Plant–arthropod interactions: who is the winner?
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Summary: Herbivorous arthropods have interacted with plants for millions of years. During feeding they release chemical cues that allow plants to detect the attack and mount an efficient defense response. A signaling cascade triggers the expression of hundreds of genes, which encode defensive proteins and enzymes for synthesis of toxic metabolites. This direct defense is often complemented by emission of volatiles that attract beneficial parasitoids. In return, arthropods have evolved strategies to interfere with plant defenses, either by producing effectors to inhibit detection and downstream signaling steps, or by adapting to their detrimental effect. In this review, we address the current knowledge on the molecular and chemical dialog between plants and herbivores, with an emphasis on co‐evolutionary aspects.
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Herbivores, pathogens, and viruses can interfere with defense hormone signaling and thereby manipulate plants for their own benefit.
“Herbivores, pathogens, and viruses can interfere with defense hormone signaling and thereby manipulate plants for their own benefit (Kazan and Lyons, 2014;Stahl et al., 2018).”
From Plant Secondary Metabolites as Defenses, Regulators, and Primary Metabolites: The Blurred Functional Trichotomy (2020) · cites this paper as Stahl et al., 2018
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Schmiesing, A., Emonet, A., Gouhier‐Darimont, C., & Reymond, P. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00031 · Cited by 70 · see citing works
Self-citationRetractedJones, J. D. G., & Dangl, J. L. (2006) · Nature · doi:10.1038/nature05286 · Cited by 13,177 · see citing works
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
Isman, M. B. (2005) · Annual Review of Entomology · doi:10.1146/annurev.ento.51.110104.151146 · Cited by 3,901 · see citing works
Howe, H. F., & Smallwood, J. (1982) · Annual Review of Ecology and Systematics · doi:10.1146/annurev.es.13.110182.001221 · Cited by 3,552 · see citing works
Boller, T., & Felix, G. (2009) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105346 · Cited by 3,395 · see citing works
Hormonal Modulation of Plant Immunity
Pieterse, C. M. J., van der Does, D., Zamioudis, C., León-Reyes, A., & Wees, S. C. M. V. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154055 · Cited by 3,021 · see citing works
Salicylic acid, a multifaceted hormone to combat disease
Vlot, A. C., Dempsey, D. A., & Klessig, D. F. (2009) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.050908.135202 · Cited by 2,568 · see citing works
JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling
Thines, B. C., Katsir, L., Melotto, M., Niu, Y., Mandaokar, A. D., Liu, G., Nomura, K., He, S. Y., Howe, G. A., & Browse, J. (2007) · Nature · doi:10.1038/nature05960 · Cited by 2,530 · see citing works
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
The JAZ family of repressors is the missing link in jasmonate signalling
Chini, A., Fonseca, S., Santos-Fernandez, G., Adie, B. A. T., Chico, J. M., Lorenzo, Ó., García‐Casado, G., López‐Vidriero, I., Lozano, F. M., Ponce, M. R., et al. (2007) · Nature · doi:10.1038/nature06006 · Cited by 2,426 · see citing works
Molecular Mechanisms of Metabolic Resistance to Synthetic and Natural Xenobiotics
Li, X., Schuler, M. A., & Berenbaum, M. R. (2006) · Annual Review of Entomology · doi:10.1146/annurev.ento.51.110104.151104 · Cited by 2,121 · 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
Regulation of pattern recognition receptor signalling in plants
Couto, D., & Zipfel, C. (2016) · Nature reviews. Immunology · doi:10.1038/nri.2016.77 · Cited by 1,400 · see citing works
Recruitment of entomopathogenic nematodes by insect-damaged maize roots
Rasmann, S., Köllner, T. G., Degenhardt, J., Hiltpold, I., Toepfer, S., Kuhlmann, U., Gershenzon, J., & Turlings, T. C. J. (2005) · Nature · doi:10.1038/nature03451 · Cited by 1,330 · 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
Self-citationWound-Induced Proteinase Inhibitor in Plant Leaves: A Possible Defense Mechanism against Insects
Green, T. R., & Ryan, C. A. (1972) · Science · doi:10.1126/science.175.4023.776 · Cited by 1,198 · 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
Natural products in crop protection.
Dayan, F., Cantrell, C., & Duke, S. (2009) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2009.01.046 · Cited by 1,187 · see citing works
Fernández‐Calvo, P., Chini, A., Fernández‐Barbero, G., Chico, J. M., Ibanez, S. G., Geerinck, J., Eeckhout, D., Schweizer, F., Godoy, M., Franco‐Zorrilla, J. M., et al. (2011) · The Plant Cell · doi:10.1105/tpc.110.080788 · Cited by 1,151 · see citing works
Self-citationBiochemistry of Plant Volatiles
Dudareva, N., Pichersky, E., & Gershenzon, J. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.049981 · Cited by 1,128 · see citing works
Staswick, P., & Tiryaki, İ. (2004) · The Plant Cell · doi:10.1105/tpc.104.023549 · Cited by 1,119 · see citing works
The genome of Tetranychus urticae reveals herbivorous pest adaptations
Grbić, M., Leeuwen, T. V., Clark, R. M., Rombauts, S., Rouzé, P., Grbić, V., Osborne, E. J., Dermauw, W., Ngoc, P. C. T., Ortego, F., et al. (2011) · Nature · doi:10.1038/nature10640 · Cited by 1,113 · see citing works
Cross Talk in Defense Signaling
Koornneef, A., & Pieterse, C. M. J. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.112029 · Cited by 1,016 · see citing works
(+)-7-iso-Jasmonoyl-L-isoleucine is the endogenous bioactive jasmonate
Fonseca, S., Chini, A., Hámberg, M., Adie, B. A. T., Porzel, A., Kramell, R., Miersch, O., Wasternack, C. H., & Solano, R. (2009) · Nature Chemical Biology · doi:10.1038/nchembio.161 · Cited by 1,008 · see citing works
Plant NBS-LRR proteins: adaptable guards.
