Transcriptome analysis revealed that AcWRKY75 transcription factor reduced the resistance of kiwifruit to Pseudomonas syringae pv. actinidiae

The kiwifruit canker disease caused by <i>Pseudomonas syringae</i> pv. <i>actinidiae</i> (Psa) seriously threatens the development of kiwifruit industry. So far, only a limited number of Psa-resistant kiwifruit varieties have been identified, and the underlying molecular mechanisms are still largely unknown. In this study, we evaluated the Psa resistance of six hybrid populations and screened a resistant segregation population R<sub>1</sub>F<sub>2</sub>. Then, transcriptome analysis on the Psa extremely high-resistant (HR) and extremely high-susceptible (HS) plants of the R<sub>1</sub>F<sub>2</sub> population was performed. KEGG enrichment analysis revealed that differentially expressed genes (DEGs) were significantly enriched in plant hormone signal transduction pathways, including auxin, abscisic acid, zeatin, jasmonic acid and salicylic acid. Furthermore, several transcription factors (TFs), especially WRKY TFs, were identified among the DEGs. The qRT-PCR showed that <i>AcWRKY75</i> was highly expressed in the HS plants. Additionally, <i>AcWRKY75</i> was significantly induced in the HS cultivar 'Hongyang' after Psa inoculation. Sequence amplification analysis showed that there was polymorphism in the DNA sequence of <i>AcWRKY75</i> gene, but no HR or HS-specific differences were observed. Subcellular localization and transcriptional activity analysis confirmed that AcWRKY75 functions as a nucleus-located transcriptional activator. Transient overexpression of <i>AcWRKY75</i> in kiwifruit leaves reduced the resistance to Psa, while silencing <i>AcWRKY75</i> by virus-induced gene silencing (VIGS) slightly enhanced the resistance to Psa. Furthermore, AcWRKY75 exhibited a weak interaction with the promoter of the ABA-related DEG <i>AcBet V1</i> (Acc27163). Our findings elucidated that AcWRKY75 may negatively regulate the Psa resistance of kiwifruit through the hormone signaling pathway, which laid a foundation for the analysis of the disease resistance mechanism of kiwifruit canker.

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Publication Details

Journal
Frontiers in Plant Science
Published
2024-10-24
DOI
https://doi.org/10.3389/fpls.2024.1488572
Citations
3
Primary Topic
Plant-Microbe Interactions and Immunity
Type
article
Field-Weighted Citation Impact
1.80

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article

Transcriptome analysis revealed that AcWRKY75 transcription factor reduced the resistance of kiwifruit to Pseudomonas syringae pv. actinidiae

Minmin Luo, Qi Chen, Lixia Ye, Fuxi Bai et al.
3 citations
Frontiers in Plant Science
Plant-Microbe Interactions and Immunity
1.80
article

Transcriptome analysis revealed that AcWRKY75 transcription factor reduced the resistance of kiwifruit to Pseudomonas syringae pv. actinidiae

Minmin Luo, Qi Chen, Lixia Ye, Fuxi Bai, Zhi Wang, Qinghong Chen, Li Li, Yafang Wang, Lei Gao, Jue Peng, Mengqi Yu, Lei Zhang, Xuan Luo, Qiong Huang
article en
3 citations

Abstract

The kiwifruit canker disease caused by <i>Pseudomonas syringae</i> pv. <i>actinidiae</i> (Psa) seriously threatens the development of kiwifruit industry. So far, only a limited number of Psa-resistant kiwifruit varieties have been identified, and the underlying molecular mechanisms are still largely unknown. In this study, we evaluated the Psa resistance of six hybrid populations and screened a resistant segregation population R<sub>1</sub>F<sub>2</sub>. Then, transcriptome analysis on the Psa extremely high-resistant (HR) and extremely high-susceptible (HS) plants of the R<sub>1</sub>F<sub>2</sub> population was performed. KEGG enrichment analysis revealed that differentially expressed genes (DEGs) were significantly enriched in plant hormone signal transduction pathways, including auxin, abscisic acid, zeatin, jasmonic acid and salicylic acid. Furthermore, several transcription factors (TFs), especially WRKY TFs, were identified among the DEGs. The qRT-PCR showed that <i>AcWRKY75</i> was highly expressed in the HS plants. Additionally, <i>AcWRKY75</i> was significantly induced in the HS cultivar 'Hongyang' after Psa inoculation. Sequence amplification analysis showed that there was polymorphism in the DNA sequence of <i>AcWRKY75</i> gene, but no HR or HS-specific differences were observed. Subcellular localization and transcriptional activity analysis confirmed that AcWRKY75 functions as a nucleus-located transcriptional activator. Transient overexpression of <i>AcWRKY75</i> in kiwifruit leaves reduced the resistance to Psa, while silencing <i>AcWRKY75</i> by virus-induced gene silencing (VIGS) slightly enhanced the resistance to Psa. Furthermore, AcWRKY75 exhibited a weak interaction with the promoter of the ABA-related DEG <i>AcBet V1</i> (Acc27163). Our findings elucidated that AcWRKY75 may negatively regulate the Psa resistance of kiwifruit through the hormone signaling pathway, which laid a foundation for the analysis of the disease resistance mechanism of kiwifruit canker.

Frontiers in Plant ScienceVol. 15
Yangtze University (CN), Wuhan Botanical Garden (CN), Sino Biological (China) (CN), Hubei Academy of Agricultural Sciences (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hubei Province
Openalex Percentile: Top 13%
Plant-Microbe Interactions and Immunity
1.80
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