Volatile organic compounds in Solanum lycopersicum leaves and their roles in plant protection

Simona Gargiulo , Michelina Ruocco , Francesco Loreto , Luigi Faino , Maurilia Maria Monti

Horticulture Research ›› 2025, Vol. 12 ›› Issue (10) : 181

PDF (1668KB)
Horticulture Research ›› 2025, Vol. 12 ›› Issue (10) :181 DOI: 10.1093/hr/uhaf181
Review Articles
research-article
Volatile organic compounds in Solanum lycopersicum leaves and their roles in plant protection
Author information +
History +
PDF (1668KB)

Abstract

Tomato (Solanum lycopersicum L.) is a species of high economic value, an essential food source, and a model organism for both applied and basic research in crop science. Tomato plants also produce and emit a wide variety of volatile organic compounds (VOCs), which are thought to play a prominent role in multitrophic interactions. This review aims to provide a comprehensive overview of the extensive literature about tomato VOCs emitted by leaves. We explored the role of VOCs in the interactions of tomato plants with the environment, focusing on VOCs that provide plant protection against herbivores, pathogen vectors, pathogens, and abiotic stresses. VOC functions in plant-plant communication and defence are less known, but new evidence is now being collected showing that VOCs sent by plants can inform neighbour plants about impending stresses. Overall, improved knowledge on VOC biochemistry and functions may soon allow their use for sustainable protection practices of tomato crops. Remaining gaps and promising areas for future research are also examined.

Cite this article

Download citation ▾
Simona Gargiulo, Michelina Ruocco, Francesco Loreto, Luigi Faino, Maurilia Maria Monti. Volatile organic compounds in Solanum lycopersicum leaves and their roles in plant protection. Horticulture Research, 2025, 12(10): 181 DOI:10.1093/hr/uhaf181

登录浏览全文

4963

注册一个新账户 忘记密码

Acknowledgements

We acknowledge the financial support under the National Recovery and Resilience Plan, Mission 4, Component 2, Investment 1.1, Call for tender No. 1409 published on 14 September 2022 by the Italian Ministry of University and Research (MUR), funded by the European Union—NextGenerationEU—Project PRIN 2022 PNRR P20229ZW4A RE-VOC CUP B53D23032030001; Grant Assignment Decree No. 1048 adopted on 14/07/2023 by the Italian Ministry of University and Research (MUR); Italian Ministry of University and Research (MUR) under the Programma Operativo Nazionale ricerca e Innovazione (PON) 2014-2020 (FSE REACT-EU) programme (grant agreement No. DOT1326JZS to S.G.); ‘Call for access to the National Research infrastructures of the Italian Plant Phenotyping network Phen-Italy’—CUP B85F19003500005.

Conflict of interest statement

The authors declare that they have no conflicts of interest regarding the publication of this manuscript.

Supplementary Data

Supplementary data is available at Horticulture Research online.

References

[1]

Rowan DD. Volatile metabolites. Metabolites. 2011; 1:41-63

[2]

Holopainen JK, Gershenzon J. Multiple stress factors and the emission of plant VOCs. Trends Plant Sci. 2010; 15:176-84

[3]

Dudareva N, Klempien A, Muhlemann JK. et al. Biosynthesis, function and metabolic engineering of plant volatile organic compounds. New Phytol. 2013; 198:16-32

[4]

Loreto F, D’Auria S. How do plants sense volatiles sent by other plants? Trends Plant Sci. 2022; 27:29-38

[5]

Pollastri S, Jorba I, Hawkins TJ. et al. Leaves of isoprene-emitting tobacco plants maintain PSII stability at high temperatures. New Phytol. 2019; 223:1307-18

[6]

Brilli F, Loreto F, Baccelli I. Exploiting plant volatile organic compounds (VOCs) in agriculture to improve sustainable defense strategies and productivity of crops. Front Plant Sci. 2019; 10:264

[7]

Nakamura S, Hatanaka A. Green-leaf-derived C6-aroma com-pounds with potent antibacterial action that act on both gram-negative and gram-positive bacteria. J Agric Food Chem. 2002; 50: 7639-44

[8]

Ricciardi V, Marcianò D, Sargolzaei M. et al. From plant resis-tance response to the discovery of antimicrobial compounds: the role of volatile organic compounds (VOCs) in grapevine downy mildew infection. Plant Physiol Biochem. 2021; 160: 294-305

[9]

Quintana-Rodriguez E, Rivera-Macias LE, Adame-Alvarez RM. et al. Shared weapons in fungus-fungus and fungus-plant inter-actions? Volatile organic compounds of plant or fungal origin exert direct antifungal activity in vitro. Fungal Ecol. 2018; 33: 115-21

[10]

Hammerbacher A, Coutinho TA, Gershenzon J. Roles of plant volatiles in defence against microbial pathogens and microbial exploitation of volatiles. Plant Cell Environ. 2019; 42: 2827-43

