scholarly journals Virus-Induced Gene Silencing-Based Functional Analyses Revealed the Involvement of Several Putative Trehalose-6-Phosphate Synthase/Phosphatase Genes in Disease Resistance against Botrytis cinerea and Pseudomonas syringae pv. tomato DC3000 in Tomato

2016 ◽  
Vol 7 ◽  
Author(s):  
Huijuan Zhang ◽  
Yongbo Hong ◽  
Lei Huang ◽  
Shixia Liu ◽  
Limei Tian ◽  
...  
Keyword(s):  
Disease Resistance ◽  
Gene Silencing ◽  
Botrytis Cinerea ◽  
Pseudomonas Syringae ◽  
Virus Induced Gene Silencing ◽  
Tomato Dc3000 ◽  
Functional Analyses ◽  
Phosphate Synthase

scholarly journals SKIP Silencing Decreased Disease Resistance Against Botrytis cinerea and Pseudomonas syringae pv. tomato DC3000 in Tomato

2020 ◽  
Vol 11 ◽  
Author(s):  
Huijuan Zhang ◽  
Longfei Yin ◽  
Fengming Song ◽  
Ming Jiang
Keyword(s):  
Disease Resistance ◽  
Botrytis Cinerea ◽  
Pseudomonas Syringae ◽  
Defense Responses ◽  
Vital Role ◽  
Pcr Analysis ◽  
Virus Induced Gene Silencing ◽  
Tomato Dc3000 ◽  
Significant Difference ◽  
Direct Genetic Evidence

SKIP, a component of the spliceosome, is involved in numerous signaling pathways. However, there is no direct genetic evidence supporting the function of SKIP in defense responses. In this paper, two SKIPs, namely, SlSKIP1a and SlSKIP1b, were analyzed in tomato. qRT-PCR analysis showed that the SlSKIP1b expression was triggered via Pseudomonas syringae pv. tomato (Pst) DC3000 and Botrytis cinerea (B. cinerea), together with the defense-associated signals. In addition, the functions of SlSKIP1a and SlSKIP1b in disease resistance were analyzed in tomato through the virus-induced gene silencing (VIGS) technique. VIGS-mediated SlSKIP1b silencing led to increased accumulation of reactive oxygen species (ROS), along with the decreased expression of defense-related genes (DRGs) after pathogen infection, suggesting that it reduced B. cinerea and Pst DC3000 resistance. There was no significant difference in B. cinerea and Pst DC3000 resistance in TRV-SlSKIP1a-infiltrated plants compared with the TRV-GUS-silencing counterparts. As suggested by the above findings, SlSKIP1b plays a vital role in disease resistance against pathogens possibly by regulating the accumulation of ROS as well as the expression of DRGs.

scholarly journals Tomato Stress-Associated Protein 4 Contributes Positively to Immunity Against Necrotrophic Fungus Botrytis cinerea

2019 ◽  
Vol 32 (5) ◽  
pp. 566-582 ◽  
Author(s):  
Shixia Liu ◽  
Xi Yuan ◽  
Yuyan Wang ◽  
Hui Wang ◽  
Jiali Wang ◽  
...  
Keyword(s):  
Botrytis Cinerea ◽  
Pseudomonas Syringae ◽  
Expression Patterns ◽  
Plant Stress ◽  
Oxygen Species ◽  
Virus Induced Gene Silencing ◽  
Tomato Dc3000 ◽  
Enhanced Resistance ◽  
Stress Associated Protein ◽  
Associated Proteins

Stress-associated proteins (SAPs) are A20 and AN1 domain–containing proteins, some of which play important roles in plant stress signaling. Here, we report the involvement of tomato SlSAP family in immunity. SlSAPs responded with different expression patterns to Botrytis cinerea and defense signaling hormones. Virus-induced gene silencing of each of the SlSAP genes and disease assays revealed that SlSAP4 and SlSAP10 play roles in immunity against B. cinerea. Silencing of SlSAP4 resulted in attenuated immunity to B. cinerea, accompanying increased accumulation of reactive oxygen species and downregulated expression of jasmonate and ethylene (JA/ET) signaling-responsive defense genes. Transient expression of SlSAP4 in Nicotiana benthamiana led to enhanced resistance to B. cinerea. Exogenous application of methyl jasmonate partially restored the resistance of the SlSAP4-silenced plants against B. cinerea. SlSAP4 interacted with three of four SlRAD23 proteins. The A20 domain in SlSAP4 and the Ub-associated domains in SlRAD23d are critical for SlSAP4-SlRAD23d interaction. Silencing of SlRAD23d led to decreased resistance to B. cinerea, but silencing of each of other SlRAD23s did not affect immunity against B. cinerea. Furthermore, silencing of SlSAP4 and each of the SlRAD23s did not affect immunity to Pseudomonas syringae pv. tomato DC3000. These data suggest that SlSAP4 contributes positively to tomato immunity against B. cinereal through affecting JA/ET signaling and may be involved in the substrate ubiquitination process via interacting with SlRAD23d.

