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Research Articles

Early Access

Assessing the infestation-induced response on the plant host by the Indian lac insect

DOI
https://doi.org/10.14719/pst.3194
Submitted
12 December 2023
Published
03-04-2024
Versions

Abstract

Lac, the only natural resin of animal origin is produced by the Indian lac insect- Kerria lacca. It is the by-product of the complex natural interaction between the lac insect and its host plant. Despite several studies on the perspectives of the chemistry of lac and its production, very little work has been carried out to understand the biology of lac and its associated plant taxa. The present work has been designed to understand the preliminary response if any, of the host plant against lac insect infestation. Structural studies and metabolic profiling such as the determination of total phenolics, flavonoids, antioxidants, FTIR, and GC-MS were carried out. The anatomical investigations revealed coagulation/deposition of metabolites in the infested sites. The infested bark showed higher phenolic, flavonoid content, and antioxidant activity in comparison to non-infested bark which was corroborated by Fourier-transform infrared spectroscopy (FTIR) and GC-MS biochemical analysis. This preliminary study will shed some light on understanding the lac plant host's physiological response and the putative mechanism used by the lac insect in overcoming the plant response.

References

  1. Schoonhoven LM. Insect-plant relationships: The whole is more than the sum of its parts. Entomologia Experimentalis et Applicata. 2005;115(1):5-6. https://doi.org/10.1111/j.1570-7458.2005.00302.x
  2. War AR, Paulraj MG, Ahmad T, Buhroo AA, Hussain B, Ignacimuthu S, Sharma HC. Mechanisms of plant defense against insect herbivores. Plant Signaling and Behavior. 2012 October;7(10):1306-20. Epub August 20, 2012. https://doi.org/10.4161/psb.21663
  3. Endara MJ, Coley PD, Ghabash G, Nicholls JA, Dexter KG, Donoso DA et al. Coevolutionary arms race versus host defense chase in a tropical herbivore–plant system. Proceedings of the National Academy of Sciences. 2017;114(36):7499-505. https://doi.org/10.1073/pnas.1707727114
  4. Galdiero S, Falanga A, Cantisani M, Tarallo R, Elena Della Pepa M, D'Oriano V, Galdiero M. Microbe-host interactions: Structure and role of Gram-negative bacterial porins. Current Protein and Peptide Science. 2012;13(8):843-54. https://doi.org/10.2174/138920312804871120
  5. Denno RF, Kaplan I. Plant-mediated interactions in herbivorous insects: Mechanisms, symmetry and challenging the paradigms of competition past. Ecological Communities: Plant Mediation in Indirect Interaction Webs. 2007;19-50. https://doi.org/10.1017/cbo9780511542701.003
  6. Karban R, Agrawal AA, Mangel M. The benefits of induced defenses against herbivores. Ecology. 1997;78(5):1351-55. https://doi.org/10.1890/0012-9658(1997)078[1351:tboida]2.0.co;2
  7. Constabel CP, Agrawal AA, Tuzun S, Bent E. A survey of herbivore-inducible defensive proteins and phytochemicals. Induced Plant Defense against Pathogens and Herbivores, Biochemistry, Ecology and Agriculture. The American Phytopathologist Society, St. Paul, MN. 1999; pp. 137-66.
  8. Mello MO, Silva-Filho MC. Plant-insect interactions: An evolutionary arms race between two distinct defense mechanisms. Brazilian Journal of Plant Physiology. 2002;14:71-81. https://doi.org/10.1590/s1677-04202002000200001
  9. Yang J, Song X, Cao M, Deng X, Zhang W, Yang X, Swenson NG. On the modelling of tropical tree growth: The importance of intra-specific trait variation, non-linear functions and phenotypic integration. Annals of Botany. 2021;127(4):533-42. https://doi.org/10.1093/aob/mcaa085