[11]

Duc NH, Vo HTN, van Doan C. et al. Volatile organic compounds shape belowground plant-fungi interactions. Front Plant Sci. 2022; 13:1046685

[12]

Rhoades DF. Responses of alder and willow to attack by tent caterpillars and webworms:evidence for pheromonal sensitiv-ity of willows. In: Plant Resistance to Insects.Vol 208. American Chemical Society Pubblication, 1983, 208, 55

[13]

Zhu J, Park K-C. Methyl salicylate, a soybean aphid-induced plant volatile attractive to the predator Coccinella septempunc-tata. JChemEcol. 2005; 31:1733-46

[14]

Burkle LA, Runyon JB. Drought and leaf herbivory influence flo-ral volatiles and pollinator attraction. Glob Change Biol. 2016; 22: 1644-54

[15]

Caparrotta S, Boni S, Taiti C. et al. Induction of priming by salt stress in neighboring plants. Environ Exp Bot. 2018; 147: 261-70

[16]

Cofer TM, Engelberth M, Engelberth J. Green leaf volatiles protect maize (Zea mays) seedlings against damage from cold stress. Plant Cell Environ. 2018; 41:1673-82

[17]

Erb M. Plant biology: evolution of volatile-mediated plant-plant interactions. Curr Biol. 2019;29:R873-5

[18]

Zhang P-J, Chan Z, Zi-Hong Y. et al. Trade-off between defense priming by herbivore-induced plant volatiles and constitutive defense in tomato. Pest Manag Sci. 2020; 76:1893-901

[19]

Ninkovic V, Markovic D, Rensing M. Plant volatiles as cues and signals in plant communication. Plant Cell Environ. 2021; 44: 1030-43

[20]

Ángeles López YI, Martínez-Gallardo NA, Ramírez-Romero R. et al. Cross-kingdom effects of plant-plant signaling via volatile organic compounds emitted by tomato (Solanum lycopersicum) plants infested by the greenhouse whitefly (Trialeurodes vapo-rariorum). JChemEcol. 2012; 38:1376-86

[21]

Zebelo S, Piorkowski J, Disi J. et al. Secretions from the ven-tral eversible gland of Spodoptera exigua caterpillars activate defense-related genes and induce emission of volatile organic compounds in tomato, Solanum lycopersicum. BMC Plant Biol. 2014; 14:140

[22]

Nagashima A, Higaki T, Koeduka T. et al. Transcriptional regu-lators involved in responses to volatile organic compounds in plants. JBiolChem. 2019; 294:2256-66

[23]

Catola S, Centritto M, Cascone P. et al. Effects of single or com-bined water deficit and aphid attack on tomato volatile organic compound (VOC) emission and plant-plant communication. Environ Exp Bot. 2018; 153:54-62

[24]

Quintana-Rodriguez E, Morales-Vargas ATM, Molina-Torres J. et al. Plant volatiles cause direct, induced and associational resistance in common bean to the fungal pathogen Col-letotrichum lindemuthianum. JEcol. 2015; 103:250-60

[25]

Brosset A, Blande JD. Volatile-mediated plant-plant interac-tions: volatile organic compounds as modulators of receiver plant defence, growth, and reproduction. JExp Bot. 2022; 73: 511-28

[26]

Murali-Baskaran RK, Mooventhan P, Das D. et al. The future of plant volatile organic compounds (pVOCs) research: advances and applications for sustainable agriculture. Environ Exp Bot. 2022; 200:104912

[27]

LavagnedOrtigue O (ESS). Agricultural production statistics 2000-2022.

[28]

FAOSTAT.Tomato Production. 2022. https://ourworldindata.org/grapher/tomatoproduction?tab=table&time=latest(accessed on 26 August 2024).

[29]

Gerszberg A, Hnatuszko-Konka K, Kowalczyk T. et al. Tomato (Solanum lycopersicum L.) in the service of biotechnology. Plant Cell Tissue Organ Cult. 2015; 120:881-902

[30]

Martina M, Tikunov Y, Portis E. et al. The genetic basis of tomato aroma. Genes. 2021; 12:226

[31]

Dehimeche N, Buatois B, Bertin N. et al. Insights into the intraspecific variability of the above and belowground emis-sions of volatile organic compounds in tomato. Molecules. 2021; 26:237

[32]

Pichersky E, Raguso RA. Why do plants produce so many ter-penoid compounds? New Phytol. 2018; 220:692-702

[33]

Karunanithi PS, Zerbe P. Terpene synthases as metabolic gate-keepers in the evolution of plant terpenoid chemical diversity. Front Plant Sci. 2019; 10:1166

[34]

Falara V, Akhtar TA, Nguyen TTH. et al. The tomato terpene synthase gene family. Plant Physiol. 2011; 157:770-89

