Biotechnology Bulletin ›› 2026, Vol. 42 ›› Issue (11): 1-10.doi: 10.13560/j.cnki.biotech.bull.1985.2026-0194
HOU Kun-peng1, XU Li-ping1, WANG Xing-bin1, ZHANG Yu-qing1, WANG Wen-qiang1, HUO Zi-han1, ZHAO Chen-yang1, XU Shuo1, ZHANG Zhi-qiang2(
), GOU Ming-yue1(
)
Received:2026-02-08
Online:2026-11-26
Published:2026-11-03
Contact:
ZHANG Zhi-qiang, GOU Ming-yue
E-mail:xiao_qiang8866@163.com;mingyuegou@henau.edu.cn
HOU Kun-peng, XU Li-ping, WANG Xing-bin, ZHANG Yu-qing, WANG Wen-qiang, HUO Zi-han, ZHAO Chen-yang, XU Shuo, ZHANG Zhi-qiang, GOU Ming-yue. Research Progress on Methyl Salicylate Esterase and Its Mediated Plant Disease Resistance[J]. Biotechnology Bulletin, 2026, 42(11): 1-10.
Fig. 3 Methyl salicylate esterase gene regulates plant disease resistanceWhen pathogens (such as fungi, bacteria, viruses, etc.) infect the lower leaves of a plant, the plant perceives the signal and activates SAMT1, which converts SA in the leaves into MeSA. SABP2 is regulated by WRKY1 and NAC2. Meanwhile, SIP428 deacetylates SABP2, enhancing its methyl salicylate esterase activity, which promotes the conversion of MeSA back to SA. This simultaneously activates the ICS pathway and the PAL pathway, collectively promoting the accumulation of SA. The accumulation of SA facilitates the binding of the transcription factor TGA with its receptor NPR1, activating the expression of PRs genes. Additionally, SABP2 indirectly regulates RBOH activity, stimulating the ROS, which induces local resistance in the lower leaves. Furthermore, WRKY1 moderately inhibits the expression of SAMT1 gene, thereby regulating the dynamic balance between MeSA and SA. When MeSA is transported to the upper leaves via the phloem, the increased MeSA level in the upper leaves activates SABP2, which reconverts MeSA into SA. This again promotes the binding of TGA with NPR1 in the upper leaves, activates the expression of PRs genes, and triggers SAR. Solid arrows indicate direct regulation, dashed arrows indicate indirect regulation, T-shaped lines indicate inhibition
Fig. 4 Methyl salicylate esterase plays a key role in MeSA-mediated airborne defense in plantsA: When non-virulent aphids infest a plant, the NAC2 transcription factor is activated, leading to increased expression of SAMT1 and activation of SAMT1, which strongly induces MeSA production. As substantial amounts of MeSA are released into the air, neighboring plants capture MeSA, activate SABP2, and convert MeSA into SA, thereby activating the NAC2-SAMT1 module and further promoting MeSA generation. This induces airborne defense (AD) in neighboring plants, protecting them against aphid infestation. B: When viruliferous aphids infest a plant, NAC2 binds to CMV1a and is degraded by the 26S proteasome, leading to inhibition of SAMT1 and subsequent suppression of MeSA production. Consequently, less MeSA is captured by neighboring plants, SABP2 activity is inhibited, and SA production is reduced. This suppresses the NAC2-SAMT1 module, inhibiting MeSA synthesis and release, thereby reducing resistance to aphids. Solid arrows indicate direct regulation, T-shaped lines indicate inhibition
基因 Genes | 物种 Species | 是否受病原物诱导 Whether induced by pathogens or not | 病原物种类 Types of pathogens | 遗传材料的表型 The phenotype of genetic material | 参考文献 References |
|---|---|---|---|---|---|
| NtSABP2 | 烟草 Nicotiana tabacum | 是 | 病毒 | NtSABP2沉默株系相较于野生型更易感烟草花叶病毒 | [ |
