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Santalum album–Host Plants Interaction: An Incomplete Story of Semi-Root Parasite


Affiliations
1 College of Forestry, Kerala Agricultural University, Thrissur 680 656, India
2 Bundhelkhand University, Jhansi 284 001, India
 

Sandal (Santalum album L.) is one of the most valuable hemiparasitic tree species cultivated for its scented heartwood and oil. The economic yield from sandal depends on the hosts associated with it. Previous studies show that the sandal–host interaction is related to certain physiological, genetic and molecular mechanisms that enable them to identify host plants, to grow invasively into the hosts, and to establish connections to withdraw water and other resources from the hosts. However, the understanding of these mechanisms is still very vague. Our observations from the three-month-old sandal seedlings–host interaction study revealed the complex and multifaceted character of the host–parasite signalling mechanism. Besides, we found numerous unsolved questions and a significant knowledge gap in this field. Therefore, this article aims to correlate and contrast our observations with previous findings and to deliver some key questions to bridge the knowledge gap in future research.

Keywords

Haustoria, HIFs, Host–Parasite Interaction, Santalum album.
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  • Kim, T. H., Ito, H., Hayashi, K., Hasegawa, T., Machiguchi, T. and Yoshida, T., Aromatic constituents from the heartwood of Santalum album L. Chem. Pharm. Bull., 2005, 53, 641–644.
  • Ochi, T., Shibata, H., Higuti, T., Kodama, K. H., Kusumi, T. and Takaishi, Y., Anti-Helicobacter pylori compounds from Santalum album. J. Nat. Prod., 2005, 68, 819–824.
  • Bhaskar, D., Viswanath, S. and Purushothaman, S., Sandal (Santalum album L.) conservation in southern India: a review of policies and their impacts. J. Trop. Agric., 2010, 48, 1–10.
  • Lu, J. K., Xu, D. P., Kang, L. H. and He, X. H., Host-species-dependent physiological characteristics of hemiparasite Santalum album in association with N2-fixing and non-N2-fixing hosts native to southern China. Tree Physiol., 2014, 34(9), 1006–1017; doi.org/10.1093/treephys/tpu073.
  • Pate, J. S., Haustoria in action: case studies of nitrogen acquisition by woody xylem-tapping hemiparasites from their hosts. Proto-plasma, 2001, 215, 204–217.
  • Bell, T. L. and Adams, M. A., Attack on all fronts: functional relationships between aerial and root parasitic plants and their woody hosts and consequences for ecosystems. Tree Physiol., 2011, 31, 3–15.
  • Yoshida, S., Cui, S., Ichihashi, Y. and Shirasu, K., The haustorium, a specialized invasive organ in parasitic plants. Annu. Rev. Plant Biol., 2016, 67, 643–667.
  • Westwood, J. H., Yoder, J. I., Timko, M. P. and Depamphilis, C. W., The evolution of parasitism in plants. Trends Plant Sci., 2010, 15, 227–235.
  • Radomiljac, A. M., McComb, J. A. and McGrath, J. F., Intermediate host influences on the root hemi-parasite Santalum album L. biomass partitioning. For. Ecol. Manage., 1999, 113, 143–153.
  • Press, M. C. and Phoenix, G. K., Impacts of parasitic plants on natural communities. New Phytol., 2005, 166(3), 737–751; doi:10.1111/j.1469-8137.2005.01358.x.
  • March, W. A. and Watson, D. M., Parasites boost productivity: effects of mistletoe on litterfall dynamics in a temperate Australian forest. Oecologia, 2007, 154(2), 339–347; http://www.jstor.org/stable/40213084.
  • Watson, D. M., Parasitic plants as facilitators: more Dryad than Dracula? J. Ecol., 2009, 97(6), 1151–1159.
  • Demey, A., De Frenne, P., Baeten, L., Verstraeten, G., Hermy, M., Boeckx, P. and Verheyen, K., The effects of hemiparasitic plant removal on community structure and seedling establishment in semi‐natural grasslands. J. Veg. Sci., 2015, 26(3), 409–420.
  • Těšitel, J., Mládek, J., Fajmon, K., Blažek, P. and Mudrák, O., Reversing expansion of Calamagrostis epigejos in a grassland biodiversity hotspot: Hemiparasitic rhinanthus major does a better job than increased mowing intensity. Appl. Veg. Sci., 2015, 21(1), 104–112.
