Detection of Genetic Diversity and Phylogenetic Relationship of Tanacetum parthenium (L.) Sch.Bip. Germplasm: Implications for Conservation and Breeding

Document Type : Research Paper

Authors

1 Department of Medicinal Plants, Arak University, Arak, Iran

2 Department of Horticulture and Landscape Engineering, Ferdowsi University of Mashhad, Iran

3 Department of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

4 Department of Horticulture Sciences and Engineering, Nahavand Higher Education Complex, Bu-Ali Sina University, Hamedan, Iran

Abstract

Feverfew (Tanacetum parthenium (L.) Sch.Bip), belonging to the family Asteraceae, is a valuable medicinal plant containing effective anti-cancer compounds. The current study was conducted to investigate the diversity of feverfew ecotypes. Ecotypes were collected from different geographical areas of Iran in 2016 and 2017. The experiment was conducted in a completely randomized design with four replications. The analysis of variance showed significant phenotypic differences among the studied ecotypes. The plant height ranged from 55.75 to 124.50 cm and shoot and capitule diameters varied from 3.81 to 8.18 and 7.51 to 15.42 mm, respectively. The aerial biomass weight ranged from 36.62 to 136.40 g, root weight ranged from 9.81 to 36.65 g, and total biomass ranged from 46.44 to 173.05 g. In addition, flower weight varied from 3.46 to 6.21 g, while flower yield ranged from 1.48 to 13.90 g per plant. The obtained results regarding the phenotypic correlation demonstrated that plant height had the highest positive correlation with functional traits. Furthermore, the aerial biomass weight was positively correlated with flower weight, flower number, and flower yield, suggesting that vegetative growth had a positive correlation with reproductive growth. In general, tall plants produced more flowers. We also found some correlations between the geographical distances of ecotypes and phenotypic diversity. The dendrogram obtained based on the measured traits revealed that the classification of ecotypes in close groups can show their kinship and genetic relationships between them.

