Plant resistance towards insect herbivores: a dynamic interaction

Gatehouse, John A.

doi:10.1046/j.1469-8137.2002.00519.x

Cited by 704Insect-Plant Interactions and ControlForest Insect Ecology and ManagementPlant biochemistry and biosynthesis

Plant resistance towards insect herbivores: a dynamic interaction

Gatehouse, John A.·2002·New Phytologist

DOI 10.1046/j.1469-8137.2002.00519.x

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Abstract

Summary: Plant defences against insect herbivores can be divided into ‘static’ or constitutive defences, and ‘active’ or induced defences, although the insecticidal compounds or proteins involved are often the same. Induced defences have aspects common to all plants, whereas the accumulation of constitutive defences is species‐specific. Insect herbivores activate induced defences both locally and systemically by signalling pathways involving systemin, jasmonate, oligogalacturonic acid and hydrogen peroxide. Plants also respond to insect attack by producing volatiles, which can be used to deter herbivores, to communicate between parts of the plant, or between plants, to induce defence responses. Plant volatiles are also an important component in indirect defence. Herbivorous insects have adapted to tolerate plant defences, and such adaptations can also be constitutive or induced. Insects whose plant host range is limited are more likely to show constitutive adaptation to the insecticidal compounds they will encounter, whereas insects which feed on a wide range of plant species often use induced adaptations to overcome plant defences. Both plant defence and insect adaptation involve a metabolic cost, and in a natural system most plant–insect interactions involving herbivory reach a ‘stand‐off’ where both host and herbivore survive but develop suboptimally. Contents Summary 145 I. Introduction 146 II. Accumulation of defensive compounds and induced resistance 146 III. Signalling pathways in wound‐induced resistance 147 IV. Insect modulation of the wounding response 155 V. Insects which evade the wounding response 156 VI. Insect‐induced emission of volatiles and tritrophic interactions 157 VII. Insect adaptation to plant defences 160 Conclusions 163 Acknowlegements 163 References 163

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When the herbivore is the initial agent, plants frequently activate metabolic pathways that produce jasmonic acid, which cascades many metabolic signals involved in disease resistance.
“Alternatively, when the herbivore is the initial agent, plants frequently activate metabolic pathways that produce jasmonic acid that, in turn, cascade many metabolic signals involved in disease resistance (1,20,23,24).”
From A Tripartite Interaction Between Spartina alterniflora, Fusarium palustre, and the Purple Marsh Crab (Sesarma reticulatum) Contributes to Sudden Vegetation Dieback of Salt Marshes in New England (2014) · cites this paper as [20]

