植物系统获得性抗性的分子机理

系统获得性抗性(systemic acquired resistance, SAR)是水杨酸(salicylic acid,SA)介导的植物对病原物的广谱抗病反应,NPR1和WRKY是SA信号传递过程中的重要转录因子.SAR的发生需要可移动信号(mobile signal)由局部到系统的长途运输,水杨酸甲酯(methyl salicylate, MeSA)和茉莉酸(jasmonic acid,JA)是两种可能的可移动信号.     

植物系统获得性抗性的信号转导

坏死病原菌（necrotizingpathogen）的侵染或者一些化学因子的处理能诱导植物的非侵染或非处理部位产生对多种病原再侵染产生抗性,即系统获得性抗性（systemicacquiredresistance,SAR）。获得系统抗性的组织中SAR基因产物的累积和防卫反应的潜在诱导增强（potentiation）是其两类抗病机制。SAR至少有通过水杨酸（salicylicacid,SA）或茉莉酸（jasmonicacid,JA）、乙烯（ethylene）为系统信号分子的两类信号转导途径。遗传分析已用于SAR产生的信号转导过程的分析,一些与SAR信号转导相关的基因已经和正在克隆,这些基因具有明显提高植物广谱抗性的潜能。     

植物系统获得性抗性的转录调控

系统获得性抗性(SAR)是植物重要的防御机制,可显著增强植株对病原微生物的抗性,且具有系统性、持久性和广谱性特征,其转录调控为抗性激活的核心环节。该文从水杨酸(SA)和Pip/NHP的合成, NPR1、NPR3/NPR4受体和Pip/NHP移动信号等的转录调控,以及TGA和WRKY转录因子家族调控等方面综述了SAR的转录调控研究进展,为深入理解植物免疫调控网络以及系统探究植物在复杂环境中平衡生长与防御的机制提供参考。     

根际细菌诱导的植物系统抗性

综述根际细菌诱导ISR的机制及其信号传递途径的研究进展。     

茉莉酸及其甲酯在植物诱导抗病性中的作用

茉莉酸类物质被认为是植物抗病防卫反应的内源及中间信号分子。本文介绍了茉莉酸及其甲酯在植物抗病性中的作用,从它们在体内激活的代谢途径及相关基因表达探讨有关作用机制以及有可能在农业上应用的前景。     

生物和非生物逆境胁迫下的植物系统信号

复杂多变的自然环境使植物进化出许多适应策略, 其中由局部胁迫引起的系统响应广泛存在, 精细调节植物的生长发育和环境适应能力。植物系统响应的诱导因素首先引起植物从局部到全株范围的信号转导, 这类信号称为系统信号。当受到外界刺激时, 植物首先在受刺激细胞内触发化学信号分子的变化, 如茉莉酸和水杨酸甲酯等在浓度和信号强度方面发生变化; 进而, 伴随着一系列复杂的信号转换, 多种信号组分共同完成系统响应的激活。植物激素、小分子肽和RNA等被认为是缓慢系统信号通路中的关键组分, 而目前也有大量研究阐释了由活性氧、钙信号和电信号相互偶联组成的快速系统信号通路。植物系统信号对其生存和繁衍至关重要, 其精确的转导机制仍值得深入研究。该文综述了植物响应环境的系统信号转导研究进展, 对关键的系统信号组分及其转导机制进行了总结, 同时对植物系统信号传递的研究方向进行了展望。     

系统获得性抗性移动信号Pip/NHP研究进展

系统获得性抗性(SAR)是一种因病原微生物初次侵染植物局部叶片而被激活的整株水平上的持久广谱抗性。在初次侵染部位快速产生的抗性信号,可通过韧皮部传输到植物其它部位,从而激活SAR。哌啶酸/N-羟基哌啶酸(Pip/NHP)作为新发现的移动信号分子,在SAR信号通路中具有重要作用。该文综述了Pip/NHP的合成、转运以及对SAR调控作用的最新研究进展。     

