Skip to main content
  • Note
  • Published:

Acaricidal and insecticidal activities of essential oils of Cinnamomum zeylanicum barks cultivated from France and India against Dermatophagoides spp., Tyrophagus putrescentiae and Ricania sp.

Abstract

The chemical composition of Cinnamomum zeylanicum bark oils cultivated from France and India was analyzed by GC–MS. The main components of C. zeylanicum oil were cinnamaldehyde (63.97 and 67.21%) and eugenol (6.84 and 19.79%) from France and India, respectively. Acaricidal and insecticidal activities of C. zeylanicum oils against Dermatophagoides sp, T. putrescentiae and Ricania sp. were evident. The LC50 values of C. zeylanicum oil were 123.77 and 93.06 mg/L in samples from France and India, respectively, against Ricania sp. adults in the spray bioassay. Using the leaf-dipping bioassay, the LC50 values of the oil from France and India were 80.99 and 57.44 mg/L, respectively, against Ricania sp. nymphs. Acaricidal activity of the C. zeylanicum oil from India in the fabric disk bioassay (LD50, 0.64, 0.51 and 1.72 μg/cm3, respectively) was greater than France oil (LD50, 0.92, 0.81 and 1.82 μg/cm3, respectively). In the filter paper bioassay, india oil (LD50, 1.82, 1.55 and 3.08 μg/cm2, respectively) was more potent than France oil (LD50, 2.07, 1.94 and 6.20 μg/cm2, respectively) against D. farinae, D. pteronyssinus and T. putrescentiae. The results indicate that the essential oils of C. zeylanicum barks could be an effective natural acaricide and insecticide for controlling house dust mites, stored food mites and fruit pests.

Introduction

In contrast to synthetic acaricides and insecticides, plant essential oils are environmentally benign, do not affect non-target organisms, are cost-effective and are convenient to handle and use [1]. Natural acaricides and insecticides are typically active against some species, are biodegradable, nonpoisonous and appropriate for use as mite and insect control agents [24]. Essential oils derived from plants could be important in protecting stored foods, fruit trees, crops and humans against mites and insects. Plant essential oils are potential sources of natural acaricides and insecticides [5].

Lauraceae is a plant family comprised mainly of evergreen shrubs and trees. The genus Cinnamomum includes about 250 species, which are generally located in Asia and Australia [6]. Cinnamomum provides diverse oils with various aromatic and chemical components, which include cinnamaldehyde, eugenol and camphor [7, 8]. Cinnamomum zeylanicum Blume is universally known as cinnamon. This economically important species is cultivated in India and Sri Lanka. C. zeylanicum leaves and barks are processed to yield a spice that has been commonly used worldwide for centuries by various cultures. C. zeylanicum has a history as a traditional medicine for gastritis, dyspepsia, inflammatory diseases and blood circulation issues [9]. Cinnamomum sp. oil has potential acaricidal and insecticidal activities against Tetranychus cinnabarinus [10] and Callosobruchus maculatus [11].

Dermatophagoides farinae (Hughes), Tyrophagus putrescentiae (Schrank) and D. pteronyssinus (Trouessart) are the most important house dust and stored food mites. House dust mites are a main source of allergens related to asthma, atopic dermatitis and perennial allergic rhinitis [12]. Stored food mites are an etiological factor of allergic illness among workers and farmers handling polluted stored products. Ingestion of mites causes systemic anaphylaxis and acute enteritis [13]. Efforts to eradicate the mites by repeated application of synthetic acaricides have triggered the development of resistance, killing of non-target organisms and raised concern about human health [13]. Ricania sp. belongs to the planthopper family Ricaniidae. Ricania sp. is a pest of important economic plants in the agriculture and forestry sectors [14]. Ricania sp. was first described in 2010 [14] and was soon reported as a sporadic pest of some fruit plants, such as persimmon, plum, chestnut and blueberry [15]. The infestation area is increasing in the absence of an active insecticide for long-term control.

In seeking a solution, the potential acaricidal and insecticidal activities of C. zeylanicum bark oils cultivated from India and France against Dermatophagoides spp., T. putrescentiae and Ricania sp. attracted our attention. This paper reports the results of the chemical composition of the essential oils of C. zeylamicum obtained from bark gathered in India and France, and their acaricidal and insecticidal activities against Dermatophagoides spp., T. putrescentiae and Ricania sp.

Materials and methods

Plant material extraction

Cinnamomum zeylanicum bark (5 kg) cultivated from France and India was obtained from a medicinal herb market in Jeonju, South Korea. Samples were authenticated by Jeong-moon Kim at Chonbuk National University. Essential oils derived from C. zeylanicum barks were obtained by steam distillation. The concentrated volatile oils were stored at 4 °C before bioassay.