  • Těšitel, J., Li, A. R., Knotková, K., McLellan, R., Bandaranayake, P. C. G. and Watson, D. M., The bright side of parasitic plants: what are they good for? Plant Physiol., 2021, 185(4), 1309–1324; doi:10.1093/plphys/kiaa069
  • Watson, M., Richard, C., McLellan, F. and Fontúrbel, E., Functional roles of parasitic plants in a warming world. Annu. Rev. Ecol. Evol. Syst., 2022, 53(1), 25–45.
  • Christopher, R., Clarke, M. P., Timko, J. I., Yoder, M. J. and Axtell, J. H., Westwood molecular dialog between parasitic plants and their hosts. Ann. Rev. Phytopathol., 2019, 57(1), 279–299.
  • Satoko, Y., Songkui, C., Yasunori, I. and Ken, S., The haustorium, a specialized invasive organ in parasitic plants. Ann. Rev. Plant Biol., 2016, 67(1), 643–667.
  • Nagaveni, H. C. and Vijayalakshmi, G., Growth performance of sandal (Santalum album L.) with different host species. Sandalwood Research Newsletter, 2003, vol. 18, pp. 1–4.
  • Annapurna, D., Rathore, T. S. and Joshi, G., Modern nursery practices in the production of quality seedlings of Indian sandalwood (Santalum album L.)-stage of host requirement and screening of primary host species. J. Sustain. For., 2006, 22, 33–55.
  • Barbour, L., Analysis of plant-host relationships in tropical sandalwood (Santalum album). Rural Industries Research and Development Corporation, 2008, p. 35.
  • Institute of Forest Genetics and Tree Breeding, Sandal (Santalum album Linn.). Envis Bulletin, 2012, p. 7.
  • Ouyang, Y., Zhang, X., Chen, Y., Teixeira da Silva, J. A. and Ma, G., Growth, photosynthesis and haustorial development of semiparasitic Santalum album L. penetrating into roots of three hosts: a comparative study. Trees, 2016, 30, 317–328; https://doi.org/10.1007/s00-468-015-1303-3.
  • Rocha, D., Ashokan, P. K., Santhoshkumar, A. V., Anoop, E. V. and Sureshkumar, P., Anatomy and functional status of haustoria in field grown sandalwood tree (Santalum album L.). Curr. Sci., 2017, 113, 130–133.
  • Cameron, D. D., Geniez, J. M., Seel, W. E. and Irving, L. J., Suppression of host photosynthesis by the parasitic plant Rhinanthus minor. Ann Bot., 2008, 101, 573–578.
  • Rümer, S., Cameron, D. D., Wacker, R., Hartung, W. and Jiang, F., An anatomical study of the haustoria of Rhinanthus minor attached to roots of different hosts. Flora: Morphol. Distrib. Funct. Ecol. Plants, 2007, 202, 194–200; https://doi.org/10.1016/j.flora.2006.07.002.
  • Jiang, F., Jeschke, W. D., Hartung, W. and Cameron, D. D., Does legume nitrogen fixation underpin host quality for the hemiparasitic plant Rhinanthus minor? J. Exp. Bot., 2008, 59, 917–925.
  • Hibberd, J. M., Quick, W. P., Press, M. C. and Scholes, J. D., The influence of the parasitic angiosperm Striga gesnerioides on the growth and photosynthesis of its host, Vigna unguiculata. J. Exp. Bot., 1996, 47, 507–512.
  • Watling, J. R. and Press, M. C., Impacts of infection by parasitic angiosperms on host photosynthesis. Plant Biol., 2001, 3, 244–250.
  • Cameron, D. D., Hwangbo, J. K., Keith, A. M., Geniez, J. M., Kraushaar, D., Rowntree, J. and Seel, W. E., Interactions between the hemiparasitic angiosperm Rhinanthus minor and its hosts: from the cell to the ecosystem. Folia Geobot., 2005, 40, 217–229.
  • Zhang, X., da Silva, J. A. T., Duan, J., Deng, R., Xu, X. and Ma, G., Endogenous hormone levels and anatomical characters of haustoria in Santalum album L. seedlings before and after attachment to the host. J. Plant Physiol., 2012, 169(9), 859–866.
  • Fisher, J. P., Phoenix, G. K., Childs, D. Z., Press, M. C., Smith, S. W., Pilkington, M. G. and Cameron, D. D., Parasitic plant litter input: a novel indirect mechanism influencing plant community structure. New Phytol., 2013, 198, 222–231.
  • Shen, H., Prider, J. N., Facelli, J. M. and Watling, J. R., The influence of the hemiparasitic angiosperm Cassytha pubescens on photosynthesis of its host Cytisus scoparius. Funct. Plant Biol., 2010, 37, 14–21.
  • Su, C., Liu, H., Wafula, E. K., Honaas, L., de Pamphilis, C. W. and Timko, M. P., SHR4z, a novel decoy effector from the haustorium of the parasitic weed Striga gesnerioides, suppresses host plant immunity. New Phytol., 2020, 226, 891–908.