McHale, L. K., Tan, X., Koehl, P., & Michelmore, R. W. (2006) · Genome biology · doi:10.1186/gb-2006-7-4-212 · Cited by 1,008 · 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
Signal Signature and Transcriptome Changes of Arabidopsis During Pathogen and Insect Attack
de Vos, M., van Oosten, V. R., Poecke, R. M. P. V., van Pelt, J. A., Pozo, M. J., Mueller, M. J., Buchala, A. J., Métraux, J., van Loon, L. C., Dicke, M., et al. (2005) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-18-0923 · Cited by 974 · see citing works
Jasmonate Passes Muster: A Receptor and Targets for the Defense Hormone
Browse, J. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.043008.092007 · Cited by 946 · 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
The evolutionary ecology of insect resistance to plant chemicals
Després, L., David, J., & Gallet, C. (2007) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2007.02.010 · Cited by 924 · see citing works
Role of phytohormones in insect-specific plant reactions
Erb, M., Meldau, S., & Howe, G. A. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2012.01.003 · Cited by 917 · see citing works
The adaptive significance of insect gall morphology
Stone, G. N., & Schönrogge, K. (2003) · Trends in Ecology & Evolution · doi:10.1016/s0169-5347(03)00247-7 · Cited by 852 · 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
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
GLUTAMATE RECEPTOR-LIKE genes mediate leaf-to-leaf wound signalling
Mousavi, S. A. R., Chauvin, A., Pascaud, F., Kellenberger, S. B., & Farmer, E. E. (2013) · Nature · doi:10.1038/nature12478 · Cited by 765 · 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
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
Silverleaf Whitefly Induces Salicylic Acid Defenses and Suppresses Effectual Jasmonic Acid Defenses
Zarate, S. I., Kempema, L. A., & Walling, L. L. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.090035 · Cited by 746 · see citing works
Kaplan, I., & Denno, R. F. (2007) · Ecology Letters · doi:10.1111/j.1461-0248.2007.01093.x · Cited by 681 · see citing works
Li, L., Zhao, Y. F., McCaig, B. C., Wingerd, B. A., Wang, J., Whalon, M. E., Pichersky, E., & Howe, G. A. (2004) · The Plant Cell · doi:10.1105/tpc.017954 · Cited by 668 · see citing works
Vetter, J. (2000) · Toxicon · doi:10.1016/s0041-0101(99)00128-2 · Cited by 665 · see citing works
Zheng, X., Spivey, N. W., Zeng, W., Liu, P., Fu, Z. Q., Klessig, D. F., He, S. Y., & Dong, X. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.04.014 · Cited by 653 · see citing works
Helping plants to deal with insects: the role of beneficial soil-borne microbes
Pineda, A., Zheng, S., van Loon, J. J. A., Pieterse, C. M. J., & Dicke, M. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.05.007 · Cited by 640 · see citing works
Dermauw, W., & Leeuwen, T. V. (2013) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2013.11.001 · Cited by 638 · see citing works
A Role for Isothiocyanates in Plant Resistance Against the Specialist Herbivore Pieris rapae
Agrawal, A. A., & Kurashige, N. S. (2003) · Journal of Chemical Ecology · doi:10.1023/a:1024265420375 · Cited by 638 · see citing works
Macroevolution and the biological diversity of plants and herbivores
Futuyma, D. J., & Agrawal, A. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904106106 · Cited by 635 · see citing works
Multitrophic effects of herbivore‐induced plant volatiles in an evolutionary context
Dicke, M., & van Loon, J. J. A. (2000) · Entomologia Experimentalis et Applicata · doi:10.1046/j.1570-7458.2000.00736.x · Cited by 597 · see citing works
Disarming the mustard oil bomb
Ratzka, A., Vogel, H., Kliebenstein, D. J., Mitchell‐Olds, T., & Kroymann, J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.172112899 · Cited by 595 · see citing works
Mattiacci, L., Dicke, M., & Posthumus, M. A. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.6.2036 · Cited by 586 · see citing works
Identification of a Plant Receptor for Extracellular ATP
Choi, J., Tanaka, K., Cao, Y., Qi, Y. A., Qiu, J., Liang, Y., Lee, S. Y., & Stacey, G. S. (2014) · Science · doi:10.1126/science.343.6168.290 · Cited by 578 · see citing works
Schweizer, F., Fernández‐Calvo, P., Zander, M., Díez-Díaz, M., Fonseca, S., Glauser, G., Lewsey, M. G., Ecker, J. R., Solano, R., & Reymond, P. (2013) · The Plant Cell · doi:10.1105/tpc.113.115139 · Cited by 548 · see citing works
Self-citationPlant α‐amylase inhibitors and their interaction with insect α‐amylases
Franco, O. L., Rigden, D. J., Melo, F. R., & Grossi‐de‐Sá, M. F. (2002) · European Journal of Biochemistry · doi:10.1046/j.0014-2956.2001.02656.x · Cited by 544 · see citing works
Carlini, C. R., & Grossi‐de‐Sá, M. F. (2002) · Toxicon · doi:10.1016/s0041-0101(02)00240-4 · Cited by 543 · see citing works
Du, B., Zhang, W., Liu, B., Hu, J., Wei, Z., Shi, Z., He, R., Zhu, L., Chen, R., Han, B., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912139106 · Cited by 542 · see citing works
Martin, D., Tholl, D., Gershenzon, J., & Bohlmann, J. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.011001 · Cited by 537 · see citing works
Jennings, C. V., West, J., Waine, C., Craik, D. J., & Anderson, M. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191366898 · Cited by 524 · see citing works
Molecular sabotage of plant defense by aphid saliva
Will, T., Tjallingii, W. F., Thönnessen, A., & van Bel, A. J. E. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703535104 · Cited by 524 · see citing works
The butterfly plant arms-race escalated by gene and genome duplications
Edger, P. P., Heidel‐Fischer, H. M., Bekaert, M., Rota, J., Glöckner, G., Platts, A. E., Heckel, D. G., Der, J. P., Wafula, E. K., Tang, M., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1503926112 · Cited by 519 · see citing works
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
Successful herbivore attack due to metabolic diversion of a plant chemical defense
Wittstock, U., Agerbirk, N., Stauber, E. J., Olsen, C. E., Hippler, M., Mitchell‐Olds, T., Gershenzon, J., & Vogel, H. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308007101 · Cited by 509 · see citing works
A Conserved Transcript Pattern in Response to a Specialist and a Generalist Herbivorew
Reymond, P., Bodenhausen, N., Poecke, R. M. P. V., Krishnamurthy, V., Dicke, M., & Farmer, E. E. (2004) · The Plant Cell · doi:10.1105/tpc.104.026120 · Cited by 503 · see citing works
Self-citationBos, J. I. B., Prince, D. C., Pitino, M., Maffei, M. E., Win, J., & Hogenhout, S. A. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001216 · Cited by 497 · see citing works
Nicotine's Defensive Function in Nature
Steppuhn, A., Gase, K., Krock, B., Halitschke, R., & Baldwin, I. T. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020217 · Cited by 492 · see citing works
Ververidis, F., Trantas, E., Douglas, C. J., Vollmer, G., Kretzschmar, G., & Panopoulos, N. J. (2007) · Biotechnology Journal · doi:10.1002/biot.200700084 · Cited by 489 · see citing works
Plant Interactions with Multiple Insect Herbivores: From Community to Genes
Stam, J. M., Kroes, A., Li, Y., Gols, R., van Loon, J. J. A., Poelman, E. H., & Dicke, M. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050213-035937 · Cited by 482 · see citing works
Dermauw, W., Wybouw, N., Rombauts, S., Menten, B., VONTAS, J. G., Grbić, M., Clark, R. M., Feyereisen, R., & Leeuwen, T. V. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1213214110 · Cited by 478 · see citing works
Effector proteins that modulate plant–insect interactions
Hogenhout, S. A., & Bos, J. I. B. (2011) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2011.05.003 · Cited by 474 · see citing works
Sugio, A., Kingdom, H. N., MacLean, A. M., Grieve, V. M., & Hogenhout, S. A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105664108 · Cited by 474 · see citing works
Insect Herbivores Drive Real-Time Ecological and Evolutionary Change in Plant Populations
Agrawal, A. A., Hastings, A. P., Johnson, M. T. J., Maron, J. L., & Salminen, J. (2012) · Science · doi:10.1126/science.1225977 · Cited by 458 · see citing works
Herbivore exploits orally secreted bacteria to suppress plant defenses
Chung, S. H., Rosa, C., Scully, E. D., Peiffer, M. L., Tooker, J. F., Hoover, K., Luthe, D. S., & Felton, G. W. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1308867110 · Cited by 456 · see citing works
Plant interactions with microbes and insects: from molecular mechanisms to ecology
Pieterse, C. M. J., & Dicke, M. (2007) · Trends in Plant Science · doi:10.1016/j.tplants.2007.09.004 · Cited by 450 · see citing works
Mewis, I., Appel, H. M., Hom, A., Raina, R., & Schultz, J. C. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.053389 · Cited by 442 · see citing works
Mechanism of action of the toxic lectins abrin and ricin
Olsnes, S., Refsnes, K., & Pihl, A. (1974) · Nature · doi:10.1038/249627a0 · Cited by 440 · see citing works
A rapid wound signal activates the systemic synthesis of bioactive jasmonates in Arabidopsis
Koo, A. J., Gao, X., Jones, A. D., & Howe, G. A. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03924.x · Cited by 437 · see citing works
Plant disease resistance genes: Current status and future directions
Gururani, M. A., Venkatesh, J., Upadhyaya, C. P., Nookaraju, A., Pandey, S. K., & Park, S. W. (2012) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2012.01.002 · Cited by 427 · see citing works
Barth, C., & Jander, G. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02716.x · Cited by 415 · see citing works
Fragments of ATP synthase mediate plant perception of insect attack
Schmelz, E. A., Carroll, M. J., LeClere, S., Phipps, S. M., Meredith, J. A., Chourey, P. S., Alborn, H. T., & Teal, P. E. A. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602328103 · Cited by 414 · see citing works
Mechanisms of Selective Action of Pyrethroid Insecticides
Casida, J. E., Gammon, D. W., Glickman, A. H., & Lawrence, L. J. (1983) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.23.040183.002213 · Cited by 414 · see citing works
Physical defences wear you down: progressive and irreversible impacts of silica on insect herbivores
Massey, F. P., & Hartley, S. E. (2008) · Journal of Animal Ecology · doi:10.1111/j.1365-2656.2008.01472.x · Cited by 402 · 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
Nombela, G., Williamson, V. M., & Muñiz, M. (2003) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2003.16.7.645 · Cited by 396 · see citing works
Mutti, N. S., Louis, J., Pappan, L. K., Pappan, K. L., Begum, K., Chen, M., Park, Y., Dittmer, N. T., Marshall, J. L., Reese, J. C., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708958105 · Cited by 394 · see citing works
Liu, Y., Wu, H., Chen, H., Liu, Y., He, J., Kang, H., Sun, Z., Pan, G., Wang, Q., Hu, J., et al. (2014) · Nature Biotechnology · doi:10.1038/nbt.3069 · Cited by 377 · see citing works
Ament, K., Kant, M. R., Sabelis, M. W., Haring, M. A., & Schuurink, R. C. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.048694 · Cited by 370 · see citing works
Molecular Bases of Plant Resistance to Arthropods
Smith, C. M., & Clement, S. L. (2011) · Annual Review of Entomology · doi:10.1146/annurev-ento-120710-100642 · Cited by 367 · see citing works
The genetic basis of a plant–insect coevolutionary key innovation
Wheat, C. W., Vogel, H., Wittstock, U., Braby, M. F., Underwood, D. L. A., & Mitchell‐Olds, T. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706229104 · Cited by 364 · see citing works
The Layers of Plant Responses to Insect Herbivores.
