抗坏血酸通过对病原菌的直接作用和通过植物防御的间接作用来控制面包和硬粒小麦的谷草分枝杆菌。

L Somai-Jemmali, M Magnin-Robert, B Randoux, A Siah, B Tisserant, P Halama, Ph Reignault, W Hamada
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引用次数: 0

摘要

小麦黑穗病(STB)是小麦分枝杆菌(Mycosphaerella graminicola)引起的最严重的叶面病害之一。由于抗杀菌剂禾草杆菌菌株的出现以及为了减少农药对环境的影响,人们对替代控制策略的兴趣越来越大。可以考虑使用天然产品,特别是通过对宿主的防御激活作用。抗坏血酸(AA)是由植物和大多数动物细胞合成的具有抗氧化特性的物质。本研究旨在:(i)评估aa基产品对面包小麦(BW)和硬粒小麦(DW)(分别为Triticum aestivum和T. durum)小麦敏感品种对M. graminicola的保护作用;(ii)探讨小麦保护的机制。因此,在3周龄的小麦植株叶面施用配方aa基产品(50 mg L-)可使体重和重降低75%以上。体外实验表明,AA对两种菌株的孢子萌发(50 mg L.(-1))和菌丝生长(16 mg L.(-1))均有较强的抑制作用,无论感染BW还是DW。在小麦叶片上进行预防性叶喷,显微镜观察发现AA对植物孢子萌发、菌丝生长、叶片渗透、气孔下定植和最终产孢均有抑制作用。此外,AA处理还降低了真菌蛋白酶和细胞壁降解酶的活性,这是假定的致病性决定因素。除了对真菌的这些作用外,AA还引起了体重和体重的防御反应。事实上,在未接种的情况下,诱导效应被观察到:(i)刺激酶活性,如脂氧合酶、过氧化物酶和过氧化氢酶,以及(ii)编码致病相关(PR)蛋白(几丁质酶IV类,过氧化物酶)的基因转录物积累。在接种条件下,aa处理叶片穿透部位的H2O2和酚类化合物积累增加。此外,AA处理通过诱导苯丙氨酸解氨酶活性影响了苯丙氨酸途径。这些结果表明,在我们的条件下,AA既具有抗真菌活性,又能触发小麦的几种植物防御,建议在DW和BW上使用它来控制稻瘟病菌。
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ASCORBIC ACID CONTROLS MYCOSPHAERELLA GRAMINICOLA IN BREAD AND DURUM WHEAT THROUGH DIRECT EFFECT ON THE PATHOGEN AND INDIRECT ACTION VIA PLANT DEFENCE.

Septoria tritici blotch (STB) caused by Mycosphaerella graminicola is one of the most devastating foliar diseases on wheat. Due to the emergence of fungicide-resistant M. graminicola strains and in an effort to reduce the impact of pesticides on the environment, considerable interest has been devoted to alternative control strategies. The use of natural products, especially through a defense-activating effect on the host, could be considered. Acid ascorbic (AA) is synthesized by plants and most animal cells with antioxidant properties. This study aimed at: (i) assessing the protective effect of an AA-based product on bread (BW) and durum (DW) wheat (Triticum aestivum and T. durum, respectively) susceptible cultivars against M. graminicola and (ii) investigating the mechanisms involved in wheat protection. Therefore, the foliar application of a formulated AA-based product (50 mg L-) on 3-week-old wheat plants reduced the infection level by more than 75% for both BW and DW. In vitro experiments revealed that AA induced a strong inhibition of spore germination (at 50 mg L.(-1)) and hyphal growth (at 16 mg L.(-1)) for both M. graminicola strains, infecting either BW or DW. Used as a preventive foliar spray on wheat leaves, microscopic observations revealed that AA inhibits in planta spore germination, hyphal growth, leaf penetration, substomatal colonization and eventually sporulation. Moreover, AA treatment also decreased fungal protease and cell wall degrading enzyme activities, putative pathogenicity determinants of M. graminicola. In addition to these effects on the fungus, AA induced defence reactions in both BW and DW. Indeed, in non-inoculated context, eliciting effect was observed on (i) stimulation of enzymatic activities such as lipoxygenase, peroxydase and catalase and (ii) transcript accumulation of genes encoding for pathogenesis-related (PR) proteins (chitinase class IV, peroxidase). In inoculated condition, accumulation of H2O2 and phenolic compounds increased at the penetration site in AA-treated leaves. In addition, AA treatment impacted the phenylpropanoid pathway through the induction of phenylalanine ammonia lyase activity. These results show that, in our conditions, AA both presents an antifungal activity and triggers several plant defences in wheat and suggest its use to control M. graminicola on both DW and BW.

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