scholarly journals Investigation of the role of AcTPR2 in kiwifruit and its response to Botrytis cinerea infection

2020 ◽  
Author(s):  
Zhexin Li ◽  
Jian-Bin Lan ◽  
Yi-Qing Liu ◽  
Li-Wang Qi ◽  
Jianmin Tang
Keyword(s):  
Disease Resistance ◽  
Botrytis Cinerea ◽  
Molecular Breeding ◽  
Regulatory Mechanism ◽  
Gray Mold ◽  
Virus Induced Gene Silencing ◽  
Induced Stress ◽  
Defensive Enzymes ◽  
Endogenous Phytohormones

Abstract Background Elucidation of the regulatory mechanism of kiwifruit response to gray mold disease caused by Botrytis cinerea can provide the basis for its molecular breeding to impart resistance against this disease. In this study, 'Hongyang' kiwifruit served as the experimental material; the TOPLESS/TOPLESS-RELATED (TPL/TPR) co-repressor gene AcTPR2 was cloned into a pTRV2 vector (AcTPR2-TRV) and the virus-induced gene silencing technique was used to establish the functions of the AcTPR2 gene in kiwifruit resistance to Botrytis cinerea. Results Virus-induced silencing of AcTPR2 enhanced the susceptibility of kiwifruit to Botrytis cinerea. Defensive enzymes such as SOD, POD, CAT, and PAL and endogenous phytohormones such as IAA, GA, ABA, and SA were detected. Kiwifruit activated these enzymes and endogenous phytohormones in response to pathogen-induced stress and injury. The expression levels of the IAA signaling genes—AcNIT, AcARF1, and AcARF2—were higher in the AcTPR2-TRV treatment group than in the control. The IAA levels were higher and the rot phenotype was more severe in AcTPR2-TRV kiwifruits than that in the control. These results suggested that AcTPR2 downregulation promotes expression of IAA and IAA signaling genes and accelerates postharvest kiwifruit senescence. Further, Botrytis cinerea dramatically upregulated AcTPR2, indicating that AcTPR2 augments kiwifruit defense against pathogens by downregulating the IAA and IAA signaling genes. Conclusions The results of the present study could help clarify the regulatory mechanisms of disease resistance in kiwifruit and furnish genetic resources for molecular breeding of kiwifruit disease resistance.

scholarly journals Investigation of the role of AcTPR2 in kiwifruit and its response to Botrytis cinerea infection

2020 ◽  
Author(s):  
Zhexin Li ◽  
Jian-Bin Lan ◽  
Yi-Qing Liu ◽  
Li-Wang Qi ◽  
Jianmin Tang
Keyword(s):  
Disease Resistance ◽  
Botrytis Cinerea ◽  
Indole Acetic Acid ◽  
Phenylalanine Ammonia Lyase ◽  
Molecular Breeding ◽  
Gray Mold ◽  
Virus Induced Gene Silencing ◽  
Defensive Enzymes ◽  
Endogenous Phytohormones

Abstract Background: Elucidation of the regulatory mechanism of kiwifruit response to gray mold disease caused by Botrytis cinerea can provide the basis for its molecular breeding to impart resistance against this disease. In this study, 'Hongyang' kiwifruit served as the experimental material; the TOPLESS/TOPLESS-RELATED (TPL/TPR) co-repressor gene AcTPR2 was cloned into a pTRV2 vector (AcTPR2-TRV) and the virus-induced gene silencing technique was used to establish the functions of the AcTPR2 gene in kiwifruit resistance to Botrytis cinerea.Results: Virus-induced silencing of AcTPR2 enhanced the susceptibility of kiwifruit to Botrytis cinerea. Defensive enzymes such as superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and phenylalanine ammonia-lyase (PAL) and endogenous phytohormones such as indole acetic acid (IAA), gibberellin (GA3), abscisic acid (ABA), and salicylic acid (SA) were detected. Kiwifruit activated these enzymes and endogenous phytohormones in response to pathogen-induced stress and injury. The expression levels of the IAA signaling genes—AcNIT, AcARF1, and AcARF2—were higher in the AcTPR2-TRV treatment group than in the control. The IAA levels were higher and the rot phenotype was more severe in AcTPR2-TRV kiwifruits than that in the control. These results suggested that AcTPR2 downregulation promotes expression of IAA and IAA signaling genes and accelerates postharvest kiwifruit senescence. Further, Botrytis cinerea dramatically upregulated AcTPR2, indicating that AcTPR2 augments kiwifruit defense against pathogens by downregulating the IAA and IAA signaling genes.Conclusions: The results of the present study could help clarify the regulatory mechanisms of disease resistance in kiwifruit and furnish genetic resources for molecular breeding of kiwifruit disease resistance.

scholarly journals Investigation of the role of AcTPR2 in kiwifruit and its response to Botrytis cinerea infection