[35]

Zhou F, Pichersky E. The complete functional characterisation of the terpene synthase family in tomato. New Phytol. 2020; 226: 1341-60

[36]

López-Gresa MP, Lisón P, Campos L. et al. A non-targeted metabolomics approach unravels the VOCs associated with the tomato immune response against Pseudomonas syringae. Front Plant Sci. 2017; 8:1188

[37]

Pazouki L, Kanagendran A, Li S. et al. Mono-and sesquiter-pene release from tomato (Solanum lycopersicum)leavesupon mild and severe heat stress and through recovery: from gene expression to emission responses. Environ Exp Bot. 2016; 132:1-15

[38]

Gutensohn M, Klempien A, Kaminaga Y. et al. Role of aromatic aldehyde synthase in wounding/herbivory response and flower scent production in different Arabidopsis ecotypes. Plant J. 2011; 66:591-602

[39]

Kumar V, Nadarajan S, Boddupally D. et al. Phenylalanine treat-ment induces tomato resistance to Tuta absoluta via increased accumulation of benzenoid/phenylpropanoid volatiles serving as defense signals. Plant J. 2024; 119:84-99

[40]

Mao G, Tian J, Li T. et al. Behavioral responses of Nagrus nilaparvatae to common terpenoids, aromatic compounds, and fatty acid derivatives from rice plants. Entomologia Exp et App. 2018; 166:483-90

[41]

Ament K, Krasikov V, Allmann S. et al. Methyl salicylate pro-duction in tomato affects biotic interactions. Plant J. 2010; 62: 124-34

[42]

Picazo-Aragonés J, Terrab A, Balao F. Plant volatile organic compounds evolution: transcriptional regulation, epigenetics and polyploidy. Int J Mol Sci. 2020; 21:8956

[43]

Upadhyay RK, Mattoo AK. Genome-wide identification of tomato (Solanum lycopersicum L.) lipoxygenases coupled with expression profiles during plant development and in response to methyl-jasmonate and wounding. J Plant Physiol. 2018; 231: 318-28

[44]

Upadhyay RK, Handa AK, Mattoo AK. Transcript abundance patterns of 9- and 13-lipoxygenase subfamily gene members in response to abiotic stresses (heat, cold, drought or salt) in tomato (Solanum lycopersicum L.) highlights member-specific dynamics relevant to each stress. Genes. 2019; 10:683

[45]

Hernández-Aparicio F, Lisón P, Rodrigo I. et al. Signaling in the tomato immunity against Fusarium oxysporum. Molecules. 2021; 26:1818

[46]

Yan L, Zhai Q, Wei J. et al. Role of tomato lipoxygenase D in wound-induced jasmonate biosynthesis and plant immunity to insect herbivores. PLoS Genet. 2013; 9:e1003964

[47]

Bleeker PM, Diergaarde PJ, Ament K. et al. The role of specific tomato volatiles in tomato-whitefly interaction. Plant Physiol. 2009; 151:925-35

[48]

Bleeker PM, Diergaarde PJ, Ament K. et al. Tomato-produced 7-epizingiberene and R-curcumene act as repellents to white-flies. Phytochemistry. 2011; 72:68-73

[49]

Freitas JA, Maluf WR, das Graças Cardoso M. et al. Inheritance of foliar zingiberene contents and their relationship to tri-chome densities and whitefly resistance in tomatoes. Euphytica. 2002; 127:275-87

[50]

Kortbeek RWJ, Galland MD, Muras A. et al. Natural variation in wild tomato trichomes; selecting metabolites that contribute to insect resistance using a random forest approach. BMC Plant Biol. 2021; 21:315

[51]

Paudel S, Lin P-A, Foolad MR. et al. Induced plant defenses against herbivory in cultivated and wild tomato. JChemEcol. 2019; 45:693-707

[52]

Arafa RA, Kamel SM, Taher DI. et al. Leaf extracts from resistant wild tomato can be used to control late blight (Phytophthora infestans) in the cultivated tomato. Plants. 2022; 11:1824

[53]

Turcotte MM, Turley NE, Johnson MTJ. The impact of domes-tication on resistance to two generalist herbivores across 29 independent domestication events. New Phytol. 2014; 204: 671-81

[54]

Chen YH, Gols R, Benrey B. Crop domestication and its impact on naturally selected trophic interactions. Annu Rev Entomol. 2015; 60:35-58

[55]

Milla R, Osborne CP, Turcotte MM. et al. Plant domestication through an ecological lens. Trends Ecol Evol. 2015; 30:463-9

[56]

Smýkal P, Nelson MN, Berger JD. et al. The impact of genetic changes during crop domestication. Agronomy. 2018; 8:119

[57]