Test insects

Cultures of Dermatophagoides spp. and T. putrescentiae were maintained without exposure to any synthetic acaricides. The mites were reared on fry feed (Korea Special Feed-Meal Co. Ltd, Jeonju, South Korea) and dried yeast and housed in circular cages (15 × 12 × 6 cm) at 26 ± 1 °C and 75% relative humidity in the dark. The feed included protein (45.9%), fiber (4.1%), lipid (2.9%), phosphate (1.8%) and calcium (1.1%). Ricania sp. adults and nymphs were gathered from Wanju, South Korea, from May to October 2016 using an insect catcher. They were classified as the fourth instar stage of Ricania sp. nymphs.

Bioassays

Acaricidal activities of essential oils derived from C. zeylanicum bark against Dermatophagoides spp. and T. putrescentiae were measured with the fabric disk and filter paper bioassays, as modified [16]. In the fabric disk bioassay, various concentrations ranging from 80 to 1.2 μg/cm3 in 10 μL acetone were applied to fabric disks (8 mm diameter and 1 mm thick). The fabric disks were dried in an air fume hood for 15 min and put in the cap of a microtube. Thirty adult mites were treated in the test and control tubes. In the filter paper bioassay, differing concentrations (80–1.2 μg/cm2) of the sample were liquefied in 50 μL and applied to filter paper (50 mm diameter, 55 μm thick). After drying in the fume hood for 15 min, the treated filter paper was put in the base of a Petri dish (50 mm × 8 mm). Thirty mites were transferred to the dish, and the lid was completely sealed. Treatments for the fabric disk and filter paper bioassays were repeated three times at 26 ± 1 °C for 24 h. Dead mites were checked by microscopy examination (×20). Acetone and benzyl benzoate were used for the negative control and the positive control, respectively.

The insecticidal activities of C. zeylanicum oils against Ricania sp. nymph and adult with the spray and leaf-dipping bioassays were determined as previously described [3]. In the leaf-dipping bioassay, several concentrations of the sample (1000–50 mg/L) in distilled water of the test samples were dissolved and althea leaf (30 mm diameter) was dipped into each concentration. After drying in the fume hood for 6 min, the dried leaf was set into bottom of a Petri dish (60 × 15 mm) and 20 nymphs were added. In the spray bioassay, various concentrations (1000–50 mg/L) of the test sample were soluble in distilled water. The samples were sprinkled into a square cage (15 × 15 × 20 cm) which held 20 adults. The spray and leaf-dipping bioassays were maintained at 23 ± 2 °C for 48 and 72 h. All tests were done three times.

Gas chromatography–mass spectrometry (GC–MS)

Essential oils of C. zeylanicum barks cultivated in France and India were analyzed with GC–MS (HP 6890 and 5973 series; Agilent, Santa Clara, CA, USA) and were separated using a DB-5 column and HP-Innowax capillary column (0.25 mm i. d. × 3000 mm L × 0.25 μm thickness). Helium was used as the carrier gas at 0.76 mL/min. Ion source temperature was 220 °C, and column temperature was 50 to 210 °C at 2 °C/min. Electron ionization obtained mass spectra at 70 eV with a scan area of 20–400 amu. The constituents of C. zeylanicum bark oil were identified by retention indices and mass spectra as compared to be spectra library (Table 1). The relative percentage (%) of constituents was measured by calculating with internal standards.

Table 1 GC–MS analyses of the essential oils derived from Cinnamomum zeylanicum cultivated from France and India by steam distillation extraction

Statistical analysis

This study used probit analysis to handle mortality data, determining the lethal concentrations (LC50 and LC90), the lethal doses (LD50 and LD90) and 95% confidence intervals. SPSS version 12 software (SPSS Inc., Chicago, IL, USA) was used to analyze all data.