| AtMES1 | 拟南芥 Arabidopsis thaliana | 是 | 细菌 | SABP2沉默系更易感丁香假单胞菌,AtMES1、AtMES7 和 AtMES9 这3个基因能完全恢复SABP2沉默系的SAR缺陷 | [ |
| AtMES7 | |||||
| AtMES9 | |||||
| AtMES2 | 否 | ||||
| AtMES4 | 否 | ||||
| CsMES1 | 柑橘 Citrus sinensis | 是 | 细菌 | 外施MeSA和SA后,野生型叶片的柑橘溃疡病菌明显减少 | [ |
| CsMES2 | |||||
| CsSABP2-1 | 是 | 细菌 | CsSABP2过表达株系相对于野生型,对柑橘溃疡病和黄龙病的抗性提高 | [ | |
| CsSABP2-2 | |||||
| CsSABP2-3 | |||||
| StMES1 | 马铃薯 Solanum tuberosum | 是 | 真菌 | StMES1沉默株系对致病疫霉的抗性相对于野生型减弱 | [ |
| PvMES1 | 普通菜豆 Phaseolus vulgaris | 是 | 真菌 | PvMES1的过表达株系提高了对尖孢镰刀菌的抗性,PvMES1的沉默株系更加易感病 | [ |
| FvMES2 | 草莓 Fragaria vesca | 是 | 真菌 | FvMES2的过表达株系增加对灰霉病的抗性 | [ |
| BnMES34 | 甘蓝型油菜 Brassica napus | 是 | 原生动物 | BnMES34过表达株系有效抵御芸苔疟原虫的侵袭 | [ |
| GmSABP2-1 | 大豆 Glycine max | 是 | 动物 | GmSABP2-1的过表达株系能有效抵抗大豆胞囊线虫 | [ |
| SlMES1 | 番茄 Solanum lycopersicum | 未知 | |||
| SlMES2 | |||||
| SlMES3 | [ | ||||
| SlMES4 | |||||
| PtSABP2 | 毛果杨 Populus trichocarpa | 未知 | [ | ||
| PpMES2 | 桃子 Prunus persica | 未知 | [ | ||
| LcSABP2 | 枸杞 Lycium chinense | 未知 | [ |
Table 1 Pathogen-induced expression and disease resistance function of methyl salicylate esterase genes
基因 Genes | 物种 Species | 是否受病原物诱导 Whether induced by pathogens or not | 病原物种类 Types of pathogens | 遗传材料的表型 The phenotype of genetic material | 参考文献 References |
|---|---|---|---|---|---|
| NtSABP2 | 烟草 Nicotiana tabacum | 是 | 病毒 | NtSABP2沉默株系相较于野生型更易感烟草花叶病毒 | [ |
| AtMES1 | 拟南芥 Arabidopsis thaliana | 是 | 细菌 | SABP2沉默系更易感丁香假单胞菌,AtMES1、AtMES7 和 AtMES9 这3个基因能完全恢复SABP2沉默系的SAR缺陷 | [ |
| AtMES7 | |||||
| AtMES9 | |||||
| AtMES2 | 否 | ||||
| AtMES4 | 否 | ||||
| CsMES1 | 柑橘 Citrus sinensis | 是 | 细菌 | 外施MeSA和SA后,野生型叶片的柑橘溃疡病菌明显减少 | [ |
| CsMES2 | |||||
| CsSABP2-1 | 是 | 细菌 | CsSABP2过表达株系相对于野生型,对柑橘溃疡病和黄龙病的抗性提高 | [ | |
| CsSABP2-2 | |||||
| CsSABP2-3 | |||||
| StMES1 | 马铃薯 Solanum tuberosum | 是 | 真菌 | StMES1沉默株系对致病疫霉的抗性相对于野生型减弱 | [ |
| PvMES1 | 普通菜豆 Phaseolus vulgaris | 是 | 真菌 | PvMES1的过表达株系提高了对尖孢镰刀菌的抗性,PvMES1的沉默株系更加易感病 | [ |
| FvMES2 | 草莓 Fragaria vesca | 是 | 真菌 | FvMES2的过表达株系增加对灰霉病的抗性 | [ |
| BnMES34 | 甘蓝型油菜 Brassica napus | 是 | 原生动物 | BnMES34过表达株系有效抵御芸苔疟原虫的侵袭 | [ |
| GmSABP2-1 | 大豆 Glycine max | 是 | 动物 | GmSABP2-1的过表达株系能有效抵抗大豆胞囊线虫 | [ |
| SlMES1 | 番茄 Solanum lycopersicum | 未知 | |||
| SlMES2 | |||||
| SlMES3 | [ | ||||
| SlMES4 | |||||
| PtSABP2 | 毛果杨 Populus trichocarpa | 未知 | [ | ||
| PpMES2 | 桃子 Prunus persica | 未知 | [ | ||
| LcSABP2 | 枸杞 Lycium chinense | 未知 | [ |
| [1] | Kumar D, Klessig DF. High-affinity salicylic acid-binding protein 2 is required for plant innate immunity and has salicylic acid-stimulated lipase activity [J]. Proc Natl Acad Sci U S A, 2003, 100(26): 16101-16106. |
| [2] | Vlot AC, Dempsey DA, Klessig DF. Salicylic acid, a multifaceted hormone to combat disease [J]. Annu Rev Phytopathol, 2009, 47: 177-206. |
| [3] | Sharma S, Prasad M. Diverse roles of phytohormonal signaling in modulating plant-virus interactions [J]. J Exp Bot, 2025, 76(7): 1921-1940. |
| [4] | Park SW, Kaimoyo E, Kumar D, et al. Methyl salicylate is a critical mobile signal for plant systemic acquired resistance [J]. Science, 2007, 318(5847): 113-116. |
| [5] | Dong LT, Chen S, Shang LY, et al. Overexpressing CsSABP2 enhances tolerance to Huanglongbing and Citrus canker in C. sinensis [J]. Front Plant Sci, 2024, 15: 1472155. |
| [6] | Lin JY, Wang WJ, Mazarei M, et al. GmSABP2-1 encodes methyl salicylate esterase and functions in soybean defense against soybean cyst nematode [J]. Plant Cell Rep, 2024, 43(6): 138. |