BUTTERFLIES AND PLANTS: A STUDY IN COEVOLUTION
Ehrlich, P. R., & Raven, P. H. (1964) · Evolution · doi:10.1111/j.1558-5646.1964.tb01674.x · Cited by 4,501 · see citing works
THE OXIDATIVE BURST IN PLANT DISEASE RESISTANCE
Lamb, C. J., & Dixon, R. A. (1997) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.48.1.251 · Cited by 3,219 · see citing works
Defensive Function of Herbivore-Induced Plant Volatile Emissions in Nature
Keßler, A., & Baldwin, I. T. (2001) · Science · doi:10.1126/science.291.5511.2141 · Cited by 2,191 · see citing works
Secondary metabolites in plant defence mechanisms
BENNETT, R. N., & WALLSGROVE, R. M. (1994) · New Phytologist · doi:10.1111/j.1469-8137.1994.tb02968.x · Cited by 1,654 · see citing works
Introduction to Ecological Biochemistry
(1993) · Elsevier eBooks · doi:10.1016/c2009-0-03518-1 · Cited by 1,508 · see citing works
SYSTEMIC ACQUIRED RESISTANCE
Sticher, L., Mauch‐Mani, B., & Métraux, A. J. (1997) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.35.1.235 · Cited by 1,436 · see citing works
The Myriad Plant Responses to Herbivores
Walling, L. L. (2000) · Journal of Plant Growth Regulation · doi:10.1007/s003440000026 · Cited by 1,405 · see citing works
Interplant communication: airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves.
Farmer, E. E., & Ryan, C. A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.19.7713 · Cited by 1,372 · see citing works
Coordinated plant defense responses in Arabidopsis revealed by microarray analysis
Schenk, P. M., Kazan, K., Wilson, I. W., Anderson, J. P., Richmond, T., Somerville, S. C., & Manners, J. M. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.21.11655 · Cited by 1,370 · see citing works
Herbivore-infested plants selectively attract parasitoids
Moraes, C. Μ. D., LEWIS, W. J., Paré, P. W., Alborn, H. T., & Tumlinson, J. H. (1998) · Nature · doi:10.1038/31219 · Cited by 1,320 · see citing works
Differential Gene Expression in Response to Mechanical Wounding and Insect Feeding in Arabidopsis
Reymond, P., Weber, H. H., Damond, M., & Farmer, E. E. (2000) · The Plant Cell · doi:10.1105/tpc.12.5.707 · Cited by 1,229 · see citing works
Plant Volatiles as a Defense against Insect Herbivores
Paré, P. W., & Tumlinson, J. H. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.121.2.325 · Cited by 1,197 · see citing works
The formation and function of plant volatiles: perfumes for pollinator attraction and defense
Pichersky, E., & Gershenzon, J. (2002) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(02)00251-0 · Cited by 1,193 · see citing works
Reactive Oxygen Intermediates Mediate a Systemic Signal Network in the Establishment of Plant Immunity
Álvarez, M. E., Pennell, R. I., Meijer, P., Ishikawa, A., Dixon, R. A., & Lamb, C. (1998) · Cell · doi:10.1016/s0092-8674(00)81405-1 · Cited by 1,154 · see citing works
INSECT P450 ENZYMES
Feyereisen, R. (1999) · Annual Review of Entomology · doi:10.1146/annurev.ento.44.1.507 · Cited by 1,070 · see citing works
Natural protein proteinase inhibitors and their interaction with proteinases
Bode, W., & Huber, R. (1992) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1992.tb16654.x · Cited by 1,044 · see citing works
Caterpillar-induced nocturnal plant volatiles repel conspecific females
Moraes, C. Μ. D., Mescher, M. C., & Tumlinson, J. H. (2001) · Nature · doi:10.1038/35069058 · Cited by 1,018 · see citing works
An Elicitor of Plant Volatiles from Beet Armyworm Oral Secretion
Alborn, H. T., Turlings, T. C. J., Jones, T. H., Stenhagen, G., Loughrin, J. H., & Tumlinson, J. H. (1997) · Science · doi:10.1126/science.276.5314.945 · Cited by 998 · see citing works
A novel mechanism of insect resistance engineered into tobacco
Hilder, V. A., Gatehouse, A. M. R., Sheerman, S. E., Barker, R. F., & Boulter, D. (1987) · Nature · doi:10.1038/330160a0 · Cited by 927 · see citing works
Hydrogen Peroxide Acts as a Second Messenger for the Induction of Defense Genes in Tomato Plants in Response to Wounding, Systemin, and Methyl Jasmonate
Orozco-Cárdenas, M. L., Narváez-Vásquez, J., & Ryan, C. A. (2001) · The Plant Cell · doi:10.1105/tpc.13.1.179 · Cited by 889 · see citing works
Hydrogen peroxide is generated systemically in plant leaves by wounding and systemin via the octadecanoid pathway
Orozco-Cárdenas, M. L., & Ryan, C. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.11.6553 · Cited by 837 · see citing works
The Arabidopsis male-sterile mutant, opr3 , lacks the 12-oxophytodienoic acid reductase required for jasmonate synthesis
Stintzi, A., & Browse, J. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.190264497 · Cited by 834 · see citing works
Jasmonate is essential for insect defense in Arabidopsis
McConn, M. M., Creelman, R. A., Bell, E., Mullet, J. E., & Browse, J. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.10.5473 · Cited by 810 · see citing works
The Root Knot Nematode Resistance Gene Mi from Tomato Is a Member of the Leucine Zipper, Nucleotide Binding, Leucine-Rich Repeat Family of Plant Genes
Milligan, S. B., Bodeau, J. P., Yaghoobi, J., Kaloshian, I., Zabel, P., & Williamson, V. M. (1998) · The Plant Cell · doi:10.1105/tpc.10.8.1307 · Cited by 804 · see citing works
Sympatric Speciation in Phytophagous Insects: Moving Beyond Controversy?
Berlocher, S. H., & Feder, J. L. (2002) · Annual Review of Entomology · doi:10.1146/annurev.ento.47.091201.145312 · Cited by 792 · see citing works
Jasmonic acid carboxyl methyltransferase: A key enzyme for jasmonate-regulated plant responses
Seo, H. S., Song, J. T., Cheong, J., Lee, Y., Lee, Y., Hwang, I., Lee, J. S., & Choi, Y. D. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081557298 · Cited by 774 · see citing works
MAPK cascades in plant defense signaling
Zhang, S., & Klessig, D. F. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(01)02103-3 · Cited by 773 · see citing works
Wound signalling in plants
León, J., Rojo, E., & Sánchez‐Serrano, J. J. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.354.1 · Cited by 773 · see citing works
Herbivory-induced volatiles elicit defence genes in lima bean leaves
Arimura, G., Ozawa, R., Shimoda, T., Nishioka, T., Boland, W., & Takabayashi, J. (2000) · Nature · doi:10.1038/35020072 · Cited by 763 · see citing works
The nematode resistance gene Mi of tomato confers resistance against the potato aphid
Rossi, M., Goggin, F. L., Milligan, S. B., Kaloshian, I., Ullman, D. E., & Williamson, V. M. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.17.9750 · Cited by 759 · see citing works
How caterpillar-damaged plants protect themselves by attracting parasitic wasps.
Turlings, T. C. J., Loughrin, J. H., McCall, P. J., Röse, U. S. R., LEWIS, W. J., & Tumlinson, J. H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.10.4169 · Cited by 757 · see citing works
The myrosinase‐glucosinolate system, its organisation and biochemistry
Bones, A. M., & Rossiter, J. T. (1996) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1996.tb00497.x · Cited by 752 · see citing works
Ethylene as a Signal Mediating the Wound Response of Tomato Plants
O'Donnell, P. J. M., Calvert, C. M., Atzorn, R., Wasternack, C. H., Leyser, O., & Bowles, D. J. (1996) · Science · doi:10.1126/science.274.5294.1914 · Cited by 744 · see citing works
Jasmonate-induced responses are costly but benefit plants under attack in native populations
Baldwin, I. T. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.14.8113 · Cited by 743 · see citing works
Plant defense in the absence of jasmonic acid: The role of cyclopentenones
Stintzi, A., Weber, H. H., Reymond, P., Browse, J., & Farmer, E. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.211311098 · Cited by 698 · see citing works
Fitness costs of induced resistance: emerging experimental support for a slippery concept
Heil, M. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(01)02186-0 · Cited by 612 · see citing works
Glucosinolate research in the Arabidopsis era
Wittstock, U., & Halkier, B. A. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(02)02273-2 · Cited by 611 · see citing works
Molecular Responses to Aphid Feeding in Arabidopsis in Relation to Plant Defense Pathways
Moran, P. J., & Thompson, G. A. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.2.1074 · Cited by 595 · see citing works
Constitutive plant toxins and their role in defense against herbivores and pathogens
Wittstock, U., & Gershenzon, J. (2002) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(02)00264-9 · Cited by 568 · see citing works
The systemin signaling pathway: differential activation of plant defensive genes
Ryan, C. A. (2000) · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · doi:10.1016/s0167-4838(99)00269-1 · Cited by 563 · see citing works
The adaptation of insects to plant protease inhibitors
Jongsma, M. A., & Bolter, C. J. (1997) · Journal of Insect Physiology · doi:10.1016/s0022-1910(97)00040-1 · Cited by 533 · see citing works
Oligosaccharide signalling for defence responses in plant
Shibuya, N., & Minami, E. (2001) · Physiological and Molecular Plant Pathology · doi:10.1006/pmpp.2001.0364 · Cited by 527 · see citing works
Molecular Interactions between the Specialist Herbivore Manduca sexta (Lepidoptera, Sphingidae) and Its Natural Host Nicotiana attenuata . III. Fatty Acid-Amino Acid Conjugates in Herbivore Oral Secretions Are Necessary and Sufficient for Herbivore-Specific Plant Responses
Halitschke, R., Schittko, U., Pohnert, G., Boland, W., & Baldwin, I. T. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.2.711 · Cited by 513 · see citing works
Caterpillar saliva beats plant defences
Musser, R. O., Hum‐Musser, S. M., Eichenseer, H., Peiffer, M. L., Ervin, G. N., Murphy, J. B., & Felton, G. W. (2002) · Nature · doi:10.1038/416599a · Cited by 510 · see citing works
Oligogalacturonides and chitosan activate plant defensive genes through the octadecanoid pathway.
Doares, S. H., Syrovets, T., Weiler, E. W., & Ryan, C. A. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.10.4095 · Cited by 481 · see citing works
De Novo Biosynthesis of Volatiles Induced by Insect Herbivory in Cotton Plants
Paré, P. W., & Tumlinson, J. H. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.4.1161 · Cited by 480 · see citing works
Fatty acid-derived signals in plants
Weber, H. H. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(02)02250-1 · Cited by 470 · see citing works
An octadecanoid pathway mutant (JL5) of tomato is compromised in signaling for defense against insect attack.
Howe, G. A., Lightner, J. E., Browse, J., & Ryan, C. A. (1996) · The Plant Cell · doi:10.1105/tpc.8.11.2067 · Cited by 456 · see citing works
Adaptation of Spodoptera exigua larvae to plant proteinase inhibitors by induction of gut proteinase activity insensitive to inhibition.
Jongsma, M. A., Bakker, P. L., Peters, J., Bosch, D., & Stiekema, W. J. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.17.8041 · Cited by 454 · see citing works
New roles for cis -jasmone as an insect semiochemical and in plant defense
Birkett, M. A., Campbell, C. A. M., Chamberlain, K., Guerrieri, E., Hick, A. J., Martin, J. L., Matthes, M. C., Napier, J. A., Pettersson, J., Pickett, J. A., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.160241697 · Cited by 454 · see citing works
Structure, Expression, and Antisense Inhibition of the Systemin Precursor Gene
McGurl, B., Pearce, G., Orozco-Cárdenas, M. L., & Ryan, C. A. (1992) · Science · doi:10.1126/science.1549783 · Cited by 446 · see citing works
C6‐volatiles derived from the lipoxygenase pathway induce a subset of defense‐related genes
Bate, N. J., & Rothstein, S. J. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00324.x · Cited by 426 · see citing works
Distinct roles for jasmonate synthesis and action in the systemic wound response of tomato
Li, L., Li, C., Lee, G. I., & Howe, G. A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.072072599 · Cited by 401 · see citing works
Disease resistance conferred by expression of a gene encoding H2O2-generating glucose oxidase in transgenic potato plants.
Wu, G., Shortt, B. J., Lawrence, E. B., Levine, E. B., Fitzsimmons, K. C., & Shah, D. M. (1995) · The Plant Cell · doi:10.1105/tpc.7.9.1357 · Cited by 391 · see citing works
