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Mechanical and Phytochemical Protection Mechanisms of Calligonum Comosum in Arid Deserts

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Journal PLoS One
Date 2018 Feb 8
PMID 29415032
Citations 11
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Abstract

Unlike animals, plants are sessile organisms, lacking circulating antibodies and specialized immune cells and are exposed to various harsh environmental conditions that make them at risk of being attacked by different pathogens and herbivores. Plants produce chemo-signals to respond to the surroundings and be able to distinguish between harmless and harmful signals. In this study, the production of phytochemicals as plant signaling mechanisms and their defensive roles in disease resistance and repelling herbivores are examined in Calligonum comosum. C. comosum is a leafless standalone perennial shrub widespread in sand dunes. The plant has the ability to survive the drastic environmental conditions of the arid/ hyperarid deserts of the Arabia. Structural anatomy and phytochemicals analyses were used to identify both mechanical and chemical defensive mechanisms in C. comosum. Microscopy-based investigations indicated that stems of this species developed hard structures in its outer layers including sclerenchyma and cluster crystals of calcium oxalate (CaOx). Sclerenchyma and CaOx are difficult to be eaten by herbivores and insects and can harm their mouthparts. On the other hand, the plant developed both short-distance (local) and long-distance (systematic over limited sphere) phytochemicals-producing cells located at its outer regions that is surrounding the inner nutrient-rich vascular system (VS). Local chemical was represented by phenolic idioblasts that were released in response to plant cutting. Systematic chemical was represented by toxic volatile oil containing ~50% benzaldehyde derivative (cuminaldehyde). The oil caused strong killing effect on both mammalian cells and microbial pathogens via either direct addition or indirect exposure to its vapor. The plants lost the oil content and allowed fungal growth once cut and dried. The localization of both defensive mechanisms to the outer region of the plant seemed to protect the inner nutrient-rich VS and hence maintained the plant survival. Surprisingly, in relation to traditional folklore use as medicine, local people use only green parts of the plant and only during the winter, where the plant found devoid of volatile oil and phenolic idioblasts. Moreover, it turns into recommendations for local people to avoid any health problems caused by the plant supply.

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References
1.
Klosterman S, Subbarao K, Kang S, Veronese P, Gold S, Thomma B . Comparative genomics yields insights into niche adaptation of plant vascular wilt pathogens. PLoS Pathog. 2011; 7(7):e1002137. PMC: 3145793. DOI: 10.1371/journal.ppat.1002137. View

2.
Genin S . Molecular traits controlling host range and adaptation to plants in Ralstonia solanacearum. New Phytol. 2010; 187(4):920-8. DOI: 10.1111/j.1469-8137.2010.03397.x. View

3.
Badria F, Ameen M, Akl M . Evaluation of cytotoxic compounds from calligonum comosum L. growing in Egypt. Z Naturforsch C J Biosci. 2007; 62(9-10):656-60. DOI: 10.1515/znc-2007-9-1005. View

4.
Mandal S, Chakraborty D, Dey S . Phenolic acids act as signaling molecules in plant-microbe symbioses. Plant Signal Behav. 2010; 5(4):359-68. PMC: 2958585. DOI: 10.4161/psb.5.4.10871. View

5.
Yap P, Yiap B, Ping H, Lim S . Essential oils, a new horizon in combating bacterial antibiotic resistance. Open Microbiol J. 2014; 8:6-14. PMC: 3950955. DOI: 10.2174/1874285801408010006. View