Yongzhong Li

Yongzhong Li


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 March 2020 in Journal of Plant Biology
Verified
Journal Article
Closed access
PDF file
MJMin Jiang
Min Jiang
CZChang-Ling Zhao
Chang-Ling Zhao
MZMingfu Zhao
Mingfu Zhao
YLYongzhong Li
Yongzhong Li
GWGuosong Wen
Guosong Wen

23 January 2012 in Journal of Phytopathology
Verified
Journal Article
Closed access
PDF file
YLYating Liu
Yating Liu
XLXiuping Lu
Xiuping Lu
LZLong Zhi
Long Zhi
YZYuanxian Zheng
Yuanxian Zheng
XCXuejiao Chen
Xuejiao Chen
YLYongzhong Li
Yongzhong Li

1 May 2013 in Journal of Virological Methods
Verified
Journal Article
Closed access
XCXuejiao Chen
Xuejiao Chen
XXXiaogang Xu
Xiaogang Xu
YLYongzhong Li
Yongzhong Li
YLYating Liu
Yating Liu

13 February 2024 in Virus Research
Verified
Journal Article
Open access
YLYanping Liang
Yanping Liang
JWJinfeng Wang
Jinfeng Wang
XZXin Zhang
Xin Zhang
KLKunming Li
Kunming Li
JSJun Su
Jun Su
YLYating Liu
Yating Liu
• Phytohormone-related metabolites were significantly altered after TSWV inoculation. • ABA and JA-Ile decreased significantly while isopentenyladenine and SA increased. • TSWV infection reduced expression of genes involved in ABA and JA pathways. • Expression of ICS1 and PR1 genes were significantly increased after TSWV infection.

22 March 2023 in Frontiers in Plant Science
Verified
Journal Article
Open access
MGMin Gui
Min Gui
HHHuaran Hu
Huaran Hu
ZJZhiqiang Jia
Zhiqiang Jia
XGXue Gao
Xue Gao
HTHongzheng Tao
Hongzheng Tao
YLYating Liu
Yating Liu
Viruses deploy numerous strategies to infect plants, typically by forming complexes with another virus, leading to more efficient infection. However, the detailed plant responses to viral infection and the underlying mechanisms of co-infection remain unclear. Previously, we found that tomato spotted wilt orthotospovirus (TSWV) and Hippeastrum chlorotic ringspot orthotospovirus (HCRV) could infect plants in the field by forming a complex. In this study, we found that TSWV infected tobacco (Nicotiana benthamiana) plants in cooperation with HCRV, leading to a more efficient infection rate of both viruses. We then used the in-depth full-length transcriptome to analyze the responses of N. benthamiana to complex infection by TSWV–HCRV (TH). We found that infection with individual TSWV and HCRV triggered plant defense responses, including the jasmonic acid signaling pathway, autophagy, and secondary metabolism. However, TH co-infection could not trigger and even suppress some genes that are involved in these basal resistance responses, suggesting that co-infection is advantageous for the virus and not for the plants. Typically, the TH complex inhibits NbPR1 expression to suppress tobacco resistance. Moreover, the TH complex could alter the expression of microRNAs (miRNAs), especially novel-m0782-3p and miR1992-3p, which directly interact with NbSAM and NbWRKY6 and suppress their expression in tobacco, leading to downregulation of NbPR1 and loss of resistance in tobacco to TSWV and HCRV viruses. Overall, our results elucidated the co-infection mechanisms of TH in tobacco by deploying the miRNA of plants to suppress plant basal resistance and contributed to developing a novel strategy to control crop disease caused by this virus complex.

1 February 2022 in Virus Research
Verified
Journal Article
Closed access
XGXue Gao
Xue Gao
ZJZhi-Qiang Jia
Zhi-Qiang Jia
HTHong-Zheng Tao
Hong-Zheng Tao
YXYe Xu
Ye Xu
YLYongzhong Li
Yongzhong Li
YLYating Liu
Yating Liu