Tenuivirus utilizes its glycoprotein as a helper component to overcome insect midgut barriers for its circulative and propagative transmission

• Published in: PLoS pathogens Vol. 15; no. 3; p. e1007655
• Main Authors: Lu, Gang, Li, Shuo, Zhou, Changwei, Qian, Xin, Xiang, Qing, Yang, Tongqing, Wu, Jianxiang, Zhou, Xueping, Zhou, Yijun, Ding, Xin S, Tao, Xiaorong
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01.03.2019; Public Library of Science (PLoS)
• Subjects: Agricultural production; Animals; Arthropods; Biology; Biology and Life Sciences; Cell fusion; Cell membranes; Crop damage; Crop production; Crystal structure; Cytosol; Development and progression; Digestive System - metabolism; Digestive System - virology; Disease transmission; Endocytosis; Endosomes; Entrances; Gene expression; Genetic vectors; Glycoproteins; Glycoproteins - metabolism; Glycoproteins - physiology; Glycosylation; Hemiptera - genetics; Insect Vectors - metabolism; Insect Vectors - virology; Insecta; Insects; Laboratories; Medicine and Health Sciences; Membrane fusion; Midgut; Molecular modelling; Oryza; Plant diseases; Plant Diseases - virology; Plant pathology; Plant viruses; Prevention; Proteins; Research and Analysis Methods; Rice; Supervision; Tenuivirus - metabolism; Tenuivirus - pathogenicity; Terminal protein; Virion; Virions; Virus Replication - physiology; Viruses; China
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1007655

Many persistent transmitted plant viruses, including rice stripe virus (RSV), cause serious damage to crop production worldwide. Although many reports have indicated that a successful insect-mediated virus transmission depends on a proper interaction between the virus and its insect vector, the mechanism(s) controlling this interaction remained poorly understood. In this study, we used RSV and its small brown planthopper (SBPH) vector as a working model to elucidate the molecular mechanisms underlying the entrance of RSV virions into SBPH midgut cells for virus circulative and propagative transmission. We have determined that this non-enveloped tenuivirus uses its non-structural glycoprotein NSvc2 as a helper component to overcome the midgut barrier(s) for RSV replication and transmission. In the absence of this glycoprotein, purified RSV virions were unable to enter SBPH midgut cells. In the RSV-infected cells, this glycoprotein was processed into two mature proteins: an amino-terminal protein (NSvc2-N) and a carboxyl-terminal protein (NSvc2-C). Both NSvc2-N and NSvc2-C interact with RSV virions. Our results showed that the NSvc2-N could bind directly to the surface of midgut lumen via its N-glycosylation sites. Upon recognition, the midgut cells underwent endocytosis followed by compartmentalization of RSV virions and NSvc2 into early and then late endosomes. The NSvc2-C triggered cell membrane fusion via its highly conserved fusion loop motifs under the acidic condition inside the late endosomes, leading to the release of RSV virions from endosomes into cytosol. In summary, our results showed for the first time that a rice tenuivirus utilized its glycoprotein NSvc2 as a helper component to ensure a proper interaction between its virions and SBPH midgut cells for its circulative and propagative transmission.