2020 ◽  
Author(s):  
Zhexin Li ◽  
Jian-Bin Lan ◽  
Yi-Qing Liu ◽  
Li-Wang Qi ◽  
Jianmin Tang
Keyword(s):  
Disease Resistance ◽  
Botrytis Cinerea ◽  
Indole Acetic Acid ◽  
Phenylalanine Ammonia Lyase ◽  
Molecular Breeding ◽  
Gray Mold ◽  
Virus Induced Gene Silencing ◽  
Defensive Enzymes ◽  
Endogenous Phytohormones

Abstract Background: Elucidation of the regulatory mechanism of kiwifruit response to gray mold disease caused by Botrytis cinerea can provide the basis for its molecular breeding to impart resistance against this disease. In this study, 'Hongyang' kiwifruit served as the experimental material; the TOPLESS/TOPLESS-RELATED (TPL/TPR) co-repressor gene AcTPR2 was cloned into a pTRV2 vector (AcTPR2-TRV) and the virus-induced gene silencing technique was used to establish the functions of the AcTPR2 gene in kiwifruit resistance to Botrytis cinerea.Results: Virus-induced silencing of AcTPR2 enhanced the susceptibility of kiwifruit to Botrytis cinerea. Defensive enzymes such as superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and phenylalanine ammonia-lyase (PAL) and endogenous phytohormones such as indole acetic acid (IAA), gibberellin (GA3), abscisic acid (ABA), and salicylic acid (SA) were detected. Kiwifruit activated these enzymes and endogenous phytohormones in response to pathogen-induced stress and injury. The expression levels of the IAA signaling genes—AcNIT, AcARF1, and AcARF2—were higher in the AcTPR2-TRV treatment group than in the control. The IAA levels were higher and the rot phenotype was more severe in AcTPR2-TRV kiwifruits than that in the control. These results suggested that AcTPR2 downregulation promotes expression of IAA and IAA signaling genes and accelerates postharvest kiwifruit senescence. Further, Botrytis cinerea dramatically upregulated AcTPR2, indicating that AcTPR2 augments kiwifruit defense against pathogens by downregulating the IAA and IAA signaling genes.Conclusions: The results of the present study could help clarify the regulatory mechanisms of disease resistance in kiwifruit and furnish genetic resources for molecular breeding of kiwifruit disease resistance.

scholarly journals Investigation of the role of AcTPR2 in kiwifruit and its response to Botrytis cinerea infection

2020 ◽  
Author(s):  
Zhexin Li ◽  
Jian-Bin Lan ◽  
Yi-Qing Liu ◽  
Li-Wang Qi ◽  
Jianmin Tang
Keyword(s):  
Disease Resistance ◽  
Botrytis Cinerea ◽  
Indole Acetic Acid ◽  
Phenylalanine Ammonia Lyase ◽  
Molecular Breeding ◽  
Gray Mold ◽  
Virus Induced Gene Silencing ◽  
Defensive Enzymes ◽  
Endogenous Phytohormones

Abstract Background: Elucidation of the regulatory mechanism of kiwifruit response to gray mold disease caused by Botrytis cinerea can provide the basis for its molecular breeding to impart resistance against this disease. In this study, 'Hongyang' kiwifruit served as the experimental material; the TOPLESS/TOPLESS-RELATED (TPL/TPR) co-repressor gene AcTPR2 was cloned into a pTRV2 vector (AcTPR2-TRV) and the virus-induced gene silencing technique was used to establish the functions of the AcTPR2 gene in kiwifruit resistance to Botrytis cinerea.Results: Virus-induced silencing of AcTPR2 enhanced the susceptibility of kiwifruit to Botrytis cinerea. Defensive enzymes such as superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and phenylalanine ammonia-lyase (PAL) and endogenous phytohormones such as indole acetic acid (IAA), gibberellin (GA3), abscisic acid (ABA), and salicylic acid (SA) were detected. Kiwifruit activated these enzymes and endogenous phytohormones in response to pathogen-induced stress and injury. The expression levels of the IAA signaling genes—AcNIT, AcARF1, and AcARF2—were higher in the AcTPR2-TRV treatment group than in the control. The IAA levels were higher and the rot phenotype was more severe in AcTPR2-TRV kiwifruits than that in the control. These results suggested that AcTPR2 downregulation promotes expression of IAA and IAA signaling genes and accelerates postharvest kiwifruit senescence. Further, Botrytis cinerea dramatically upregulated AcTPR2, indicating that AcTPR2 augments kiwifruit defense against pathogens by downregulating the IAA and IAA signaling genes.Conclusions: The results of the present study could help clarify the regulatory mechanisms of disease resistance in kiwifruit and furnish genetic resources for molecular breeding of kiwifruit disease resistance.

scholarly journals Investigation of the role of AcTPR2 in kiwifruit and its response to Botrytis cinerea infection