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  1. Pareek A., Suthar M., Rathore G.S., Bansal V. Feverfew (Tanacetum parthenium L.): A systematic review. Pharmacogn Rev. 2011; 5: 103-110.
  2. Freund R.R., Gobrecht P., Fischer D., Arndt H.D. Advances in chemistry and bioactivity of parthenolide. Nat Prod Rep. 2019; 37: 541-565.
  3. Kaye A.D., Sabar R., Clarke R.C., Vig S., Hofbauer R. Nutraceuticals-current concepts and the role of the anesthesiologist (part 2). Am J Anesth. 2000; 467-471.
  4. Zhang F., Zhou J., Shi Y., Karaisz K. Identification of antioxidative ingredients from feverfew (Tanacetum Parthenium) extract substantially free of parthenolide and other alpha-unsaturated gamma-lactones. Open J Anall Bioanal Chem. 2019; 3: 076-082.
  5. Alenzi K.A., Alharbi F.H., Tawhari F.M., Fradees G.S. Alteration of coagulation test results and vaginal bleeding associated with the use of feverfew (Tanacetum parthenium). J Med Cases. 2021; 12: 9.
  6. Duke J.A. CRC Handbook of Medicinal Herbs. Boca Raton, FL: CRC Press.1985.
  7. Jackson B., McDonald R.L. In: Dobelis IN, editor. Magic and Medicine of Plants. Pleasantville, NY: Reader's Digest Assoc. 1986.
  8. Meyer J.E. The Herbalist. Hammond, IN: Hammond Book Co. 1934.
  9. Majdi M., Charnikhova T., Bouwmeester H. Genetical, developmental and spatial factors influencing parthenolide and its precursor costunolide in feverfew (Tanacetum parthenium L. Schulz Bip.). Ind Crops Prod. 2013; 47: 270-276.
  10. Maxia A., Sanna C., Piras A., Porcedda S., Falconieri D., Goncalves M.J., Salgueiro L. Chemical composition and biological activity of Tanacetum audibertii (Req.) D.C. (Asteraceae), an endemic species of Sardinia Island, Italy. Ind Crops Prod. 2015; 65: 472-476.
  11. Maggi F. Feverfew (Tanacetum parthenium (L.) Sch. Bip.). In Nonvitamin and nonmineral nutritional supplements. Academic Press. 2019; 223-225.
  12. Sadat-Hosseini M., Farajpour M., Boroomand N., Solaimani-Sardou F. Ethnopharmacological studies of indigenous medicinal plants in the south of Kerman, Iran. J Ethnopharmacol. 2017; 199: 194-204.
  13. Connell J.H., Slatyer R.O. Mechanisms of succession in natural communities and their role in community stability and organization. Am Natur. 1977; 111: 1119-1144.
  14. Hacker S.D., Gaines S.D. Some implications of direct positive interactions for community species diversity. Ecol. 1997; 78: 1990-2003. https://doi.org/10.1890/0012-9658(1997)078[1990: SIODPI]2.0.CO;2
  15. Cavieres L.A., Badano, E.I. Do facilitative interactions increase species richness at the entire community level? J Ecol. 97; 2009: 1181-1191.
  16. Maestre F.T., Callaway R.M., Valladares F., Lortie C.J. Refining the stress‐gradient hypothesis for competition and facilitation in plant communities. J Ecol. 2009; 97: 199-205.
  17. Bartels S.F., Chen, H.Y. Interactions between overstorey and understorey vegetation along an overstorey compositional gradient. J Veg Sci. 2012; 24: 543-552.
  18. Falk D.A., Knapp E.E., Guerrant E.O. An introduction to restoration genetics. Plant conservation alliance, bureau of land management. US Department of Interior, US Environmental Protection Authority. 2001.
  19. Frankham R. Genetics and extinction. Biol Conserv. 2005; 126: 131-140.
  20. Baricevic D., Mathe A., Bartol T. Conservation of wild crafted medicinal and aromatic plants and their habitats. In medicinal and aromatic plants of the world. Springer, Dordrecht. 2015; 131-144.
  21. Hoban S., Archer F.I., Bertola L.D., Bragg J.G., Breed M.F., Bruford M.W., Hunter M.E. Global genetic diversity status and trends: towards a suite of essential biodiversity variables (EBVs) for genetic composition. Biol Rev. 2022; 97: 1511-1538.
  22. Bhandari H.R., Bhanu A.N., Srivastava K., Singh M.N., Shreya H.A. Assessment of genetic diversity in crop plants-an overview. Adv Plants Agric Res. 2017; 7: 279-286.
  23. Helmstetter A.J., Oztolan‐Erol N., Lucas S.J., Buggs R.J. Genetic diversity and domestication of hazelnut (Corylus avellana L.) in Turkey. Plants People Planet. 2020; 2: 326-339.
  24. Mezaka I., Kronberga A., Nakurte I., Taskova I., Jakovels D., Primavera A. Genetic chemical and morphological variability of chamomile (Chamomilla recutita L.) populations of Latvia. Ind Crops Prod. 2020; 154: 112614.
  25. Begna, T. Role and economic importance of crop genetic diversity in food security. Inter J Agric Sci Food Technol. 2021; 7: 164-169.
  26. Mathe A. An ecological approach to medicinal plant introduction. Herbs, Spices and Medicinal Plants: Recent Advances in Botany, Horticulture, and Pharmacology. Oryx Press. 1988; 3: 175-205.
