Proteomic composition of the acrostyle: Novel approaches to identify cuticular proteins involved in virus–insect interactions
The acrostyle is a distinct anatomical region present on the cuticle at the inner face of the common food/salivary canal at the tip of aphid maxillary stylets. This conserved structure is of particular interest as it harbors the protein receptors of at least 1 plant virus, Cauliflower mosaic virus,...
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Veröffentlicht in: | Insect science 2017-12, Vol.24 (6), p.990-1002 |
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description | The acrostyle is a distinct anatomical region present on the cuticle at the inner face of the common food/salivary canal at the tip of aphid maxillary stylets. This conserved structure is of particular interest as it harbors the protein receptors of at least 1 plant virus, Cauliflower mosaic virus, and presumably has other roles in plant–insect interactions. Previously we reported immunolabeling of a highly conserved motif of cuticular proteins from the CPR family (named for the presence of a Rebers and Riddiford consensus) within the acrostyle. Here we report the development of novel tools to further study the proteomic composition of this region and to identify proteins involved in insect‐virus interactions. Using a series of antibodies against cuticular proteins from the RR‐2 subfamily, we identified additional peptides present within the acrostyle. Our results demonstrated that the acrostyle is a complex structure containing multiple domains of cuticular proteins accessible for interaction. In addition, an array of overlapping peptides, which covers the diversity of the majority of the RR‐2 subfamily, was developed as a generic tool to characterize cuticular protein/pathogen interactions. Upon probing this array with Cucumber mosaic virus particles, consensus peptide sequences from hybridizing peptides were identified. Use of these novel tools has extended our knowledge of the proteomic composition of insect maxillary stylets and identified sequences that could be involved in virus binding, thus contributing to further elucidation of the various properties and functions of the acrostyle. |
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This conserved structure is of particular interest as it harbors the protein receptors of at least 1 plant virus, Cauliflower mosaic virus, and presumably has other roles in plant–insect interactions. Previously we reported immunolabeling of a highly conserved motif of cuticular proteins from the CPR family (named for the presence of a Rebers and Riddiford consensus) within the acrostyle. Here we report the development of novel tools to further study the proteomic composition of this region and to identify proteins involved in insect‐virus interactions. Using a series of antibodies against cuticular proteins from the RR‐2 subfamily, we identified additional peptides present within the acrostyle. Our results demonstrated that the acrostyle is a complex structure containing multiple domains of cuticular proteins accessible for interaction. In addition, an array of overlapping peptides, which covers the diversity of the majority of the RR‐2 subfamily, was developed as a generic tool to characterize cuticular protein/pathogen interactions. Upon probing this array with Cucumber mosaic virus particles, consensus peptide sequences from hybridizing peptides were identified. Use of these novel tools has extended our knowledge of the proteomic composition of insect maxillary stylets and identified sequences that could be involved in virus binding, thus contributing to further elucidation of the various properties and functions of the acrostyle.</description><identifier>ISSN: 1672-9609</identifier><identifier>EISSN: 1744-7917</identifier><identifier>DOI: 10.1111/1744-7917.12469</identifier><identifier>PMID: 28421675</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>acrostyle ; Amino Acid Sequence ; Animals ; Antibodies ; aphid ; Aphidoidea ; Aphids - metabolism ; Aphids - virology ; Cauliflower mosaic virus ; Conserved sequence ; Cucumber mosaic virus ; Cucumovirus - metabolism ; Cuticles ; cuticular protein ; Hybridization ; immunolabeling ; Insect Proteins - metabolism ; Insect Vectors - metabolism ; Insect Vectors - virology ; Insects ; Life Sciences ; Maxilla ; Original ; pathogens ; peptide array ; Peptides ; Plant viruses ; plant-insect relations ; Proteins ; proteomics ; Receptors ; Sequences ; stylet ; stylets ; virion ; Viruses</subject><ispartof>Insect science, 2017-12, Vol.24 (6), p.990-1002</ispartof><rights>2017 The Authors. Insect Science published by John Wiley & Sons Australia, Ltd on behalf of Institute of Zoology, Chinese Academy of Sciences</rights><rights>2017 The Authors. Insect Science published by John Wiley & Sons Australia, Ltd on behalf of Institute of Zoology, Chinese Academy of Sciences.