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Fatty alcohols, a minor component of the tree tobacco surface wax, are associated with defence against caterpillar herbivory.
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- Author(s): Negin B;Negin B;Negin B; Shachar L; Shachar L; Meir S; Meir S; Ramirez CC; Ramirez CC; Rami Horowitz A; Rami Horowitz A; Rami Horowitz A; Rami Horowitz A; Jander G; Jander G; Aharoni A; Aharoni A
- Source:
Plant, cell & environment [Plant Cell Environ] 2024 Feb; Vol. 47 (2), pp. 664-681. Date of Electronic Publication: 2023 Nov 06.- Publication Type:
Journal Article- Language:
English - Source:
- Additional Information
- Source: Publisher: John Wiley & Sons Ltd Country of Publication: United States NLM ID: 9309004 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-3040 (Electronic) Linking ISSN: 01407791 NLM ISO Abbreviation: Plant Cell Environ Subsets: MEDLINE
- Publication Information: Publication: Hoboken, NJ : John Wiley & Sons Ltd.
Original Publication: Oxford, UK : Blackwell Scientific Publications - Subject Terms:
- Abstract: Despite decades of research resulting in a comprehensive understanding of epicuticular wax metabolism, the function of these almost ubiquitous metabolites in plant-herbivore interactions remains unresolved. In this study, we examined the effects of CRISPR-induced knockout mutations in four Nicotiana glauca (tree tobacco) wax metabolism genes. These mutations cause a wide range of changes in epicuticular wax composition, leading to altered interactions with insects and snails. Three interaction classes were examined: chewing herbivory by seven caterpillars and one snail species, phloem feeding by Myzus persicae (green peach aphid) and oviposition by Bemisia tabaci (whitefly). Although total wax load and alkane abundance did not affect caterpillar growth, a correlation across species, showed that fatty alcohols, a minor component of N. glauca surface waxes, negatively affected the growth of both a generalist caterpillar (Spodoptera littoralis) and a tobacco-feeding specialist (Manduca sexta). This negative correlation was overshadowed by the stronger effect of anabasine, a nicotine isomer, and was apparent when fatty alcohols were added to an artificial lepidopteran diet. By contrast, snails fed more on waxy leaves. Aphid reproduction and feeding activity were unaffected by wax composition but were potentially affected by altered cutin composition. Wax crystal morphology could explain the preference of B. tabaci to lay eggs on waxy wild-type plants relative to both alkane and fatty alcohol-deficient mutants. Together, our results suggest that the varied responses among herbivore classes and species are likely to be a consequence of the co-evolution that shaped the specific effects of different surface wax components in plant-herbivore interactions.
(© 2023 The Authors. Plant, Cell & Environment published by John Wiley & Sons Ltd.) - References: Aarts, M.G.M., Keijzer, C.J., Stiekema, W.J., Pereira, A., Aarts, M.G., Keijzer, C.J. et al. (1995) Molecular characterization of the CER1 gene of Arabidopsis involved in epicuticular wax biosynthesis and pollen fertility. The Plant Cell, 7, 2115-2127.
Adasme-Carreño, F., Muñoz-Gutiérrez, C., Salinas-Cornejo, J. & Ramírez, C.C. (2015) A2EPG: a new software for the analysis of electrical penetration graphs to study plant probing behaviour of hemipteran insects. Computers and Electronics in Agriculture, 113, 128-135.
Aharoni, A., Dixit, S., Jetter, R., Thoenes, E., van Arkel, G. & Pereira, A. (2004) The SHINE clade of AP2 domain transcription factors activates wax biosynthesis, alters cuticle properties, and confers drought tolerance when overexpressed in Arabidopsis. The Plant Cell, 16, 2463-2480.
Alcerito, T., Barbo, F.E., Negri, G., Santos, D.Y.A.C., Meda, C.I., Young, M.C.M. et al. (2002) Foliar epicuticular wax of Arrabidaea brachypoda: flavonoids and antifungal activity. Biochemical Systematics and Ecology, 30, 677-683.
Ali, J.G. & Agrawal, A.A. (2012) Specialist versus generalist insect herbivores and plant defense. Trends in Plant Science, 17, 293-302.