Schuman, M., & Baldwin, I. (2016) · Annual Review of Entomology · doi:10.1146/annurev-ento-010715-023851 · Cited by 362 · 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
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
Plant Responses to Insect Egg Deposition
Hilker, M., & Fatouros, N. E. (2014) · Annual Review of Entomology · doi:10.1146/annurev-ento-010814-020620 · Cited by 358 · see citing works
Plant lectins as defense proteins against phytophagous insects
Vandenborre, G., Smagghe, G. J., & Damme, E. J. M. V. (2011) · Phytochemistry · doi:10.1016/j.phytochem.2011.02.024 · Cited by 350 · 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
Glauser, G., Grata, E., Dubugnon, L., Rudaz, S. L., Farmer, E. E., & Wolfender, J. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m801760200 · Cited by 334 · see citing works
Different Lepidopteran Elicitors Account for Cross-Talk in Herbivory-Induced Phytohormone Signaling
Diezel, C., von Dahl, C. C., Gaquerel, E., & Baldwin, I. T. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.139550 · Cited by 330 · see citing works
Catch me if you can: bacterial effectors and plant targets
Deslandes, L., & Rivas, S. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2012.06.011 · Cited by 326 · see citing works
HOST RACE RADIATION IN THE SOAPBERRY BUG: NATURAL HISTORY WITH THE HISTORY
Carroll, S. P., & Boyd, C. (1992) · Evolution · doi:10.1111/j.1558-5646.1992.tb00619.x · Cited by 325 · 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
Physical and chemical interactions between aphids and plants
Will, T., & van Bel, A. J. E. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erj089 · Cited by 319 · see citing works
Transcriptional Regulation of Pattern-Triggered Immunity in Plants
Li, B., Meng, X., Shan, L., & He, P. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.04.011 · Cited by 317 · see citing works
Ellis, C., Karafyllidis, I., & Turner, J. G. (2002) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2002.15.10.1025 · Cited by 314 · see citing works
Whiteflies interfere with indirect plant defense against spider mites in Lima bean
Zhang, P., Zheng, S., van Loon, J. J. A., Boland, W., David, A., Mumm, R., & Dicke, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907890106 · Cited by 313 · see citing works
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
Breakdown of an Ant-Plant Mutualism Follows the Loss of Large Herbivores from an African Savanna
Palmer, T. M., Stanton, M. L., Young, T. P., Goheen, J. R., Pringle, R. M., & Karban, R. (2008) · Science · doi:10.1126/science.1151579 · Cited by 304 · see citing works
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
Heil, M. (2015) · Annual Review of Entomology · doi:10.1146/annurev-ento-010814-020753 · Cited by 292 · see citing works
Pechan, T., Cohen, A. C., Williams, W. P., & Luthe, D. S. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.202224899 · Cited by 290 · see citing works
Insect herbivore counteradaptations to the plant glucosinolate–myrosinase system
Winde, I. B., & Wittstock, U. (2011) · Phytochemistry · doi:10.1016/j.phytochem.2011.01.016 · Cited by 286 · see citing works
Vein-Cutting Behavior: Insect Counterploy to the Latex Defense of Plants
Dussourd, D. E., & Eisner, T. (1987) · Science · doi:10.1126/science.3616620 · Cited by 285 · see citing works
Ibanez, S. G., Botër, M., Fernández‐Barbero, G., Chini, A., Rathjen, J. P., & Solano, R. (2014) · PLoS Biology · doi:10.1371/journal.pbio.1001792 · Cited by 276 · see citing works
Phytohormone-based activity mapping of insect herbivore-produced elicitors
Schmelz, E. A., Engelberth, J., Alborn, H. T., Tumlinson, J. H., & Teal, P. E. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811861106 · Cited by 275 · see citing works
Identity, regulation, and activity of inducible diterpenoid phytoalexins in maize
Schmelz, E. A., Kaplan, F., Huffaker, A., Dafoe, N. J., Vaughan, M. M., Ni, X., Rocca, J. R., Alborn, H. T., & Teal, P. E. A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1014714108 · Cited by 274 · see citing works
Dobler, S., Dalla, S., Wagschal, V., & Agrawal, A. A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1202111109 · Cited by 271 · see citing works
Li, R., Weldegergis, B. T., Li, J., Jung, C., Qu, J., Sun, Y., Qian, H., Tee, C.-S., van Loon, J. J. A., Dicke, M., et al. (2014) · The Plant Cell · doi:10.1105/tpc.114.133181 · Cited by 271 · see citing works
Yan, Y., Christensen, S. A., Isakeit, T., Engelberth, J., Meeley, R. B., Hayward, A., Emery, R. J. N., & Kolomiets, M. V. (2012) · The Plant Cell · doi:10.1105/tpc.111.094151 · Cited by 270 · see citing works
de Vos, M., & Jander, G. (2009) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2009.02019.x · Cited by 266 · see citing works
The Impact of the Absence of Aliphatic Glucosinolates on Insect Herbivory in Arabidopsis
Beekwilder, J., van Leeuwen, W., van Dam, N. M., Bertossi, M., Grandi, V. D., Mizzi, L., Soloviev, M., Szabados, L., Molthoff, J. W., Schipper, B., et al. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002068 · Cited by 266 · see citing works
Jasmonate and salicylate induce expression of herbivore cytochrome P450 genes
Li, X., Schuler, M. A., & Berenbaum, M. R. (2002) · Nature · doi:10.1038/nature01003 · Cited by 265 · see citing works
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
Yang, J., Iwasaki, M., Machida, C., Machida, Y., Zhou, X., & Chua, N. (2008) · Genes & Development · doi:10.1101/gad.1682208 · Cited by 264 · see citing works
Bleeker, P., Mirabella, R., Diergaarde, P. J., VanDoorn, A., Tissier, A. F., Kant, M. R., Prins, M., de Vos, M., Haring, M. A., & Schuurink, R. C. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208756109 · Cited by 262 · see citing works
Bruchins: Insect-derived plant regulators that stimulate neoplasm formation
Doss, R. P., Oliver, J. E., Proebsting, W. M., Potter, S. W., Kuy, S., Clement, S. L., Williamson, R. T., Carney, J. R., & Devilbiss, E. D. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.110054697 · Cited by 258 · see citing works
Cues from chewing insects — the intersection of DAMPs, HAMPs, MAMPs and effectors
Acevedo, F. E., Rivera-Vega, L. J., Chung, S. H., Ray, S., & Felton, G. W. (2015) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2015.05.029 · Cited by 258 · see citing works
Regulation of growth–defense balance by the JASMONATE ZIM‐DOMAIN (JAZ)‐MYC transcriptional module
Major, I. T., Yoshida, Y., Campos, M. L., Kapali, G. P., Xin, X., Sugimoto, K., Ferreira, D. D. O., He, S. Y., & Howe, G. A. (2017) · New Phytologist · doi:10.1111/nph.14638 · Cited by 256 · see citing works
Tsuji, J., Jackson, E. P., Gage, D. A., Hammerschmidt, R., & Somerville, S. C. (1992) · PLANT PHYSIOLOGY · doi:10.1104/pp.98.4.1304 · Cited by 255 · see citing works
Signaling Pathways Controlling Induced Resistance to Insect Herbivores in Arabidopsis
Bodenhausen, N., & Reymond, P. (2007) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-20-11-1406 · Cited by 255 · see citing works