Ferrero V, Baeten L, Blanco-Sánchez L. et al. Complex patterns in tolerance and resistance to pests and diseases underpin the domestication of tomato. New Phytol. 2020; 226:254-66

[58]

Raghava T, Ravikumar P, Hegde R. et al. Spatial and temporal volatile organic compound response of select tomato cultivars to herbivory and mechanical injury. Plant Sci. 2010; 179:520-6

[59]

D’Esposito D, Guadagno A, Amoroso CG. et al. Genomic and metabolic profiling of two tomato contrasting cultivars for tolerance to Tuta absoluta. Planta. 2023; 257:47

[60]

Coppola M, Cascone P, Madonna V. et al. Plant-to-plant com-munication triggered by systemin primes anti-herbivore resis-tance in tomato. Sci Rep. 2017; 7:15522

[61]

Kutty NN, Mishra M. Dynamic distress calls: volatile info chem-icals induce and regulate defense responses during herbivory. Front Plant Sci. 2023; 14:1135000

[62]

Sasso R, Iodice L, Cristina Digilio M. et al. Host-locating response by the aphid parasitoid Aphidius ervi to tomato plant volatiles. J Plant Interact. 2007; 2:175-83

[63]

Sasso R, Iodice L, Woodcock CM. et al. Electrophysiological and behavioural responses of Aphidius ervi (Hymenoptera: Braconidae) to tomato plant volatiles. Chemoecology. 2009; 19: 195-201

[64]

Digilio MC, Cascone P, Iodice L. et al. Interactions between tomato volatile organic compounds and aphid behaviour. J Plant Interact. 2012; 7:322-5

[65]

Cascone P, Iodice L, Maffei ME. et al. Tobacco overexpressing β-ocimene induces direct and indirect responses against aphids in receiver tomato plants. J Plant Physiol. 2015; 173:28-32

[66]

Takemoto H, Takabayashi J. Parasitic wasps Aphidius ervi are more attracted to a blend of host-induced plant volatiles than to the independent compounds. JChemEcol. 2015; 41:801-7

[67]

Ayelo PM, Yusuf AA, Pirk CWW. et al. The role of Trialeurodes vaporariorum-infested tomato plant volatiles in the attraction of Encarsia formosa (hymenoptera: Aphelinidae). JChemEcol. 2021; 47:192-203

[68]

Ayelo PM, Yusuf AA, Pirk CW. et al. Terpenes from herbivore-induced tomato plant volatiles attract (Hemiptera: Miridae), a predator of major tomato pests. Pest Manag Sci. 2021; 77:5255-67

[69]

Tan X-L, Liu T-X. Aphid-induced plant volatiles affect the attractiveness of tomato plants to Bemisia tabaci and associated natural enemies. Entomol Exp Appl. 2014; 151:259-69

[70]

Pagadala Damodaram KJ, Gadad HS, Parepally SK. et al. Low moisture stress influences plant volatile emissions affecting herbivore interactions in tomato. Ecol Entomol. 2021; 46:637-50

[71]

Mas F, Vereijssen J, Suckling DM. Influence of the pathogen Candidatus Liberibacter solanacearum on tomato host plant volatiles and psyllid vector settlement. JChemEcol. 2014; 40: 1197-202

[72]

Luan J-B, Yao D-M, Zhang T. et al. Suppression of terpenoid synthesis in plants by a virus promotes its mutualism with vectors. Ecol Lett. 2013; 16:390-8

[73]

Fereres A, Peñaflor MFGV, Favaro CF. et al. Tomato infec-tion by whitefly-transmitted circulative and non-circulative viruses induce contrasting changes in plant volatiles and vec-tor behaviour. Viruses. 2016; 8:225

[74]

Ghosh S, Didi-Cohen S, Cna’ani A. et al. Comparative analysis of volatiles emitted from tomato and pepper plants in response to infection by two whitefly-transmitted persistent viruses. Insects. 2022; 13:840

[75]

Shi X-B, Wang X-Z, Zhang D-Y. et al. Silencing of odorant-binding protein gene OBP3 using RNA interference reduced virus transmission of tomato chlorosis virus. Int J Mol Sci. 2019; 20:4969

[76]

Yu J, Gonzalez JM, Dong Z. et al. Integrative proteomic and phosphoproteomic analyses of pattern-and effector-triggered immunity in tomato. Front Plant Sci. 2021; 12:768693

[77]

Sharifi R, Lee S-M, Ryu C-M. Microbe-induced plant volatiles. New Phytol. 2018; 220:684-91

[78]

Ortiz A, Sansinenea E. Phenylpropanoid derivatives and their role in plants’ health and as antimicrobials. Curr Microbiol. 2023; 80:380

[79]

Hassan B, Soumya E, Amal EA. et al. Antifungal activities of B-ionone, carvone and 1,8-cineole essential oil components against Aspergillus Niger spores. J Chem Pharm Res. 2017; 9:52-6