Altesor, P., García, Á., Font, E., Rodríguez-Haralambides, A., Vilaró, F., Oesterheld, M. et al. (2014) Glycoalkaloids of wild and cultivated solanum: effects on specialist and generalist insect herbivores. Journal of Chemical Ecology, 40, 599-608.
Bach, L., Michaelson, L.V., Haslam, R., Bellec, Y., Gissot, L., Marion, J. et al. (2008) The very-long-chain hydroxy fatty acyl-CoA dehydratase PASTICCINO2 is essential and limiting for plant development. Proceedings of the National Academy of Sciences of the United States of America, 105, 14727-14731.
Barthlott, W. & Neinhuis, C. (1997) Purity of the sacred lotus, or escape from contamination in biological surfaces. Planta, 202, 1-8.
Beaudoin, F., Wu, X., Li, F., Haslam, R.P., Markham, J.E., Zheng, H. et al. (2009) Functional characterization of the Arabidopsis β-ketoacyl-coenzyme a reductase candidates of the fatty acid elongase. Plant Physiology, 150, 1174-1191.
Bergman, D.K., Dillwith, J.W., Zarrabi, A.A., Caddel, J.L. & Berberet, R.C. (1991) Epicuticular lipids of alfalfa relative to its susceptibility to spotted alfalfa aphids (Homoptera: Aphididae). Environmental Entomology, 20, 781-785.
Bernaola, L., Butterfield, T.S., Tai, T.H. & Stout, M.J. (2021) Epicuticular wax rice mutants show reduced resistance to rice water weevil (Coleoptera: Curculionidae) and fall armyworm (Lepidoptera: Noctuidae). Environmental Entomology, 50, 948-957.
Bewick, T.A., Shilling, D.G. & Querns, R. (1993) Evaluation of epicuticular wax removal from whole leaves with chloroform. Weed Technology, 7, 706-716.
Bourdenx, B., Bernard, A., Domergue, F., Pascal, S., Léger, A., Roby, D. et al. (2011) Overexpression of Arabidopsis ECERIFERUM1 promotes wax very-long-chain alkane biosynthesis and influences plant response to biotic and abiotic stresses. Plant Physiology, 156, 29-45.
Chen, X., Goodwin, S.M., Boroff, V.L., Liu, X. & Jenks, M.A. (2003) Cloning and characterization of the WAX2 gene of Arabidopsis involved in cuticle membrane and wax production. The Plant Cell, 15, 1170-1185.
Clarke, J.M. & Richards, R.A. (1988) The effects of glaucousness, epicuticular wax, leaf age, plant height, and growth environment on water loss rates of excised wheat leaves. Canadian Journal of Plant Science, 68, 975-982.
Cohen, H., Dong, Y., Szymanski, J., Lashbrooke, J., Meir, S., Almekias-Siegl, E. et al. (2019) A multilevel study of melon fruit reticulation provides insight into skin ligno-suberization hallmarks. Plant Physiology, 179, 1486-1501.
Cornell, H.V. & Hawkins, B.A. (2003) Herbivore responses to plant secondary compounds: a test of phytochemical coevolution theory. The American Naturalist, 161, 507-522.
Dahan-Meir, T., Filler-Hayut, S., Melamed-Bessudo, C., Bocobza, S., Czosnek, H., Aharoni, A. et al. (2018) Efficient in planta gene targeting in tomato using geminiviral replicons and the CRISPR/Cas9 system. The Plant Journal, 95, 5-16.
Daoust, S.P., Mader, B.J., Bauce, E., Despland, E., Dussutour, A. & Albert, P.J. (2010) Influence of epicuticular-wax composition on the feeding pattern of a phytophagous insect: implications for host resistance. The Canadian Entomologist, 142, 261-270.
Daszkowska-Golec, A. (2020) Degrade or silence?-RNA turnover takes control of epicuticular wax synthesis. Trends in Plant Science, 25, 950-952.
Edwards, P.B. (1982) Do waxes on eucalyptus leaves provide protection from grazing insects? Austral Ecology, 7, 347-352.
Eigenbrode, S.D. (2004) The effects of plant epicuticular waxy blooms on attachment and effectiveness of predatory insects. Arthropod Structure & Development, 33, 91-102.
