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REFERENCESAgut, B., Gamir, J., Jaques, J. A., & Flors, V. (2016). Systemic resistance in citrus to Tetranychus urticae induced by conspecifics is transmitted by grafting and mediated by mobile amino acids. Journal of Experimental Botany, 67, 5711–5723.Ali, J. G., Alborn, H. T., Campos-Herrera, R., Kaplan, F., Duncan, L. W., Rodriguez-Saona, C., … Stelinski, L. L. (2012). Subterranean, herbivore-induced plant volatile increases biological control activity of multiple beneficial nematode species in distinct habitats. PLoS ONE, 7, 1–7.Ali, J. G., Alborn, H. T., & Stelinski, L. L. (2010). Subterranean herbivore-induced volatiles released by citrus roots upon feeding by Diaprepes abbreviatus recruit entomopathogenic nematodes. Journal of Chemical Ecology, 36, 361–368.Ali, J. G., Alborn, H. T., & Stelinski, L. L. (2011). Constitutive and induced subterranean plant volatiles attract both entomopathogenic and plant parasitic nematodes. Journal of Ecology, 99, 26–35.Aratchige, N. S., Lesna, I., & Sabelis, M. W. (2004). Below-ground plant parts emit herbivore-induced volatiles: Olfactory responses of a predatory mite to tulip bulbs infested by rust mites. Experimental and Applied Acarology, 33, 21–30.Aritua, V., Achor, D., Gmitter, F. G., Albrigo, G., & Wang, N. (2013). Transcriptional and microscopic analyses of citrus stem and root responses to Candidatus Liberibacter asiaticus infection. PLoS ONE, 8, 4–8.Barbercheck, M. E., Wang, J., & Hirsh, I. (1995). Host plant effects on entomopathogenic nematodes. Journal of Invertebrate Pathology, 66, 169–177.Bezemer, T. M., & Van Dam, N. M. (2005). Linking aboveground and belowground interactions via induced plant defenses. Trends in Ecology and Evolution, 20, 617–624.Bommarco, R., Kleijn, D., & Potts, S. G. (2013). Ecological intensification: Harnessing ecosystem services for food security. Trends in Ecology and Evolution, 28, 230–238.Cui, J., Jander, G., Racki, L. R., Kim, P. D., Pierce, N. E., & Ausubel, F. M. (2002). Signals involved in arabidopsis resistance to Trichoplusia ni Caterpillars induced by virulent and avirulent strains of the phytopathogen Pseudomonas syringae. Plant Physiology, 129, 551–564.daGraca, J. V., Douhan, G. W., Halbert, S. E., Keremane, M. L., Lee, R. F., Vidalakis, G., & Zhao, H. (2016). Huanglongbing: An overview of a complex pathosystem ravaging the world's citrus. Journal of Integrative Plant Biology, 58, 373–387.De Moraes, C. M., Mescher, M. C., & Tumlinson, J. H. (2001). Caterpillar-induced nocturnal plant volatiles repel conspecific females. Nature, 410, 577–580.Degenhardt, J., Hiltpold, I., Köllner, T. G., Frey, M., Gierl, A., Gershenzon, J., … Turlings, T. C. J. (2009). Restoring a maize root signal that attracts insect-killing nematodes to control a major pest. Proceedings of the National Academy of Sciences of the United States of America, 106, 13213–13218.Dicke, M. (2016). Plant phenotypic plasticity in the phytobiome: A volatile issue. Current Opinion in Plant Biology, 32, 17–23.Dicke, M., & Baldwin, I. T. (2010). The evolutionary context for herbivore-induced plant volatiles: Beyond the “cry for help”. Trends in Plant Science, 15, 167–175.Duncan, L. W., Graham, J. H., Zellers, J., Bright, D., Dunn, D. C., El-Borai, F. E., & Porazinska, D. L. (2007). Food web responses to augmenting the entomopathogenic nematodes in bare and animal manure-mulched soil. Journal of Nematology, 39, 176–189.Filgueiras, C. C., Willett, D. S., Junior, A. M., & Pareja, M. (2016). Stimulation