茉莉酸与植物抗性相关基因的表达

茉莉酸(jasmonic acid,JA)及其甲酯(MeJA)是调节高等植物的发育、应答外界刺激、调节基因表达的天然高等植物激素.JA最初是从真菌Lasiodiplodia theobromae培养液中分离到的.已研究过的所有高等植物中都有JA,估计其正常水平＜10μmol·L-1.植物组织中JA的水平在花和果实等繁殖器官特别是未成熟的果皮中最高,根和成熟的叶片中则低得多.JA在植物组织中的液相和气相中可快速运动.1nmol·L-1的JA和1μmol·L-1的MeJA就能诱导植物基因表达水平的变化[1].     

水杨酸诱导植物抗性的研究进展

水杨酸是一种重要的内源信号分子,能够激活一系列植物抗性防卫反应.为了研究这种抗性反应,对水杨酸诱导植物抗病性、抗旱性、抗盐性及与乙烯作用的新进展作了概述,并从水杨酸与过氧化氢及其代谢酶类相互作用的角度探讨了水杨酸诱导植物抗性生理的分子机理.     

水杨酸对芒果炭疽病的诱导抗性作用

大田试验结果表明,水杨酸叶面喷雾可减轻芒果炭疽病的发生,100—200mgL-1均有极显著的效果,病情指数分别比对照下降了23％－41．1％,以浓度为100mgL-1的效果最好,而在马铃薯培养基（PDA）中平板培养时,100mgL-1水杨酸对芒果炭疽菌菌丝生长和孢子萌发均无抑制作用．因此认为,水杨酸处理芒果后感病指数下降,是由于水杨酸处理提高了芒果幼果的抗病性,即幼果产生了诱导抗性而引起的．     

Induced systemic resistance (ISR) against pathogens in the context of induced plant defences

Induced systemic resistance (ISR) of plants against pathogens is a widespread phenomenon that has been intensively investigated with respect to the underlying signalling pathways as well as to its potential use in plant protection. Elicited by a local infection, plants respond with a salicylic-dependent signalling cascade that leads to the systemic expression of a broad spectrum and long-lasting disease resistance that is efficient against fungi, bacteria and viruses. Changes in cell wall composition, de novo production of pathogenesis-related-proteins such as chitinases and glucanases, and synthesis of phytoalexins are associated with resistance, although further defensive compounds are likely to exist but remain to be identified. In this Botanical Briefing we focus on interactions between ISR and induced resistance against herbivores that is mediated by jasmonic acid as a central signalling molecule. While many studies report cross-resistance, others have found trade-offs, i.e. inhibition of one resistance pathway by the other. Here we propose a framework that explains many of the thus far contradictory results. We regard elicitation separately from signalling and from production, i.e. the synthesis of defensive compounds. Interactions on all three levels can act independently from each other.     

Kinetics of the Accumulation of Jasmonic Acid and Its Derivatives in Systemic Leaves of Tobacco (Nicotiana tabacum cv. Xanthi nc) and Translocation of Deuterium-Labeled Jasmonic Acid from the Wounding Site to the Systemic Site

In plants, the mobile signal needed for wound-induced systemic acquired resistance (WSR) has been elusive. The signal compound involved in WSR is supposed to be JA or its derivatives. On the basis of kinetic study of the accumulation of JA or its derivatives, it was discovered that JA, JA-Ile, tuberonic acid (TA, 12-OH epi-JA), and tuberonic acid glucoside (TAG) accumulated in systemic tissues in response to mechanical wounding stress in the tobacco plant (Nicotiana tabacum). Attempts to recover deuterium-labeled JA in systemic leaves after feeding the wounded leaves with deuterium-labeled JA were successfully done. It was also found that the translocated deuterium-labeled JA was metabolized to TA in systemic leaves under feeding of deuterium-labeled JA to the wounding leaves.     