Eigenbrode, S.D. & Espelie, K.E. (1995) Effects of plant epicuticular lipids on insect herbivores. Annual Review of Entomology, 40, 171-194.
Fauser, F., Schiml, S. & Puchta, H. (2014) Both CRISPR/Cas-based nucleases and nickases can be used efficiently for genome engineering in Arabidopsis thaliana. The Plant Journal, 79, 348-359.
Federle, W., Maschwitz, U., Fiala, B., Riederer, M. & Hölldobler, B. (1997) Slippery ant-plants and skilful climbers: selection and protection of specific ant partners by epicuticular wax blooms in Macaranga (Euphorbiaceae). Oecologia, 112, 217-224.
Gog, L., Vogel, H., Hum-Musser, S., Tuter, J. & Musser, R. (2014) Larval Helicoverpa zea transcriptional, growth and behavioral responses to nicotine and Nicotiana tabacum. Insects, 5, 668-688.
Greer, S., Wen, M., Bird, D., Wu, X., Samuels, L., Kunst, L. et al. (2007) The cytochrome P450 enzyme CYP96A15 is the midchain alkane hydroxylase responsible for formation of secondary alcohols and ketones in stem cuticular wax of Arabidopsis. Plant Physiology, 145, 653-667.
Guo, Y., Li, J.J., Busta, L. & Jetter, R. (2018) Coverage and composition of cuticular waxes on the fronds of the temperate ferns Pteridium aquilinum, Cryptogramma crispa, Polypodium glycyrrhiza, Polystichum munitum and Gymnocarpium dryopteris. Annals of Botany, 122, 555-568.
Hegebarth, D. & Jetter, R. (2017) Cuticular waxes of Arabidopsis thaliana shoots: cell-type-specific composition and biosynthesis. Plants, 6, 27.
Huesing, J.E. & Jones, D. (1987) A new form of antibiosis in nicotiana. Phytochemistry, 26, 1381-1384.
Islam, M.A., Du, H., Ning, J., Ye, H. & Xiong, L. (2009) Characterization of Glossy1-homologous genes in rice involved in leaf wax accumulation and drought resistance. Plant Molecular Biology, 70, 443-456.
Jaime, C., Muchut, S.E., Reutemann, A.G., Gieco, J.O. & Dunger, G. (2020) Morphological changes, alteration of photosynthetic parameters and chlorophyll production induced by infection with alfalfa dwarf virus in Medicago sativa plants. Plant Pathology, 69, 393-402.
Johnson, A. & Severson, R. (1984) Leaf surface chemistry of tobacco budworm resistant tobacco. Journal of Agricultural Entomology, 1, 23-32.
Karmakar, A., Malik, U. & Barik, A. (2016) Effects of leaf epicuticular wax compounds from Solena amplexicaulis (Lam.) gandhi on olfactory responses of a generalist insect herbivore. Allelopathy Journal, 37, 253-272.
Koch, K. & Ensikat, H.J. (2008) The hydrophobic coatings of plant surfaces: epicuticular wax crystals and their morphologies, crystallinity and molecular self-assembly. Micron, 39, 759-772.
Kong, L., Liu, Y., Zhi, P., Wang, X., Xu, B., Gong, Z. et al. (2020) Origins and evolution of cuticle biosynthetic machinery in land plants. Plant Physiology, 184, 1998-2010.
Koornneef, M., Hanhart, C.J. & Thiel, F. (1989) A genetic and phenotypic description of Eceriferum (cer) mutants in Arabidopsis thaliana. Journal of Heredity, 80, 118-122.
Korenblum, E., Dong, Y., Szymanski, J., Panda, S., Jozwiak, A., Massalha, H. et al. (2020) Rhizosphere microbiome mediates systemic root metabolite exudation by root-to-root signaling. Proceedings of the National Academy of Sciences of the United States of America, 117, 3874-3883.
Lange, H., Ndecky, S.Y.A., Gomez-Diaz, C., Pflieger, D., Butel, N., Zumsteg, J. et al. (2019) RST1 and RIPR connect the cytosolic RNA exosome to the ski complex in Arabidopsis. Nature Communications, 10, 3871.