of the salicylic acid pathway aboveground recruits entomopathogenic nematodes belowground. PLoS ONE, 1–10.Garcia-Lor, A., Curk, F., Snoussi-Trifa, H., Morillon, R., Ancillo, G., Luro, F., … Ollitrault, P. (2013). A nuclear phylogenetic analysis: SNPs, indels and SSRs deliver new insights into the relationships in the “true citrus fruit trees” group (Citrinae, Rutaceae) and the origin of cultivated species. Annals of Botany, 111, 1–19.Goldschmidt, E. E. (2014). Plant grafting: New mechanisms, evolutionary implications. Frontiers in Plant Science, 5, 1–9.Groen, S. C., Whiteman, N. K., Bahrami, A. K., Wilczek, A. M., Cui, J., Russell, J. A., … Pierce, N. E. (2013). Pathogen-triggered ethylene signaling mediates systemic-induced susceptibility to herbivory in Arabidopsis. The Plant cell, 25, 1–13.Hazir, S., Shapiro-Ilan, D. I., Hazir, C., Leite, L. G., Cakmak, I., & Olson, D. (2016). Multifaceted effects of host plants on entomopathogenic nematodes. Journal of Invertebrate Pathology, 135, 53–59.Heil, M., Ibarra-Laclette, E., Adame-Álvarez, R. M., Martínez, O., Ramirez-Chávez, E., Molina-Torres, J., & Herrera-Estrella, L. (2012). How plants sense wounds: Damaged-self recognition is based on plant-derived elicitors and induces octadecanoid signaling. PLoS One, 7, 1–9.Hiltpold, I., Baroni, M., Toepfer, S., Kuhlmann, U., & Turlings, T. C. J. (2010). Selective breeding of entomopathogenic nematodes for enhanced attraction to a root signal did not reduce their establishment or persistence after field release. Plant Signaling & Behavior, 5, 1450–1452.Huang, M., Sanchez-Moreiras, A. M., Abel, C., Sohrabi, R., Lee, S., Gershenzon, J., & Tholl, D. (2012). The major volatile organic compound emitted from Arabidopsis thaliana flowers, the sesquiterpene (E)-B-caryophyllene, is a defense against a bacterial pathogen. New Phytologist, 193, 997–1008.Jablonka, E. (2002). Information: Its interpretation, its inheritance, and its sharing. Philosophy of Science, 69, 578–605.Johnson, E. G., Wu, J., Bright, D. B., & Graham, J. H. (2013). Association of “Candidatus Liberibacter asiaticus” root infection, but not phloem plugging with root loss on huanglongbing-affected trees prior to appearance of foliar symptoms. Plant Physiology, 63, 290–298.Kaplan, I., Halitschke, R., Kessler, A., Sardanelli, S., & Denno, R. F. (2008). Constitutive and induced defenses to herbivory in above- and belowground plant tissues. Ecology, 89, 392–406.Kaya, H. K., & Stock, S. P. (1997). Techniques in insect nematology. In L.Lacey (Ed.), Manual of techniques in insect pathology (pp. 281–324). SanDiego, CA: Academic Press.Kessler, A., & Baldwin, I. T. (2000). Defensive function of herbivore-induced plant volatile emissions in nature. Science, 41, 415–450.Kim, J.-S., Sagaram, U. S., Burns, J. K., Li, J.-L., & Wang, N. (2009). Response of sweet orange (Citrus sinensis) to “Candidatus Liberibacter asiaticus” infection: Microscopy and microarray analyses. Phytopathology, 99, 50–57.Lapointe, S. L., & Shapiro, J. P. (1999). Effect of soil moisture on development of Diaprepes abbreviatus (Coleoptera: Curculionidae). Florida Entomologist, 82, 291–299.Liu, Y., Heying, E., & Tanumihardjo, S. A. (2012). History, global distribution, and nutritional importance of citrus fruits. Comprehensive Reviews in Food Science and Food Safety, 11, 530–545.Mann, R. S., Ali, J. G., Hermann, S. L., Tiwari, S., Pelz-Stelinski, K. S., Alborn, H. T., & Stelinski, L. L. (2012). Induced release of a plant-defense volatile “deceptively” attracts