Self-citationSuppression of Plant Defenses by a Myzus persicae (Green Peach Aphid) Salivary Effector Protein
Elzinga, D. A., de Vos, M., & Jander, G. (2014) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-01-14-0018-r · Cited by 253 · see citing works
Maize landraces recruit egg and larval parasitoids in response to egg deposition by a herbivore
Tamiru, A., Bruce, T. J. A., Woodcock, C. M., Caulfield, J. C., Midega, C. A. O., OGOL, C. K. P. O., Mayon, P., Birkett, M. A., Pickett, J. A., & Khan, Z. R. (2011) · Ecology Letters · doi:10.1111/j.1461-0248.2011.01674.x · Cited by 245 · see citing works
Paschold, A., Halitschke, R., & Baldwin, I. T. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03119.x · Cited by 239 · see citing works
Alborn, H. T., Hansen, T. V., Jones, T. H., Bennett, D. C., Tumlinson, J. H., Schmelz, E. A., & Teal, P. E. A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705947104 · Cited by 239 · see citing works
Lozano‐Durán, R., Rosas‐Díaz, T., Gusmaroli, G., Luna, A. P., Soubigou‐Taconnat, L., Deng, X. W., & Bejarano, E. R. (2011) · The Plant Cell · doi:10.1105/tpc.110.080267 · Cited by 236 · see citing works
GroEL from the endosymbiont Buchnera aphidicola betrays the aphid by triggering plant defense
Chaudhary, R., Atamian, H. S., Shen, Z., Briggs, S. P., & Kaloshian, I. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1407687111 · Cited by 233 · see citing works
Herbivore-associated elicitors: FAC signaling and metabolism
Bonaventure, G., VanDoorn, A., & Baldwin, I. T. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2011.01.006 · Cited by 232 · see citing works
Insect egg deposition induces Pinus sylvestris to attract egg parasitoids
Hilker, M., Kobs, C., Varama, M., & Schrank, K. (2002) · Journal of Experimental Biology · doi:10.1242/jeb.205.4.455 · Cited by 232 · see citing works
Insect eggs suppress plant defence against chewing herbivores
Bruessow, F., Gouhier‐Darimont, C., Buchala, A. J., Métraux, J., & Reymond, P. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04200.x · Cited by 230 · see citing works
Self-citationSYSTEMIN: 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
Molecular biology of insect neuronal GABA receptors
Hosie, A. M., Sattelle, D. B., Aronstein, K., & ffrench‐Constant, R. H. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01127-2 · Cited by 227 · see citing works
Oviposition by Pierid Butterflies Triggers Defense Responses in Arabidopsis
Little, D., Gouhier‐Darimont, C., Bruessow, F., & Reymond, P. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.090837 · Cited by 227 · see citing works
Self-citationPlant cyclotides disrupt epithelial cells in the midgut of lepidopteran larvae
Barbeta, B. L., Marshall, A. T., Gillon, A. D., Craik, D. J., & Anderson, M. A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710338104 · Cited by 226 · see citing works
Aphid Protein Effectors Promote Aphid Colonization in a Plant Species-Specific Manner
Pitino, M., & Hogenhout, S. A. (2012) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-07-12-0172-fi · Cited by 223 · 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
Sugio, A., Dubreuil, G., Giron, D., & Simon, J.-C. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru435 · Cited by 214 · see citing works
Wink, M., Schmeller, T., & Latz-Brüning, B. (1998) · Journal of Chemical Ecology · doi:10.1023/a:1022315802264 · Cited by 212 · see citing works
Long-distance plant signaling pathways in response to multiple stressors: the gap in knowledge
Huber, A. E., & Bauerle, T. L. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw099 · Cited by 210 · see citing works
Korth, K. L., Doege, S. J., Park, S., Goggin, F. L., Wang, Q., Gomez, S. K., Liu, G., Jia, L., & Nakata, P. A. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.076737 · Cited by 210 · see citing works
Pegadaraju, V., Knepper, C., Reese, J. C., & Shah, J. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.070433 · Cited by 207 · see citing works
Tamura, Y., Hattori, M., Yoshioka, H., Yoshioka, M., Takahashi, A., Wu, J., Sentoku, N., & Yasui, H. (2014) · Scientific Reports · doi:10.1038/srep05872 · Cited by 205 · see citing works
Suppression of terpenoid synthesis in plants by a virus promotes its mutualism with vectors
Luan, J., Yao, D., Zhang, T., Walling, L. L., Yang, M., Wang, Y., & Liu, S. (2012) · Ecology Letters · doi:10.1111/ele.12055 · Cited by 205 · see citing works
Onkokesung, N., Reichelt, M., van Doorn, A., Schuurink, R. C., van Loon, J. J. A., & Dicke, M. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru096 · Cited by 202 · see citing works
Vinca drug components accumulate exclusively in leaf exudates of Madagascar periwinkle
Roepke, J., Salim, V., Wu, M., Thamm, A. M. K., Murata, J., Ploss, K., Boland, W., & Luca, V. D. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911451107 · Cited by 201 · see citing works
Arabidopsis Vegetative Storage Protein Is an Anti-Insect Acid Phosphatase
Liu, Y., Ahn, J., Datta, S., Salzman, R. A., Moon, J., Huyghues‐Despointes, B. M. P., Pittendrigh, B. R., Murdock, L. L., Koiwa, H., & Zhu‐Salzman, K. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.066837 · Cited by 199 · see citing works
Schlaeppi, K., Bodenhausen, N., Buchala, A. J., Mauch, F., & Reymond, P. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03545.x · Cited by 199 · see citing works
Self-citationVincent, T. R., Avramova, M., Canham, J., Higgins, P., Bilkey, N., Mugford, S. T., Pitino, M., Toyota, M., Gilroy, S., Miller, T., et al. (2017) · The Plant Cell · doi:10.1105/tpc.17.00136 · Cited by 199 · see citing works
Disruption of Two Defensive Signaling Pathways by a Viral RNA Silencing Suppressor
Lewsey, M. G., Murphy, A. M., MacLean, D., Dalchau, N., Westwood, J. H., Macaulay, K., Bennett, M. H., Moulin, M., Hanke, D. E., Powell, G., et al. (2010) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-23-7-0835 · Cited by 196 · see citing works
Tay, W. T., Mahon, R. J., Heckel, D. G., Walsh, T., Downes, S. J., James, W. J., Lee, S.-F., Reineke, A., Williams, A. K., & Gordon, K. H. J. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005534 · Cited by 196 · see citing works
Zhao, C., Navarro-Escalante, L., Chen, H., Benatti, T. R., Qu, J., Chellapilla, S., Waterhouse, R. M., Wheeler, D., Andersson, M. N., Bao, R., et al. (2015) · Current Biology · doi:10.1016/j.cub.2014.12.057 · Cited by 194 · see citing works
The cabbage aphid: a walking mustard oil bomb
Kazana, E., Pope, T. W., Tibbles, L., Bridges, M., Pickett, J. A., Bones, A. M., Powell, G., & Rossiter, J. T. (2007) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2007.0237 · Cited by 191 · see citing works
Major, I. T., & Constabel, C. P. (2006) · New Phytologist · doi:10.1111/j.1469-8137.2006.01877.x · Cited by 189 · see citing works
Bridges, M., Jones, A. M. E., Bones, A. M., Hodgson, C., Cole, R., Bartlet, E., Wallsgrove, R., Karapapa, V. K., Watts, N., & Rossiter, J. T. (2002) · Proceedings of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rspb.2001.1861 · Cited by 186 · see citing works
Gamma-aminobutyrate: defense against invertebrate pests?