Lee, S.B. & Suh, M.C. (2015) Advances in the understanding of cuticular waxes in Arabidopsis thaliana and crop species. Plant Cell Reports, 34, 557-572.
Lei, Y., Lu, L., Liu, H.-Y., Li, S., Xing, F. & Chen, L.-L. (2014) CRISPR-P: a web tool for synthetic single-guide RNA design of CRISPR-system in plants. Molecular Plant, 7, 1494-1496.
Li, G. & Ishikawa, Y. (2006) Leaf epicuticular wax chemicals of the Japanese knotweed Fallopia japonica as oviposition stimulants for Ostrinia latipennis. Journal of Chemical Ecology, 32, 595-604.
Li, F., Wu, X., Lam, P., Bird, D., Zheng, H., Samuels, L. et al. (2008) Identification of the wax ester synthase/acyl-coenzyme a: diacylglycerol acyltransferase WSD1 required for stem wax ester biosynthesis in Arabidopsis. Plant Physiology, 148, 97-107.
Long, L.M., Patel, H.P., Cory, W.C. & Stapleton, A.E. (2003) The maize epicuticular wax layer provides UV protection. Functional Plant Biology, 30, 75-81.
Lü, S., Song, T., Kosma, D.K., Parsons, E.P., Rowland, O. & Jenks, M.A. (2009) Arabidopsis CER8 encodes LONG-CHAIN ACYL-COA SYNTHETASE 1 (LACS1) that has overlapping functions with LACS2 in plant wax and cutin synthesis. The Plant Journal, 59, 553-564.
Markstädter, C., Federle, W., Jetter, R., Riederer, M. & Hölldobler, B. (2000) Chemical composition of the slippery epicuticular wax blooms on macaranga (Euphorbiaceae) ant-plants. Chemoecology, 10, 33-40.
Mayeux, H.S., Jordan, W.R., Meyer, R.E. & Meola, S.M. (1981) Epicuticular wax on goldenweed (Isocoma spp.) leaves: variation with species and season. Weed Science, 29, 389-393.
Millar, A.A., Clemens, S., Zachgo, S., Giblin, E.M., Taylor, D.C. & Kunst, L. (1999) CUT1, an Arabidopsis gene required for cuticular wax biosynthesis and pollen fertility, encodes a very-long-chain fatty acid condensing enzyme. The Plant Cell, 11, 825-838.
Millar, A.A. & Kunst, L. (1997) Very-long-chain fatty acid biosynthesis is controlled through the expression and specificity of the condensing enzyme. The Plant Journal, 12, 121-131.
Mori, M. (1982) N-Hexacosanol and n-octacosanol: feeding stimulants for larvae of the silkworm, Bombyx mori. Journal of Insect Physiology, 28, 969-973.
Mortimer, C.L., Bramley, P.M. & Fraser, P.D. (2012) The identification and rapid extraction of hydrocarbons from Nicotiana glauca: a potential advanced renewable biofuel source. Phytochemistry Letters, 5, 455-458.
Mozo, T. & Hooykaas, J.J. (1992) Factors affecting the rate of T-DNA transfer from Agrobacterium tumefaciens to Nicotiana glauca plant cells. Plant Molecular Biology, 19, 1019-1030.
Negin, B., Hen-Avivi, S., Almekias-Siegl, E., Shachar, L., Jander, G. & Aharoni, A. (2023) Tree tobacco (Nicotiana glauca) cuticular wax composition is essential for leaf retention during drought, facilitating a speedy recovery following rewatering. New Phytologist, 237, 1574-1589.
Ohnmeiss, T.E. & Baldwin, I.T. (2000) Optimal defense theory predicts the ontogeny of an induced nicotine defense. Ecology, 81, 1765-1783.
Oros, D.R., Standley, L.J., Chen, X. & Simoneit, B.R.T. (1999) Epicuticular wax compositions of predominant conifers of Western North America. Zeitschrift für Naturforschung C, 54, 17-24.
Oshima, Y., Shikata, M., Koyama, T., Ohtsubo, N., Mitsuda, N. & Ohme-Takagi, M. (2013) MIXTA-like transcription factors and WAX INDUCER1/SHINE1 coordinately regulate cuticle development in Arabidopsis and Torenia fournieri. The Plant Cell, 25, 1609-1624.