[80]

Kasal-Slavik T, Eschweiler J, Kleist E. et al. Early biotic stress detection in tomato (Solanum lycopersicum) by BVOC emissions. Phytochemistry. 2017; 144:180-8

[81]

El Oirdi M, El Rahman TA, Rigano L. et al. Botrytis cinerea manip-ulates the antagonistic effects between immune pathways to promote disease development in tomato. Plant Cell. 2011; 23: 2405-21

[82]

McDowell JM, Dangl JL. Signal transduction in the plant immune response. Trends Biochem Sci. 2000; 25:79-82

[83]

Ameye M, Allmann S, Verwaeren J. et al. Green leaf volatile production by plants: a meta-analysis. New Phytol. 2018; 220: 666-83

[84]

López-Gresa MP, Payá C, Ozáez M. et al. A new role for green leaf volatile esters in tomato stomatal defense against Pseudomonas syringe pv. tomato. Front Plant Sci. 2018; 9:1855

[85]

Xin Z, Zhang L, Zhang Z. et al.A tea hydroperoxide lyase gene, CsiHPL1, regulates tomato defense response against Pro-denia litura (Fabricius) and Alternaria alternata f. sp. Lycopersici by modulating green leaf volatiles (GLVs) release and jas-monic acid (JA) gene expression. Plant Mol Biol Report. 2014; 32: 62-9

[86]

Jansen RMC, Hofstee JW, Wildt J. et al. Induced plant volatiles allow sensitive monitoring of plant health status in green-houses. Plant Signal Behav. 2009; 4:824-9

[87]

Jansen RMC, Miebach M, Kleist E. et al. Release of lipoxygenase products and monoterpenes by tomato plants as an indicator of Botrytis cinerea-induced stress. Plant Biol. 2009; 11:859-68

[88]

Boncan DAT, Tsang SSK, Li C. et al. Terpenes and terpenoids in plants: interactions with environment and insects. Int J Mol Sci. 2020; 21:7382

[89]

Sultan K, Perveen S. Plant stress responses:past, present, and future. In:Molecular Dynamics of Plant Stress and its Management. Springer: Singapore, 2024,93-119

[90]

Choudhury FK, Rivero RM, Blumwald E. et al. Reactive oxygen species, abiotic stress and stress combination. Plant J. 2017; 90: 856-67

[91]

Velikova V, Várkonyi Z, Szabó M. et al. Increased thermostability of thylakoid membranes in isoprene-emitting leaves probed with three biophysical techniques. Plant Physiol. 2011; 157: 905-16

[92]

Loreto F, Schnitzler J-P. Abiotic stresses and induced BVOCs. Trends Plant Sci. 2010; 15:154-66

[93]

Nagalingam S, Seco R, Musaev K. et al. Impact of heat stress on foliar biogenic volatile organic compound emission and gene expression in tomato (Solanum lycopersicum) seedlings. Elem Sci Anth. 2022; 10:00096

[94]

Copolovici L, Kännaste A, Pazouki L. et al. Emissions of green leaf volatiles and terpenoids from Solanum lycopersicum are’quantitatively related to the severity of cold and heat shock treatments. J Plant Physiol. 2012; 169:664-72

[95]

Loreto F, Pollastri S, Fineschi S. et al. Volatile isoprenoids and their importance for protection against environmental con-straints in the Mediterranean area. Environ Exp Bot. 2014; 103: 99-106

[96]

Tomescu D, ¸Sum ˘alan R, Copolovici L. et al. The influence of soil salinity on volatile organic compounds emission and photo-synthetic parameters of Solanum lycopersicum L. varieties. Open Life Sci. 2017; 12:135-42

[97]

Ormeño E, Mévy JP, Vila B. et al. Water deficit stress induces different monoterpene and sesquiterpene emission changes in Mediterranean species. Relationship between terpene emis-sions and plant water potential. Chemosphere. 2007; 67:276-84

[98]

Morshedloo MR, Craker LE, Salami A. et al. Effect of prolonged water stress on essential oil content, compositions and gene expression patterns of mono-and sesquiterpene synthesis in two oregano (Origanum vulgare L.) subspecies. PPB. 2017; 111: 119-28

[99]

Monson RK, Weraduwage SM, Rosenkranz M. et al. Leaf isoprene emission as a trait that mediates the growth-defense tradeoff in the face of climate stress. Oecologia. 2021; 197:885-902

[100]

Ngumbi E, Dady E, Calla B. Flooding and herbivory: the effect of concurrent stress factors on plant volatile emissions and gene expression in two heirloom tomato varieties. BMC Plant Biol. 2022; 22:536

[101]

Lin P-A, Paudel S, Bin Zainuddin N. et al. Low water availability enhances volatile-mediated direct defences but disturbs indi-rect defences against herbivores. JEcol. 2022; 110:2759-71

