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
Hauptverfasser: Webster, Craig Graham, Thillier, Mäelle, Pirolles, Elodie, Cayrol, Bastien, Blanc, Stéphane, Uzest, Marilyne
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container_end_page 1002
container_issue 6
container_start_page 990
container_title Insect science
container_volume 24
creator Webster, Craig Graham
Thillier, Mäelle
Pirolles, Elodie
Cayrol, Bastien
Blanc, Stéphane
Uzest, Marilyne
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.
doi_str_mv 10.1111/1744-7917.12469
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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. 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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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