10
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Cuticular Structure Proteomics in the Pea Aphid Acyrthosiphon pisum Reveals New Plant Virus Receptor Candidates at the Tip of Maxillary Stylets

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Aphids are phloem-feeding insects known as major pests in agriculture that are able to transmit hundreds of plant viruses. The majority of these viruses, classified as noncirculative, are retained and transported on the inner surface of the cuticle of the needle-like mouthparts while the aphids move from plant to plant. Identification of receptors of viruses within insect vectors is a key challenge because they are promising targets for alternative control strategies. The acrostyle, an organ discovered earlier within the common food/salivary canal at the tip of aphid maxillary stylets, displays proteins at the cuticle–fluid interface, some of which are receptors of noncirculative viruses. To assess the presence of stylet- and acrostyle-specific proteins and identify putative receptors, we have developed a comprehensive comparative analysis of the proteomes of four cuticular anatomical structures of the pea aphid, stylets, antennae, legs, and wings. In addition, we performed systematic immunolabeling detection of the cuticular proteins identified by mass spectrometry in dissected stylets. We thereby establish the first proteome of stylets of an insect and determine the minimal repertoire of the cuticular proteins composing the acrostyle. Most importantly, we propose a short list of plant virus receptor candidates, among which RR-1 proteins are remarkably predominant. The data are available via ProteomeXchange (PXD016517).

          Related collections

          Most cited references63

          • Record: found
          • Abstract: found
          • Article: not found

          T-Coffee: a web server for the multiple sequence alignment of protein and RNA sequences using structural information and homology extension

          This article introduces a new interface for T-Coffee, a consistency-based multiple sequence alignment program. This interface provides an easy and intuitive access to the most popular functionality of the package. These include the default T-Coffee mode for protein and nucleic acid sequences, the M-Coffee mode that allows combining the output of any other aligners, and template-based modes of T-Coffee that deliver high accuracy alignments while using structural or homology derived templates. These three available template modes are Expresso for the alignment of protein with a known 3D-Structure, R-Coffee to align RNA sequences with conserved secondary structures and PSI-Coffee to accurately align distantly related sequences using homology extension. The new server benefits from recent improvements of the T-Coffee algorithm and can align up to 150 sequences as long as 10 000 residues and is available from both http://www.tcoffee.org and its main mirror http://tcoffee.crg.cat.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Insect vector interactions with persistently transmitted viruses.

            The majority of described plant viruses are transmitted by insects of the Hemipteroid assemblage that includes aphids, whiteflies, leafhoppers, planthoppers, and thrips. In this review we highlight progress made in research on vector interactions of the more than 200 plant viruses that are transmitted by hemipteroid insects beginning a few hours or days after acquisition and for up to the life of the insect, i.e., in a persistent-circulative or persistent-propagative mode. These plant viruses move through the insect vector, from the gut lumen into the hemolymph or other tissues and finally into the salivary glands, from which these viruses are introduced back into the plant host during insect feeding. The movement and/or replication of the viruses in the insect vectors require specific interactions between virus and vector components. Recent investigations have resulted in a better understanding of the replication sites and tissue tropism of several plant viruses that propagate in insect vectors. Furthermore, virus and insect proteins involved in overcoming transmission barriers in the vector have been identified for some virus-vector combinations.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Insect vector-mediated transmission of plant viruses.

              The majority of plant-infecting viruses are transmitted to their host plants by vectors. The interactions between viruses and vector vary in duration and specificity but some common themes in vector transmission have emerged: 1) plant viruses encode structural proteins on the surface of the virion that are essential for transmission, and in some cases additional non-structural helper proteins that act to bridge the virion to the vector binding site; 2) viruses bind to specific sites in or on vectors and are retained there until they are transmitted to their plant hosts; and 3) viral determinants of vector transmission are promising candidates for translational research aimed at disrupting transmission or decreasing vector populations. In this review, we focus on well-characterized insect vector-transmitted viruses in the following genera: Caulimovirus, Crinivirus, Luteovirus, Geminiviridae, Reovirus, Tospovirus, and Tenuivirus. New discoveries regarding these genera have increased our understanding of the basic mechanisms of virus transmission by arthropods, which in turn have enabled the development of innovative strategies for breaking the transmission cycle. Copyright © 2015 Elsevier Inc. All rights reserved.
                Bookmark

                Author and article information

                Journal
                J Proteome Res
                J. Proteome Res
                pr
                jprobs
                Journal of Proteome Research
                American Chemical Society
                1535-3893
                1535-3907
                28 January 2020
                06 March 2020
                : 19
                : 3
                : 1319-1337
                Affiliations
                [§ ]BGPI, University of Montpellier, INRAE , CIRAD, Montpellier SupAgro, 34000 Montpellier, France
                [# ]Plateforme BioPark d’Archamps , 74160 Archamps, France
                []CR University of Grenoble-Alpes , Institute for Advances Biosciences, Inserm U1209, CNRS UMR 5309, 38058 Grenoble, France
                []INRAE, INSA Lyon , UMR5240 MAP CNRS-UCBL, 69622 Villeurbanne, France
                []University of Lyon , 69007 Lyon, France
                Author notes
                [* ]Email: marilyne.uzest@ 123456inra.fr . Phone: +(33) 499 624 857. For pea aphid model.
                [* ]Email: philippe.bulet@ 123456univ-grenoble-alpes.fr . Phone: +(33) 450 432 521. For proteomics studies.
                Article
                10.1021/acs.jproteome.9b00851
                7063574
                31991085
                e0b79873-8abc-4086-9f92-37ce76bd75fb
                Copyright © 2020 American Chemical Society

                This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.

                History
                : 20 December 2019
                Categories
                Article
                Custom metadata
                pr9b00851
                pr9b00851

                Molecular biology
                cuticle,cuticular proteins,stylets,acrostyle,virus receptor,proteomics,aphid
                Molecular biology
                cuticle, cuticular proteins, stylets, acrostyle, virus receptor, proteomics, aphid

                Comments

                Comment on this article