</rights><rights>Copyright © 2017 Institute of Zoology, Chinese Academy of Sciences</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5349-3bb45a16721694476907970528f969b2cd2a87728501a5e9e4d5c54f5f553dac3</citedby><cites>FETCH-LOGICAL-c5349-3bb45a16721694476907970528f969b2cd2a87728501a5e9e4d5c54f5f553dac3</cites><orcidid>0000-0002-7459-8434 ; 0000-0002-3412-0989 ; 0009-0001-4645-8709</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1744-7917.12469$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1744-7917.12469$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,778,782,883,1414,27907,27908,45557,45558</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28421675$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01606347$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Webster, Craig Graham</creatorcontrib><creatorcontrib>Thillier, Mäelle</creatorcontrib><creatorcontrib>Pirolles, Elodie</creatorcontrib><creatorcontrib>Cayrol, Bastien</creatorcontrib><creatorcontrib>Blanc, Stéphane</creatorcontrib><creatorcontrib>Uzest, Marilyne</creatorcontrib><title>Proteomic composition of the acrostyle: Novel approaches to identify cuticular proteins involved in virus–insect interactions</title><title>Insect science</title><addtitle>Insect Sci</addtitle><description>The acrostyle is a distinct anatomical region present on the cuticle at the inner face of the common food/salivary canal at the tip of aphid maxillary stylets. This conserved structure is of particular interest as it harbors the protein receptors of at least 1 plant virus, Cauliflower mosaic virus, and presumably has other roles in plant–insect interactions. Previously we reported immunolabeling of a highly conserved motif of cuticular proteins from the CPR family (named for the presence of a Rebers and Riddiford consensus) within the acrostyle. Here we report the development of novel tools to further study the proteomic composition of this region and to identify proteins involved in insect‐virus interactions. Using a series of antibodies against cuticular proteins from the RR‐2 subfamily, we identified additional peptides present within the acrostyle. Our results demonstrated that the acrostyle is a complex structure containing multiple domains of cuticular proteins accessible for interaction. In addition, an array of overlapping peptides, which covers the diversity of the majority of the RR‐2 subfamily, was developed as a generic tool to characterize cuticular protein/pathogen interactions. Upon probing this array with Cucumber mosaic virus particles, consensus peptide sequences from hybridizing peptides were identified. Use of these novel tools has extended our knowledge of the proteomic composition of insect maxillary stylets and identified sequences that could be involved in virus binding, thus contributing to further elucidation of the various properties and functions of the acrostyle.</description><subject>acrostyle</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Antibodies</subject><subject>aphid</subject><subject>Aphidoidea</subject><subject>Aphids - metabolism</subject><subject>Aphids - virology</subject><subject>Cauliflower mosaic virus</subject><subject>Conserved sequence</subject><subject>Cucumber mosaic virus</subject><subject>Cucumovirus - metabolism</subject><subject>Cuticles</subject><subject>cuticular protein</subject><subject>Hybridization</subject><subject>immunolabeling</subject><subject>Insect Proteins - metabolism</subject><subject>Insect Vectors - metabolism</subject><subject>Insect Vectors - virology</subject><subject>Insects</subject><subject>Life Sciences</subject><subject>Maxilla</subject><subject>Original</subject><subject>pathogens</subject><subject>peptide array</subject><subject>Peptides</subject><subject>Plant viruses</subject><subject>plant-insect relations</subject><subject>Proteins</subject><subject>proteomics</subject><subject>Receptors</subject><subject>Sequences</subject><subject>stylet</subject><subject>stylets</subject><subject>virion</subject><subject>Viruses</subject><issn>1672-9609</issn><issn>1744-7917</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNqFUk1v1DAQjRCIlsKZG7LEhR7S2o4_Yg5IVVVopVVBAs6W13FYV0kcbCfVnsp_4B_2l9QmZQW91BeP3rx5Mx6_oniN4BFK5xhxQkouED9CmDDxpNjfIU9TzDguBYNir3gRwhWElcACPy_2cE1wStL94uaLd9G43mqgXT-6YKN1A3AtiBsDlPYuxG1n3oNLN5sOqHH0TumNCSA6YBszRNtugZ6i1VOnPBiznB0CsMPsutk0KQCz9VO4_fU74UbHhETjlc6NwsviWau6YF7d3wfF949n307Py9XnTxenJ6tS04qIslqvCVX5PYgJQjgTkAsOKa5bwcQa6warmnNcU4gUNcKQhmpKWtpSWjVKVwfFh0V3nNa9aXQa3KtOjt72ym-lU1b-nxnsRv5ws6Q8L5YlgcNFYPOg7PxkJTMGEYOsInxGifvuvpl3PycTouxt0Kbr1GDcFCSGhPIacywepaK6FpwxLnCivn1AvXKTH9LWJBKsrirISBY8Xlj564I37W5YBGX2jMwOkdkh8o9nUsWbf1ez4_81SSLQhXBtO7N9TE9eXH5dhO8A1LTN8A</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Webster, Craig Graham</creator><creator>Thillier, Mäelle</creator><creator>Pirolles, Elodie</creator><creator>Cayrol, Bastien</creator><creator>Blanc, Stéphane</creator><creator>Uzest, Marilyne</creator><general>Wiley Subscription Services, Inc</general><general>Wiley</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><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>7QG</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7459-8434</orcidid><orcidid>https://orcid.org/0000-0002-3412-0989</orcidid><orcidid>https://orcid.org/0009-0001-4645-8709</orcidid></search><sort><creationdate>201712</creationdate><title>Proteomic