Reduced toxicity and broad spectrum resistance to viral and fungal infection in transgenic plants expressing pokeweed antiviral protein II

Pokeweed antiviral protein II (PAPII), a 30 kDa protein isolated from leaves of Phytolacca americana, inhibits translation by catalytically removing a specific adenine residue from the large rRNA of the 60S subunit of eukaryotic ribosomes. The protein sequence of PAPII shows only 41% identity to PAP and PAP-S, two other antiviral proteins isolated from pokeweed. We isolated a cDNA corresponding to PAPII and introduced it into tobacco plants. PAPII expressed in transgenic tobacco was correctly processed to the mature form as in pokeweed and accumulated to at least 10-fold higher levels than wild-type PAP. We had previously observed a significant decrease in transformation frequency with PAP and recovered only two transgenic lines expressing 1–2 ng per mg protein. In contrast, eight different transgenic lines expressing up to 250 ng/mg PAPII were recovered, indicating that PAPII is less toxic than PAP. Two symptomless transgenic lines expressing PAPII were resistant to tobacco mosaic virus, potato virus X and the fungal pathogen Rhizoctonia solani. The level of viral and fungal resistance observed correlated well with the amount of PAPII protein accumulated. Pathogenesis-related protein PR1 was constitutively expressed in transgenic lines expressing PAPII. Although PR1 was constitutively expressed, no increase in salicylic acid levels was detected, indicating that PAPII may elicit a salicylic acid-independent signal transduction pathway.     

Induction of Systemic Acquired Resistance by Heat Shock Treatment in Arabidopsis

A 3,6-di-O-benzylated demethylallosamizoline derivative was glycosylated at the 4-position with an N, N′-diphthaloylchitobiosyl moiety by using the thioglycoside method. After de-protections, the resulting demethylallosamidin-like pseudotrisaccharide was evaluated as an inhibitor against a couple of chitinases.     

Bacillus amyloliquefaciens FZB42 represses plant miR846 to induce systemic resistance via a jasmonic acid‐dependent signalling pathway

Bacillus amyloliquefaciens FZB42 is a type of plant growth‐promoting rhizobacterium (PGPR) which activates induced systemic resistance (ISR) in Arabidopsis. Blocking of the synthesis of cyclic lipopeptides and 2,3‐butanediol by FZB42, which have been demonstrated to be involved in the priming of ISR, results in the abolishment of the plant defence responses. To further clarify the ISR activated by PGPRs at the microRNA (miRNA) level, small RNA (sRNA) libraries from Arabidopsis leaves after root irrigation with FZB42, FZB42ΔsfpΔalsS and control were constructed and sequenced. After fold change selection, promoter analysis and target prediction, miR846‐5p and miR846‐3p from the same precursor were selected as candidate ISR‐associated miRNAs. miR846 belongs to the non‐conserved miRNAs, specifically exists in Arabidopsis and its function in the plant defence response remains unclear. The disease severity of transgenic Arabidopsis overexpressing miR846 (OEmiR846) or knockdown miR846 (STTM846) against Pseudomonas syringae DC3000 suggests that the miR846 expression level in Arabidopsis is negatively correlated with disease resistance. Moreover, miR846 in Arabidopsis Col‐0 is repressed after methyl jasmonate treatment. In addition, jasmonic acid (JA) signalling‐related genes are up‐regulated in STTM846, and the stomatal apertures of STTM846 are also less than those in Arabidopsis Col‐0 after methyl jasmonate treatment. Furthermore, the disease resistance of STTM846 transgenic Arabidopsis against Pseudomonas syringae pv. tomato DC3000 (Pst DC3000) is blocked by the addition of the JA biosynthetic inhibitor diethyldiethiocarbamic acid (DIECA). Taken together, our results suggest that B. amyloliquefaciens FZB42 inoculation suppresses miR846 expression to induce Arabidopsis systemic resistance via a JA‐dependent signalling pathway.     