| [7] | Soares JM, Weber KC, Qiu WM, et al. Overexpression of the salicylic acid binding protein 2 (SABP2) from tobacco enhances tolerance against Huanglongbing in transgenic Citrus [J]. Plant Cell Rep, 2022, 41(12): 2305-2320. |
| [8] | Jia RM, Yu LG, Chen J, et al. Molecular evolution of methylesterase family genes and the BnMES34 is a positive regulator of Plasmodiophora brassicae stress response in Arabidopsis [J]. Int J Biol Macromol, 2024, 260: 129333. |
| [9] | Manosalva PM, Park SW, Forouhar F, et al. Methyl esterase 1 (StMES1) is required for systemic acquired resistance in potato [J]. Mol Plant Microbe Interac, 2010, 23(9): 1151-1163. |
| [10] | Xue RF, Feng M, Chen J, et al. A methyl esterase 1 (PvMES1) promotes the salicylic acid pathway and enhances Fusarium wilt resistance in common beans [J]. Theor Appl Genet, 2021, 134(8): 2379-2398. |
| [11] | Gong Q, Wang YJ, He LF, et al. Molecular basis of methyl-salicylate-mediated plant airborne defence [J]. Nature, 2023, 622(7981): 139-148. |
| [12] | Nardini M, Dijkstra BW. α/β Hydrolase fold enzymes: the family keeps growing [J]. Curr Opin Struct Biol, 1999, 9(6): 732-737. |
| [13] | Forouhar F, Yang Y, Kumar D, et al. Structural and biochemical studies identify tobacco SABP2 as a methyl salicylate esterase and implicate it in plant innate immunity [J]. Proc Natl Acad Sci U S A, 2005, 102(5): 1773-1778. |
| [14] | Frick EM, Sapkota M, Pereira L, et al. A family of methyl esterases converts methyl salicylate to salicylic acid in ripening tomato fruit [J]. Plant Physiol, 2023, 191(1): 110-124. |
| [15] | Li Q, Wang G, Guan CF, et al. Overexpression of LcSABP, an orthologous gene for salicylic acid binding protein 2, enhances drought stress tolerance in transgenic tobacco [J]. Front Plant Sci, 2019, 10: 200. |
| [16] | Vlot AC, Liu PP, Cameron RK, et al. Identification of likely orthologs of tobacco salicylic acid-binding protein 2 and their role in systemic acquired resistance in Arabidopsis thaliana [J]. Plant J, 2008, 56(3): 445-456. |
| [17] | de Lima Silva CC, Shimo HM, de Felício R, et al. Structure-function relationship of a Citrus salicylate methylesterase and role of salicylic acid in Citrus canker resistance [J]. Sci Rep, 2019, 9: 3901. |
| [18] | Zhao N, Guan J, Forouhar F, et al. Two poplar methyl salicylate esterases display comparable biochemical properties but divergent expression patterns [J]. Phytochemistry, 2009, 70(1): 32-39. |
| [19] | Cao XM, Duan WY, Wei CY, et al. Genome-wide identification and functional analysis of carboxylesterase and methylesterase gene families in peach (Prunus persica L. batsch) [J]. Front Plant Sci, 2019, 10: 1511. |
| [20] | Jia RM, Xing KY, Tian L, et al. Analysis of methylesterase gene family in Fragaria vesca unveils novel insights into the role of FvMES2 in methyl salicylate-mediated resistance against strawberry gray mold [J]. J Agric Food Chem, 2024, 72(20): 11392-11404. |
| [21] | Kopertekh L. Improving transient expression in N. benthamiana by suppression of the Nb-SABP2 and Nb-COI1 plant defence response related genes [J]. Front Plant Sci, 2024, 15: 1453930. |
| [22] | Delaney TP, Friedrich L, Ryals JA. Arabidopsis signal transduction mutant defective in chemically and biologically induced disease resistance [J]. Proc Natl Acad Sci U S A, 1995, 92(14): 6602-6606. |
| [23] | Glazebrook J, Rogers EE, Ausubel FM. Isolation of Arabidopsis mutants with enhanced disease susceptibility by direct screening [J]. Genetics, 1996, 143(2): 973-982. |