  • Delavault, P., Are root parasitic plants like any other plant pathogens? New Phytol., 2020, 226, 641–643; https://doi.org/10.1111/nph.16504.
  • Flor, H. H., Inheritance of pathogenicity in Melampsora lini. Phytopathology, 1942, 32, 653–669.
  • Li, J. and Timko, M. P., Gene-for-gene resistance in striga-cowpea associations. Science, 2009, 325, 1094–1094; https://doi.org/10.1126/science.1174754.
  • Swarbrick, P. J., Huang, K., Liu, G., Slate, J., Press, M. C. and Scholes, J. D., Global patterns of gene expression in rice cultivars undergoing a susceptible or resistant interaction with the parasitic plant Striga hermonthica. New Phytol., 2008, 179, 515–529; https://doi.org/10.1111/j.1469-8137.2008.02484.x.
  • Yoshida, S. and Shirasu, K., Multiple layers of incompatibility to the parasitic witchweed, Striga hermonthica. New Phytol., 2009, 183, 180–189; https://doi.org/10.1111/j.1469-8137.2009.02840.x
  • Mutuku, J. M. et al., The WRKY45-dependent signaling pathway is required for resistance against Striga hermonthica parasitism. Plant Physiol., 2015, 168, 1152–1163; https://doi.org/10.1104/pp.114.256404.
  • Botanga, C. J. and Timko, M. P., Genetic structure and analysis of host and nonhost interactions of Striga gesnerioides (witchweed) from central Florida. Phytopathology, 2005, 95, 1166–1173.
  • Pérez‐de‐Luque, A. et al., Understanding Orobanche and Phelipanche–host plant interactions and developing resistance. Weed Res., 2009, 49, 8–22.
  • Bouwmeester, H., Li, C., Thiombiano, B., Rahimi, M. and Dong, L., Adaptation of the parasitic plant lifecycle: germination is controlled by essential host signaling molecules. Plant Physiol., 2021, 185, 1292–1308; https://doi.org/10.1093/plphys/kiaa066
  • Sahai, A. and Shivanna, K. R., Seed germination, seedling growth and haustorial induction in Santalum album, a semi-root parasite. Proc. Plant. Sci., 1984, 93, 571–580.
  • Nagaveni, H. C. and Srimathi, R. A., Germinative capacity of floating and sinking sandal seeds. Indian For., 1985, 111(8), 615–618.
  • Barrett, D. R. and John, E. F., Santalum album: kernel composition, morphological and nutrient characteristics of pre-parasitic seedlings under various nutrient regimes. Ann. Bot., 1997, 79(1), 59–66.
  • Meng, S., Ma, H. B., Li, Z. S., Yang, F. C., Wang, S. K. and Lu, J. K., Impacts of nitrogen on physiological interactions of the hemi-parasitic Santalum album and its N2-fixing host Dalbergia odorifera. Trees, 2021, 35(3), 1039–1051.
  • Li, Y. L., Study on introduction of Sandalwood (Santalum album L.). Science Press, Beijing, China, 2003.
  • Atsatt, P. R. and Strong, D. R., The population biology of annual grassland hemiparasites. ‘The host environment’. Evolution, 1970, 24(2), 278–291.
  • Marvier, M. A., Parasitic plant–host interactions: plant performance and indirect effects on parasite‐feeding herbivores. Ecology, 1996, 77, 1398–1409.
  • Keyes, W. J., O’malley, R. C., Kim, D. and Lynn, D. G., Signaling organogenesis in parasitic angiosperms: xenognosin generation, perception, and response. J. Plant Growth Regul., 2000, 19, 217–231; https://doi.org/10.1007/s003440000024
  • Goyet, V. et al., Haustorium inducing factors for parasitic Orobanchaceae. Front. Plant Sci., 2019, 10, 1056.
  • Tomilov, A. A., Tomilova, N. B., Abdallah, I. and Yoder, J., Localized hormone fluxes and early haustorium development in the hemi-parasitic plant Triphysaria versicolor. Plant Physiol., 2005, 138, 1469–1480; doi:10.1104/pp.104.057836.
  • Hamilton, L. and Conrad, C. E., In Proceeding of the Symposium on Sandalwood in the Pacific, Honolulu, Hawaii, US Forest Service General Technical Paper PSW-122, 9–11 April 1990, p. 84.
  • Yoder, J. I., A species–specific recognition system directs haustorium development in the parasitic plant Triphysaria (Scrophulariaceae). Planta, 1997, 202, 407–413; https://doi.org/10.1007/s00425-0050144
  • Jamison, D. S. and Yoder, J. I., Heritable variation in quinone-induced haustorium development in the parasitic plant Triphysaria. Plant Physiol., 2001, 125, 1870–1879; https://doi.org/10.1104/pp.125.4.1870