Petschenka, G. & Agrawal, A.A. (2015) Milkweed butterfly resistance to plant toxins is linked to sequestration, not coping with a toxic diet. Proceedings of the Royal Society B: Biological Sciences, 282, 20151865.
Pollard, M., Beisson, F., Li, Y. & Ohlrogge, J.B. (2008) Building lipid barriers: biosynthesis of cutin and suberin. Trends in Plant Science, 13, 236-246.
Proctor, M.C.F. (1979) Surface wax on the leaves of some mosses. Journal of Bryology, 10, 531-538.
Rahim Khan, M., Ghani, I.A., Rafique Khan, M., Ghaffar, A. & Tamkeen, A. (2011) Host plant selection and oviposition behaviour of whitefly Bemisia tabaci (Gennadius) in a mono and simulated polyculture crop habitat. African Journal of Biotechnology, 10, 1467-1472.
Ramsey, J.S., Elzinga, D.A., Sarkar, P., Xin, Y.R., Ghanim, M. & Jander, G. (2014) Adaptation to nicotine feeding in Myzus persicae. Journal of Chemical Ecology, 40, 869-877.
Ramsey, J.S., Wilson, A.C., de Vos, M., Sun, Q., Tamborindeguy, C., Winfield, A. et al. (2007) Genomic resources for Myzus persicae: EST sequencing, SNP identification, and microarray design. BMC Genomics, 8, 423.
Rid, M., Markheiser, A., Hoffmann, C. & Gross, J. (2018) Waxy bloom on grape berry surface is one important factor for oviposition of european grapevine moths. Journal of Pest Science, 91, 1225-1239.
Riederer, M. & Schreiber, L. (2001) Protecting against water loss: analysis of the barrier properties of plant cuticles. Journal of Experimental Botany, 52, 2023-2032.
Roth-Nebelsick, A., Fernández, V., Peguero-Pina, J.J., Sancho-Knapik, D. & Gil-Pelegrín, E. (2013) Stomatal encryption by epicuticular waxes as a plastic trait modifying gas exchange in a Mediterranean evergreen species (Quercus coccifera L.). Plant, Cell & Environment, 36, 579-589.
Rowland, O., Zheng, H., Hepworth, S.R., Lam, P., Jetter, R. & Kunst, L. (2006) CER4 encodes an alcohol-forming fatty acyl-coenzyme A reductase involved in cuticular wax production in Arabidopsis. Plant Physiology, 142, 866-877.
Saleem, M., Gopalakrishna, N.K., Tippannavar, P.S. & Nadaf, H.l. (2019) Biophysical and biochemical mechanism of resistance to Spodoptera litura in groundnut (Arachis hypogaea L.). Journal of Entomology and Zoology Studies, 7, 86-96.
Sarria, E., Cid, M., Garzo, E. & Fereres, A. (2009) Excel workbook for automatic parameter calculation of EPG data. Computers and Electronics in Agriculture, 67, 35-42.
Sarrion-Perdigones, A., Vazquez-Vilar, M., Palaci, J., Castelijns, B., Forment, J., Ziarsolo, P. et al. (2013) GoldenBraid 2.0: a comprehensive DNA assembly framework for plant synthetic biology. Plant Physiology, 162, 1618-1631.
Schnurr, J., Shockey, J. & Browse, J. (2004) The Acyl-CoA synthetase encoded by LACS2 is essential for normal cuticle development in Arabidopsis. The Plant Cell, 16, 629-642.
Schreiber, L. (2010) Transport barriers made of cutin, suberin and associated waxes. Trends in Plant Science, 15, 546-553.
Self, L.S., Guthrie, F.E. & Hodgson, E. (1964) Adaptation of tobacco hornworms to the ingestion of nicotine. Journal of Insect Physiology, 10, 907-914.
Seo, P.J., Lee, S.B., Suh, M.C., Park, M.J., Go, Y.S. & Park, C.M. (2011) The MYB96 transcription factor regulates cuticular wax biosynthesis under drought conditions in Arabidopsis. The Plant Cell, 23, 1138-1152.
