Arboviruses antagonize insect Toll antiviral immune signaling to facilitate the coexistence of viruses with their vectors

• Published in: PLoS pathogens Vol. 20; no. 6; p. e1012318
• Main Authors: Jia, Dongsheng, Luo, Guozhong, Guan, Heran, Yu, Tingting, Sun, Xinyan, Du, Yu, Wang, Yiheng, Chen, Hongyan, Wei, Taiyun
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 12.06.2024; Public Library of Science (PLoS)
• Subjects: Adapters; Adaptor proteins; Antiviral activity; Apoptosis; Arboviruses; Attenuation; Capsid protein; Cellular signal transduction; Coexistence; Defensins; Degradation; Dengue fever; Disease transmission; Dwarf disease; Expression vectors; Homeostasis; Immune response; Immune system; Infections; Insects; Insects as carriers of disease; Mitochondria; MyD88 protein; Physiological aspects; Plant virus diseases; Plant viruses; Proteasomes; Proteins; Toll-like receptors; Transcription factors; Tubules; Ubiquitin-protein ligase; Viral infections; Viral proteins; Virus diseases of plants; Virus research; Viruses; China
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1012318

Many plant arboviruses are persistently transmitted by piercing-sucking insect vectors. However, it remains largely unknown how conserved insect Toll immune response exerts antiviral activity and how plant viruses antagonize it to facilitate persistent viral transmission. Here, we discover that southern rice black-streaked dwarf virus (SRBSDV), a devastating planthopper-transmitted rice reovirus, activates the upstream Toll receptors expression but suppresses the downstream MyD88-Dorsal-defensin cascade, resulting in the attenuation of insect Toll immune response. Toll pathway-induced the small antibacterial peptide defensin directly interacts with viral major outer capsid protein P10 and thus binds to viral particles, finally blocking effective viral infection in planthopper vector. Furthermore, viral tubular protein P7-1 directly interacts with and promotes RING E3 ubiquitin ligase-mediated ubiquitinated degradation of Toll pathway adaptor protein MyD88 through the 26 proteasome pathway, finally suppressing antiviral defensin production. This virus-mediated attenuation of Toll antiviral immune response to express antiviral defensin ensures persistent virus infection without causing evident fitness costs for the insects. E3 ubiquitin ligase also is directly involved in the assembly of virus-induced tubules constructed by P7-1 to facilitate viral spread in planthopper vector, thereby acting as a pro-viral factor. Together, we uncover a previously unknown mechanism used by plant arboviruses to suppress Toll immune response through the ubiquitinated degradation of the conserved adaptor protein MyD88, thereby facilitating the coexistence of arboviruses with their vectors in nature.