[102]

Beckett M, Loreto F, Velikova V. et al. Photosynthetic limitations and volatile and non-volatile isoprenoids in the poikilochloro-phyllous resurrection plant Xerophyta humilis during dehydra-tion and rehydration. Plant Cell Environ. 2012; 35:2061-74

[103]

Fabbri B, Valt M, Parretta C. et al. Correlation of gaseous emis-sions to water stress in tomato and maize crops: from field to laboratory and back. Sens Actuators B Chem. 2020; 303:127227

[104]

Kataria S, Chandel M, Kumar P. et al. Irrigation-friendly sensor to manage drought in crops through carbon-based signature volatile sensing. Sens Actuators B Chem. 2024; 403:134975

[105]

Runyon JB, Mescher MC, De Moraes CM. Volatile chemical cues guide host location and host selection by parasitic plants. Science. 2006; 313:1964-7

[106]

Arimura G, Uemura T. Cracking the plant VOC sensing code and its practical applications. Trends Plant Sci. 2024; 30:105-15

[107]

Sheard LB, Tan X, Mao H. et al. Jasmonate perception by inositol-phosphate-potentiated COI1-JAZ co-receptor. Nature. 2010; 468:400-5

[108]

Park S-W, Kaimoyo E, Kumar D. et al. Methyl salicylate is a critical mobile signal for plant systemic acquired resistance. Science. 2007; 318:113-6

[109]

Frank L, Wenig M, Ghirardo A. et al. Isoprene and β-caryophyllene confer plant resistance via different plant inter-nal signalling pathways. Plant Cell Environ. 2021; 44:1151-64

[110]

Zebelo SA, Matsui K, Ozawa R. et al. Plasma membrane poten-tial depolarization and cytosolic calcium flux are early events involved in tomato (Solanum lycopersicum) plant-to-plant com-munication. Plant Sci. 2012; 196:93-100

[111]

Aratani Y, Uemura T, Hagihara T. et al. Green leaf volatile sensory calcium transduction in Arabidopsis. Nat Commun. 2023; 14:6236

[112]

Yamauchi Y, Kunishima M, Mizutani M. et al. Reactive short-chain leaf volatiles act as powerful inducers of abiotic stress-related gene expression. Sci Rep. 2015; 5:8030

[113]

Tian S, Guo R, Zou X. et al. Priming with the green leaf volatile (Z)-3-hexeny-1-yl acetate enhances salinity stress tol-erance in peanut (Arachis hypogaea L.)seedlings. Front Plant Sci. 2019; 10:785

[114]

Engelberth J. Green leaf volatiles: a new player in the protection against abiotic stresses? Int J Mol Sci. 2024; 25:9471

[115]

Heil M, Karban R. Explaining evolution of plant communication by airborne signals. Trends Ecol Evol. 2010; 25:137-44

[116]

Desmedt W, Vanholme B, Kyndt T. Chapter 5—Plant defense priming in the field:a review. In: Maienfisch P, Mangelinckx S, Academic Press,eds. Recent Highlights in the Discovery and Optimization of Crop Protection Products. 2021,87-124

[117]

Wang L, Einig E, Almeida-Trapp M. et al. The systemin recep-tor SYR1 enhances resistance of tomato against herbivorous insects. Nat Plants. 2018; 4:152-6

[118]

Heldt H-W, Piechulla B. 19- Multiple signals regulate the growth and development of plant organs and enable their adaptation to environmental conditions. In: Heldt H-W, Piechulla B,eds. Plant Biochemistry. 4th ed. Elsevier: San Diego, 2011,451-85

[119]

Degenhardt DC, Refi-Hind S, Stratmann JW. et al. Systemin and jasmonic acid regulate constitutive and herbivore-induced systemic volatile emissions in tomato, Solanum lycopersicum. Phytochemistry. 2010; 71:2024-37

[120]

Corrado G, Sasso R, Pasquariello M. et al. Systemin regulates both systemic and volatile signaling in tomato plants. JChem Ecol. 2007; 33:669-81

[121]

Sun J-Q, Jiang H-L, Li C-Y. Systemin/jasmonate-mediated sys-temic defense signaling in tomato. Mol Plant. 2011; 4:607-15

[122]

Savary S, Willocquet L, Pethybridge SJ. et al. The global burden of pathogens and pests on major food crops. Nat Ecol Evol. 2019; 3:430-9

[123]

Maurya AK. Application of plant volatile organic compounds (VOCs) in agriculture. In: Rakshit A, Singh HB, Singh AK. et al.eds., New Frontiers in Stress Management for Durable Agriculture. Springer: Singapore, 2020,369-88

[124]

Razo-Belman R, Ozuna C. Volatile organic compounds: a review of their current applications as pest biocontrol and disease management. Horticulturae. 2023; 9:441