scholarly journals Ectopic Expression of Grapevine Gene VaRGA1 in Arabidopsis Improves Resistance to Downy Mildew and Pseudomonas syringae pv. tomato DC3000 But Increases Susceptibility to Botrytis cinerea

2019 ◽  
Vol 21 (1) ◽  
pp. 193
Author(s):  
Shanshan Tian ◽  
Xiangjing Yin ◽  
Peining Fu ◽  
Wei Wu ◽  
Jiang Lu
Keyword(s):  
Disease Resistance ◽  
Botrytis Cinerea ◽  
Pseudomonas Syringae ◽  
Broad Spectrum ◽  
Ectopic Expression ◽  
Vitis Amurensis ◽  
Transcriptional Level ◽  
Tomato Dc3000 ◽  
Resistance Function ◽  
Broad Spectrum Resistance

The protein family with nucleotide binding sites and leucine-rich repeat (NBS-LRR) in plants stimulates immune responses caused by effectors and can mediate resistance to hemi-biotrophs and biotrophs. In our previous study, a Toll-interleukin-1(TIR)-NBS-LRR gene cloned from Vitis amurensis “Shuanghong”, VaRGA1, was induced by Plasmopara viticola and could improve the resistance of tobacco to Phytophthora capsici. In this study, VaRGA1 in “Shuanghong” was also induced by salicylic acid (SA), but inhibited by jasmonic acid (JA). To investigate whether VaRGA1 confers broad-spectrum resistance to pathogens, we transferred this gene into Arabidopsis and then treated with Hyaloperonospora arabidopsidis (Hpa), Botrytis cinerea (B. cinerea), and Pseudomonas syringae pv. tomato DC3000 (PstDC3000). Results showed that VaRGA1 improved transgenic Arabidopsis thaliana resistance to the biotrophic Hpa and hemi-biotrophic PstDC3000, but decreased resistance to the necrotrophic B. cinerea. Additionally, qPCR assays showed that VaRGA1 plays an important role in disease resistance by activating SA and inhibiting JA signaling pathways. A 1104 bp promoter fragment of VaRGA1 was cloned and analyzed to further elucidate the mechanism of induction of the gene at the transcriptional level. These results preliminarily confirmed the disease resistance function and signal regulation pathway of VaRGA1, and contributed to the identification of R-genes with broad-spectrum resistance function.

scholarly journals A detached petal disc assay and virus-induced gene silencing facilitate the study of Botrytis cinerea resistance in rose flowers

2019 ◽  
Vol 6 (1) ◽  
Author(s):  
Xiaoqian Cao ◽  
Huijun Yan ◽  
Xintong Liu ◽  
Dandan Li ◽  
Mengjie Sui ◽  
...  
Keyword(s):  
Jasmonic Acid ◽  
Gene Silencing ◽  
Botrytis Cinerea ◽  
High Throughput ◽  
Regulatory Protein ◽  
Gray Mold ◽  
Virus Induced Gene Silencing ◽  
Potential Benefits ◽  
Rose Petals ◽  
Disc Assay

AbstractFresh-cut roses (Rosa hybrida) are one of the most important ornamental crops worldwide, with annual trade in the billions of dollars. Gray mold disease caused by the pathogen Botrytis cinerea is the most serious fungal threat to cut roses, causing extensive postharvest losses. In this study, we optimized a detached petal disc assay (DPDA) for artificial B. cinerea inoculation and quantification of disease symptoms in rose petals. Furthermore, as the identification of rose genes involved in B. cinerea resistance could provide useful genetic and genomic resources, we devised a virus-induced gene silencing (VIGS) procedure for the functional analysis of B. cinerea resistance genes in rose petals. We used RhPR10.1 as a reporter of silencing efficiency and found that the rose cultivar ‘Samantha’ showed the greatest decrease in RhPR10.1 expression among the cultivars tested. To determine whether jasmonic acid and ethylene are required for B. cinerea resistance in rose petals, we used VIGS to silence the expression of RhLOX5 and RhEIN3 (encoding a jasmonic acid biosynthesis pathway protein and an ethylene regulatory protein, respectively) and found that petal susceptibility to B. cinerea was affected. Finally, a VIGS screen of B. cinerea-induced rose transcription factors demonstrated the potential benefits of this method for the high-throughput identification of gene function in B. cinerea resistance. Collectively, our data show that the combination of the DPDA and VIGS is a reliable and high-throughput method for studying B. cinerea resistance in rose.

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