Abscisic acid modulates salicylic acid biosynthesis for systemic acquired resistance in tomato

Among the regulatory mechanisms of systemic acquired resistance (SAR) in tomato, antagonistic interaction between salicylic acid (SA) and abscisic acid (ABA) signaling pathways was investigated. Treatment with 1,2-benzisothiazol-3(2H)-one1,1-dioxide (BIT) induced SAR in tomato thorough SA biosynthesis. Pretreatment of ABA suppressed BIT-induced SAR including SA accumulation, suggesting that ABA suppressed SAR by inhibiting SA biosynthesis.     

Different mechanisms of Trichoderma virens‐mediated resistance in tomato against Fusarium wilt involve the jasmonic and salicylic acid pathways

In the present study, we investigated the role of Trichoderma virens (TriV_JSB100) spores or cell‐free culture filtrate in the regulation of growth and activation of the defence responses of tomato (Solanum lycopersicum) plants against Fusarium oxysporum f. sp. lycopersici by the development of a biocontrol–plant–pathogen interaction system. Two‐week‐old tomato seedlings primed with TriV_JSB100 spores cultured on barley grains (BGS) or with cell‐free culture filtrate (CF) were inoculated with Fusarium pathogen under glasshouse conditions; this resulted in significantly lower disease incidence in tomato Oogata‐Fukuju plants treated with BGS than in those treated with CF. To dissect the pathways associated with this response, jasmonic acid (JA) and salicylic acid (SA) signalling in BGS‐ and CF‐induced resistance was evaluated using JA‐ and SA‐impaired tomato lines. We observed that JA‐deficient mutant def1 plants were susceptible to Fusarium pathogen when they were treated with BGS. However, wild‐type (WT) BGS‐treated tomato plants showed a higher JA level and significantly lower disease incidence. SA‐deficient mutant NahG plants treated with CF were also found to be susceptible to Fusarium pathogen and displayed low SA levels, whereas WT CF‐treated tomato plants exhibited moderately lower disease levels and substantially higher SA levels. Expression of the JA‐responsive defensin gene PDF1 was induced in WT tomato plants treated with BGS, whereas the SA‐inducible pathogenesis‐related protein 1 acidic (PR1a) gene was up‐regulated in WT tomato plants treated with CF. These results suggest that TriV_JSB100 BGS and CF differentially induce JA and SA signalling cascades for the elicitation of Fusarium oxysporum resistance in tomato.     

Stimulation and attenuation of induced resistance by elicitors and inhibitors of chemical induction in tomato (Lycopersicon esculentum) foliage

Elicitors and inhibitors of chemical induction were used to manipulate the activities of several putative defense-related proteins in leaves of the tomato, Lycopersicon esculentum Mill. The four presumptive defenses manipulated were proteinase inhibitors, polyphenol oxidase, peroxidase, and lipoxygenase. The elicitors used were jasmonic acid, methyl jasmonate, ultraviolet light, and feeding by larvae of the noctuid, Helicoverpa zea Boddie; the inhibitors used were salicylic acid and acetylsalicylic acid. These chemical manipulations were combined with short-term growth assays using larvae of the generalist noctuid, Spodoptera exigua Hubner, in order to assess the relative roles of the proteins in induced resistance to S. exigua. When activities of proteinase inhibitors and/or polyphenol oxidase in leaf tissue were high (e.g., in damaged or elicited plants), growth rates of larvae of S. exigua were low; when activities of polyphenol oxidase and proteinase inhibitors were low (e.g., in undamaged or damaged, inhibited plants), growth rates of larvae were high. In contrast, high activities of peroxidase and lipoxygenase were not associated with decreases in suitability of leaf tissue for S. exigua. The association of high levels of proteinase inhibitors and polyphenol oxidase with resistance to S. exigua – irrespective of the presence or absence of damage – strongly implicates these proteins as causal agents in induced resistance to S. exigua.