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  • Santalum album–Host Plants Interaction: An Incomplete Story of Semi-Root Parasite

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Authors

Vishnu Raju
College of Forestry, Kerala Agricultural University, Thrissur 680 656, India
Ashish Agashe
Bundhelkhand University, Jhansi 284 001, India
Mushineni Ashajyothi
College of Forestry, Kerala Agricultural University, Thrissur 680 656, India
Kunasekaran Rajarajan
College of Forestry, Kerala Agricultural University, Thrissur 680 656, India
Naresh Kumar
College of Forestry, Kerala Agricultural University, Thrissur 680 656, India
Ayyanadar Arunachalam
College of Forestry, Kerala Agricultural University, Thrissur 680 656, India

Abstract


Sandal (Santalum album L.) is one of the most valuable hemiparasitic tree species cultivated for its scented heartwood and oil. The economic yield from sandal depends on the hosts associated with it. Previous studies show that the sandal–host interaction is related to certain physiological, genetic and molecular mechanisms that enable them to identify host plants, to grow invasively into the hosts, and to establish connections to withdraw water and other resources from the hosts. However, the understanding of these mechanisms is still very vague. Our observations from the three-month-old sandal seedlings–host interaction study revealed the complex and multifaceted character of the host–parasite signalling mechanism. Besides, we found numerous unsolved questions and a significant knowledge gap in this field. Therefore, this article aims to correlate and contrast our observations with previous findings and to deliver some key questions to bridge the knowledge gap in future research.

Keywords


Haustoria, HIFs, Host–Parasite Interaction, Santalum album.

References





DOI: https://doi.org/10.18520/cs%2Fv125%2Fi2%2F130-137