Results and discussion

Composition of C. zeylanicum essential oil

Essential oil extracted by steam distillation was obtained with a yield of 1.27% for bark from India and 1.05% for bark from France. Fourteen components were identified, accounting for 98.59% of the oil in samples from France, with 11 components obtained from samples from India, accounting for 97.90%. The chemical constituents of the essential oils of two countries are shown in Table 1. The two essential oils comprised monoterpene alcohol, monoterpene ether, monoterpene hydrocarbon, monoterpene ketone, phenolic, phenylpropanoid ester, phenylpropanoid ether, phenylpropanoid hydrocarbon and sesquiterpene hydrocarbon. The compounds derived from the C. zeylanicum oil from France were 2 monoterpene alcohols (linalool and α-terpineol), 1 monoterpene ether (eucalyptol), 4 monoterpene hydrocarbons (α-pinene, α-phellandrene, (±)-limonene and o-cymene), 1 monoterpene ketone (camphor), 1 phenolic (benzaldehyde), 1 phenylpropanoid ester (cinnamyl acetate), 1 phenylpropanoid ether (eugenol), 1 phenylpropanoid hydrocarbon (cinnamaldehyde) and 2 sesquiterpene hydrocarbons (α-humulene and β-caryophyllene). The main components of the C. zeylanicum oil from France were cinnamaldehyde (63.97%), eugenol (6.84%), β-caryophyllene (6.40%), linalool (6.30%), cinnamyl acetate (3.90%), o-cymene (3.45%), α-humulene (1.92%), α-terpineol (1.40%), α-pinene (1.15%), benzaldehyde (0.87%), α-phellandrene (0.75%), (±)-limonene (0.68%), eucalyptol (0.48%) and camphor (0.48%). Most of the oil for France was phenylpropanoids (74.71%) and only 14.69% monoterpenoids and 8.32% sesquiterpenoids.

The composition of C. zeylanicum oil from India included 3 monoterpene alcohols (linalool, α-terpineol and geraniol), 1 monoterpene ether (eucalyptol), 3 monoterpene hydrocarbons (α-pinene, (±)-limonene and o-cymene), 1 phenylpropanoid ester (cinnamyl acetate), 1 phenylpropanoid ether (eugenol), 1 phenylpropanoid hydrocarbon (cinnamaldehyde) and 1 sesquiterpene hydrocarbon (β-caryophyllene). The main composition of C. zeylanicum oil from India included cinnamaldehyde (67.21%), eugenol (19.79%), cinnamyl acetate (4.34%), linalool (1.88%), α-terpineol (1.13%), geraniol (0.79%), β-caryophyllene (0.75%), eucalyptol (0.60%), α-pinene (0.56%), (±)-limonene (0.52%) and o-cymene (0.33%). Most of the Indian oil was phenylpropanoids (91.34%), with only 5.81% monoterpenoids and 0.75% sesquiterpenoids. The oil from India was richer in phenylpropanoids (91.34%) than that from France (74.71%). Eugenol comprised 19.79% of the oil from India and 6.84% of the oil from France. C. zeylanicum bark oil constituents differ according to the tree chemotype, climate, year and region. Chalchat and Valade [7] reported that the main compounds of C. zeylanicum oil from Madagascar were cinnamaldehyde and camphor. Jirovetz et al. [8] reported that eugenol (85%) was the main component of the oil from Cameroon.

Insecticidal activities of C. zeylanicum oil

The insecticidal activities of C. zeylanicum oils from France and India against Ricania sp. adults and nymphs were analyzed using spray and leaf-dipping bioassays (Table 2). In the spray bioassay, the LC50 values against Ricania sp. adults of C. zeylanicum oil from France were 160.39 mg/L at 48 h and 123.77 mg/L at 72 h. The respective values from the oil from India were 109.72 and 93.06 mg/L. Using the leaf-dipping bioassay, the LC50 values against Ricania sp. nymphs of C. zeylanicum oil from France were LC50 104.95 mg/L at 48 h and 80.99 mg/L at 72 h. The respective values of the oil from India were 76.89 and 57.44 mg/L. The activities of C. zeylanicum oil from India were about 1.33–1.46 times greater than that of the oil from France. The negative control displayed no activity against Ricania sp. Lee et al. [4] reported that eugenol had great insecticidal activity (143.24 and 124.44 mg/L, respectively) against Ricania sp. adults and nymphs. Taken together with GC–MS data of C. zeylanicum oils, it is assumed that the difference in insecticidal activity between the oils cultivated from France and India was related to the chemical content of eugenol. In addition, variation in the insecticidal activities of essential oil from different region may reflect chemical composition, phytochemicals and the size and weight of Ricania sp. adults and nymphs [17]. Santos et al. [17] described different activities of Copaifera reticulata oils from Acre and Para against bacteria.