Foliar oxidative stress and insect herbivory: Primary compounds, secondary metabolites, and reactive oxygen species as components of induced resistance
Bi, J. L., & Felton, G. W. (1995) · Journal of Chemical Ecology · doi:10.1007/bf02035149 · Cited by 376 · see citing works
Oligogalacturonic Acid and Chitosan Reduce Stomatal Aperture by Inducing the Evolution of Reactive Oxygen Species from Guard Cells of Tomato and Commelina communis
Lee, S., Choi, H., Suh, S., Doo, I.-S., Oh, K.-Y., Choi, E. J., Taylor, A., Low, P. S., & Lee, Y. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.121.1.147 · Cited by 362 · see citing works
Cost of Resistance to Natural Enemies in Field Populations of the Annual Plant Arabidopsis thaliana
Mauricio, R. (1998) · The American Naturalist · doi:10.1086/286099 · Cited by 360 · see citing works
Herbivore-Induced Volatile Production by Arabidopsis thaliana Leads to Attraction of the Parasitoid Cotesia rubecula: Chemical, Behavioral, and Gene-Expression Analysis
Poecke, R. M. P. V., Posthumus, M. A., & Dicke, M. (2001) · Journal of Chemical Ecology · doi:10.1023/a:1012213116515 · Cited by 358 · see citing works
Differentially regulated inhibitor-sensitive and insensitive protease genes from the phytophagous insect pest, Helicoverpa armigera, are members of complex multigene families
Bown, D. P., Wilkinson, H. S., & Gatehouse, J. A. (1997) · Insect Biochemistry and Molecular Biology · doi:10.1016/s0965-1748(97)00043-x · Cited by 352 · see citing works
Self-citation
Systemin activates synthesis of wound-inducible tomato leaf polyphenol oxidase via the octadecanoid defense signaling pathway.
Constabel, C. P., Bergey, D. R., & Ryan, C. A. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.2.407 · Cited by 351 · see citing works
The tomato Mi-1 gene confers resistance to both root-knot nematodes and potato aphids
Vos, P., Simons, G., Jesse, T., Wijbrandi, J., Heinen, L., Hogers, R. C. J., Frijters, A. C. J., Groenendijk, J., Diergaarde, P. J., Reijans, M., et al. (1998) · Nature Biotechnology · doi:10.1038/4350 · Cited by 350 · see citing works
PREDATORS EXERT TOP-DOWN CONTROL OF SOYBEAN APHID ACROSS A GRADIENT OF AGRICULTURAL MANAGEMENT SYSTEMS
Costamagna, A. C., & Landis, D. A. (2006) · Ecological Applications · doi:10.1890/1051-0761(2006)016[1619:petcos]2.0.co;2 · Cited by 350 · see citing works
Herbivore-induced ethylene suppresses a direct defense but not a putative indirect defense against an adapted herbivore
Kahl, J., Siemens, D. H., Aerts, R. J., Gäbler, R., Kühnemann, F., Preston, C. A., & Baldwin, I. T. (2000) · Planta · doi:10.1007/pl00008142 · Cited by 345 · see citing works
Experimental evidence that plants under caterpillar attack may benefit from attracting parasitoids
Hoballah, M. E., & Turlings, T. C. J. (2001) · Evolutionary ecology research · Cited by 340 · see citing works
Signals involved in wound-induced proteinase inhibitor II gene expression in tomato and potato plants.
Peña‐Cortés, H., Fisahn, J., & Willmitzer, L. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.10.4106 · Cited by 337 · see citing works
Allene oxide synthase: a major control point in Arabidopsis thaliana octadecanoid signalling
Laudert, D., & Weiler, E. W. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00245.x · Cited by 329 · see citing works
Enzymes of the biosynthesis of octadecanoid‐derived signalling molecules
Schaller, F. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.354.11 · Cited by 326 · see citing works
Advances In Insect Control: The Role Of Transgenic Plants
Carozzi, N. B., & Koziel, M. G. (2007) · Cited by 314 · see citing works
Jasmonate‐mediated induced plant resistance affects a community of herbivores
Thaler, J. S., Stout, M. J., Karban, R., & Duffey, S. S. (2001) · Ecological Entomology · doi:10.1046/j.1365-2311.2001.00324.x · Cited by 311 · see citing works
Resistance to an Herbivore Through Engineered Cyanogenic Glucoside Synthesis
Tattersall, D. B., Bak, S., Jones, P. R., Olsen, C. E., Nielsen, J. K., Hansen, M. L., Høj, P. B., & Møller, B. L. (2001) · Science · doi:10.1126/science.1062249 · Cited by 310 · see citing works
Molecular Interactions between the Specialist Herbivore Manduca sexta (Lepidoptera, Sphingidae) and Its Natural Host Nicotiana attenuata . I. Large-Scale Changes in the Accumulation of Growth- and Defense-Related Plant mRNAs
Hermsmeier, D., Schittko, U., & Baldwin, I. T. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.2.683 · Cited by 308 · see citing works
Impact of oxidized plant phenolics on the nutritional quality of dietar protein to a noctuid herbivore, Spodoptera exigua
Felton, G. W., Donato, K. K., Broadway, R. M., & Duffey, S. S. (1992) · Journal of Insect Physiology · doi:10.1016/0022-1910(92)90128-z · Cited by 299 · see citing works
Monitoring of Methyl Jasmonate-responsive Genes in Arabidopsis by cDNA Macroarray: Self-activation of Jasmonic Acid Biosynthesis and Crosstalk with Other Phytohormone Signaling Pathways
Sasaki, Y. (2001) · DNA Research · doi:10.1093/dnares/8.4.153 · Cited by 293 · see citing works
Volatile Semiochemicals Released from Undamaged Cotton Leaves (A Systemic Response of Living Plants to Caterpillar Damage)
Röse, U. S. R., Manukian, A., Heath, R. R., & Tumlinson, J. H. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.2.487 · Cited by 291 · see citing works
Hydrogen peroxide and lignification
Olson, P., & Varner, J. E. (1993) · The Plant Journal · doi:10.1046/j.1365-313x.1993.04050887.x · Cited by 290 · see citing works
An herbivore elicitor activates the gene for indole emission in maize
Frey, M., Stettner, C., Paré, P. W., Schmelz, E. A., Tumlinson, J. H., & Gierl, A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.260499897 · Cited by 289 · see citing works
Production of multiple plant hormones from a single polyprotein precursor
Pearce, G., de Moura, D. S., Stratmann, J. W., & Ryan, C. A. (2001) · Nature · doi:10.1038/35081107 · Cited by 283 · see citing works
Hydroperoxide lyase depletion in transgenic potato plants leads to an increase in aphid performance
Vancanneyt, G., Sanz, C., Farmaki, T., Paneque, M., Ortego, F., Castañera, P., & Sánchez‐Serrano, J. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.141079498 · Cited by 277 · see citing works
Herbivory and caterpillar regurgitants amplify the wound-induced increases in jasmonic acid but not nicotine in Nicotiana sylvestris
McCLOUD, E. S., & Baldwin, I. T. (1997) · Planta · doi:10.1007/s004250050210 · Cited by 275 · see citing works
Activation of Host Defense Mechanisms by Elevated Production of H2O2 in Transgenic Plants
Wu, G., Shortt, B. J., Lawrence, E. B., León, J., Fitzsimmons, K. C., Levine, E. B., Raskin, I., & Shah, D. M. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.115.2.427 · Cited by 274 · see citing works
Introduction to ecological biochemistry:
Bell, E. A. (1989) · Phytochemistry · doi:10.1016/s0031-9422(00)97958-5 · Cited by 272 · see citing works
Inverse relationship between systemic resistance of plants to microorganisms and to insect herbivory
Felton, G. W., Korth, K. L., Bi, J. L., Wesley, S. V., Huhman, D. V., Mathews, M. C., Murphy, J. B., Lamb, C. J., & Dixon, R. A. (1999) · Current Biology · doi:10.1016/s0960-9822(99)80140-7 · Cited by 271 · see citing works
Ontogeny Constrains Systemic Protease Inhibitor Response in Nicotiana attenuata
van Dam, N. M., Horn, M., Mareš, M., & Baldwin, I. T. (2001) · Journal of Chemical Ecology · doi:10.1023/a:1010341022761 · Cited by 267 · see citing works
Induced Plant Defense Responses against Chewing Insects. Ethylene Signaling Reduces Resistance of Arabidopsis against Egyptian Cotton Worm But Not Diamondback Moth
Stotz, H. U., Pittendrigh, B. R., Kroymann, J., Weniger, K., Fritsche, J., Bauke, A., & Mitchell‐Olds, T. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.124.3.1007 · Cited by 265 · see citing works
Jasmonate-Based Wound Signal Transduction Requires Activation of WIPK, a Tobacco Mitogen-Activated Protein Kinase
Seo, S., Sano, H., & Ohashi, Y. (1999) · The Plant Cell · doi:10.1105/tpc.11.2.289 · Cited by 264 · see citing works
A Gene Encoding a Chloroplast-Targeted Lipoxygenase in Tomato Leaves Is Transiently Induced by Wounding, Systemin, and Methyl Jasmonate
Heitz, T., Bergey, D. R., & Ryan, C. A. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.3.1085 · Cited by 262 · see citing works
Characterization of the Oligogalacturonide-Induced Oxidative Burst in Cultured Soybean (Glycine max) Cells
Legendre, L., Rueter, S. M., Heinstein, P. F., & Low, P. S. (1993) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.1.233 · Cited by 262 · see citing works
Are insects resistant to plant proteinase inhibitors?
Broadway, R. M. (1995) · Journal of Insect Physiology · doi:10.1016/0022-1910(94)00101-l · Cited by 255 · see citing works
Herbivore‐induced emissions of maize volatiles repel the corn leaf aphid, Rhopalosiphum maidis
Bernasconi, M. L., Turlings, T. C. J., Ambrosetti, L., Bassetti, P., & Dorn, S. (1998) · Entomologia Experimentalis et Applicata · doi:10.1046/j.1570-7458.1998.00315.x · Cited by 252 · see citing works
Cytochrome P450-Dependent Metabolism of Oxylipins in Tomato. Cloning and Expression of Allene Oxide Synthase and Fatty Acid Hydroperoxide Lyase
Howe, G. A., Lee, G. I., Itoh, A., Li, L., & DeRocher, A. E. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.123.2.711 · Cited by 246 · see citing works
The oxidative burst protects plants against pathogen attack: Mechanism and role as an emergency signal for plant bio-defence — a review
Noriyuki Doke, A., Miura, Y., Sanchez, L. M., Park, H. J., Noritake, T., Yoshioka, H., & Kawakita, K. (1996) · Gene · doi:10.1016/s0378-1119(96)00423-4 · Cited by 243 · see citing works
An Ecologically Motivated Analysis of Plant-Herbivore Interactions in Native Tobacco
Baldwin, I. T. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.010762 · Cited by 238 · see citing works
Ecophysiological comparison of direct and indirect defenses in Nicotiana attenuata
Halitschke, R., Keßler, A., Kahl, J., Lorenz, A., & Baldwin, I. T. (2000) · Oecologia · doi:10.1007/s004420000389 · Cited by 233 · see citing works
Molecular Cloning of Allene Oxide Cyclase
Ziegler, J., Stenzel, I., Hause, B., Maucher, H. P., Hámberg, M., Grimm, R., Ganal, M. W., & Wasternack, C. H. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002133200 · Cited by 232 · see citing works
Herbivore‐induced volatiles induce the emission of ethylene in neighboring lima bean plants
Arimura, G., Ozawa, R., Nishioka, T., Boland, W., Koch, T., Kühnemann, F., & Takabayashi, J. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01198.x · Cited by 229 · see citing works
SYSTEMIN: A Polypeptide Signal for Plant Defensive Genes
Ryan, C. A., & Pearce, G. (1998) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.14.1.1 · Cited by 228 · see citing works
Polypeptide Hormones
Ryan, C. A., Pearce, G., Scheer, J., & Moura, D. S. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.1.65 · Cited by 228 · see citing works
Expression of multiple insecticidal genes confers broad resistance against a range of different rice pests
Maqbool, S. B., Riazuddin, S. A., Loc, N. T., Gatehouse, A. M. R., Gatehouse, J. A., & Christou, P. (2001) · Molecular Breeding · doi:10.1023/a:1009644712157 · Cited by 227 · see citing works
Self-citation
Overexpression of the prosystemin gene in transgenic tomato plants generates a systemic signal that constitutively induces proteinase inhibitor synthesis.
McGurl, B., Orozco-Cárdenas, M. L., Pearce, G., & Ryan, C. A. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.21.9799 · Cited by 227 · see citing works
Prooxidant effects of phenolic acids on the generalist herbivore Helicoverpa zea (Lepidoptera: Noctuidae): Potential mode of action for phenolic compounds in plant anti-herbivore chemistry
Summers, C. B., & Felton, G. W. (1994) · Insect Biochemistry and Molecular Biology · doi:10.1016/0965-1748(94)90023-x · Cited by 225 · see citing works
Specificity of induced resistance in the tomato, Lycopersicon esculentum
Stout, M. J., Workman, K. V., Bostock, R. M., & Duffey, S. S. (1997) · Oecologia · doi:10.1007/s004420050355 · Cited by 223 · see citing works
Strategies Involved in the Location of Hosts by the ParasitoidAphidius erviHaliday (Hymenoptera: Braconidae: Aphidiinae)