  10. Isah T. Stress and defense responses in plant secondary metabolites production. Biological Research. 2019;52. https://doi.org/10.1186/s40659-019-0246-3
  11. Sharma KK, Jaiswal AK, Kumar KK. Role of lac culture in biodiversity conservation: Issues at stake and conservation strategy. Curr Sci. 2006;91(7):894-98.
  12. Ahmad A, Kaushik S, Ramamurthy VV, Lakhanpaul S, Ramani R, Sharma KK, Vidyarthi AS. Mouthparts and stylet penetration of the lac insect Kerria lacca (Kerr.). (Hemiptera: Tachardiidae). Arthropod Structure and Development. 2012;41(5):435-41. https://doi.org/10.1016/j.asd.2012.04.001
  13. Cook SC, Eubanks MD, Gold RE, Behmer ST. Colony-level macronutrient regulation in ants: Mechanisms, hoarding and associated costs. Animal Behaviour. 2010;79:429-37. https://doi.org/10.1016/j.anbehav.2009.11.022
  14. Behmer ST, Grebenok RJ, Douglas AE. Plant sterols and host plant suitability for a phloem-feeding insect. Functional Ecology. 2011;25(3):484-91. https://doi.org/10.1111/j.1365-2435.2010.01810.x
  15. Singh P, Arif Y, Bajguz A, Hayat S. The role of quercetin in plants. Plant Physiology and Biochemistry. 2021;166:10-19. https://doi.org/10.1016/j.plaphy.2021.05.023
  16. Singleton VL, Orthofer R, Lamuela-Raventós RM. Analysis of totalphenols and other oxidation substrates and antioxidants by means of folin-ciocalteu reagent. Methods in Enzymology. 1999;299:152-78. https://doi.org/10.1016/S0076-6879(99)99017-1
  17. Chang CC, Yang MH, Wen HM, Chem JC. Estimation of total flavonoid content in propolis by two complementary colorimetric methods. Journal of Food and Drug Analysis. 2002;10:178-82. https://doi.org/10.38212/2224-6614.2748
  18. Govindarajan R, Rastogi S, Vijayakumar M, Shirwaikar A, Rawat AK, Mehrotra S, Pushpangadan P. Studies on the antioxidant activities of Desmodium gangeticum. Biological and Pharmaceutical Bulletin. 2003;26(10):1424-27. https://doi.org/10.1248/bpb.26.1424
  19. Subhasree B, Baskar R, Laxmi Keerthana R, Lijina Susan R, Rajasekaran P. Evaluation of antioxidant potential in selected green leafy vegetables. Food Chemistry. 2009;115(4):1213-20. https://doi.org/10.1016/j.foodchem.2009.01.029
  20. Semwal P, Painuli S. Antioxidant, antimicrobial and GC-MS profiling of Saussurea obvallata (Brahma Kamal) from Uttarakhand Himalaya. Clinical Phytoscience. 2019;5(1):12. https://doi.org/10.1186/s40816-019-0105-3
  21. Pushker AK, Kaushik S, Lakhanpaul S, Sharma KK, Ramani R. Preliminary phytochemical investigation on the bark of some of the important host plants of Kerria lacca – The Indian lac insect. Botany Research International. 2011;4(3):48-51.
  22. Kaushik S, Vashishtha A, Shweta S, KK Sharma, S Lakhanpaul. Essential amino acid profiling of the four lac hosts belonging to genus Flemingia: Its implications on lac productivity. Physiol Mol Biol Plants. 2020;26:1867-74. https://doi.org/10.1007/s12298-020-00860-9
  23. Fürstenberg-Hägg J, Zagrobelny M, Bak S. Plant defense against insect herbivores. International Journal of Molecular Sciences. 2013;14(5):10242-297. https://doi.org/10.3390/ijms140510242
  24. Aharoni A, Galili G. Metabolic engineering of the plant primary–secondary metabolism interface. Current Opinion in Biotechnology. 2011;22(2):239-44. https://doi.org/10.1016/j.copbio.2010.11.004
  25. Eckardt NA. Myo-inositol biosynthesis genes in Arabidopsis: Differential patterns of gene expression and role in cell death. Plant Cell. 2010;22(3):537. https://doi.org/10.1105/tpc.110.220310