  27. Tetenyi P. Chemical variation (chemo differentiation) in medicinal and aromatic plant. Acta Hortic. 2002; 576: 15-23.
  28. Joshi K., Chavan P., Warude D., Patwardhan B. Molecular markers in herbal drug technology. Curr Sci. 2004; 87: 159-165.
  29. Hadi N., Shojaeiyan A., Sefidkon F., Jafari A.A., Misic D., Banjanac T., Siler B. Assessment of infraspecific genetic diversity in Nepeta kotschyi Boiss., a native Iranian medicinal plant. J Agric Sci Technol. 2020; 22: 1327-1342.
  30. Cirak C., Radusiene J., Karabuk B., Janulis V., Ivanauskas L. Variation of bioactive compounds in Hypericum perforatum growing in Turkey during its phenological cycle. J Integr Plant Biol. 2007; 49: 615-620.
  31. Swarup S., Cargill E.J., Crosby K., Flagel L., Kniskern J., Glenn K.C. Genetic diversity is indispensable for plant breeding to improve crops. Crop Sci. 2021; 61: 839-852.
  32. Cruz V.M.V., Dierig D.A., Lynch A., Hunnicutt K., Sullivan T.R., Wang G., Zhu J. Assessment of phenotypic diversity in the USDA, National Plant Germplasm System (NPGS) guayule germplasm collection. Ind Crops Prod. 2022; 175: 114303.
  33. Heidari P., Rezaei M., Sahebi M., Khadivi, A. Phenotypic variability of Pyrus boissieriana Buhse: Implications for conservation and breeding. Sci Hortic. 2019; 247: 1-8.
  34. Khadivi A., Mirheidari F., Moradi Y., Paryan S. Phenotypic variability of oleaster (Elaeagnus angustifolia L.) as revealed by morphological characteristics. Ind Crops Prod. 2020; 149: 112322.
  35. Samsampour D., Kazemzadeh-Beneh H., Damizadeh G.R., Mirzaei Z. Morphological and biochemical classification of Iranian mango germplasm collection by multivariate analysis: implications for breeding. Adv Hortic Sci 2020; 34: 381-395.
  36. Khadivi-Khub A., Etemadi-Khah A. Phenotypic diversity and relationships between morphological traits in selected almond (Prunus amygdalus) germplasm. Agrofor Syst. 2015; 89: 205-216.
  37. Hibberd J.M., Quick W.P. Characteristics of C4 photosynthesis in stems and petioles of C3 flowering plants. Nature. 2002; 415: 451-454.
  38. Qi Y., Wei W., Chen C., Chen L. Plant root-shoot biomass allocation over diverse biomes: A global synthesis. Global Ecol Conserv. 2019; 18: e00606.
  39. Foust C.M., Preite V., Schrey, A.W., Alvarez, M., Robertson M.H., Verhoeven K.J.F., Richards C.L. 2016. Genetic and epigenetic differences associated with environmental gradients in replicate populations of two salt marsh perennials. Molecular Ecol. 2016; 25: 1639-1652. https://doi.org/10.1111/mec.13522
  40. Xiong F., Nie X., Yang L., Wang L., Li J., Zhou G. Non-target metabolomics revealed the differences between Rh. tanguticum plants growing under canopy and open habitats. BMC Plant Boil. 2021; 21: 1-13.
  41. Richards C.L., Pennings S.C., Donovan L.A. Habitat range and phenotypic variation in salt marsh plants. Plant Ecol. 2005; 176: 263-273.
  42. Otto S.P., Whitton J. Polyploid incidence and evolution. Annu Rev Genet. 2000; 34: 401-437.
  43. Beaulieu J.M., Leitch I.J., Patel S., Pendharkar A., Knight C.A. Genome size is a strong predictor of cell size and stomatal density in angiosperms. New Phyto. 2008; 179: 975-986.
  44. Stahlberg D. Habitat differentiation, hybridization and gene flow patterns in mixed populations of diploid and autotetraploid Dactylorhiza maculata sl (Orchidaceae). Evol Ecol. 2009; 23: 295-328.
  45. Kim S., Rayburn A.L., Boe A., Lee D.K. Neopolyploidy in Spartina pectinata Link: 1. Morphological analysis of tetraploid and hexaploid plants in a mixed natural population. Plant Syst Evol. 2012; 298: 1073-1083. https://doi.org/10.1007/s00606-012-0617-5
  46. Laport R.G., Ramsey J. Morphometric analysis of the North American creosote bush (Larrea tridentata, Zygophyllaceae) and the microspatial distribution of its chromosome races. Plant Syst Evol. 2015; 301: 1581-1599.
  47. Pastorino M.J., Marchelli P. Genetic resources: The base material for managing nature. Conserv. 2021; 77-87.
  48. Babazadeh Darjazi, B. Comparison of vitamin C in mandarin (Citrus Blanco.) cultivars. Eco-phyto J Med Plant. 2013; 3: 82-93.
  49. Zarabiyan M., Majidi M.M., Bahrami, F. Relationship of morphological and agronomic traits in Iranian and exotic sainfoin populations using multivariate statistical analysis. Iran J Rang for Plant Breed Genet Res. 2014; 22: 278-290.
  50. Birchler J.A., Yao H., Chudalayandi S. Unraveling the genetic basis of hybrid vigor. Proc Natl Acad Sci. 2006; 103: 12957-12958.
  51. Pank F. Adaptation of medicinal and aromatic plants to contemporary quality and technological demands by breeding: aims, methods and trends. Rev Bras Plant Med. Botucatu. 2006; 8: 39-42.