insect vectors to plants infected with a bacterial pathogen. PLoS Pathogens, 8, 1–13.Mauck, K. E., De Moraes, C. M., & Mescher, M. C. (2010). Deceptive chemical signals induced by a plant virus attract insect vectors to inferior hosts. Proceedings of the National Academy of Sciences of the United States of America, 107, 3600–3605.Mauck, K. E., Moraes, C. M. De, & Mescher, M. C. (2016). Effects of pathogens on sensory-mediated interactions between plants and insect vectors. Current Opinion in Plant Biology, 32, 53–61.Meiners, T., & Hilker, M. (1997). Host location in Oomyzus gallerucae (Hymenoptera: Eulophidae), an egg parasitoid of the elm leaf beetle Xanthogaleruca luteola (Coleoptera: Chrysomelidae). Oecologia, 112, 87–93.Metlen, K. L., Aschehoug, E. T., & Callaway, R. M. (2009). Plant behavioural ecology: Dynamic plasticity in secondary metabolites. Plant, Cell and Environment, 32, 641–653.Mumm, R., & Dicke, M. (2010a). Variation in natural plant products and the attraction of bodyguards involved in indirect plant defense. Canadian Journal of Zoology, 88, 628–667.Mumm, R., & Dicke, M. (2010b). Variation in natural plant products and the attraction of bodyguards involved in indirect plant defense. Canadian Journal of Zoology, 88, 628–667.Nwugo, C. C., Duan, Y., & Lin, H. (2013). Study on citrus response to huanglongbing highlights a down-regulation of defense-related proteins in lemon plants upon “Ca. Liberibacter asiaticus” infection. PLoS ONE, 8, 1–13.Ozawa, R., Arimura, G., Takabayashi, J., Shimoda, T., & Nishioka, T. (2000). Involvement of jasmonate- and salicylate-related signaling pathways for the production of specific herbivore-induced volatiles in plants. Plant & Cell Physiology, 41, 391–398.Pieterse, C. M. J., & Dicke, M. (2007). Plant interactions with microbes and insects: From molecular mechanisms to ecology. Trends in Plant Science, 12, 564–569.Preisser, E. L., Dugaw, C. J., Dennis, B., & Strong, D. R. (2006). Plant facilitation of a belowground predator. Ecology, 87, 1116–1123.Price, P. W., Bouton, C. E., Gross, P., McPheron, B. A., Thompson, J. N., & Weis, A. E. (1980). Interactions among three trophic levels: Influence of plants on interactions between insect herbivores and natural enemies. Annual Review of Ecology and Systematics, 11, 41–65.Rasmann, S., Ali, J. G., Helder, J., & van derPutten, W. H. (2012). Ecology and evolution of soil nematode chemotaxis. Journal of Chemical Ecology, 38, 615–628.Rasmann, S., Köllner, T. G., Degenhardt, J., Hiltpold, I., Toepfer, S., Kuhlmann, U., … Turlings, T. C. J. (2005). Recruitment of entomopathogenic nematodes by insect-damaged maize roots. Nature, 434, 732–737.Tatineni, S., Sagaram, U. S., Gowda, S., Robertson, C. J., Dawson, W. O., Iwanami, T., & Wang, N. (2008). In planta distribution of “Candidatus Liberibacter asiaticus” as revealed by polymerase chain reaction (PCR) and real-time PCR. Phytopathology, 98, 592–599.vanDam, N. M., Qiu, B.-L., Hordijk, C. A., Vet, L. E. M., & Jansen, J. J. (2010). Identification of biologically relevant compounds in aboveground and belowground induced volatile blends. Journal of Chemical Ecology, 36, 1006–1016.vanTol, R. W. H. M., van derSommen, A. T. C., Boff, M. I. C., vanBezooijen, J., Sabelis, M. W., & Smits, P. H. (2001). Plants protect their roots by alerting the enemies of grubs. Ecology Letters, 4, 292–294.Turlings, T. C. J., Hiltpold, I., & Rasmann, S. (2012). The importance of root-produced volatiles as foraging cues for entomopathogenic nematodes. Plant and