. ; Seufferheld, Manfredo J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4711-a78ab449ae15f110068ae6dab086425a1c5ea86d78c04b8c4ed4a97f15840ba73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adults</topic><topic>Agricultural practices</topic><topic>Behavior</topic><topic>Cathepsin L</topic><topic>Cereal crops</topic><topic>contemporary evolution</topic><topic>Corn</topic><topic>Crop rotation</topic><topic>Cysteine proteinase</topic><topic>Diabrotica</topic><topic>Diabrotica virgifera</topic><topic>Diagnostic systems</topic><topic>Diet</topic><topic>Digestive system</topic><topic>Egg laying</topic><topic>Eggs</topic><topic>Enzymatic activity</topic><topic>Enzyme activity</topic><topic>Evolution</topic><topic>Foliage</topic><topic>Gastrointestinal tract</topic><topic>Gene expression</topic><topic>Glycine max</topic><topic>Herbivory</topic><topic>Heterogeneity</topic><topic>Insects</topic><topic>Land area</topic><topic>Landscape</topic><topic>landscape heterogeneity</topic><topic>Larvae</topic><topic>Leaves</topic><topic>Motility</topic><topic>Original Research</topic><topic>Pest resistance</topic><topic>plant defenses</topic><topic>plant–insect interactions</topic><topic>Protease</topic><topic>Protease inhibitors</topic><topic>Proteinase inhibitors</topic><topic>Proteolysis</topic><topic>Soybeans</topic><topic>Vegetables</topic><topic>Zea mays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Curzi, Matías J.</creatorcontrib><creatorcontrib>Zavala, Jorge A.</creatorcontrib><creatorcontrib>Spencer, Joseph L.</creatorcontrib><creatorcontrib>Seufferheld, Manfredo J.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</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>Biotechnology and BioEngineering Abstracts</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>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Sustainability Science Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Ecology and evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Curzi, Matías J.</au><au>Zavala, Jorge A.</au><au>Spencer, Joseph L.</au><au>Seufferheld, Manfredo J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Abnormally high digestive enzyme activity and gene expression explain the contemporary evolution of a Diabrotica biotype able to feed on soybeans</atitle><jtitle>Ecology and evolution</jtitle><addtitle>Ecol Evol</addtitle><date>2012-08</date><risdate>2012</risdate><volume>2</volume><issue>8</issue><spage>2005</spage><epage>2017</epage><pages>2005-2017</pages><issn>2045-7758</issn><eissn>2045-7758</eissn><abstract>Western corn rootworm (Diabrotica virgifera) (WCR) depends on the continuous availability of corn. Broad adoption of annual crop rotation between corn (Zea mays) and nonhost soybean (Glycine max) exploited WCR biology to provide excellent WCR control, but this practice dramatically reduced landscape heterogeneity in East‐central Illinois and imposed intense selection pressure. This selection resulted in behavioral changes and “rotation‐resistant” (RR) WCR adults. Although soybeans are well defended against Coleopteran insects by cysteine protease inhibitors, RR‐WCR feed on soybean foliage and remain long enough to deposit eggs that will hatch the following spring and larvae will feed on roots of planted corn. Other than documenting changes in insect mobility and egg laying behavior, 15 years of research have failed to identify any diagnostic differences between wild‐type (WT)‐ and RR‐WCR or a mechanism that allows for prolonged RR‐WCR feeding and survival in soybean fields. We documented differences in behavior, physiology, digestive protease activity (threefold to fourfold increases), and protease gene expression in the gut of RR‐WCR adults. Our data suggest that higher constitutive activity levels of cathepsin L are part of the mechanism that enables populations of WCR to circumvent soybean defenses, and thus, crop rotation. These new insights into the mechanism of WCR tolerance of soybean herbivory transcend the issue of RR‐WCR diagnostics and management to link changes in insect gut proteolytic activity and behavior with landscape heterogeneity. The RR‐WCR illustrates how agro‐ecological factors can affect the evolution of insects in human‐altered ecosystems.
Western corn rootworm (Diabrotica virgifera) (WCR) depends on the continuous availability of corn. Broad adoption of annual crop rotation between corn (Zea mays) and nonhost soybean (Glycine max) exploited WCR biology to provide excellent WCR control, but this practice dramatically reduced landscape heterogeneity in East‐central Illinois and imposed intense selection pressure. This selection resulted in behavioral changes and ‘rotation‐resistant’ (RR) WCR adults. Our data strongly suggest that higher constitutive activity of cathepsin L and differential gene expression are components of the mechanism that enables U.S. Corn Belt populations of WCR that enter soybean fields to circumvent soybean defenses, and thus, crop rotation. These new insights into the mechanism of WCR tolerance of soybean herbivory transcend the issue of RR WCR diagnostics and management to link changes in insect gut proteolytic activity and behavior with landscape heterogeneity. The RR WCR illustrates how agro‐ecological factors can affect the evolution of insects in human‐altered ecosystems.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>22957201</pmid><doi>10.1002/ece3.331</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2045-7758 |
ispartof | Ecology and evolution, 2012-08, Vol.2 (8), p.2005-2017 |
issn | 2045-7758 2045-7758 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3434003 |
source | Wiley Online Library Open Access; DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Adults Agricultural practices Behavior Cathepsin L Cereal crops contemporary evolution Corn Crop rotation Cysteine proteinase Diabrotica Diabrotica virgifera Diagnostic systems Diet Digestive system Egg laying Eggs Enzymatic activity Enzyme activity Evolution Foliage Gastrointestinal tract Gene expression Glycine max Herbivory Heterogeneity Insects Land area Landscape landscape heterogeneity Larvae Leaves Motility Original Research Pest resistance plant defenses plant–insect interactions Protease Protease inhibitors Proteinase inhibitors Proteolysis Soybeans Vegetables Zea mays |
title | Abnormally high digestive enzyme activity and gene expression explain the contemporary evolution of a Diabrotica biotype able to feed on soybeans |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T14%3A42%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Abnormally%20high%20digestive%20enzyme%20activity%20and%20gene%20expression%20explain%20the%20contemporary%20evolution%20of%20a%20Diabrotica%20biotype%20able%20to%20feed%20on%20soybeans&rft.jtitle=Ecology%20and%20evolution&rft.au=Curzi,%20Mat%C3%ADas%20J.&rft.date=2012-08&rft.volume=2&rft.issue=8&rft.spage=2005&rft.epage=2017&rft.pages=2005-2017&rft.issn=2045-7758&rft.eissn=2045-7758&rft_id=info:doi/10.1002/ece3.331&rft_dat=%3Cproquest_pubme%3E2290305954%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2290305954&rft_id=info:pmid/22957201&rfr_iscdi=true |