Powell, W., Pennacchio, F., Poppy, G. M., & Tremblay, E. (1998) · Biological Control · doi:10.1006/bcon.1997.0584 · Cited by 222 · see citing works
Signal interactions in pathogen and insect attack: expression of lipoxygenase, proteinase inhibitor II, and pathogenesis-related protein P4 in the tomato,Lycopersicon esculentum
Fidantsef, A. L., Stout, M. J., Thaler, J. S., Duffey, S. S., & Bostock, R. M. (1999) · Physiological and Molecular Plant Pathology · doi:10.1006/pmpp.1998.0192 · Cited by 219 · see citing works
A survey of wound- and methyl jasmonate-induced leaf polyphenol oxidase in crop plants
Constabel, C. P., & Ryan, C. A. (1998) · Phytochemistry · doi:10.1016/s0031-9422(97)00539-6 · Cited by 219 · see citing works
Monoterpene Synthases from Grand Fir (Abies grandis)
Bohlmann, J., Steele, C. L., & Croteau, R. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.35.21784 · Cited by 219 · see citing works
Expression of an antisense prosystemin gene in tomato plants reduces resistance toward Manduca sexta larvae.
Orozco-Cárdenas, M. L., McGurl, B., & Ryan, C. A. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.17.8273 · Cited by 218 · see citing works
Tissue‐specific oxylipin signature of tomato flowers: allene oxide cyclase is highly expressed in distinct flower organs and vascular bundles
Hause, B., Stenzel, I., Miersch, O., Maucher, H. P., Kramell, R., Ziegler, J., & Wasternack, C. H. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00861.x · Cited by 217 · see citing works
Induction of Plant Synomones by Oviposition of a Phytophagous Insect
Meiners, T., & Hilker, M. (2000) · Journal of Chemical Ecology · doi:10.1023/a:1005453830961 · Cited by 216 · see citing works
Parasitoid‐plant mutualism: parasitoid attack of herbivore increases plant reproduction
van Loon, J. J. A., de Boer, J. G., & Dicke, M. (2000) · Entomologia Experimentalis et Applicata · doi:10.1046/j.1570-7458.2000.00733.x · Cited by 216 · see citing works
The degrees of polymerization and N-acetylation of chitosan determine its ability to elicit callose formation in suspension cells and protoplasts of Catharanthus roseus
Kauss, H., Jeblick, W., & Domard, A. (1989) · Planta · doi:10.1007/bf00391866 · Cited by 212 · see citing works
Evidence for Chewing Insect-Specific Molecular Events Distinct from a General Wound Response in Leaves
Korth, K. L., & Dixon, R. A. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.115.4.1299 · Cited by 211 · see citing works
Relative importance of semiochemicals from first and second trophic levels in host foraging behavior ofAphidius ervi
Du, Y., Poppy, G. M., & Powell, W. (1996) · Journal of Chemical Ecology · doi:10.1007/bf02272400 · Cited by 210 · see citing works
Expression of Allene Oxide Synthase Determines Defense Gene Activation in Tomato
Sivasankar, S., Bay, S., & Rothstein, S. J. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.122.4.1335 · Cited by 205 · see citing works
Merging molecular and ecological approaches in plant–insect interactions
Baldwin, I. T., Halitschke, R., Keßler, A., & Schittko, U. (2001) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00184-9 · Cited by 202 · see citing works
Colorado potato beetles (leptinotarsa decemlineata) adapt to proteinase inhibitors induced in potato leaves by methyl jasmonate
Bolter, C. J., & Jongsma, M. A. (1995) · Journal of Insect Physiology · doi:10.1016/0022-1910(95)00073-4 · Cited by 202 · see citing works
OPTIMAL DEFENSE THEORY PREDICTS THE ONTOGENY OF AN INDUCED NICOTINE DEFENSE
Ohnmeiss, T. E., & Baldwin, I. T. (2000) · Ecology · doi:10.1890/0012-9658(2000)081[1765:odtpto]2.0.co;2 · Cited by 201 · see citing works
Systemic wound induction of potato (Solanum tuberosum) polyphenol oxidase
Thipyapong, P., Hunt, M. D., & Steffens, J. C. (1995) · Phytochemistry · doi:10.1016/0031-9422(95)00359-f · Cited by 196 · see citing works
Terpenoid-based defenses in conifers: cDNA cloning, characterization, and functional expression of wound-inducible ( E )-α-bisabolene synthase from grand fir ( Abies grandis )
Bohlmann, J., Crock, J. E., Jetter, R., & Croteau, R. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.12.6756 · Cited by 192 · see citing works
EXOGENOUS METHYL JASMONATE INDUCES VOLATILE EMISSIONS IN COTTON PLANTS
Rodriguez‐Saona, C., Crafts‐Brandner, S. J., Paré, P. W., & Henneberry, T. J. (2001) · Journal of Chemical Ecology · doi:10.1023/a:1010393700918 · Cited by 188 · see citing works
Transport of [2- 14 C]jasmonic acid from leaves to roots mimics wound-induced changes in endogenous jasmonic acid pools in Nicotiana sylvestris
Baldwin, I. T., & Zhang, Z. (1997) · Planta · doi:10.1007/s004250050211 · Cited by 185 · see citing works
Patterns of induced and constitutive monoterpene production in conifer needles in relation to insect herbivory
Litvak, M. E., & Monson, R. K. (1998) · Oecologia · doi:10.1007/s004420050477 · Cited by 182 · see citing works
Isolation and characterization of the proteinase inhibitor-inducing factor from tomato leaves. Identity and activity of poly- and oligogalacturonide fragments.
Bishop, P. D., Pearce, G., Bryant, J., & Ryan, C. A. (1984) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)90673-3 · Cited by 181 · see citing works
Insect Glutathione S-Transferases
Yu, S. J. (1996) · Cited by 180 · see citing works
Long-Distance Phloem Transport of Glucosinolates in Arabidopsis
Chen, S., Petersen, B. L., Olsen, C. E., Schulz, A., & Halkier, B. A. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.127.1.194 · Cited by 176 · see citing works
Enzymes involved in jasmonic acid biosynthesis
Mueller, M. J. (1997) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1997.tb03072.x · Cited by 175 · see citing works
Activation of Salicylic Acid–Induced Protein Kinase, a Mitogen-Activated Protein Kinase, Induces Multiple Defense Responses in Tobacco
Zhang, S., & Liu, Y. (2001) · The Plant Cell · doi:10.1105/tpc.010044 · Cited by 172 · see citing works
Antisense-mediated depletion of a potato lipoxygenase reduces wound induction of proteinase inhibitors and increases weight gain of insect pests
Royo, J., León, J., Vancanneyt, G., Albar, J. P., Rosahl, S., Ortego, F., Castañera, P., & Sánchez‐Serrano, J. J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.3.1146 · Cited by 167 · see citing works
Successive Use of Non-Host Plant Proteinase Inhibitors Required for Effective Inhibition of Helicoverpa armigera Gut Proteinases and Larval Growth
Harsulkar, A., Giri, A. P., Patankar, A. G., Gupta, V. S., Sainani, M. N., Ranjekar, P. K., & DESHPANDE, V. V. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.121.2.497 · Cited by 166 · see citing works
A wound- and systemin-inducible polygalacturonase in tomato leaves
Bergey, D. R., Orozco-Cárdenas, M. L., de Moura, D. S., & Ryan, C. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.4.1756 · Cited by 165 · see citing works
Soluble phospholipase A2 activity is induced before oxylipin accumulation in tobacco mosaic virus‐infected tobacco leaves and is contributed by patatin‐like enzymes
Dhondt‐Cordelier, S., Geoffroy, P., Stelmach, B. A., Legrand, M., & Heitz, T. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00802.x · Cited by 162 · see citing works
Concerted biosynthesis of an insect elicitor of plant volatiles
Paré, P. W., Alborn, H. T., & Tumlinson, J. H. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.23.13971 · Cited by 161 · see citing works
Plant-insect interactions
Stotz, H. U., Kroymann, J., & Mitchell‐Olds, T. (1999) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(99)80048-x · Cited by 158 · see citing works
Volatiles from damaged plants as major cues in long‐range host‐searching by the specialist parasitoid Cotesia rubecula
Geervliet, J. B. F., Vet, L. E. M., & Dicke, M. (1994) · Entomologia Experimentalis et Applicata · doi:10.1111/j.1570-7458.1994.tb01866.x · Cited by 154 · see citing works
Molecular Cloning and Characterization of 12-Oxophytodienoate Reductase, an Enzyme of the Octadecanoid Signaling Pathway fromArabidopsis thaliana
Schaller, F., & Weiler, E. W. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.44.28066 · Cited by 153 · see citing works
Genetics Of Resistance To Insects In Crop Plants
Khush, G. S., & Brar, D. S. (1991) · Advances in agronomy · doi:10.1016/s0065-2113(08)60042-5 · Cited by 151 · see citing works
Site fidelity in habitats with contrasting levels of nest predation and brood parasitism
Schmidt, K. A. (2001) · Evolutionary ecology research · Cited by 149 · see citing works
Systemin induces rapid ion fluxes and ethylene biosynthesis in Lycopersicon peruvianum cells
Felix, G., & Boller, T. (1995) · The Plant Journal · doi:10.1046/j.1365-313x.1995.7030381.x · Cited by 146 · see citing works
Reversible protein phosphorylation regulates jasmonic acid‐dependent and ‐independent wound signal transduction pathways in Arabidopsis thaliana
Rojo, E., Titarenko, E., León, J., Berger, S., Vancanneyt, G., & Sánchez‐Serrano, J. J. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00020.x · Cited by 146 · see citing works
Gut Bacteria May Be Involved in Interactions between Plants, Herbivores and Their Predators: Microbial Biosynthesis of N-Acylglutamine Surfactants as Elicitors of Plant Volatiles
Spiteller, D., Dettner, K., & Boland, W. (2000) · Biological Chemistry · doi:10.1515/bc.2000.096 · Cited by 145 · see citing works
A 160-kD Systemin Receptor on the Surface of Lycopersicon peruvianum Suspension-Cultured Cells
Scheer, J. M., & Ryan, C. A. (1999) · The Plant Cell · doi:10.1105/tpc.11.8.1525 · Cited by 144 · see citing works
Differential induction of tomato foliar proteins by arthropod herbivores
Stout, M. J., Workman, J., & Duffey, S. S. (1994) · Journal of Chemical Ecology · doi:10.1007/bf02036193 · Cited by 141 · see citing works
Gene Responses in Bean Leaves Induced by Herbivory and by Herbivore-Induced Volatiles
Arimura, G., Tashiro, K., Kuhara, S., Nishioka, T., Ozawa, R., & Takabayashi, J. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.3672 · Cited by 140 · see citing works
Demonstration and characterization of ( E )-nerolidol synthase from maize: a herbivore-inducible terpene synthase participating in (3 E )-4,8-dimethyl-1,3,7-nonatriene biosynthesis
Degenhardt, J., & Gershenzon, J. (2000) · Planta · doi:10.1007/s004250050684 · Cited by 138 · see citing works
Signal Interactions in Induced Resistance to Pathogens and Insect Herbivores
Bostock, R. M., Karban, R., Thaler, J. S., Weyman, P. D., & Gilchrist, D. G. (2001) · European Journal of Plant Pathology · doi:10.1023/a:1008703904253 · Cited by 137 · see citing works
Induced plant defenses breached? Phytochemical induction protects an herbivore from disease
Hunter, M. D., & Schultz, J. C. (1993) · Oecologia · doi:10.1007/bf00341317 · Cited by 134 · see citing works
Structure and regulation of the Arabidopsis thaliana allene oxide synthase gene
Kubigsteltig, I. I., Laudert, D., & Weiler, E. W. (1999) · Planta · doi:10.1007/s004250050583 · Cited by 134 · see citing works
Compound effects of induced plant responses on insect herbivores and parasitoids: implications for tritrophic interactions
Havill, N. P., & Raffa, K. F. (2000) · Ecological Entomology · doi:10.1046/j.1365-2311.2000.00247.x · Cited by 133 · see citing works
Applications of Tagging and Mapping Insect Resistance Loci in Plants
Yencho, G. C., Cohen, M. B., & Byrne, P. F. (2000) · Annual Review of Entomology · doi:10.1146/annurev.ento.45.1.393 · Cited by 132 · see citing works
Activation of Salicylic Acid-Induced Protein Kinase, a Mitogen-Activated Protein Kinase, Induces Multiple Defense Responses in Tobacco
Zhang, S. (2001) · The Plant Cell · doi:10.1105/tpc.13.8.1877 · Cited by 132 · see citing works
Spider Mite-Induced (3S)-(E)-Nerolidol Synthase Activity in Cucumber and Lima Bean. The First Dedicated Step in Acyclic C11-Homoterpene Biosynthesis
Bouwmeester, H. J., Verstappen, F. W. A., Posthumus, M. A., & Dicke, M. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.121.1.173 · Cited by 122 · see citing works
A Calcium-Dependent Protein Kinase Is Systemically Induced upon Wounding in Tomato Plants
Chico, J. M. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.128.1.256 · Cited by 121 · see citing works
