Wu Jian, Bisaro David M
State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agroproducts, Institute of Plant Virology, Ningbo University, Ningbo, 315211, China; Key Laboratory of Biotechnology in Plant Protection of MARA and Zhejiang Province, Institute of Plant Virology, Ningbo University, Ningbo, 315211, China; Department of Molecular Genetics, Center for Applied Plant Sciences, Center for RNA Biology, and Infectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
Department of Molecular Genetics, Center for Applied Plant Sciences, Center for RNA Biology, and Infectious Diseases Institute, The Ohio State University, Columbus, OH, USA.
Virology. 2024 Sep;597:110137. doi: 10.1016/j.virol.2024.110137. Epub 2024 Jun 15.
Variations in infection progression with concurrent or prior infections by different viruses, viroids, or their strains are evident, but detailed investigations into viroid variant interactions are lacking. We studied potato spindle tuber viroid intermediate strain (PSTVd-I) to explore variant interactions. Two mutants, U177A/A182U (AU, replication- and trafficking-competent) and U178G/U179G (GG, replication-competent but trafficking-defective) on loop 27 increased cell-to-cell movement of wild-type (WT) PSTVd without affecting replication. In mixed infection assays, both mutants accelerated WT phloem unloading, while only AU promoted it in separate leaf assays, suggesting that enhancement of WT infection is not due to systemic signals. The mutants likely enhance WT infection due to their loop-specific functions, as evidenced by the lack of impact on WT infection seen with the distantly located G347U (UU) mutant. This study provides the first comprehensive analysis of viroid variant interactions, highlighting the prolonged phloem unloading process as a significant barrier to systemic spread.
不同病毒、类病毒或其毒株同时感染或先前感染时感染进程的变化是明显的,但对类病毒变体相互作用的详细研究却很缺乏。我们研究了马铃薯纺锤块茎类病毒中间株(PSTVd-I)以探索变体相互作用。27环上的两个突变体U177A/A182U(AU,具有复制和转运能力)和U178G/U179G(GG,具有复制能力但转运缺陷)增加了野生型(WT)PSTVd的细胞间运动,而不影响复制。在混合感染试验中,两个突变体都加速了WT韧皮部卸载,而在单独叶片试验中只有AU促进了韧皮部卸载,这表明WT感染的增强不是由于系统信号。这些突变体可能因其环特异性功能增强了WT感染,这一点由位于较远位置的G347U(UU)突变体对WT感染没有影响所证明。本研究首次对类病毒变体相互作用进行了全面分析,突出了延长的韧皮部卸载过程是系统传播的一个重要障碍。