composition of the acrostyle: Novel approaches to identify cuticular proteins involved in virus–insect interactions</title><author>Webster, Craig Graham ; Thillier, Mäelle ; Pirolles, Elodie ; Cayrol, Bastien ; Blanc, Stéphane ; Uzest, Marilyne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5349-3bb45a16721694476907970528f969b2cd2a87728501a5e9e4d5c54f5f553dac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>acrostyle</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Antibodies</topic><topic>aphid</topic><topic>Aphidoidea</topic><topic>Aphids - metabolism</topic><topic>Aphids - virology</topic><topic>Cauliflower mosaic virus</topic><topic>Conserved sequence</topic><topic>Cucumber mosaic virus</topic><topic>Cucumovirus - metabolism</topic><topic>Cuticles</topic><topic>cuticular protein</topic><topic>Hybridization</topic><topic>immunolabeling</topic><topic>Insect Proteins - metabolism</topic><topic>Insect Vectors - metabolism</topic><topic>Insect Vectors - virology</topic><topic>Insects</topic><topic>Life Sciences</topic><topic>Maxilla</topic><topic>Original</topic><topic>pathogens</topic><topic>peptide array</topic><topic>Peptides</topic><topic>Plant viruses</topic><topic>plant-insect relations</topic><topic>Proteins</topic><topic>proteomics</topic><topic>Receptors</topic><topic>Sequences</topic><topic>stylet</topic><topic>stylets</topic><topic>virion</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Webster, Craig Graham</creatorcontrib><creatorcontrib>Thillier, Mäelle</creatorcontrib><creatorcontrib>Pirolles, Elodie</creatorcontrib><creatorcontrib>Cayrol, Bastien</creatorcontrib><creatorcontrib>Blanc, Stéphane</creatorcontrib><creatorcontrib>Uzest, Marilyne</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Insect science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Webster, Craig Graham</au><au>Thillier, Mäelle</au><au>Pirolles, Elodie</au><au>Cayrol, Bastien</au><au>Blanc, Stéphane</au><au>Uzest, Marilyne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proteomic composition of the acrostyle: Novel approaches to identify cuticular proteins involved in virus–insect interactions</atitle><jtitle>Insect science</jtitle><addtitle>Insect Sci</addtitle><date>2017-12</date><risdate>2017</risdate><volume>24</volume><issue>6</issue><spage>990</spage><epage>1002</epage><pages>990-1002</pages><issn>1672-9609</issn><eissn>1744-7917</eissn><abstract>The acrostyle is a distinct anatomical region present on the cuticle at the inner face of the common food/salivary canal at the tip of aphid maxillary stylets. This conserved structure is of particular interest as it harbors the protein receptors of at least 1 plant virus, Cauliflower mosaic virus, and presumably has other roles in plant–insect interactions. Previously we reported immunolabeling of a highly conserved motif of cuticular proteins from the CPR family (named for the presence of a Rebers and Riddiford consensus) within the acrostyle. Here we report the development of novel tools to further study the proteomic composition of this region and to identify proteins involved in insect‐virus interactions. Using a series of antibodies against cuticular proteins from the RR‐2 subfamily, we identified additional peptides present within the acrostyle. Our results demonstrated that the acrostyle is a complex structure containing multiple domains of cuticular proteins accessible for interaction. In addition, an array of overlapping peptides, which covers the diversity of the majority of the RR‐2 subfamily, was developed as a generic tool to characterize cuticular protein/pathogen interactions. Upon probing this array with Cucumber mosaic virus particles, consensus peptide sequences from hybridizing peptides were identified. Use of these novel tools has extended our knowledge of the proteomic composition of insect maxillary stylets and identified sequences that could be involved in virus binding, thus contributing to further elucidation of the various properties and functions of the acrostyle.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28421675</pmid><doi>10.1111/1744-7917.12469</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-7459-8434</orcidid><orcidid>https://orcid.org/0000-0002-3412-0989</orcidid><orcidid>https://orcid.org/0009-0001-4645-8709</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | acrostyle Amino Acid Sequence Animals Antibodies aphid Aphidoidea Aphids - metabolism Aphids - virology Cauliflower mosaic virus Conserved sequence Cucumber mosaic virus Cucumovirus - metabolism Cuticles cuticular protein Hybridization immunolabeling Insect Proteins - metabolism Insect Vectors - metabolism Insect Vectors - virology Insects Life Sciences Maxilla Original pathogens peptide array Peptides Plant viruses plant-insect relations Proteins proteomics Receptors Sequences stylet stylets virion Viruses |
title | Proteomic composition of the acrostyle: Novel approaches to identify cuticular proteins involved in virus–insect interactions |
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