文献类型： 外文期刊

作者： Guo, Wei ¹ ; Li, Chenyang ² ; Zeng, Bo ³ ; Li, Jie ² ; Wang, Zhaoyun ² ; Ma, Shuhui ² ; Du, Linlin ² ; Lan, Ying ² ; Sun, Feng ² ; Lu, Chengye ¹ ; Li, Shuo ² ; Zhou, Yijun ² ; Wang, Yunyue ¹ ; Zhou, Tong ² ;

作者机构： 1.Yunnan Agr Univ, Coll Plant Protect, Key Lab Agr Biodivers Plant Dis Management,Minist, State Key Lab Conservat & Utilizat Bioresources Y, Kunming 650201, Yunnan, Peoples R China

2.Jiangsu Acad Agr Sci, Inst Plant Protect, Key Lab Food Qual & Safety, Nanjing 210014, Peoples R China

3.Natl Agr Technol Extens & Serv Ctr, Beijing 100125, Peoples R China

4.Nanjing Agr Univ, Coll Plant Protect, Dept Plant Pathol, Nanjing 210095, Peoples R China

5.Jiangsu Acad Agr Sci, Int Rice Res Inst, Joint Lab, Nanjing 210014, Peoples R China

关键词： Rice stripe virus; Rice black streaked dwarf virus; small brown planthopper; viral infection process; spatiotemporal expression of defense genes

期刊名称：PATHOGENS （ 影响因子：4.531； 五年影响因子：4.58 ）

ISSN：

年卷期： 2022 年 11 卷 2 期

页码：

收录情况： SCI

摘要： Rice viral diseases adversely affect crop yield and quality. Most rice viruses are transmitted through insect vectors. However, the traditional whole-plant inoculation method cannot control the initial inoculation site in rice plants because the insect feeding sites in plants are random. To solve this problem, we established a determined-part inoculation approach in this study that restricted the insect feeding sites to specific parts of the rice plant. Rice stripe virus (RSV) was used as the model virus and was inoculated at the bottom of the stem using our method. Quantitative real-time PCR and Western blot analyses detected RSV only present at the bottom of the Nipponbare (NPB) stem at 1 day post-inoculation (dpi), indicating that our method successfully controlled the inoculation site. With time, RSV gradually moved from the bottom of the stem to the leaf in NPB rice plants, indicating that systemic viral spread can also be monitored using this method. In addition, a cultivar resistant to RSV, Zhendao 88 (ZD88), was inoculated using this method. We found that RSV accumulation in ZD88 was significantly lower than in NPB. Additionally, the expression level of the resistant gene STV11 in ZD88 was highly induced at the initial invasion stage of RSV (1 dpi) at the inoculation site, whereas it remained relatively stable at non-inoculated sites. This finding indicated that STV11 directly responded to RSV invasion to inhibit virus accumulation at the invasion site. We also proved that this approach is suitable for other rice viruses, such as Rice black-streaked dwarf virus (RBSDV). Interestingly, we determined that systemic infection with RSV was faster than that with RBSDV in NPB, which was consistent with findings in field trails. In summary, this approach is suitable for characterizing the viral infection process in rice plants, comparing the local viral accumulation and spread among different cultivars, analyzing the spatiotemporal expression pattern of resistance-associated genes, and monitoring the infection rate for different viruses.