  26. Valluru R, Van den Ende W. Myo-inositol and beyond–emerging networks under stress. Plant Science. 2011;181(4):387-400. https://doi.org/10.1016/j.plantsci.2011.07.009
  27. Leiss KA, Maltese F, Choi YH, Verpoorte R, Klinkhamer PGL. Identification of chlorogenic acid as a resistance factor for thrips in Chrysanthemum. Plant Physiology. 2009;150(3):1567-75. https://doi.org/10.1104/pp.109.138131
  28. Kumar S, Stecher G, Tamura K. MEGA7: Molecular evolutionary genetics analysis version 7.0 for Bigger Datasets. Molecular Biology and Evolution. 2016;33:1870-74. https://doi.org/10.1093/molbev/msw054
  29. Mallikarjuna N, Kranthi KR, Jadhav DR, Kranthi S, Chandra S. Influence of foliar chemical compounds on the development of Spodoptera litura (Fab.) in interspecific derivatives of groundnut. Journal of Applied Entomology. 2004;128(5):321-28. https://doi.org/10.1111/j.1439-0418.2004.00834.x
  30. Lee G, Joo Y, Diezel C, Lee EJ, Baldwin IT, Kim SG. Trichobaris weevils distinguish amongst toxic host plants by sensing volatiles that do not affect larval performance. Molecular Ecology. 2016;25(14):3509-19. https://doi.org/10.1111/mec.13686
  31. Wang Y, Mostafa S, Zeng W, Jin B. Function and mechanism of jasmonic acid in plant responses to abiotic and biotic stresses. International Journal of Molecular Sciences. 2021;22(16):8568. https://doi.org/10.3390/ijms22168568
  32. Pasteels JM, Rowell-Rahier M. Proximate and ultimate causes for host plant influence on chemical defense of leaf beetles (Coleoptera: Chrysomelidae). Entomologia Generalis. 1991;15(4):227-35. https://doi.org/10.1127/entom.gen/15/1991/227
  33. Lortzing V, Oberländer J, Lortzing T, Tohge T, Steppuhn A, Kunze R, Hilker M. Insect egg deposition renders plant defence against hatching larvae more effective in a salicylic acid-dependent manner. Plant, Cell and Environment. 2019;42(3):1019-32. https://doi.org/10.1111/pce.13447
  34. Mansoori A, Singh N, Dubey SK, Thakur TK, Alkan N, Das SN, Kumar A. Phytochemical characterization and assessment of crude extracts from Lantana camara L. for antioxidant and antimicrobial activity. Frontiers in Agronomy. 2020;2:582268. https://doi.org/10.3389/fagro.2020.582268
  35. Marinescu M, Popa CV. Pyridine compounds with antimicrobial and antiviral activities. International Journal of Molecular Sciences. 2020;23(10):5659. https://doi.org/10.3390/ijms23105659,
  36. Zhu F, Liu D, Chen Z. Recent advances in biological production of 1,3-propanediol: New routes and engineering strategies. Green Chemistry. 2022;24(4):1390-403. https://doi.org/10.1039/d1gc04288b
  37. Peng Y, Wu P, Schartup AT, Zhang Yanxu. Plastic waste release caused by COVID-19 and its fate in the global ocean. Proceedings of the National Academy of Sciences of the United States of America. 2021;118(47):e2111530118. https://doi.org/10.1073/pnas.2111530118
  38. Nishad R, Ahmed T, Rahman VJ, Kareem A. Modulation of plant defense system in response to microbial interactions. Frontiers in Microbiology. 2020;11:1298. https://doi.org/10.3389/fmicb.2020.01298
  39. Fraser CM, Chapple C. The phenylpropanoid pathway in Arabidopsis. Arabidopsis Book. 2011;9:e0152. https://doi.org/10.1199/tab.0152
  40. Vashishtha A, Sharma KK, Lakhanpaul S. Co-existence, phylogeny and putative role of Wolbachia and Yeast-Like Symbiont (YLS) in Kerria lacca (Kerr.). Curr Microbiol. 2011;63:206-12. https://doi.org/10.1007/s00284-011-9961-x41.
  41. Kaushik S, Sharma KK, Ramani R, Lakhanpaul S. Detection of Wolbachia phage (WO) in Indian lac insect [Kerria lacca (Kerr.)] and its implications. Indian Journal of Microbiology. 2019;59(2):237-40. https://doi.org/10.1007/s12088-018-0763-8

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