[125]

Munawar A, Zhu Z, Machado RAR. et al. Beyond “push-pull”: unraveling the ecological pleiotropy of plant volatile organic compounds for sustainable crop pest management. Crop Health. 2023; 1:18

[126]

Szczech M, Kowalska B, Wurm FR. et al. The effects of tomato intercropping with medicinal aromatic plants combined with trichoderma applications in organic cultivation. Agronomy. 2024; 14:2572

[127]

Togni PHB, Laumann RA, Medeiros MA. et al. Odour masking of tomato volatiles by coriander volatiles in host plant selection of Bemisia tabaci biotype B. Entomologia Exp et App. 2010; 136:164-73

[128]

Hilje L, Stansly PA. Living ground covers for management of Bemisia tabaci (Gennadius) (Homoptera: Aleyrodidae) and tomato yellow mottle virus (ToYMoV) in Costa Rica. Crop Prot. 2008; 27:10-6

[129]

Medeiros MA, Sujii ER, Morais HC. Effect of plant diversification on abundance of south American tomato pinworm and preda-tors in two cropping systems. Hortic Bras. 2009; 27:300-6

[130]

Togni PH, Frizzas MR, Medeiros MA. et al. Dinâmica popula-cional de Bemisia tabaci biótipo B em tomate monocultivo e consorciado com coentro sob cultivo orgânico e convencional. Hortic Bras. 2009; 27:183-8

[131]

Padala VK, Saravan Kumar P, Ramya N. et al. Aromatic plant odours of Anethum graveolens and Coriandrum sativum repel whitefly, Bemisia tabaci in tomato. Curr Sci. 2023; 124:231-8

[132]

Conboy NJA, McDaniel T, Ormerod A. et al. Companion planting with French marigolds protects tomato plants from glasshouse whiteflies through the emission of airborne limonene. PLoS One. 2019; 14:e0213071

[133]

Zhou X, Zhang J, Shi J. et al. Volatile-mediated interspe-cific plant interaction promotes root colonization by benefi-cial bacteria via induced shifts in root exudation. Microbiome. 2024; 12:207

[134]

Lee YS, Lee H, Lee HJ. et al. Push-pull strategy for control of sweet-potato whitefly, Bemisia tabaci (Hemiptera: Aleyrodi-dae) in a tomato greenhouse. Korean J Appl Entomol. 2019; 58: 209-18

[135]

Mangrio GQ. Pull-push strategy for the management of Tuta absoluta (Lepidoptera: Gelechiidae) in tomatoes. Pakistan J Zool. 2024;1-8

[136]

Anastasaki E, Drizou F, Milonas PG. Electrophysiological and oviposition responses of Tuta absoluta females to herbivore-induced volatiles in tomato plants. JChemEcol. 2018; 44:288-98

[137]

Msisi D, Matojo ND, Kimbokota F. Attraction of female tomato leaf miner, Tuta absoluta (Meyrick, 1917) (Lepidoptera: Gelechi-idae) to shared compounds from hosts. Phytoparasitica. 2021; 49: 153-62

[138]

Pouët C, Deletre E, Rhino B. Repellency of wild oregano plant volatiles, Plectranthus amboinicus, and their essential oils to the Silverleaf whitefly, Bemisia tabaci, on tomato. Neotrop Entomol. 2022; 51:133-42

[139]

Pérez-Hedo M, Riahi C, Urbaneja A. Use of zoophytophagous mirid bugs in horticultural crops: current challenges and future perspectives. Pest Manag Sci. 2021; 77:33-42

[140]

Fullana AM, Giné A, Urbaneja A. et al. Nesidiocoris tenuis, Macrolophus pygmaeus (Hemiptera: Miridae) and (Z)-3-hexenyl propanoate induce systemic resistance against the root-knot nematode Meloidogyne spp. in tomatoes. BioControl. 2025; 70: 357-68

[141]

Depalo L, Gallego C, Ortells-Fabra R. et al. Advancing tomato crop protection: green leaf volatile-mediated defense mech-anisms against Nesidiocoris tenuis plant damage. Biol Control. 2024; 192:105517

[142]

Chen C-S, Zhao C, Wu Z-Y. et al. Whitefly-induced tomato volatiles mediate host habitat location of the parasitic wasp Encarsia formosa, and enhance its efficacy as a bio-control agent. Pest Manag Sci. 2021; 77:749-57

[143]

Conboy NJA, McDaniel T, George D. et al. Volatile organic com-pounds as insect repellents and plant elicitors: an Integrated Pest Management (IPM) strategy for glasshouse whitefly (Tri-aleurodes vaporariorum). JChemEcol. 2020; 46:1090-104

[144]