The Plant Wound Hormone Systemin Binds with the N-Terminal Part to Its Receptor but Needs the C-Terminal Part to Activate It
Meindl, T., Boller, T., & Felix, G. (1998) · The Plant Cell · doi:10.1105/tpc.10.9.1561 · Cited by 121 · see citing works
Wound Signaling in Tomato Plants1
Birkenmeier, G. F., & Ryan, C. A. (1998) · PLANT PHYSIOLOGY · doi:10.1104/pp.117.2.687 · Cited by 117 · see citing works
Jasmonic acid-dependent and -independent wound signal transduction pathways are differentially regulated by Ca2+/calmodulin in Arabidopsis thaliana
León, J., Rojo, E., Titarenko, E., & Sánchez‐Serrano, J. J. (1998) · Molecular and General Genetics MGG · doi:10.1007/s004380050749 · Cited by 116 · see citing works
Cell signalling by oligosaccharides
John, M., Röhrig, H., Schmidt, J., Walden, R. M., & Schell, J. (1997) · Trends in Plant Science · doi:10.1016/s1360-1385(97)01005-4 · Cited by 115 · see citing works
Molecular cloning and expression of CYP6B8: a xanthotoxin-inducible cytochrome P450 cDNA from Helicoverpa zea1The sequence data are deposited in GenBank under the accession number AF102263.1
Li, X., Berenbaum, M. R., & Schuler, M. A. (2000) · Insect Biochemistry and Molecular Biology · doi:10.1016/s0965-1748(99)00102-2 · Cited by 113 · see citing works
Effects of some leaf-emitted volatile compounds on aphid population increase
Hildebrand, D. F., Brown, G. C., Jackson, D. M., & Hamilton–Kemp, T. R. (1993) · Journal of Chemical Ecology · doi:10.1007/bf00983793 · Cited by 112 · see citing works
A Calcium-Dependent Protein Kinase Is Systemically Induced upon Wounding in Tomato Plants
Chico, J. M., Raı́ces, M., Téllez-Iñón, M. T., et al. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.010649 · Cited by 112 · see citing works
A maize sesquiterpene cyclase gene induced by insect herbivory and volicitin: Characterization of wild-type and mutant alleles
Shen, B., Zheng, Z., & Dooner, H. K. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.240284097 · Cited by 110 · see citing works
Variability in the Response ofMacrosiphum euphorbiaeandMyzus persicae(Hemiptera: Aphididae) to the Tomato Resistance GeneMi
Goggin, F. L., Williamson, V. M., & Ullman, D. E. (2001) · Environmental Entomology · doi:10.1603/0046-225x-30.1.101 · Cited by 110 · see citing works
Wound‐induced increases in the glucosinolate content of oilseed rape and their effect on subsequent herbivory by a crucifer specialist
Bartlet, E., Kiddle, G. A., Williams, I. H., & Wallsgrove, R. M. (1999) · Entomologia Experimentalis et Applicata · doi:10.1046/j.1570-7458.1999.00479.x · Cited by 107 · see citing works
Antioxidant defenses in caterpillars: role of the ascorbate-recycling system in the midgut lumen
Barbehenn, R. V., Bumgarner, S. L., Roosen, E. F., & Martin, M. M. (2001) · Journal of Insect Physiology · doi:10.1016/s0022-1910(00)00125-6 · Cited by 107 · see citing works
Abscisic acid and jasmonic acid activate wound‐inducible genes in potato through separate, organ‐specific signal transduction pathways
Dammann, C., Rojo, E., & Sánchez‐Serrano, J. J. (1997) · The Plant Journal · doi:10.1046/j.1365-313x.1997.11040773.x · Cited by 107 · see citing works
The immobility of pectic substances in injured tomato leaves and its bearing on the identity of the wound hormone
Baydoun, E., & Fry, S. C. (1985) · Planta · doi:10.1007/bf00395050 · Cited by 107 · see citing works
TACHINID PARASITOIDS AFFECT HOST PLANT CHOICE BY CATERPILLARS TO INCREASE CATERPILLAR SURVIVAL
Karban, R., & English‐Loeb, G. M. (1997) · Ecology · doi:10.1890/0012-9658(1997)078[0603:tpahpc]2.0.co;2 · Cited by 106 · see citing works
Methyl jasmonate‐induced nicotine production in Nicotiana attenuata: inducing defenses in the field without wounding
Baldwin, I. T. (1996) · Entomologia Experimentalis et Applicata · doi:10.1111/j.1570-7458.1996.tb00921.x · Cited by 105 · see citing works
Plant Secondary Compounds and Grasshoppers: Beyond Plant Defenses
Bernays, E. A., & Chapman, R. F. (2000) · Journal of Chemical Ecology · doi:10.1023/a:1005578804865 · Cited by 103 · see citing works
Eating the evidence? Manduca sexta larvae can not disrupt specific jasmonate induction in Nicotiana attenuata by rapid consumption
Schittko, U., Preston, C. A., & Baldwin, I. T. (2000) · Planta · doi:10.1007/pl00008143 · Cited by 103 · see citing works
Evolutionary aspects of defense by recycled plant compounds in herbivorous insects
Dobler, S. (2001) · Basic and Applied Ecology · doi:10.1078/1439-1791-00032 · Cited by 103 · see citing works
The TASTY Locus on Chromosome 1 of Arabidopsis Affects Feeding of the Insect Herbivore Trichoplusia ni
Jander, G., Cui, J., Nhan, B., Pierce, N. E., & Ausubel, F. M. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.126.2.890 · Cited by 102 · see citing works
A novel tomato gene that rapidly responds to wound‐ and pathogen‐related signals
O'Donnell, P. J. M., Truesdale, M. R., Calvert, C. M., Dorans, A., ROBERTS, M. R., & Bowles, D. J. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00110.x · Cited by 98 · see citing works
Tomato prosystemin promoter confers wound-inducible, vascular bundle-specific expression of the β-glucuronidase gene in transgenic tomato plants
Jacinto, T., McGurl, B., Franceschi, V. R., Delano-Freier, J., & Ryan, C. A. (1997) · Planta · doi:10.1007/s004250050207 · Cited by 97 · see citing works
H2O2 activates a MAP kinase-like enzyme in Arabidopsis thaliana suspension cultures
Desikan, R., Clarke, A., Hancock, J. T., & Neill, S. J. (1999) · Journal of Experimental Botany · doi:10.1093/jxb/50.341.1863 · Cited by 94 · see citing works
R ESISTANCE OF D ROSOPHILA TO T OXINS
Wilson, T. G. (2001) · Annual Review of Entomology · doi:10.1146/annurev.ento.46.1.545 · Cited by 92 · see citing works
Plant Phenolics as Dietary Antioxidants for Herbivorous Insects: A Test with Genetically Modified Tobacco
Johnson, K. S., & Felton, G. W. (2001) · Journal of Chemical Ecology · doi:10.1023/a:1013691802028 · Cited by 90 · see citing works
Molecular biology of jasmonic acid biosynthesis in plants
León, J., & Sánchez‐Serrano, J. J. (1999) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(99)80043-6 · Cited by 90 · see citing works
Costs of Inducible Defense: Protein Limitation, Growth, and Detoxification in Parsnip Webworms
Berenbaum, M. R., & Zangerl, A. R. (1994) · Ecology · doi:10.2307/1940886 · Cited by 87 · see citing works
Characterization of 12-Oxo-Phytodienoic Acid Reductase in Corn
Vick, B. A., & Zimmerman, D. C. (1986) · PLANT PHYSIOLOGY · doi:10.1104/pp.80.1.202 · Cited by 87 · see citing works
Enzymatic decomposition of elicitors of plant volatiles in Heliothis virescens and Helicoverpa zea
Mori, N., Alborn, H. T., Teal, P. E. A., & Tumlinson, J. H. (2001) · Journal of Insect Physiology · doi:10.1016/s0022-1910(00)00171-2 · Cited by 83 · see citing works
Characterization and localization of a wound-inducible type I serine-carboxypeptidase from leaves of tomato plants ( Lycopersicon esculentum Mill.)
de Moura, D. S., Bergey, D. R., & Ryan, C. A. (2001) · Planta · doi:10.1007/s004250000380 · Cited by 82 · see citing works
The ecology and evolution of host-plant resistance to insects
Simms, E. L., & Fritz, R. S. (1990) · Trends in Ecology & Evolution · doi:10.1016/0169-5347(90)90094-t · Cited by 81 · see citing works
Induction of systemic acquired resistance in cotton by BTH has a negligible effect on phytophagous insects
Inbar, M., Doostdar, H., Gerling, D., & Mayer, R. T. (2001) · Entomologia Experimentalis et Applicata · doi:10.1046/j.1570-7458.2001.00802.x · Cited by 76 · see citing works
Hypersensitivity as a Phenotypic Basis of Plant Induced Resistance against a Galling Insect (Diptera: Cecidomyiidae)
Fernandes, G. W. (1998) · Environmental Entomology · doi:10.1093/ee/27.2.260 · Cited by 75 · see citing works
Localization of hydrogen peroxide during the defence response of Arabidopsis thaliana against the plant-parasitic nematode Heterodera glycines
Waetzig, G. H., Sobczak, M., & Grundler, F. M. W. (1999) · Nematology · doi:10.1163/156854199508702 · Cited by 74 · see citing works
Abscisic acid-deficient plants do not accumulate proteinase inhibitor II following systemin treatment
Pe�a-Cort�s, H., Prat, S., Atzorn, R., Wasternack, C. H., & Willmitzer, L. (1996) · Planta · doi:10.1007/bf00620062 · Cited by 73 · see citing works
Insect-Induced Synthesis of Phytoecdysteroids in Spinach, Spinacia oleracea
Schmelz, E. A., Grebenok, R. J., Galbraith, D. W., & Bowers, W. S. (1999) · Journal of Chemical Ecology · doi:10.1023/a:1020969413567 · Cited by 72 · see citing works
Methyl jasmonate is blowing in the wind, but can it act as a plant–plant airborne signal?
Preston, C. A., Laue, G., & Baldwin, I. T. (2001) · Biochemical Systematics and Ecology · doi:10.1016/s0305-1978(01)00047-3 · Cited by 72 · see citing works
Putative protein digestion in a sap-sucking homopteran plant pest (rice brown plant hopper; Nilaparvata lugens: Delphacidae)—identification of trypsin-like and cathepsin B-like proteases
Foissac, X., Edwards, M. G., Du, J., Gatehouse, A. M. R., & Gatehouse, J. A. (2002) · Insect Biochemistry and Molecular Biology · doi:10.1016/s0965-1748(02)00033-4 · Cited by 72 · see citing works
Self-citation
Metabolic fate of the allelochemical nicotine in the tobacco hornworm Manduca sexta
Snyder, M. J., Walding, J. K., & Feyereisen, R. (1994) · Insect Biochemistry and Molecular Biology · doi:10.1016/0965-1748(94)90112-0 · Cited by 71 · see citing works
Feeding preferences ofSpodoptera exiguain response to form and concentration of selenium
Vickerman, D. B., & Trumble, J. T. (1999) · Archives of Insect Biochemistry and Physiology · doi:10.1002/(sici)1520-6327(199909)42:1 · Cited by 71 · see citing works
Systemin Potentiates the Oxidative Burst in Cultured Tomato Cells1
Stennis, M. J., Chandra, S. S., Ryan, C. A., & Low, P. S. (1998) · PLANT PHYSIOLOGY · doi:10.1104/pp.117.3.1031 · Cited by 70 · see citing works
Induction of cytochrome P-450 activities by nicotine in the tobacco hornworm,Manduca sexta
Snyder, M. J., Hsu, E. L., & Feyereisen, R. (1993) · Journal of Chemical Ecology · doi:10.1007/bf00980591 · Cited by 69 · see citing works
Responses of the flea beetles Phyllotreta nemorum and P. cruciferae to metabolically engineered Arabidopsis thaliana with an altered glucosinolate profile
Nielsen, J. K., Hansen, M. L., Agerbirk, N., Petersen, B. L., & Halkier, B. A. (2001) · Chemoecology · doi:10.1007/pl00001835 · Cited by 67 · see citing works
Induction by alkaloids and phenobarbital of Family 4 Cytochrome P450s in Drosophila : evidence for involvement in host plant utilization
Danielson, P. B., Foster, J. L. M., McMahill, M. M., Smith, M., & Fogleman, J. C. (1998) · Molecular and General Genetics MGG · doi:10.1007/s004380050788 · Cited by 67 · see citing works
Chemical information transfer between wounded and unwounded plants: backing up the future
de Bruin, J. P. C., & Dicke, M. (2001) · Biochemical Systematics and Ecology · doi:10.1016/s0305-1978(01)00053-9 · Cited by 62 · see citing works
Does Salicylic Acid Act as a Signal in Cotton for Induced Resistance to Helicoverpa zea?
Bi, J. L., Murphy, J. B., & Felton, G. W. (1997) · Journal of Chemical Ecology · doi:10.1023/b:joec.0000006452.81324.b8 · Cited by 59 · see citing works
Depolarization of tomato leaf cells by oligogalacturonide elicitors
Thain, J. F., Gubb, I. R., & Wildon, D. C. (1995) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1995.tb00355.x · Cited by 58 · see citing works
Characterization of the constitutive and wound-inducible monoterpene cyclases of grand fir (Abies grandis)
Gijzen, M., Lewinsohn, E., & Croteau, R. (1991) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(91)90471-t · Cited by 57 · see citing works
The Root Knot Nematode Resistance Gene Mi from Tomato Is a Member of the Leucine Zipper, Nucleotide Binding, Leucine-Rich Repeat Family of Plant Genes
Milligan, S. B., Bodeau, J. P., Yaghoobi, J., Kaloshian, I., Zabel, P., & Williamson, V. M. (1998) · The Plant Cell · doi:10.2307/3870642 · Cited by 57 · see citing works
Overexpression of a cytoplasm-localized allene oxide synthase promotes the wound-induced accumulation of jasmonic acid in transgenic tobacco
Wang, C., Avdiushko, S. A., & Hildebrand, D. F. (1999) · Plant Molecular Biology · doi:10.1023/a:1006253927431 · Cited by 55 · see citing works