Bown, A. W., MacGregor, K. B., & Shelp, B. J. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2006.07.002 · Cited by 185 · see citing works
Macroevolutionary chemical escalation in an ancient plant–herbivore arms race
Becerra, J. X., Noge, K., & Venable, D. L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904456106 · Cited by 184 · see citing works
Kant, M. R., Sabelis, M. W., Haring, M. A., & Schuurink, R. C. (2007) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2007.1277 · Cited by 184 · see citing works
Huang, T., Jander, G., & de Vos, M. (2011) · Phytochemistry · doi:10.1016/j.phytochem.2011.03.019 · Cited by 182 · see citing works
Effectors of biotrophic fungi and oomycetes: pathogenicity factors and triggers of host resistance
Dodds, P. N., Rafiqi, M., Gan, P., Hardham, A. R., Jones, D. A., & Ellis, J. G. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2009.02922.x · Cited by 181 · see citing works
The ecology of herbivore‐induced silicon defences in grasses
Hartley, S. E., & DeGabriel, J. L. (2016) · Functional Ecology · doi:10.1111/1365-2435.12706 · Cited by 179 · see citing works
Bede, J. C., Musser, R. O., Felton, G. W., & Korth, K. L. (2006) · Plant Molecular Biology · doi:10.1007/s11103-005-4923-y · Cited by 174 · see citing works
Changing Pollinators as a Means of Escaping Herbivores
Kessler, D., Diezel, C., & Baldwin, I. T. (2010) · Current Biology · doi:10.1016/j.cub.2009.11.071 · Cited by 173 · see citing works
Atamian, H. S., Chaudhary, R., Cin, V. D., Bao, E., Girke, T., & Kaloshian, I. (2012) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-06-12-0144-fi · Cited by 173 · see citing works
Williams, K. S., & Gilbert, L. E. (1981) · Science · doi:10.1126/science.212.4493.467 · Cited by 172 · see citing works
Prince, D. C., Drurey, C., Zipfel, C., & Hogenhout, S. A. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.235598 · Cited by 169 · see citing works
Kang, J.-H., Liu, G., Shi, F., Jones, A. D., Beaudry, R. M., & Howe, G. A. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.160192 · Cited by 168 · see citing works
A gene horizontally transferred from bacteria protects arthropods from host plant cyanide poisoning
Wybouw, N., Dermauw, W., Tirry, L., Stevens, C. V., Grbić, M., Feyereisen, R., & Leeuwen, T. V. (2014) · eLife · doi:10.7554/elife.02365 · Cited by 164 · see citing works
Singh, V., Louis, J., Ayre, B. G., Reese, J. C., & Shah, J. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04583.x · Cited by 163 · 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
Casteel, C. L., Alwis, M. D., Bak, A., Dong, H., Whitham, S. A., & Jander, G. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.00332 · Cited by 160 · see citing works
Insect oral secretions suppress wound-induced responses in Arabidopsis
Consales, F., Schweizer, F., Erb, M., Gouhier‐Darimont, C., Bodenhausen, N., Bruessow, F., Sobhy, I. S., & Reymond, P. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err308 · Cited by 154 · see citing works
Self-citationA burst of ABC genes in the genome of the polyphagous spider mite Tetranychus urticae
Dermauw, W., Osborne, E. J., Clark, R. M., Grbić, M., Tirry, L., & Leeuwen, T. V. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-317 · Cited by 153 · see citing works
New fatty acid amides from regurgitant of Lepidopteran (Noctuidae, Geometridae) caterpillars
Pohnert, G., Jung, V., Haukioja, E., Lempa, K., & Boland, W. (1999) · Tetrahedron · doi:10.1016/s0040-4020(99)00639-0 · Cited by 152 · see citing works
Bricchi, I., Leitner, M., Foti, M., Mithöfer, A., Boland, W., & Maffei, M. E. (2010) · Planta · doi:10.1007/s00425-010-1203-0 · Cited by 150 · see citing works
A Secreted MIF Cytokine Enables Aphid Feeding and Represses Plant Immune Responses
Naessens, É., Dubreuil, G., Giordanengo, P., Baron, O. L., Kebdani-Minet, N., Keller, H., & Coustau, C. (2015) · Current Biology · doi:10.1016/j.cub.2015.05.047 · Cited by 149 · see citing works
Gall Midges (Hessian Flies) as Plant Pathogens
Stuart, J. J., Chen, M., Shukle, R. H., & Harris, M. O. (2012) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-072910-095255 · Cited by 149 · see citing works
Zhurov, V. V., Navarro, M., Bruinsma, K. A., Arbona, V., Santamaria, M. E., Cazaux, M., Wybouw, N., Osborne, E. J., Ens, C., Rioja, C., et al. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.231555 · Cited by 147 · see citing works
Long distance run in the wound response – jasmonic acid is pulling ahead
Stratmann, J. W. (2003) · Trends in Plant Science · doi:10.1016/s1360-1385(03)00106-7 · Cited by 147 · see citing works
Perception, signaling and molecular basis of oviposition-mediated plant responses
Reymond, P. (2013) · Planta · doi:10.1007/s00425-013-1908-y · Cited by 147 · see citing works
Self-citationVillarroel, C. A., Jonckheere, W., Alba, J. M., Glas, J. J., Dermauw, W., Haring, M. A., Leeuwen, T. V., Schuurink, R. C., & Kant, M. R. (2016) · The Plant Journal · doi:10.1111/tpj.13152 · Cited by 146 · see citing works
The squeeze cell hypothesis for the activation of jasmonate synthesis in response to wounding
Farmer, E. E., Gasperini, D., & Acosta, I. F. (2014) · New Phytologist · doi:10.1111/nph.12897 · Cited by 145 · see citing works
A Plasma Membrane Protein from Zea mays Binds with the Herbivore Elicitor Volicitin
Truitt, C. L., Wei, H., & Paré, P. W. (2004) · The Plant Cell · doi:10.1105/tpc.017723 · Cited by 145 · see citing works
Induced Jasmonate Signaling Leads to Contrasting Effects on Root Damage and Herbivore Performance
Lu, J., Robert, C. A. M., Riemann, M., Cosme, M., Mène‐Saffrané, L., Codina, J. M., Stout, M. J., Lou, Y., Gershenzon, J., & Erb, M. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.252700 · Cited by 141 · see citing works
Holzinger, F., & Wink, M. (1996) · Journal of Chemical Ecology · doi:10.1007/bf02028512 · Cited by 140 · see citing works
Behavior and biology of the tomato psyllid, Bactericerca cockerelli, in response to the Mi‐1.2 gene
Casteel, C. L., Walling, L. L., & Paine, T. D. (2006) · Entomologia Experimentalis et Applicata · doi:10.1111/j.1570-8703.2006.00458.x · Cited by 139 · see citing works
Root-Feeding Insects and Their Interactions with Organisms in the Rhizosphere
Johnson, S. N., & Rasmann, S. (2015) · Annual Review of Entomology · doi:10.1146/annurev-ento-010814-020608 · Cited by 139 · see citing works
Intensified agriculture favors evolved resistance to biological control
Tomasetto, F., Tylianakis, J. M., Reale, M., Wratten, S. D., & Goldson, S. L. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1618416114 · Cited by 138 · see citing works
Biological targets of isothiocyanates
Brown, K., & Hampton, M. B. (2011) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2011.06.004 · Cited by 137 · see citing works
Synchronous coadaptation in an ancient case of herbivory
Becerra, J. X. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2133013100 · Cited by 137 · see citing works
Krempl, C., Sporer, T., Reichelt, M., Ahn, S., Heidel‐Fischer, H. M., Vogel, H., Heckel, D. G., & Joußen, N. (2016) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2016.02.005 · Cited by 135 · see citing works
Molecular strategies of plant defense and insect counter-defense
Zhu‐Salzman, K., Bi, J., & Liu, T. (2005) · Insect Science · doi:10.1111/j.1672-9609.2005.00002.x · Cited by 134 · see citing works
Excretion of Alkaloids by Malpighian Tubules of Insects
Maddrell, S. H. P., & Gardiner, B. O. C. (1976) · Journal of Experimental Biology · doi:10.1242/jeb.64.2.267 · Cited by 134 · see citing works
Lipase Activity in Insect Oral Secretions Mediates Defense Responses in Arabidopsis
Schäfer, M. K. H., Fischer, C., Meldau, S., Seebald, E., Oelmüller, R., & Baldwin, I. T. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.173567 · Cited by 134 · see citing works
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Erb, M., & Kliebenstein, D. J. (2020) · Plant Physiology · doi:10.1104/pp.20.00433 · Cited by 1,333 · see citing works
Molecular Interactions Between Plants and Insect Herbivores
Erb, M., & Reymond, P. (2019) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050718-095910 · Cited by 751 · see citing works
Self-citationThe role of volatiles in plant communication
Bouwmeester, H. J., Schuurink, R. C., Bleeker, P., & Schiestl, F. P. (2019) · The Plant Journal · doi:10.1111/tpj.14496 · Cited by 393 · see citing works
Endophytic Fungi: From Symbiosis to Secondary Metabolite Communications or Vice Versa?
