Abstract
Plant viruses transmitted by insects cause tremendous losses in most important crops around the world. The identification of receptors of plant viruses within their insect vectors is a key challenge to understanding the mechanisms of transmission and offers an avenue for future alternative control strategies to limit viral spread. We here report the identification of two cuticular proteins within aphid mouthparts, and we provide experimental support for the role of one of them in the transmission of a noncirculative virus. These two proteins, named Stylin-01 and Stylin-02, belong to the RR-1 cuticular protein subfamily and are highly conserved among aphid species. Using an immunolabeling approach, they were localized in the maxillary stylets of the pea aphid Acyrthosiphon pisum and the green peach aphid Myzus persicae, in the acrostyle, an organ earlier shown to harbor receptors of a noncirculative virus. A peptide motif present at the C termini of both Stylin-01 and Stylin-02 is readily accessible all over the surface of the acrostyle. Competition for in vitro binding to the acrostyle was observed between an antibody targeting this peptide and the helper component protein P2 of Cauliflower mosaic virus Furthermore, silencing the stylin-01 but not stylin-02 gene through RNA interference decreased the efficiency of Cauliflower mosaic virus transmission by Myzus persicae These results identify the first cuticular proteins ever reported within arthropod mouthparts and distinguish Stylin-01 as the best candidate receptor for the aphid transmission of noncirculative plant viruses.IMPORTANCE Most noncirculative plant viruses transmitted by insect vectors bind to their mouthparts. They are acquired and inoculated within seconds when insects hop from plant to plant. The receptors involved remain totally elusive due to a long-standing technical bottleneck in working with insect cuticle. Here we characterize the role of the two first cuticular proteins ever identified in arthropod mouthparts. A domain of these proteins is directly accessible at the surface of the cuticle of the acrostyle, an organ at the tip of aphid stylets. The acrostyle has been shown to bind a plant virus, and we consistently demonstrated that one of the identified proteins is involved in viral transmission. Our findings provide an approach to identify proteins in insect mouthparts and point at an unprecedented gene candidate for a plant virus receptor.
Highlights
Plant viruses transmitted by insects cause tremendous losses in most important crops around the world
In that case, the decrease in stylin-02 mRNA did not lead to a significant change in Cauliflower mosaic virus (CaMV) transmission efficiency (Fig. 5D). Even though both stylin-01 and stylin-02 transcript levels were significantly reduced, only Stylin-01-silenced aphids showed a significant decrease in their ability to transmit CaMV. While these results suggest that reducing the stylin-01 mRNA level may have a direct impact on CaMV transmission by decreasing the amount of Stylin-01 protein in aphid stylets, the above-described experiments do not exclude a possible indirect effect of silencing on aphid feeding behavior and on virus acquisition
The coat protein of Pea enation mosaic virus (PEMV) directly interacts with aminopeptidase N (APN) of the aphid gut cell membrane [46, 47]
Summary
Plant viruses transmitted by insects cause tremendous losses in most important crops around the world. We here report the identification of two cuticular proteins within aphid mouthparts, and we provide experimental support for the role of one of them in the transmission of a noncirculative virus. Silencing the stylin-01 but not stylin-02 gene through RNA interference decreased the efficiency of Cauliflower mosaic virus transmission by Myzus persicae These results identify the first cuticular proteins ever reported within arthropod mouthparts and distinguish Stylin-01 as the best candidate receptor for the aphid transmission of noncirculative plant viruses. IMPORTANCE Most noncirculative plant viruses transmitted by insect vectors bind to their mouthparts. Noncirculative viruses do not penetrate the aphid body but are retained on the cuticle of the insect They reversibly attach to the insect feeding apparatus during acquisition from an infected plant. A few species in the genera Sequivirus and Closterovirus are retained upstream in the foregut, either in the precibarium or in the cibarium [11, 12]
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