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2 of the 222 references couldn’t be matched to a known paper.

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Plant Immunity to Insect Herbivores
Howe, G. A., & Jander, G. (2007) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092825 · Cited by 2,445 · see citing works
Plant Defense Against Herbivores: Chemical Aspects
Mithöfer, A., & Boland, W. (2012) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042110-103854 · Cited by 1,621 · see citing works
Silencing a cotton bollworm P450 monooxygenase gene by plant-mediated RNAi impairs larval tolerance of gossypol
Mao, Y.-B., Cai, W.-J., Wang, J.-W., Hong, G.-J., Tao, X.-Y., Wang, L.-J., Huang, Y.-P., & Chen, X.-Y. (2007) · Nature Biotechnology · doi:10.1038/nbt1352 · Cited by 1,358 · see citing works
Bacterial Volatiles Induce Systemic Resistance in Arabidopsis
Ryu, C.-M., Farag, M. A., Hu, C.-H., Reddy, M. S., Kloepper, J. W., & Paré, P. W. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.026583 · Cited by 1,308 · see citing works
Plant Defense against Insect Herbivores
Fürstenberg-Hägg, J., Zagrobelny, M., & Bak, S. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140510242 · Cited by 933 · see citing works
New Insights into Plant Responses to the Attack from Insect Herbivores
Wu, J., & Baldwin, I. T. (2010) · Annual Review of Genetics · doi:10.1146/annurev-genet-102209-163500 · Cited by 929 · see citing works
Plant-based insect repellents: a review of their efficacy, development and testing
Maia, M. F., & Moore, S. (2011) · Malaria Journal · doi:10.1186/1475-2875-10-s1-s11 · Cited by 769 · see citing works
Indirect defence via tritrophic interactions
Heil, M. (2007) · New Phytologist · doi:10.1111/j.1469-8137.2007.02330.x · Cited by 756 · see citing works
Arthropod Pest Management in Organic Crops
Zehnder, G., Gurr, G. M., Kühne, S., Wade, M. R., Wratten, S. D., & Wyss, E. (2006) · Annual Review of Entomology · doi:10.1146/annurev.ento.52.110405.091337 · Cited by 620 · see citing works
RNAi-mediated crop protection against insects
Price, D. R. G., & Gatehouse, J. A. (2008) · Trends in biotechnology · doi:10.1016/j.tibtech.2008.04.004 · Cited by 585 · see citing works
Self-citation
Ecological and Evolutionary Consequences of Multispecies Plant-Animal Interactions
Strauss, S. Y., & Irwin, R. E. (2004) · Annual Review of Ecology Evolution and Systematics · doi:10.1146/annurev.ecolsys.35.112202.130215 · Cited by 579 · see citing works
Systemic signaling in the wound response
Schilmiller, A. L., & Howe, G. A. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.05.008 · Cited by 544 · see citing works
PLANT-MEDIATED INTERACTIONS BETWEEN PATHOGENIC MICROORGANISMS AND HERBIVOROUS ARTHROPODS
Stout, M. J., Thaler, J. S., & Thomma, B. P. H. J. (2006) · Annual Review of Entomology · doi:10.1146/annurev.ento.51.110104.151117 · Cited by 463 · see citing works
Indirect plant defense against insect herbivores: a review
Aljbory, Z., & Chen, M. (2016) · Insect Science · doi:10.1111/1744-7917.12436 · Cited by 444 · see citing works
Effects of Feeding Spodoptera littoralis on Lima Bean Leaves. II. Continuous Mechanical Wounding Resembling Insect Feeding Is Sufficient to Elicit Herbivory-Related Volatile Emission
Mithöfer, A., Wanner, G., & Boland, W. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.054460 · Cited by 433 · see citing works
Biotic and heavy metal stress response in plants: evidence for common signals
Mithöfer, A., Schulze, B., & Boland, W. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.04.011 · Cited by 423 · see citing works
Silicon‐augmented resistance of plants to herbivorous insects: a review
Reynolds, O. L., Keeping, M. G., & Meyer, J. H. (2009) · Annals of Applied Biology · doi:10.1111/j.1744-7348.2009.00348.x · Cited by 403 · see citing works
Differential Timing of Spider Mite-Induced Direct and Indirect Defenses in Tomato Plants
Kant, M. R., Ament, K., Sabelis, M. W., Haring, M. A., & Schuurink, R. C. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.038315 · Cited by 395 · see citing works
The molecular bases of plant resistance and defense responses to aphid feeding: current status
Smith, C. M., & Boyko, E. V. (2006) · Entomologia Experimentalis et Applicata · doi:10.1111/j.1570-7458.2006.00503.x · Cited by 395 · see citing works
Defensive symbiosis in the real world – advancing ecological studies of heritable, protective bacteria in aphids and beyond
Oliver, K. M., Smith, A., & Russell, J. A. (2013) · Functional Ecology · doi:10.1111/1365-2435.12133 · Cited by 371 · see citing works
Jasmonate-inducible plant enzymes degrade essential amino acids in the herbivore midgut
Chen, H., Wilkerson, C. G., Kuchar, J. A., Phinney, B. S., & Howe, G. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509026102 · Cited by 360 · see citing works
Jasmonates as Signals in the Wound Response
Howe, G. A. (2004) · Journal of Plant Growth Regulation · doi:10.1007/bf02637263 · Cited by 347 · see citing works
Sites of synthesis, biochemistry and functional role of plant volatiles
Maffei, M. E. (2010) · South African Journal of Botany · doi:10.1016/j.sajb.2010.03.003 · Cited by 343 · see citing works
Molecular mechanisms of insect adaptation to plant secondary compounds
Heidel‐Fischer, H. M., & Vogel, H. (2015) · Current Opinion in Insect Science · doi:10.1016/j.cois.2015.02.004 · Cited by 341 · see citing works
Induced resistance to pests and pathogens in trees
Eyles, A., Bonello, P., Ganley, R. J., & Mohammed, C. L. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2009.03127.x · Cited by 319 · see citing works
Recognition of Herbivory-Associated Molecular Patterns
Mithöfer, A., & Boland, W. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.113118 · Cited by 319 · see citing works
Shared signals –‘alarm calls’ from plants increase apparency to herbivores and their enemies in nature
Halitschke, R., Stenberg, J. A., Kessler, D., Keßler, A., & Baldwin, I. T. (2007) · Ecology Letters · doi:10.1111/j.1461-0248.2007.01123.x · Cited by 312 · see citing works
Towards global understanding of plant defence against aphids – timing and dynamics of early Arabidopsis defence responses to cabbage aphid (Brevicoryne brassicae) attack
Kuśnierczyk, A., Winge, P., Jørstad, T. S., Troczyńska, J., Rossiter, J. T., & Bones, A. M. (2008) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2008.01823.x · Cited by 305 · see citing works
Structural and functional divergence of insect CYP6B proteins: From specialist to generalist cytochrome P450
Li, X., Baudry, J. Y., Berenbaum, M. R., & Schuler, M. A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308691101 · Cited by 300 · see citing works
Recent developments and future prospects in insect pest control in transgenic crops
Christou, P., Capell, T., Kohli, A., Gatehouse, J. A., & Gatehouse, A. M. R. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2006.04.001 · Cited by 289 · see citing works
Self-citation
The wound response in tomato – Role of jasmonic acid
Wasternack, C. H., Stenzel, I., Hause, B., Hause, G., Kutter, C., Maucher, H. P., Neumerkel, J., Feußner, I., & Miersch, O. (2005) · Journal of Plant Physiology · doi:10.1016/j.jplph.2005.10.014 · Cited by 284 · see citing works
The Nutritional Physiology of Aphids
Douglas, A. E. (2003) · Advances in insect physiology · doi:10.1016/s0065-2806(03)31002-1 · Cited by 275 · see citing works
Herbivory‐induced signalling in plants: perception and action
Wu, J., & Baldwin, I. T. (2009) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2009.01943.x · Cited by 278 · see citing works
Exploiting Allee effects for managing biological invasions
Tobin, P. C., Berec, L., & Liebhold, A. M. (2011) · Ecology Letters · doi:10.1111/j.1461-0248.2011.01614.x · Cited by 269 · see citing works
Cotton plants expressing CYP6AE14 double-stranded RNA show enhanced resistance to bollworms
Mao, Y., Tao, X., Xue, X., Wang, L.-J., & Chen, X. (2010) · Transgenic Research · doi:10.1007/s11248-010-9450-1 · Cited by 263 · see citing works
The rhizobacterial elicitor acetoin induces systemic resistance in Arabidopsis thaliana
Rudrappa, T., Biedrzycki, M. L., Kunjeti, S. G., Donofrio, N. M., Czymmek, K. J., Paré Paul, W., & Bais, H. P. (2010) · Communicative & Integrative Biology · doi:10.4161/cib.3.2.10584 · Cited by 259 · see citing works
Jasmonate response decay and defense metabolite accumulation contributes to age-regulated dynamics of plant insect resistance
Mao, Y., Liu, Y.-Q., Chen, D.-Y., Chen, F., Fang, X., Hong, G., Wang, L.-J., Wang, J., & Chen, X. (2017) · Nature Communications · doi:10.1038/ncomms13925 · Cited by 256 · see citing works
The Tomato Suppressor of prosystemin-mediated responses2 Gene Encodes a Fatty Acid Desaturase Required for the Biosynthesis of Jasmonic Acid and the Production of a Systemic Wound Signal for Defense Gene Expression
Li, C., Liu, G., Xu, C., Lee, G. I., Bauer, P., Ling, H., Ganal, M. W., & Howe, G. A. (2003) · The Plant Cell · doi:10.1105/tpc.012237 · Cited by 255 · see citing works
R2R3-NaMYB8 Regulates the Accumulation of Phenylpropanoid-Polyamine Conjugates, Which Are Essential for Local and Systemic Defense against Insect Herbivores in Nicotiana attenuata
Kaur, H., Heinzel, N., Schöttner, M., Baldwin, I. T., & Gális, I. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.151738 · Cited by 254 · see citing works
Proton-Transfer-Reaction Mass Spectrometry as a New Tool for Real Time Analysis of Root-Secreted Volatile Organic Compounds in Arabidopsis
Steeghs, M. M. L., Bais, H. P., de Gouw, J. A., Goldan, P. D., Kuster, W. C., Northway, M. J., Fall, R., & Vivanco, J. M. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.038703 · Cited by 251 · see citing works
Plant–insect interactions: molecular approaches to insect resistance
Ferry, N., Edwards, M. G., Gatehouse, J. A., & Gatehouse, A. M. R. (2004) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2004.01.008 · Cited by 248 · see citing works
Self-citation
Jasmonate‐ and salicylate‐mediated plant defense responses to insect herbivores, pathogens and parasitic plants
Smith, J. L., Moraes, C. Μ. D., & Mescher, M. C. (2009) · Pest Management Science · doi:10.1002/ps.1714 · Cited by 243 · see citing works
Trends in insect repellent formulations: A review
Tavares, M., da Silva, M. R. M., de Siqueira, L. B. D. O., Schuenck-Rodrigues, R. A., Bodjolle-d'Almeida, L., dos Santos, E. P., & Ricci‐Júnior, E. (2018) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2018.01.046 · Cited by 228 · see citing works
Review Jasmonates are phytohormones with multiple functions, including plant defense and reproduction
Avanci, N. C., Luche, D. D., Goldman, G. H., & Goldman, M. H. S. (2010) · Genetics and Molecular Research · doi:10.4238/vol9-1gmr754 · Cited by 217 · see citing works
Direct and indirect defences induced by piercing‐sucking and chewing herbivores in Medicago truncatula
Leitner, M., Boland, W., & Mithöfer, A. (2005) · New Phytologist · doi:10.1111/j.1469-8137.2005.01426.x · Cited by 217 · see citing works
Systemin/Jasmonate-Mediated Systemic Defense Signaling in Tomato
Sun, J., Jiang, H., & Li, C. (2011) · Molecular Plant · doi:10.1093/mp/ssr008 · Cited by 203 · see citing works
Convergent Responses to Stress. Solar Ultraviolet-B Radiation and Manduca sexta Herbivory Elicit Overlapping Transcriptional Responses in Field-Grown Plants of Nicotiana longiflora
Izaguirre, M. M., Scopel, A. L., Baldwin, I. T., & Ballaré, C. L. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.024323 · Cited by 200 · see citing works
Priming of indirect defences
Heil, M., & Kost, C. (2006) · Ecology Letters · doi:10.1111/j.1461-0248.2006.00932.x · Cited by 192 · see citing works
Effects of Feeding Spodoptera littoralis on Lima Bean Leaves. I. Membrane Potentials, Intracellular Calcium Variations, Oral Secretions, and Regurgitate Components
Maffei, M. E., Bossi, S., Spiteller, D., Mithöfer, A., & Boland, W. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.034165 · Cited by 193 · see citing works
Molecular analysis of poplar defense against herbivory: comparison of wound‐ and insect elicitor‐induced gene expression
Major, I. T., & Constabel, C. P. (2006) · New Phytologist · doi:10.1111/j.1469-8137.2006.01877.x · Cited by 189 · see citing works
The interaction of plant genotype and herbivory decelerate leaf litter decomposition and alter nutrient dynamics
Schweitzer, J. A., Bailey, J. K., Hart, S. C., Wimp, G. M., Chapman, S., & Whitham, T. G. (2005) · Oikos · doi:10.1111/j.0030-1299.2005.13650.x · Cited by 184 · see citing works
Innate immune memory in plants