Alam, B., Lǐ, J., Gě, Q., Khan, M. A., Gōng, J., Mehmood, S., Yuán, Y., & Gǒng, W. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.791033 · Cited by 282 · see citing works
Plant chitinases and their role in plant defense: A comprehensive review
Vaghela, B. D., Vashi, R., Rajput, K. N., & Joshi, R. G. (2022) · Enzyme and Microbial Technology · doi:10.1016/j.enzmictec.2022.110055 · Cited by 245 · see citing works
Molecular tug-of-war: Plant immune recognition of herbivory
Snoeck, S., Palacios, N. G., & Steinbrenner, A. D. (2022) · The Plant Cell · doi:10.1093/plcell/koac009 · Cited by 162 · see citing works
A Reference Genome Sequence for Giant Sequoia
Scott, A. D., Zimin, A. V., Puiu, D., Workman, R., Britton, M., Zaman, S., Caballero, M., Read, A. C., Bogdanove, A. J., Burns, E., et al. (2020) · G3 Genes Genomes Genetics · doi:10.1534/g3.120.401612 · Cited by 120 · see citing works
Plant Defenses Against Tetranychus urticae: Mind the Gaps
Santamaria, M. E., Arnáiz, A., Rosa‐Diaz, I., González‐Melendi, P., Romero‐Hernandez, G., Ojeda-Martinez, D., Garcia, A., Contreras, E., Martínez, M., & Dı́az, I. (2020) · Plants · doi:10.3390/plants9040464 · Cited by 107 · see citing works
Niu, J., Shen, G., Christiaens, O., Smagghe, G. J., He, L., & Wang, J. (2018) · Pest Management Science · doi:10.1002/ps.5071 · Cited by 83 · see citing works
Murali‐Baskaran, R. K., Mooventhan, P., Das, D., Dixit, A., Sharma, K. C., Senthil‐Nathan, S., Kaushal, P., & Ghosh, P. K. (2022) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2022.104912 · Cited by 79 · see citing works
Rethink RNAi in Insect Pest Control: Challenges and Perspectives
Niu, J., Taning, C. N. T., Christiaens, O., Smagghe, G. J., & Wang, J. (2018) · Advances in insect physiology · doi:10.1016/bs.aiip.2018.07.003 · Cited by 76 · see citing works
Plant defense resistance in natural enemies of a specialist insect herbivore
Zhang, X., van Doan, C., Arce, C. C. M., Hu, L., Grünig, S., Parisod, C., Hibbard, B. E., Hervé, M. R., Nielson, C., Robert, C. A. M., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1912599116 · Cited by 70 · see citing works
Favery, B., Dubreuil, G., Chen, M., Giron, D., & Abad, P. (2020) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-010820-012722 · Cited by 68 · see citing works
Ali, J., Tonğa, A., Islam, T., Mir, S. H., Mukarram, M., Konôpková, A., & Chen, R. (2024) · Frontiers in Plant Science · doi:10.3389/fpls.2024.1376917 · Cited by 66 · see citing works
Why Do Herbivorous Mites Suppress Plant Defenses?
Blaazer, C. J. H., Perez, E. V., Chafi, R., Leeuwen, T. V., Kant, M. R., & Schimmel, B. C. J. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.01057 · Cited by 65 · see citing works
Convergent molecular evolution among ash species resistant to the emerald ash borer
Kelly, L. J., Plumb, W. J., Carey, D. W., Mason, M. E., Cooper, E. D., Crowther, W., Whittemore, A. T., Rossiter, S. J., Koch, J. L., & Buggs, R. J. A. (2020) · Nature Ecology & Evolution · doi:10.1038/s41559-020-1209-3 · Cited by 59 · see citing works
Phosphatidylcholines from Pieris brassicae eggs activate an immune response in Arabidopsis
Stahl, E., Brillatz, T., Queiroz, E. F., Marcourt, L., Schmiesing, A., Hilfiker, O., Riezman, I., Riezman, H., Wolfender, J., & Reymond, P. (2020) · eLife · doi:10.7554/elife.60293 · Cited by 59 · see citing works
Self-citationAdaptive Plasticity of Insect Eggs in Response to Environmental Challenges
Hilker, M., Salem, H., & Fatouros, N. E. (2022) · Annual Review of Entomology · doi:10.1146/annurev-ento-120120-100746 · Cited by 56 · see citing works
Snoeck, S., Wybouw, N., Leeuwen, T. V., & Dermauw, W. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200585 · Cited by 56 · see citing works
Erb, M., & Kliebenstein, D. J. (2020) · Plant Physiology · doi:10.31219/osf.io/6ba7r · Cited by 51 · see citing works
Nilaparvata lugens salivary protein NlG14 triggers defense response in plants
Gao, H., Zou, J., Lin, X., Zhang, H., Yu, N., & Liu, Z. (2022) · Journal of Experimental Botany · doi:10.1093/jxb/erac354 · Cited by 50 · see citing works
Garantonakis, N., Pappas, M. L., Varikou, K., Skiada, V., Broufas, G. D., Kavroulakis, Ν., & Papadopoulou, K. Κ. (2018) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2018.00126 · Cited by 47 · see citing works
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Reymond, P. (2021) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2021.04.004 · Cited by 46 · see citing works
Self-citationHuang, J., Zhang, N., Shan, J., Peng, Y., Guo, J., Zhou, C., Shi, S., Zheng, X., Wu, D., Guan, W., et al. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.571280 · Cited by 42 · see citing works
Kallure, G. S., Kumari, A., Shinde, B. A., & Giri, A. P. (2021) · Phytochemistry · doi:10.1016/j.phytochem.2021.113008 · Cited by 39 · see citing works
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Schimmel, B. C. J., Alba, J. M., Wybouw, N., Glas, J. J., Meijer, T. T., Schuurink, R. C., & Kant, M. R. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19103265 · Cited by 35 · see citing works
Metabolomics‐driven investigation of plant defense response against pest and pathogen attack
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Kuai, P., Lin, N., Ye, M., Ye, M., Chen, L., Chen, S., Zu, H., Hu, L., Gatehouse, A. M. R., & Lou, Y. (2024) · Nature Food · doi:10.1038/s43016-024-01044-4 · Cited by 34 · see citing works
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Arena, G. D., Ramos‐González, P. L., Rogerio, L. A., Alves, M. R., Casteel, C. L., Freitas‐Astúa, J., & Machado, M. A. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.01147 · Cited by 34 · see citing works
Advances in molecular interactions between rice and insect herbivores
Kuai, P., & Lou, Y. (2024) · Crop Health · doi:10.1007/s44297-024-00027-y · Cited by 32 · see citing works
Stahl, E., Martin, A. F., Glauser, G., Guillou, M., Aubourg, S., Renou, J., & Reymond, P. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.852808 · Cited by 30 · see citing works
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Ribeiro, L. D. P., Santana, A. L., Filho, J. A. W., Tramontin, M. A., Almeida-Trapp, M., Mithöfer, A., & Nansen, C. (2018) · Plant Methods · doi:10.1186/s13007-018-0322-7 · Cited by 29 · see citing works
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Rosa‐Diaz, I., Rowe, J. H., López, A. C., Arbona, V., Dı́az, I., & Jones, A. M. (2024) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiae215 · Cited by 26 · see citing works
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Jin, M., Cheng, Y., Guo, X., Li, M., Chakrabarty, S., Liu, K., Wu, K., & Xiao, Y. (2020) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2020.103387 · Cited by 25 · see citing works
Dong, Y., Huang, X., Yang, Y., Li, J., Zhang, M., Shen, H., Ren, Y., Li, X., Tian, J., Shen, D., et al. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.912603 · Cited by 25 · see citing works
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Martínez, M., & Dı́az, I. (2024) · Plants · doi:10.3390/plants13091239 · Cited by 24 · see citing works
Secret Weapon of Insects: The Oral Secretion Cocktail and Its Modulation of Host Immunity
