The P2 nucleic acid binding protein of Sugarcane bacilliform virus is a viral pathogenic factor
Xiongbiao Xu,
Yinian Lou,
Kaili Liang,
Jingying Liu,
Zhiyuan Wang,
Baoshan Chen,
Wenlan Li
Affiliations
Xiongbiao Xu
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi key Laboratory of Sugarcane biology, Province and Ministry Co-sponsored Collaborative Innovation Center of Canesugar Industry, College of Agriculture, Guangxi University, Nanning, Guangxi, China
Yinian Lou
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi key Laboratory of Sugarcane biology, Province and Ministry Co-sponsored Collaborative Innovation Center of Canesugar Industry, College of Agriculture, Guangxi University, Nanning, Guangxi, China
Kaili Liang
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi key Laboratory of Sugarcane biology, Province and Ministry Co-sponsored Collaborative Innovation Center of Canesugar Industry, College of Agriculture, Guangxi University, Nanning, Guangxi, China
Jingying Liu
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi key Laboratory of Sugarcane biology, Province and Ministry Co-sponsored Collaborative Innovation Center of Canesugar Industry, College of Agriculture, Guangxi University, Nanning, Guangxi, China
Zhiyuan Wang
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi key Laboratory of Sugarcane biology, Province and Ministry Co-sponsored Collaborative Innovation Center of Canesugar Industry, College of Agriculture, Guangxi University, Nanning, Guangxi, China
Baoshan Chen
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi key Laboratory of Sugarcane biology, Province and Ministry Co-sponsored Collaborative Innovation Center of Canesugar Industry, College of Agriculture, Guangxi University, Nanning, Guangxi, China
Wenlan Li
College of Life Science and Technology, Guangxi University, Nanning, Guangxi, China
Background Saccharum spp. is the primary source of sugar and plays a significant role in global renewable bioenergy. Sugarcane bacilliform virus (SCBV) is one of the most important viruses infecting sugarcane, causing severe yield losses and quality degradation. It is of great significance to reveal the pathogenesis of SCBV and resistance breeding. However, little is known about the viral virulence factors or RNA silencing suppressors and the molecular mechanism of pathogenesis. Methods To systematically investigate the functions of the unknown protein P2 encoded by SCBV ORF2. Phylogenetic analysis was implemented to infer the evolutionary relationship between the P2 of SCBV and other badnaviruses. The precise subcellular localization of P2 was verified in the transient infiltrated Nicotiana benthamiana epidermal mesophyll cells and protoplasts using the Laser scanning confocal microscope (LSCM). The post-transcriptional gene silencing (PTGS) and transcriptional gene silencing (TGS) RNA silencing suppressor activity of P2 was analyzed, respectively. Furthermore, restriction digestion and RT-qPCR assays were conducted to verify the probable mechanism of P2 on repressing DNA methylation. To explore the pathogenicity of P2, a potato virus X-based viral vector was used to heterologously express SCBV P2 and the consequent H2O2 accumulation was detected by the 3,3′-diaminobenzidine (DAB) staining method. Results Phylogenetic analysis shows that SCBV has no obvious sequence similarity and low genetic relatedness to Badnavirus and Tungrovirus representatives. LSCM studies show that P2 is localized in both the cytoplasm and nucleus. Moreover, P2 is shown to be a suppressor of PTGS and TGS, which can not only repress ssRNA-induced gene silencing but also disrupt the host RNA-directed DNA methylation (RdDM) pathway. In addition, P2 can trigger an oxidative burst and cause typical hypersensitive-like response (HLR) necrosis in systemic leaves of N. benthamiana when expressed by PVX. Overall, our results laid a foundation for deciphering the molecular mechanism of SCBV pathogenesis and made progress for resistance breeding.