Yang F, Zhang Q, Yao Q. et al. Direct and indirect plant defenses induced by (Z)-3-hexenol in tomato against whitefly attack. J Pest Sci. 2020; 93:1243-54

[145]

Nuñez-Gómez V, Baenas N, Navarro-González I. et al. Sea-sonal variation of health-promoting bioactives in broccoli and methyl-jasmonate pre-harvest treatments to enhance their contents. Foods. 2020; 9:1371

[146]

Baenas N, García-Viguera C, Moreno DA. Elicitation: a tool for enriching the bioactive composition of foods. Molecules. 2014; 19:13541-63

[147]

Zhou H, Ashworth K, Dodd IC. Exogenous monoterpenes mit-igate H2O2-induced lipid damage but do not attenuate pho-tosynthetic decline during water deficit in tomato. JExp Bot. 2023; 74:5327-40

[148]

Chen L, Liao P. Current insights into plant volatile organic compound biosynthesis. Curr Opin Plant Biol. 2025; 85:102708

[149]

Zhou S, Jander G. Molecular ecology of plant volatiles in inter-actions with insect herbivores. JExp Bot. 2022; 73:449-62

[150]

Mahmood MA, Awan MJA, Naqvi RZ. et al. Methyl-salicylate (MeSA)-mediated airborne defence. Trends Plant Sci. 2024; 29: 391-3

[151]

Taggar GK, Rains GC, Tayal M. et al. Bioengineering plant volatile emissions: prospects for plant protection against insect herbi-vores. Entomol Gen. 2024; 44:749-64

[152]

Vu TV, Das S, Tran MT. et al. Precision genome engineering for the breeding of tomatoes: recent progress and future perspec-tives. Front Genome Ed. 2020; 2:612137

[153]

Tariq S, Gul A, Negri S. et al.Chapter 6—Genetic engineering in tomato. In: Gul A, in Plants. Academic press,ed. Targeted Genome Engineering via CRISPR/-Cas 9 2024,101-33

[154]

Yang F, Zhu L, Liu Z. et al. CAS1-synthesized β-caryophyllene enhances broad-spectrum stress resistance in tomatoes. Plant Physiol Biochem. 2025; 222:109726

[155]

Gutensohn M, Henry LK, Gentry SA. et al. Overcoming bottle-necks for metabolic engineering of sesquiterpene production in tomato fruits. Front Plant Sci. 2021; 12:691754

[156]

Lew TTS, Koman VB, Gordiichuk P. et al. The emergence of plant nanobionics and living plants as technology. Adv Mater Technol. 2020; 5:1900657

[157]

Pace R, Schiano Di Cola V, Monti MM. et al. Artificial intelli-gence in soil microbiome analysis: a potential application in predicting and enhancing soil health—a review. Discov Appl Sci. 2025; 7:85

[158]

Gan Z, Zhou Q, Zheng C. et al. Challenges and applications of volatile organic compounds monitoring technology in plant disease diagnosis. Biosens Bioelectron. 2023; 237:115540

[159]

Li Z, Paul R, Saville AC. et al. Non-invasive plant disease diag-nostics enabled by smartphone-based fingerprinting of leaf volatiles. Nat Plants. 2019; 5:856-66

[160]

Li Z, Liu Y, Hossain O. et al. Real-time monitoring of plant stresses via chemiresistive profiling of leaf volatiles by a wear-able sensor. Matter. 2021; 4:2553-70

[161]

Hong X, Wang J, Qi G. E-nose combined with chemometrics to trace tomato-juice quality. J Food Eng. 2015; 149:38-43

[162]

Gómez AH, Hu G, Wang J. et al. Evaluation of tomato maturity by electronic nose. Comput Electron Agr. 2006; 54: 44-52

[163]

Messina V, Domínguez PG, Sancho AM. et al. Tomato quality during short-term storage assessed by colour and electronic nose. Int J Electrochem. 2012; 2012:687429

[164]

Cui S, Cao L, Acosta N. et al. Development of portable E-nose system for fast diagnosis of whitefly infestation in tomato plant in greenhouse. Chemosensors. 2021; 9:297

[165]

Sun Y, Wang J, Cheng S. Differentiation of tomato seedlings with different mechanical damage severities using E-nose and GC-MS. Trans ASABE. 2016; 59:1069-78

[166]

Sun Y, Zheng Y. Prediction of tomato plants infected by fungal pathogens at different disease severities using E-nose and GC-MS. J Plant Dis Prot. 2024; 131:835-46

[167]

Feng H, Gonzalez Viejo C, Vaghefi N. et al. Early detection of Fusarium oxysporum infection in processing tomatoes (Solanum lycopersicum) and pathogen-soil interactions using a low-cost portable electronic nose and machine learning modeling. Sen-sors. 2022; 22:8645

PDF (1668KB)

158

Accesses

0

Citation

Detail

Sections
Recommended

/