Shepherd, T., Robertson, G.W., Griffiths, D.W. & Birch, A.N.E. (1999) Epicuticular wax composition in relation to aphid infestation and resistance in red raspberry (Rubus idaeus L.). Phytochemistry, 52, 1239-1254.
Shitan, N., Hayashida, M. & Yazaki, K. (2015) Translocation and accumulation of nicotine via distinct spatio-temporal regulation of nicotine transporters in Nicotiana tabacum. Plant Signaling & Behavior, 10, 1035852.
Simpson, J.P. & Ohlrogge, J.B. (2016) A novel pathway for triacylglycerol biosynthesis is responsible for the accumulation of massive quantities of glycerolipids in the surface wax of bayberry (Myrica pensylvanica) fruit. The Plant Cell, 28, 248-264.
Städler, E. & Buser, H.R. (1984) Defense chemicals in leaf surface wax synergistically stimulate oviposition by a phytophagous insect. Experientia, 40, 1157-1159.
Steppuhn, A., Gase, K., Krock, B., Halitschke, R. & Baldwin, I.T. (2004) Nicotine's defensive function in nature. PLoS Biology, 2, e217.
Tjallingii, W.F. & Esch, T.H. (1993) Fine structure of aphid stylet routes in plant tissues in correlation with EPG signals. Physiological Entomology, 18, 317-328.
Udayagiri, S. & Mason, C.E. (1997) Epicuticular wax chemicals in Zea mays influence oviposition in Ostrinia nubilalis. Journal of Chemical Ecology, 23, 1675-1687.
Uematsu, H. & Sakanoshita, A. (1989) Possible role of cabbage leaf wax bloom in suppressing diamondback moth Plutella xylostella (Lepidoptera: Yponomeutidae) oviposition. Applied Entomology and Zoology, 24, 253-257.
Usadel, B., Tohge, T., Scossa, F., Sierro, N., Schmidt, M. & Vogel, A. et al. (2018) The genome and metabolome of the tobacco tree, nicotiana glauca: a potential renewable feedstock for the bioeconomy. bioRxiv, 351429.
Via, S. (1991) Specialized host plant performance of pea aphid clones is not altered by experience. Ecology, 72, 1420-1427.
Voelckel, C., Krügel, T., Gase, K., Heidrich, N., van Dam, N.M., Winz, R. et al. (2001) Anti-sense expression of putrescine N-methyltransferase confirms defensive role of nicotine in Nicotiana sylvestris against Manduca sexta. Chemoecology, 11, 121-126.
Wójcicka, A. (2013) Importance of epicuticular wax cover for plant/insect interactions: experiment with cereal aphids. Polish Journal of Ecology, 61, 183-186.
Zammit, M., Shoemake, C., Attard, E. & Azzopardi, L.M. (2014) The effects of anabasine and the alkaloid extract of Nicotiana glauca on lepidopterous larvae. International Journal of Biology, 6, 46.
Zheng, H., Rowland, O. & Kunst, L. (2005) Disruptions of the Arabidopsis enoyl-CoA reductase gene reveal an essential role for very-long-chain fatty acid synthesis in cell expansion during plant morphogenesis. The Plant Cell, 17, 1467-1481.
Žnidarčič, D., Valič, N. & Trdan, S. (2008) Epicuticular wax content in the leaves of cabbage (Brassica oleracea L. var. capitata) as a mechanical barrier against three insect pests. Acta Agriculturae Slovenica, 91, 361-370. - Grant Information: 2089/18 Israel Science Foundation; FR-36-2018 United States - Israel Binational Agricultural Research and Development Fund; United States - Israel Binational Science Foundation; 2020-76013-30896 U.S. Department of Agriculture; Weizmann Institute of Science; 2022-67012-36739 USDA postdoctoral fellowship
- Contributed Indexing: Keywords: Nicotiana glauca; epicuticular wax; insect herbivory; snail
- Accession Number: 0 (Fatty Alcohols)
0 (Waxes)
0 (Alkanes) - Publication Date: Date Created: 20231106 Date Completed: 20240104 Latest Revision: 20240304
- Publication Date: 20240304
- Accession Number: 10.1111/pce.14752
- Accession Number: 37927215
- Source:
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