Soil, 358, 51–60.Walling, L. L. L. L. (2000). The myriad plant responses to herbivores. Journal of Plant Growth Regulation, 19, 195–216.Willett, D. S., Alborn, H. T., Duncan, L. W., & Stelinski, L. L. (2015). Social networks of educated nematodes. Scientific Reports, 5, 14388.Wu, J., & Baldwin, I. T. (2009). Herbivory-induced signalling in plants: Perception and action. Plant, Cell & Environment, 32, 1161–1174.Zangerl, A. R., & Berenbaum, M. R. (1990). Furanocoumarin induction in wild parsnip: Evidence for an induced defense against herbivores. Ecology, 71, 1933–1940.Zarate, S. I., Kempema, L. A., & Walling, L. L. (2007). Silverleaf whitefly induces salicylic acid defenses and suppresses effectual jasmonic acid defenses. Plant Physiology, 143, 866–875.Zipfel, C. (2014). Plant pattern-recognition receptors. Trends in Immunology, 35, 345–351.
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Plants can defend themselves against herbivores through activation of defensive pathways and attraction of third-trophic-level predators and parasites. Trophic cascades that mediate interactions in the phytobiome are part of a larger dynamic including the pathogens of the plant itself, which are known to greatly influence plant defenses. As such, we investigated the impact of a phloem-limited bacterial pathogen, Candidatus Liberibacter asiaticus (CLas), in cultivated citrus rootstock on a well-studied belowground tritrophic interaction involving the attraction of an entomopathogenic nematode (EPN), Steinernema diaprepesi, to their root-feeding insect hosts, Diaprepes abbreviatus larvae. Using belowground olfactometers, we show how CLas infection interferes with this belowground interaction by similarly inducing the release of a C12 terpene, pregeijerene, and disconnecting the association of the terpene with insect presence. D. abbreviatus larvae that were not feeding but in the presence of a CLas-infected plant were more likely to be infected by EPN than those near uninfected plants. Furthermore, nonfeeding larvae associated with CLas-infected plants were just as likely to be infected by EPN as those near noninfected plants with D. abbreviatus larval damage. Larvae of two weevil species, D. abbreviatus and Pachnaeus litus, were also more attracted to plants with infection than to uninfected plants. D. abbreviatus larvae were most active when exposed to pregeijerene at a concentration of 0.1 µg/µl. We attribute this attraction to CLas-infected plants to the same signal previously thought to be a herbivore-induced plant volatile specifically induced by root-feeding insects, pregeijerene, by assessing volatiles collected from the roots of infected plants and uninfected plants with and without feeding D. abbreviatus. Synthesis. Phytopathogens can influence the structuring of soil communities extending to the third trophic level. Field populations of EPN may be less effective at host-finding using pregeijerene as a cue in citrus grove agroecosystems with high presence of CLas infection.
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Rivera, Monique J 1
; Pelz-Stelinski, Kirsten S 1 ; Martini, Xavier 2 ; Stelinski, Lukasz L 1
1 Entomology and Nematology Department, Citrus Research and Education Center, University of Florida, Lake Alfred, FL, USA
2 Entomology and Nematology Department, Citrus Research and Education Center, University of Florida, Lake Alfred, FL, USA; Entomology and Nematology Department, North Florida Research and Education Center, University of Florida, Quincy, FL, USA