Prajapati, V. K., Vijayan, V., & Vadassery, J. (2024) · Plant and Cell Physiology · doi:10.1093/pcp/pcae059 · Cited by 23 · see citing works
Wang, Y., Zhu, C., Chen, G., Li, X., Zhu, M., Alariqi, M., Hussian, A., Ma, W., Lindsey, K., Zhang, X., et al. (2024) · Advanced Science · doi:10.1002/advs.202407826 · Cited by 23 · see citing works
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Jia, M., Li, Q., Hua, J., Liu, J., Zhou, W., Qu, B., & Luo, S. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.580155 · Cited by 23 · see citing works
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Arnáiz, A., Rosa‐Diaz, I., Romero‐Puertas, M. C., Sandalio, L. M., & Dı́az, I. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2020.620086 · Cited by 20 · see citing works
Steinbrenner, A. D., Saldivar, E. V., Hodges, N., Palacios, N. G., Chaparro, A. F., & Schmelz, E. A. (2022) · The Plant Journal · doi:10.1111/tpj.15732 · Cited by 20 · see citing works
Shan, S., Huang, Y., Guo, C., Hu, B., Zhang, H., Li, Y., Chen, J., Wei, Z., & Sun, Z. (2023) · Molecular Plant Pathology · doi:10.1111/mpp.13323 · Cited by 18 · see citing works
Zheng, X., Yong, C., Zhao, L., Chen, Y., Zheng, L., Zheng, K., Mu, Y., Zhao, X., Gao, Y., & Zhang, J. (2019) · Arthropod-Plant Interactions · doi:10.1007/s11829-019-09683-2 · Cited by 18 · see citing works
Müller, N. A., Kersten, B., Fladung, M., & Schroeder, H. (2019) · BMC Genomics · doi:10.1186/s12864-019-6048-8 · Cited by 18 · see citing works
Hafeez, M., Li, X., Chen, L., Ullah, F., Huang, J., Zhang, Z., Zhang, J., Siddiqui, J. A., Zhou, S., Ren, X., et al. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1079442 · Cited by 18 · see citing works
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Kanda, Y., Shinya, T., Maeda, S., Mujiono, K., Hojo, Y., Tomita, K., Okada, K., Kamakura, T., Gális, I., & Mori, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210395 · Cited by 17 · see citing works
Yang, J., Wang, G., Zhou, Q., Lu, W., Ma, J., & Huang, J. (2019) · Experimental and Applied Acarology · doi:10.1007/s10493-019-00387-z · Cited by 17 · see citing works
Zhou, W., Jia, M., Zhang, G., Sun, J., Li, Q., Wang, X., Hua, J., & Luo, S. (2020) · Tree Physiology · doi:10.1093/treephys/tpaa132 · Cited by 17 · see citing works
Zhi, J., Liu, L., Hou, X., Xie, W., Yue, W., & Zeng, G. (2021) · Entomologia Experimentalis et Applicata · doi:10.1111/eea.13074 · Cited by 16 · see citing works
Plant Defense Genes against Biotic Stresses
Dı́az, I. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19082446 · Cited by 15 · see citing works
Plant defences for enhanced integrated pest management in tomato
Tortorici, S., Biondi, A., Pérez‐Hedo, M., Larbat, R., & Zappalà, L. (2022) · Annals of Applied Biology · doi:10.1111/aab.12750 · Cited by 14 · see citing works
Li, S., Li, H., Wang, J., Chen, C., & Hao, D. (2022) · Journal of Pest Science · doi:10.1007/s10340-022-01509-0 · Cited by 14 · see citing works
New insights into the transcriptional regulation of benzoxazinoid biosynthesis in wheat
Stahl, E. (2022) · Journal of Experimental Botany · doi:10.1093/jxb/erac244 · Cited by 14 · see citing works
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Reymond, P. (2022) · CHIMIA International Journal for Chemistry · doi:10.2533/chimia.2022.914 · Cited by 14 · see citing works
Self-citationPandharikar, G., Gatti, J., Simon, J., Frendo, P., & Poirié, M. (2020) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2020.1493 · Cited by 13 · see citing works
Ngom, B., Mamati, E. G., Goudiaby, M. F., Kimatu, J. N., Sarr, I., Diouf, D., & Kane, N. A. (2018) · Journal of Plant Interactions · doi:10.1080/17429145.2018.1473515 · Cited by 13 · see citing works
The involvement of cyclotides in mutual interactions of violets and the two-spotted spider mite
Ślązak, B., Jędrzejska, A., Badyra, B., Sybilska, A., Lewandowski, M., Kozak, M., Kapusta, M., Shariatgorji, M., Nilsson, A., Andrén, P. E., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-05461-y · Cited by 13 · see citing works
Plant biotic interactions: from conflict to collaboration
Glazebrook, J., & Roby, D. (2018) · The Plant Journal · doi:10.1111/tpj.13812 · Cited by 13 · see citing works
Zhou, J., Yin, Z., Shen, D., Zhang, Q., OYang, Y., Li, X., Ma, Y., Ding, L., Pei, Y., Ai, G., et al. (2024) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiae468 · Cited by 12 · see citing works
Samal, I., Dhillon, M. K., & Singh, N. (2021) · The Indian Journal of Agricultural Sciences · doi:10.56093/ijas.v91i9.116085 · Cited by 12 · see citing works
Caarls, L., Bassetti, N., Verbaarschot, P., Mumm, R., van Loon, J. J. A., Schranz, M. E., & Fatouros, N. E. (2023) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2022.1070859 · Cited by 12 · see citing works
Root-exuded specialized metabolites reduce arsenic toxicity in maize
Caggìa, V., Waelchli, J., Deslandes‐Hérold, G., Mateo, P., Robert, C. A. M., Guan, H., Bigalke, M., Spielvogel, S., Mestrot, A., Schlaeppi, K., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2314261121 · Cited by 12 · see citing works
Malik, M. A., Poveda, J., Zuluaga, D. L., Boccaccio, L., Hassan, Z., akram, M., & Ali, J. (2025) · Industrial Crops and Products · doi:10.1016/j.indcrop.2025.120945 · Cited by 11 · see citing works
An increased risk of parasitism mediated by the facultative symbiont Regiella insecticola
Luo, C., Gatti, J., Monticelli, L. S., Poirié, M., Desneux, N., Zhao, H., & Hu, Z. (2020) · Journal of Pest Science · doi:10.1007/s10340-019-01189-3 · Cited by 11 · see citing works
Lawrence, S. D., Novak, N. G., Shao, J. Y., Ghosh, S. K. B., & Blackburn, M. B. (2020) · MicrobiologyOpen · doi:10.1002/mbo3.994 · Cited by 11 · see citing works
Ye, M., Kuai, P., Chen, S., Lin, N., Ye, M., Hu, L., & Lou, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222212182 · Cited by 11 · see citing works
Li, S., Li, H., Chen, C., & Hao, D. (2023) · BMC Genomics · doi:10.1186/s12864-023-09117-7 · Cited by 11 · see citing works
Mealybug salivary microbes inhibit induced plant defenses
Zhao, J., Liu, Y., Xu, S., Wang, J., Zhang, Z., Wang, M., Turlings, T. C. J., Zhang, P., & Zhou, A. (2023) · Pest Management Science · doi:10.1002/ps.7600 · Cited by 11 · see citing works
Arnáiz, A., Romero‐Puertas, M. C., Santamaria, M. E., Rosa‐Diaz, I., Arbona, V., Muñoz, A., Grbić, V., González‐Melendi, P., Castellano, M. M., Sandalio, L. M., et al. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102902 · Cited by 11 · see citing works
Liao, H., Zhou, Z., Liu, Y., Luo, Y., Zhang, C., Feng, Y., Shu, Y., & Wang, J. (2024) · European Journal of Agronomy · doi:10.1016/j.eja.2024.127118 · Cited by 11 · see citing works
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Barbier, M., Perrot, T., Salzet, G., Amusant, N., Dumarçay, S., Gérardin, P., Morel‐Rouhier, M., Sormani, R., & Gelhaye, É. (2020) · Journal of Natural Products · doi:10.1021/acs.jnatprod.0c00480 · Cited by 11 · see citing works
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Stahl, E., Maier, L.-P., & Reymond, P. (2023) · PLoS Pathogens · doi:10.1371/journal.ppat.1011072 · Cited by 10 · see citing works
Self-citationHost adaptation and specialization in Tetranychidae mites
