Seed pretreatment with brassinosteroids stimulates sunflower immunity against parasitic weed (Orobanche cumana) infection

生物 向日葵 奥罗班切 向日葵 超氧化物歧化酶 植物对草食的防御 植物 园艺 生物化学 抗氧化剂 基因
作者
Na Zhang,Sehrish Ali,Qian Huang,Chong Yang,Basharat Ali,Weiqi Chen,Kangni Zhang,Sharafat Ali,Zaid Ulhassan,Weijun Zhou
出处
期刊:Physiologia Plantarum [Wiley]
卷期号:176 (3)
标识
DOI:10.1111/ppl.14324
摘要

Abstract Broomrape ( Orobanche cumana ) negatively affects sunflower, causing severe yield losses, and thus, there is a need to control O. cumana infestation . Brassinosteroids (BRs) play key roles in plant growth and provide resilience to weed infection. This study aims to evaluate the mechanisms by which BRs ameliorate O. cumana infection in sunflower ( Helianthus annuus ). Seeds were pretreated with BRs (1, 10, and 100 nM) and O. cumana inoculation for 4 weeks under soil conditions. O. cumana infection significantly reduced plant growth traits, photosynthesis, endogenous BRs and regulated the plant defence ( POX , GST ), BRs signalling ( BAK1, BSK1 to BSK4 ) and synthesis ( BRI1 , BR6OX2 ) genes. O. cumana also elevated the levels of malondialdehyde (MDA), hydroxyl radical (OH − ), hydrogen peroxide (H 2 O 2 ) and superoxide (O 2 •– ) in leaves/roots by 77/112, 63/103, 56/97 and 54/89%, as well as caused ultrastructural cellular damages in both leaves and roots. In response, plants activated a few enzymes, superoxide dismutase (SOD), peroxidase (POD) and reduced glutathione but were unable to stimulate the activity of ascorbate peroxidase (APX) and catalase (CAT) enzymes. The addition of BRs (especially at 10 nM) notably recovered the ultrastructural cellular damages, lowered the production of oxidative stress, activated the key enzymatic antioxidants and induced the phenolic and lignin contents. The downregulation in the particular genes by BRs is attributed to the increased resilience of sunflower via a susceptible reaction. In a nutshell, BRs notably enhanced the sunflower resistance to O. cumana infection by escalating the plant immunity responses, inducing systemic acquired resistance, reducing oxidative or cellular damages, and modulating the expression of BR synthesis or signalling genes.

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