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Zhe-Xin Li ◽  
Jian-Bin Lan ◽  
Yi-Qing Liu ◽  
Li-Wang Qi ◽  
Jian-Min Tang
Keyword(s):  
Disease Resistance ◽  
Botrytis Cinerea ◽  
Indole Acetic Acid ◽  
Phenylalanine Ammonia Lyase ◽  
Molecular Breeding ◽  
Gray Mold ◽  
Virus Induced Gene Silencing ◽  
Defensive Enzymes ◽  
Endogenous Phytohormones

Abstract Background Elucidation of the regulatory mechanism of kiwifruit response to gray mold disease caused by Botrytis cinerea can provide the basis for its molecular breeding to impart resistance against this disease. In this study, ‘Hongyang’ kiwifruit served as the experimental material; the TOPLESS/TOPLESS-RELATED (TPL/TPR) co-repressor gene AcTPR2 was cloned into a pTRV2 vector (AcTPR2-TRV) and the virus-induced gene silencing technique was used to establish the functions of the AcTPR2 gene in kiwifruit resistance to Botrytis cinerea. Results Virus-induced silencing of AcTPR2 enhanced the susceptibility of kiwifruit to Botrytis cinerea. Defensive enzymes such as superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and phenylalanine ammonia-lyase (PAL) and endogenous phytohormones such as indole acetic acid (IAA), gibberellin (GA3), abscisic acid (ABA), and salicylic acid (SA) were detected. Kiwifruit activated these enzymes and endogenous phytohormones in response to pathogen-induced stress and injury. The expression levels of the IAA signaling genes—AcNIT, AcARF1, and AcARF2—were higher in the AcTPR2-TRV treatment group than in the control. The IAA levels were higher and the rot phenotype was more severe in AcTPR2-TRV kiwifruits than that in the control. These results suggested that AcTPR2 downregulation promotes expression of IAA and IAA signaling genes and accelerates postharvest kiwifruit senescence. Further, Botrytis cinerea dramatically upregulated AcTPR2, indicating that AcTPR2 augments kiwifruit defense against pathogens by downregulating the IAA and IAA signaling genes. Conclusions The results of the present study could help clarify the regulatory mechanisms of disease resistance in kiwifruit and furnish genetic resources for molecular breeding of kiwifruit disease resistance.

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.

scholarly journals Ubiquitin Extension Protein UEP1 Modulates Cell Death and Resistance to Various Pathogens in Tobacco

2019 ◽  
Vol 109 (7) ◽  
pp. 1257-1269
Author(s):  
You-Ping Xu ◽  
Yuan Zhao ◽  
Xiao-Yi Song ◽  
Yun-Feng Ye ◽  
Ren-Gang Wang ◽  
...  
Keyword(s):  
Cell Death ◽  
Disease Resistance ◽  
Ribosomal Protein ◽  
Mosaic Virus ◽  
Amine Oxidase ◽  
Active Species ◽  
26S Proteasome ◽  
Virus Induced Gene Silencing ◽  
Copper Amine Oxidase

Ubiquitin (Ub) extension proteins (UEPs) are fusion proteins of a Ub at the N terminus to a ribosomal protein. They are the main source of Ub and the only source of extension ribosomal protein. Although important roles of the Ub-26S proteasome system in various biological processes have been well established, direct evidence for the role of UEP genes in plant defense is rarely reported. In this study, we cloned a Ub-S27a-type UEP gene (NbUEP1) from Nicotiana benthamiana and demonstrated its function in cell death and disease resistance. Virus-induced gene silencing of NbUEP1 led to intensive cell death, culminating in whole-seedling withering. Transient RNA interference (RNAi) of NbUEP1 caused strong cell death in infiltrated areas, while stable NbUEP1-RNAi tobacco plants constitutively formed necrotic lesions in leaves. NbUEP1-RNAi plants exhibited increased resistance to the oomycete Pythium aphanidermatum and viruses Tobacco mosaic virus and Cucumber mosaic virus while displaying decreased resistance to the nematode Meloidogyne incognita compared with non-RNAi control plants. Transcription profiling analysis indicated that jasmonate and ethylene pathways, lipid metabolism, copper amine oxidase-mediated active species generation, glycine-rich proteins, vacuolar processing enzyme- and RD21-mediated cell death and defense regulation, and autophagy might be associated with NbUEP1-mediated cell death and resistance. Our results provided evidence for the important roles of plant UEPs in modulating plant cell death and disease resistance.

Disease resistance in rice and the role of molecular breeding in protecting rice crops against diseases

2014 ◽  
Vol 36 (7) ◽  
pp. 1407-1420 ◽  
Author(s):  
Shah Fahad ◽  
Lixiao Nie ◽  
Faheem Ahmed Khan ◽  
Yutiao Chen ◽  
Saddam Hussain ◽  
...  
Keyword(s):  
Disease Resistance ◽  
Molecular Breeding
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