Bruinsma, K. A., Rioja, C., Zhurov, V., Santamaria, M. E., Arbona, V., Navarro, M., Cazaux, M., Auger, P., Migeon, A., Wybouw, N., et al. (2023) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiad412 · Cited by 10 · see citing works
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Han, C., Su, H., Zhang, S., Jing, T., Liu, Z., & Yi-zhong, Y. (2022) · Insects · doi:10.3390/insects13040391 · Cited by 10 · see citing works
Wurlitzer, W. B., Labudda, M., da Silveira, J. A. G., Matthes, R. D., Schneider, J. R., & Ferla, N. J. (2024) · International Journal of Plant Biology · doi:10.3390/ijpb15030043 · Cited by 9 · see citing works
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Fuentes-Lopez, K., Olivero‐Verbel, J., & Caballero-Gallardo, K. (2025) · Journal of Pest Science · doi:10.1007/s10340-025-01953-8 · Cited by 9 · see citing works
Somers, D. J., Kushner, D. B., McKinnis, A. R., Mehmedovic, D., Flame, R. S., & Arnold, T. M. (2023) · PLoS ONE · doi:10.1371/journal.pone.0293075 · Cited by 9 · see citing works
Balakrishnan, D., Srivastava, V., & Kariyat, R. (2024) · Plant Stress · doi:10.1016/j.stress.2024.100667 · Cited by 8 · see citing works
Zhang, X., Zhu, X., Zhang, Y., Wu, Z., Fan, S., & Zhang, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113519 · Cited by 8 · see citing works
Early transcriptomic responses of rice leaves to herbivory by Spodoptera frugiperda
Leclerc, L., Nguyen, T. H., Duval, P., Mariotti, V., Petitot, A., Orjuela, J., Ogier, J.-C., Gaudriault, S., Champion, A., & Negre, N. N. (2024) · Scientific Reports · doi:10.1038/s41598-024-53348-x · Cited by 8 · see citing works
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Rosa‐Diaz, I., Santamaria, M. E., Acién, J. M., & Dı́az, I. (2023) · Plant Science · doi:10.1016/j.plantsci.2023.111784 · Cited by 8 · see citing works
Haeger, W., Wielsch, N., Shin, N. R., Gebauer-Jung, S., Pauchet, Y., & Kirsch, R. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.660430 · Cited by 8 · see citing works
Wu, S., Chen, L., Zhou, Y., Xiao, F., Liu, D., & Wang, Y. (2022) · Environmental Entomology · doi:10.1093/ee/nvac108 · Cited by 7 · see citing works
Changes in "natural antibiotic" metabolite composition during tetraploid wheat domestication
Ben-Abu, Y., & Itsko, M. (2021) · Scientific Reports · doi:10.1038/s41598-021-98764-5 · Cited by 7 · see citing works
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Chen, X., Peiffer, M. L., Tan, C., & Felton, G. W. (2020) · Arthropod-Plant Interactions · doi:10.1007/s11829-020-09767-4 · Cited by 7 · see citing works
Regulatory role of phytohormones in the interaction of plants with insect herbivores
Kundu, P., Bera, P., Mishra, S., & Vadassery, J. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-91886-2.00003-3 · Cited by 6 · see citing works
Molecular insights into stress-responsive genes in the mitigation of environmental stresses
Kumar, N., Verma, S., Kumar, A., Dasila, H., Suyal, D. C., Kumari, G., Rawat, S., Jeena, N., Singh, M., & Kumar, A. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99896-3.00005-9 · Cited by 6 · see citing works
Caarls, L., Bassetti, N., van Doesburg, F., Verbaarschot, P., van Loon, J. J. A., Schranz, M. E., & Fatouros, N. E. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.29.437462 · Cited by 6 · see citing works
Shangguan, L., Chen, R., Zhang, Y., Ye, S., Hong, C., Cui, H., Yu, H., Zuo, C., Pan, J., Hu, J., et al. (2025) · Molecular Plant Pathology · doi:10.1111/mpp.70112 · Cited by 5 · see citing works
Cell surface receptors integrate plant immunity, stress adaptation, and nutrient acquisition
Xie, Y., Shan, L., & He, P. (2026) · Trends in Plant Science · doi:10.1016/j.tplants.2026.04.013 · Cited by 5 · see citing works
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Dev, D., Sawant, S. B., Gupta, P. K., Bhargava, P., Singh, P., Nandni, S., Mishra, U. N., Sankarganesh, E., & Ghatak, A. (2026) · Plant Science · doi:10.1016/j.plantsci.2026.113186 · Cited by 5 · see citing works
Host Plant Resistance to Insects in Vegetable Crops
Kumaraswamy, S., Nasif, S. O., Siddique, A. B., Karuppannasamy, A., Chowdary, R., Mohan, M., & Chaitanya, A. K. (2024) · Springer eBooks · doi:10.1007/978-981-99-7520-4_9 · Cited by 5 · see citing works
Śmigała, M., Winiarczyk, K., Dąbrowska, A., Domaciuk, M., & Gancarz, M. (2021) · Sensors · doi:10.3390/s21062209 · Cited by 5 · see citing works
Avoidance of previously infested cabbage by MEAM1 cryptic species of Bemisia tabaci species complex
Hu, J., Lu, J., Yang, N., Liu, B., Fu, P., Yang, J., Zhang, Y., & Jiao, X. (2022) · Journal of Pest Science · doi:10.1007/s10340-022-01480-w · Cited by 5 · see citing works
Genetic Warfare: The Plant Genome's Role in Fending Off Insect Invaders
Alam, A., Abbas, S., Waheed, N., Abbas, A., Qin, W., Huang, J., Khan, K. A., Ghramh, H. A., Ali, J., & Zhao, C. R. (2024) · Archives of Insect Biochemistry and Physiology · doi:10.1002/arch.70021 · Cited by 5 · see citing works
Plant defense resistance in natural enemies of a specialist insect herbivorePreprint
Zhang, X., van Doan, C., Arce, C. C. M., Hu, L., Grünig, S., Parisod, C., Hibbard, B. E., Hervé, M. R., Robert, C. A. M., Machado, R. A. R., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/710681 · Cited by 5 · see citing works
Qiu, C., Jin, X., Zhao, Y., Kuai, P., & Lou, Y. (2024) · Plants · doi:10.3390/plants13233275 · Cited by 4 · see citing works
Yu, S., Li, S., Li, J., Wang, C., Yang, L., Li, J., Meng, Y. D., Tan, X., Jing, M., Luo, G., et al. (2025) · Plant Cell & Environment · doi:10.1111/pce.15386 · Cited by 4 · see citing works
Gholami, N., Aleosfoor, M., Hosseini, M., & Fekrat, L. (2021) · Biocontrol Science and Technology · doi:10.1080/09583157.2021.2009771 · Cited by 4 · see citing works
- Authors
- Stahl, E., Hilfiker, O., & Reymond, P.
- Affiliations
- University of Lausanne (CH)
- Corresponding author
- Reymond, Philippe
- Venue
- The Plant Journal
- Publisher
- Wiley
- Published
- 2017-12-20
- Volume
- 93
- Issue
- 4
- Pages
- 703-728
- ISSN
- 0960-7412 (ISSN-L)
- 1365-313X
- OpenAlex
- W2770133701
- Cited by
- 164
- References
- 304
- Citations by year
- 2026: 10 · 2025: 18 · 2024: 35 · 2023: 21 · 2022: 21 · 2021: 18 · 2020: 19 · 2019: 9 · 2018: 13
- FWCI
- 1.24
- Type
- journal article
- Language
- en
- Open access
- green
- serval.unil.ch
- Licence
- Locations
- The Plant Journal (publishedVersion)
- PubMed (publishedVersion)
- SERVAL (Université de Lausanne) (acceptedVersion, other-oa)
- IRIS (submittedVersion)
- Funders
- National Science Foundation
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (169278)
- Université de Lausanne
- Topics
- Life Sciences › Agricultural and Biological Sciences › Insect Science › Insect-Plant Interactions and Control
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant-Microbe Interactions and Immunity
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
- Keywords
- plant-arthropod interactions, herbivorous arthropods, plant defense response, chemical communication, plant volatiles, parasitoid attraction, effectors, plant defense gene expression, toxic metabolites
- MeSH terms
- Animals, Arthropods, Biological Evolution, Insecta, Plant Proteins, Plants, Plant Physiological Phenomena, Phytoplasma, Receptors, Pattern Recognition, Herbivory
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