Reimer-Michalski, E.-M., & Conrath, U. (2016) · Seminars in Immunology · doi:10.1016/j.smim.2016.05.006 · Cited by 178 · see citing works
The Interplay Between Ozone and Urban Vegetation—BVOC Emissions, Ozone Deposition, and Tree Ecophysiology
Fitzky, A. C., Sandén, H., Karl, T., Fares, S., Calfapietra, C., Grote, R., Saunier, A., & Rewald, B. (2019) · Frontiers in Forests and Global Change · doi:10.3389/ffgc.2019.00050 · Cited by 181 · see citing works
Silicon enhances natural enemy attraction and biological control through induced plant defences
Kvedaras, O. L., An, M., Choi, Y. S., & Gurr, G. M. (2009) · Bulletin of Entomological Research · doi:10.1017/s0007485309990265 · Cited by 176 · see citing works
Resource allocation to defence and growth are driven by different responses to generalist and specialist herbivory in an invasive plant
Huang, W., Siemann, E., Wheeler, G. S., Zou, J., Carrillo, J., & Ding, J. (2010) · Journal of Ecology · doi:10.1111/j.1365-2745.2010.01704.x · Cited by 174 · see citing works
Horticultural applications of jasmonates
Rohwer, C. L., & Erwin, J. E. (2008) · The Journal of Horticultural Science and Biotechnology · doi:10.1080/14620316.2008.11512381 · Cited by 175 · see citing works
Plant invaders and their novel natural enemies: who is naïve?
Verhoeven, K. J. F., Biere, A., Harvey, J. A., & van der Putten, W. H. (2008) · Ecology Letters · doi:10.1111/j.1461-0248.2008.01248.x · Cited by 171 · see citing works
Algal Chemical Ecology
Amsler, C. D. (2007) · Springer eBooks · doi:10.1007/978-3-540-74181-7 · Cited by 285 · see citing works
Developmental and stimulus-induced expression patterns of Arabidopsis calmodulin-like genes CML37, CML38 and CML39
Vanderbeld, B., & Snedden, W. A. (2007) · Plant Molecular Biology · doi:10.1007/s11103-007-9189-0 · Cited by 166 · see citing works
Identification of Volatile Synomones, Induced by Nezara viridula Feeding and Oviposition on Bean spp., That Attract the Egg Parasitoid Trissolcus basalis
Colazza, S., McElfresh, J. S., & Millar, J. G. (2004) · Journal of Chemical Ecology · doi:10.1023/b:joec.0000028460.70584.d1 · Cited by 165 · see citing works
The genetic adaptations of fall armyworm Spodoptera frugiperda facilitated its rapid global dispersal and invasion
Xiao, H., Ye, X., Xu, H., Yang, M., Yang, Y., Chen, X., Yang, Y., Liu, T., Yu, Y., Yang, W., et al. (2020) · Molecular Ecology Resources · doi:10.1111/1755-0998.13182 · Cited by 163 · see citing works
Systemic response to aphid infestation by Myzus persicae in the phloem of Apium graveolens
Divol, F., Vilaine, F., Thibivilliers, S., Amselem, J., Palauqui, J., Kusiak, C., & Dinant, S. (2005) · Plant Molecular Biology · doi:10.1007/s11103-005-0338-z · Cited by 162 · see citing works
Transcriptional responses of Arabidopsis thaliana ecotypes with different glucosinolate profiles after attack by polyphagous Myzus persicae and oligophagous Brevicoryne brassicae
Kuśnierczyk, A., Winge, P., Midelfart, H., Armbruster, W. S., Rossiter, J. T., & Bones, A. M. (2007) · Journal of Experimental Botany · doi:10.1093/jxb/erm043 · Cited by 162 · see citing works
Stability of Plant Defense Proteins in the Gut of Insect Herbivores
Chen, H., Gonzales‐Vigil, E., Wilkerson, C. G., & Howe, G. A. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.095588 · Cited by 159 · see citing works
MAPK signaling: A key element in plant defense response to insects
Hettenhausen, C., Schuman, M. C., & Wu, J. (2014) · Insect Science · doi:10.1111/1744-7917.12128 · Cited by 157 · see citing works
Transcriptome analysis reveals a comprehensive insect resistance response mechanism in cotton to infestation by the phloem feeding insect Bemisia tabaci (whitefly)
Li, J., Zhu, L., Hull, J. J., Liang, S., Daniell, H., Jin, S., & Zhang, X. (2016) · Plant Biotechnology Journal · doi:10.1111/pbi.12554 · Cited by 157 · see citing works
In Defense of Roots: A Research Agenda for Studying Plant Resistance to Belowground Herbivory
Rasmann, S., & Agrawal, A. A. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.112045 · Cited by 154 · see citing works
Isoprenoid metabolism and plastid reorganization in arbuscular mycorrhizal roots
Strack, D., & Fester, T. (2006) · New Phytologist · doi:10.1111/j.1469-8137.2006.01837.x · Cited by 155 · see citing works
Silicon and acibenzolar-S-methyl as resistance inducers in cucumber, against the whitefly Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) biotype B
Corrêa, R. S. B., Moraes, J. C., Auad, A. M., & Carvalho, G. A. (2005) · Neotropical Entomology · doi:10.1590/s1519-566x2005000300011 · Cited by 151 · see citing works
Can phylogeny predict chemical diversity and potential medicinal activity of plants? A case study of amaryllidaceae
Rønsted, N., Symonds, M. R. E., Birkholm, T., Christensen, S. B., MEEROW, A. W., Molander, M., Mølgaard, P., Petersen, G., Rasmussen, N., van Staden, J., et al. (2012) · BMC Evolutionary Biology · doi:10.1186/1471-2148-12-182 · Cited by 150 · see citing works
Priming of Wheat with the Green Leaf Volatile Z-3-Hexenyl Acetate Enhances Defense against Fusarium graminearum But Boosts Deoxynivalenol Production
Ameye, M., Audenaert, K., Zutter, N. D., Steppe, K., Meulebroek, L. V., Vanhaecke, L., Vleesschauwer, D. D., Haesaert, G., & Smagghe, G. J. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.00107 · Cited by 150 · see citing works
The Significance of Background Odour for an Egg Parasitoid to Detect Plants with Host Eggs
Mumm, R., & Hilker, M. (2005) · Chemical Senses · doi:10.1093/chemse/bji028 · Cited by 143 · see citing works
Chemical Defence Strategies of Higher Fungi
Spiteller, P. (2008) · Chemistry - A European Journal · doi:10.1002/chem.200800292 · Cited by 136 · see citing works
An Intimate Relationship Between Eriophyoid Mites and Their Host Plants – A Review
de Lillo, E., Pozzebon, A., Valenzano, D., & Duso, C. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.01786 · Cited by 125 · see citing works
Insect Elicitors and Exposure to Green Leafy Volatiles Differentially Upregulate Major Octadecanoids and Transcripts of 12-Oxo Phytodienoic Acid Reductases in Zea mays
Engelberth, J., Seidl‐Adams, I., Schultz, J. C., & Tumlinson, J. H. (2007) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-20-6-0707 · Cited by 124 · see citing works
Multivariate Analysis of Multiple Datasets: a Practical Guide for Chemical Ecology
Hervé, M. R., Nicolè, F., & Cao, K. L. (2018) · Journal of Chemical Ecology · doi:10.1007/s10886-018-0932-6 · Cited by 120 · see citing works
Insect-resistant biotech crops and their impacts on beneficial arthropods
Gatehouse, A. M. R., Ferry, N., Edwards, M. G., & Bell, H. A. (2011) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2010.0330 · Cited by 119 · see citing works
Morphogenesis of insect-induced plant galls: facts and questions
Raman, A. (2011) · Flora · doi:10.1016/j.flora.2010.08.004 · Cited by 117 · see citing works
In the light of new greenhouse technologies: 1. Plant‐mediated effects of artificial lighting on arthropods and tritrophic interactions
Vänninen, I., Pinto‐Zevallos, D. M., Nissinen, A., Johansen, N. S., & Shipp, L. (2010) · Annals of Applied Biology · doi:10.1111/j.1744-7348.2010.00438.x · Cited by 114 · see citing works
Selenium hyperaccumulation offers protection from cell disruptor herbivores
Quinn, C. F., Freeman, J. L., Reynolds, R. J., Cappa, J. J., Fakra, S. C., Marcus, M. A., Lindblom, S. D., Quinn, E. K., Bennett, L. E., & Pilon-Smits, E. A. (2010) · BMC Ecology · doi:10.1186/1472-6785-10-19 · Cited by 112 · see citing works
Direct Defenses in Plants and Their Induction by Wounding and Insect Herbivores
Howe, G. A., & Schaller, A. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8182-8_1 · Cited by 112 · see citing works
Induced resistance in the indeterminate growth of aspen (Populus tremuloides)
Stevens, M. T., & Lindroth, R. L. (2005) · Oecologia · doi:10.1007/s00442-005-0128-y · Cited by 112 · see citing works
Synergizing biological control: Scope for sterile insect technique, induced plant defences and cultural techniques to enhance natural enemy impact
Gurr, G. M., & Kvedaras, O. L. (2009) · Biological Control · doi:10.1016/j.biocontrol.2009.02.013 · Cited by 111 · see citing works
Polyphenoloxidase Silencing Affects Latex Coagulation in Taraxacum Species
Wahler, D., Gronover, C. S., Richter, C. G., Foucu, F., Twyman, R. M., Moerschbacher, B. M., Fischer, R., Muth, J. R., & Prüfer, D. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.138743 · Cited by 107 · see citing works
A Kunitz proteinase inhibitor from Archidendron ellipticum seeds: Purification, characterization, and kinetic properties
Bhattacharyya, A., Mazumdar, S., Mazumdar–Leighton, S., & Babu, C. R. (2005) · Phytochemistry · doi:10.1016/j.phytochem.2005.11.010 · Cited by 107 · see citing works
Plant-Based Insect Repellents
Moore, S. (2006) · CRC Press eBooks · doi:10.1201/9781420006650.ch14 · Cited by 109 · see citing works
Volatiles Mediating a Plant-Herbivore-Natural Enemy Interaction in Resistant and Susceptible Soybean Cultivars
Michereff, M. F. F., Laumann, R. A., Borges, M., Michereff‐Filho, M., Diniz, I. R., Neto, A. L. F., & Blassioli‐Moraes, M. C. (2011) · Journal of Chemical Ecology · doi:10.1007/s10886-011-9917-4 · Cited by 107 · see citing works
Plant and animal rhabdovirus host range: a bug's view
Hogenhout, S. A., Redinbaugh, M. G., & Ammar, E. (2003) · Trends in Microbiology · doi:10.1016/s0966-842x(03)00120-3 · Cited by 106 · see citing works
Significance and Role of Si in Crop Production
Haynes, R. J. (2017) · Advances in agronomy · doi:10.1016/bs.agron.2017.06.001 · Cited by 103 · see citing works
Alarm Pheromones—Chemical Signaling in Response to Danger
Verheggen, F. J., Haubruge, É., & Mescher, M. C. (2010) · Vitamins and hormones · doi:10.1016/s0083-6729(10)83009-2 · Cited by 103 · see citing works
Chitosan-induced biotic stress tolerance and crosstalk with phytohormones, antioxidants, and other signalling molecules
Mukarram, M., Ali, J., Dadkhah-Aghdash, H., Kurjak, D., Kačík, F., & Ďurkovič, J. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1217822 · Cited by 102 · see citing works
Inducible expression of a fusion gene encoding two proteinase inhibitors leads to insect and pathogen resistance in transgenic rice
Quilis, J., López‐García, B., Meynard, D., Guiderdoni, E., & Segundo, B. S. (2013) · Plant Biotechnology Journal · doi:10.1111/pbi.12143 · Cited by 100 · see citing works
The maize transcription factor EREB 58 mediates the jasmonate‐induced production of sesquiterpene volatiles
Li, S., Wang, H., Li, F., Chen, Z., Li, X., Zhu, L., Wang, G., Yu, J., Huang, D., & Lang, Z. (2015) · The Plant Journal · doi:10.1111/tpj.12994 · Cited by 98 · see citing works
Efflux Transporters as a Novel Herbivore Countermechanism to Plant Chemical Defenses
Forbey, J. S., & Dearing, M. D. (2006) · Journal of Chemical Ecology · doi:10.1007/s10886-006-9079-y · Cited by 91 · see citing works
Nickel hyperaccumulation as an elemental defense of Streptanthus polygaloides (Brassicaceae): influence of herbivore feeding mode
Jhee, E. M., Boyd, R. S., & Eubanks, M. D. (2005) · New Phytologist · doi:10.1111/j.1469-8137.2005.01504.x · Cited by 93 · see citing works
Multidimensional approaches for studying plant defence against insects: from ecology to omics and synthetic biology
Barah, P., & Bones, A. M. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru489 · Cited by 93 · see citing works
Involvement of the xyloglucan endotransglycosylase/hydrolases encoded by celery XTH1 and Arabidopsis XTH33 in the phloem response to aphids
Divol, F., Vilaine, F., Thibivilliers, S., Kusiak, C., Sauge, M. H., & Dinant, S. (2007) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2006.01618.x · Cited by 92 · see citing works
3-β-d-Glucopyranosyl-6-methoxy-2-benzoxazolinone (MBOA-N-Glc) is an insect detoxification product of maize 1,4-benzoxazin-3-ones
Maag, D., Dalvit, C., Thévenet, D., Köhler, A., Wouters, F. C., Vassão, D. G., Gershenzon, J., Wolfender, J., Turlings, T. C. J., Erb, M., et al. (2014) · Phytochemistry · doi:10.1016/j.phytochem.2014.03.018 · Cited by 91 · see citing works
Early Transcriptome Analyses of Z-3-Hexenol-Treated Zea mays Revealed Distinct Transcriptional Networks and Anti-Herbivore Defense Potential of Green Leaf Volatiles
Engelberth, J., Contreras, C. F., Dalvi, C., Li, T., & Engelberth, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077465 · Cited by 90 · see citing works
Gut microbiota degrades toxic isothiocyanates in a flea beetle pest
Shukla, S. P., & Beran, F. (2020) · Molecular Ecology · doi:10.1111/mec.15657 · Cited by 85 · see citing works