| [24] | Cao H, Bowling SA, Gordon AS, et al. Characterization of an Arabidopsis mutant that is nonresponsive to inducers of systemic acquired resistance [J]. Plant Cell, 1994: 1583-1592. |
| [25] | Yan J, Li Q, Geng DY, et al. The potato StNAC2-StSABP2 module enhanced resistance to Phytophthora infestans through activating the salicylic acid pathway [J]. Mol Plant Pathol, 2025, 26(5): e70081. |
| [26] | Lefevere H, Bauters L, Gheysen G. Salicylic acid biosynthesis in plants [J]. Front Plant Sci, 2020, 11: 338. |
| [27] | Wildermuth MC, Dewdney J, Wu G, et al. Isochorismate synthase is required to synthesize salicylic acid for plant defence [J]. Nature, 2001, 414(6863): 562-565. |
| [28] | Mauch-Mani B, Slusarenko AJ. Production of salicylic acid precursors is a major function of phenylalanine ammonia-lyase in the resistance of Arabidopsis to Peronospora parasitica [J]. Plant Cell, 1996: 203-212. |
| [29] | Zou XP, Zhao K, Liu YN, et al. Overexpression of salicylic acid carboxyl methyltransferase (CsSAMT1) enhances tolerance to Huanglongbing disease in wanjincheng orange (Citrus sinensis (L.) osbeck) [J]. Int J Mol Sci, 2021, 22(6): 2803. |
| [30] | Li YX, Zhang W, Dong HX, et al. Salicylic acid in Populus tomentosa is a remote signalling molecule induced by Botryosphaeria dothidea infection [J]. Sci Rep, 2018, 8: 14059. |
| [31] | Dong HX, Zhang W, Li YX, et al. Overexpression of salicylic acid methyltransferase reduces salicylic acid-mediated pathogen resistance in poplar [J]. Front Plant Sci, 2022, 13: 973305. |
| [32] | 袁亮, 郭慧娟, 孙玉诚, 等. 蚜虫诱导的植物免疫反应 [J]. 应用昆虫学报, 2015, 52(1): 23-31. |
| Yuan L, Guo HJ, Sun YC, et al. Plant immunity responses to aphid [J]. Chin J Appl Entomol, 2015, 52(1): 23-31. | |
| [33] | Baldwin IT, Halitschke R, Paschold A, et al. Volatile signaling in plant-plant interactions: “talking trees” in the genomics era [J]. Science, 2006, 311(5762): 812-815. |
| [34] | Shulaev V, Silverman P, Raskin I. Airborne signalling by methyl salicylate in plant pathogen resistance [J]. Nature, 1997, 385(6618): 718-721. |
| [35] | Mahmood MA, Awan MJA, Naqvi RZ, et al. Methyl-salicylate (MeSA)-mediated airborne defence [J]. Trends Plant Sci, 2024, 29(4): 391-393. |
| [36] | 袁民航, 辛秀芳. 烽火狼烟: 水杨酸甲酯介导的植物间通讯和气传性免疫的机制解析 [J]. 植物学报, 2023, 58(5): 682-686. |
| Yuan MH, Xin XF. Study uncovers a new signaling circuit mediating airborne defense of plants against aphids and viruses [J]. Chin Bull Bot, 2023, 58(5): 682-686. | |
| [37] | Ooka H. Comprehensive analysis of NAC family genes in Oryza sativa and Arabidopsis thaliana [J]. DNA Res, 2003, 10(6): 239-247. |
| [38] | Yang PZ, Chen ZX. A family of dispersed repetitive DNA sequences in tobacco contain clusters of W-box elements recognized by pathogen-induced WRKY DNA-binding proteins [J]. Plant Sci, 2001, 161(4): 655-664. |
| [39] | Lan LM, Zhang LL, Cao LF, et al. WRKY1-mediated interconversion of MeSA and SA in neighbouring apple plants enhances defence against powdery mildew [J]. Plant Cell Environ, 2025, 48(5): 3105-3117. |
| [40] | Haq MI, Thakuri BKC, Hobbs T, et al. Tobacco SABP2-interacting protein SIP428 is a SIR2 type deacetylase [J]. Plant Physiol Biochem, 2020, 152: 72-80. |
| [41] | Nicolas-Francès V, Grandperret V, Liegard B, et al. Evolutionary diversification of type-2 HDAC structure, function and regulation in Nicotiana tabacum [J]. Plant Sci, 2018, 269: 66-74. |
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