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Fürstenberg-Hägg, J., Zagrobelny, M., & Bak, S. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140510242 · Cited by 933 · see citing works
www.mdpi.com/journal/ijms Plant Defense against Insect Herbivores
Fürstenberg-Hägg, J., Zagrobelny, M., & Bak, S. (2013)
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Chaudhary, A., Bala, K., Thakur, S., Kamboj, R., & Dumra, N. (2018) · International Journal of Chemical Studies · Cited by 17 · see citing works
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Borkataki, S., Nanda, S. P., Reddy, M. D., & Taye, R. R. (2020) · Journal of Entomological Research · doi:10.5958/0974-4576.2020.00032.8 · Cited by 4 · see citing works
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Abdi, G., Samanta, S., Rani, A., Mondol, M. S. A., & Basak, A. (2026) · Apple Academic Press eBooks · doi:10.1201/9781779644282-9

Authors: Gatehouse, J. A.
Affiliations: Durham University (GB)
Corresponding author: Gatehouse, John A.
ORCID: Gatehouse, John A.
Venue: New Phytologist
Publisher: Wiley
Published: 2002-10-21
Volume: 156
Issue: 2
Pages: 145-169
ISSN: 0028-646X (ISSN-L)
1469-8137
DOI: 10.1046/j.1469-8137.2002.00519.x
OpenAlex: W2160819466
Cited by: 704
References: 222
Citations by year: 2026: 32 · 2025: 44 · 2024: 49 · 2023: 41 · 2022: 40 · 2021: 27 · 2020: 34 · 2019: 27 · 2018: 27 · 2017: 28 · 2016: 16 · 2015: 23 · 2014: 32 · 2013: 32 · 2012: 28
FWCI: 1.58
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: New Phytologist (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Agricultural and Biological Sciences › Insect Science › Insect-Plant Interactions and Control
Physical Sciences › Environmental Science › Ecology › Forest Insect Ecology and Management
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
Keywords: plant-insect interactions, phytophagous insects, induced plant defense, systemin, jasmonates, oligogalacturonides, hydrogen peroxide, plant volatiles, indirect defense, tritrophic interactions, insecticidal compounds

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Plant resistance towards insect herbivores: a dynamic interaction

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