Table 2 Insecticidal activities of the essential oil of C. zeylanicum cultivated from France and India against Ricania sp. adults and nymphsa

Acaricidal activity of C. zeylanicum oil

The acaricidal activities of C. zeylanicum oil from France and India against house dust and stored food mites were tested using fabric disk and filter paper bioassays and compared with that of the benzyl benzoate positive control (Tables 3). In the fabric disk bioassay, the LD50 values against D. farinae, D. pteronyssinus and T. putrescentiae of the essential oil from France were 0.92, 0.81 and 1.82 μg/cm3, respectively, and those of the essential oil from India were 0.64, 0.51 and 1.72 μg/cm3, respectively. The LD50 values against D. farinae, D. pteronyssinus and T. putrescentiae of C. zeylanicum oil from France in the filter paper bioassay were 2.07, 1.94 and 6.20 μg/cm2, respectively, and those of the oil from India were 1.82, 1.55 and 3.08 μg/cm2, respectively. Relative toxicity (RT) was expressed as the ratio of benzyl benzoate LD50 value/each test material LD50 value. In the fabric disk bioassay, the RT values for D. farinae, D. pteronyssinus and T. putrescentiae of C. zeylanicum oils from bark obtained from India (14.78, 16.57 and 6.73) were greater than France oil (10.92, 10.41 and 6.36). In the filter paper bioassay, the RT values of C. zeylanicum india oils (4.26, 4.22 and 3.28 times) were higher than France oil (3.75, 3.37 and 1.63 times) against D. farinae, D. pteronyssinus and T. putrescentiae, respectively. Based on the LD50 values, C. zeylanicum oil from India was more sensitive than the oil from France against house dust and stored food mites. The acaricidal activities of C. zeylanicum oils are impacted by type and proportion of constituent from plant oil, detoxification enzyme activity and biological conditions of mites [16]. In a previous study, the acaricidal activities of eugenol and cinnamaldehyde, which is the main component of C. zeylanicum oil, were potent against house dust and stored food mites [18, 19].

Table 3 Acaricidal activities of C. zeylanicum oils cultivated from France and India against Dermatophagoides spp. and Tyrophagus putrescentiae a

Cinnamon oil and eugenol may deleteriously affect cell membrane permeability and inhibit growth due to disruption of intracellular enzymes [20]. Cinnamon oil is safe when ingested and has been granted GRAS (generally recognized as safe) status by the United States Food and Drug Administration. Cinnamon displays varied pharmacological activities including antiallergic [21] and antimicrobial [22] activities. The present findings implicate the essential oils of C. zeylanicum bark as an effective natural acaricide and insecticide for controlling house dust mites, stored food mites and sporadic pests.

References

  1. Belmain SR, Neal GE, Ray DE, Golob P (2001) Insecticidal and vertebrate toxicity associated with ethnobotanicals used as post-harvest protectants in Ghana. Food Chem Toxicol 39:287–291

    Article  CAS  Google Scholar 

  2. Isman MB (1995) Leads and prospects for the development of new botanical insecticides. Rev Pestic Toxicol 3:1–20

    CAS  Google Scholar 

  3. Lee HK, Lee HS (2016) Toxicities of active constituent isolated from Thymus vulgaris flowers and its structural derivatives against Tribolium castaneum (Herbst). Appl Biol Chem 59:821–826

    Article  CAS  Google Scholar 

  4. Lee HW, Lee SG, Lee HS (2016) Active component isolated from Eugenia caryophyllata. Appl Biol Chem 59:609–614

    Article  CAS  Google Scholar 

  5. Singh G, Upadhyay RK (1993) Essential oils-a potent source of natural pesticides. J Sci Ind Res 52:676–683

    CAS  Google Scholar 

  6. The Wealth of India (1992) A dictionary of Indian raw materials and industrial products, vol 3. Publication and Information Directorate, New Delhi, p 589

    Google Scholar 

  7. Chalchat JC, Valade I (2000) Chemical composition of leaf oils of Cinnamomum from Madagascar: C. zeylanicum Blume, C. camphora L., C fragrans Baillon and C. angustifolium. J Essent Oil Res 12(5):537–540

    Article  CAS  Google Scholar 

  8. Jirovetz L, Buchbaner G, Ngassoum MB, Eberhardt R (1998) Analysis and quality control of the essential oil of the leaves of Cinnamomum zeylanicum from Cameroon. Ernahrung 22(10):443–445

    CAS  Google Scholar 

  9. Lou ZQ, Qin B (1995) Species systemization and quality evaluation of commonly used Chinese tradition drugs. Edition North 1:203–251

    Google Scholar 

  10. Chen Y, Dai G (2015) Acaricidal activity of compounds from Cinnamomum camphora (L.) Presl against the carmine spider mite, Tetranychus cinnabarinus. Pest Manag Sci 71(11):1561–1571

    Article  CAS  Google Scholar 

  11. Islam R, Khan RI, Al-Reza SM, Jeong YT, Song CH, Khalequzzaman M (2009) Chemical composition and insecticidal properties of Cinnamomum aromaticum (Nees) essential oil against the stored product beetle Callosobruchus maculatus (F.). J Sci Food Agric 89:1241–1246

    Article  CAS  Google Scholar 

  12. Arlian LG (1989) Biology and ecology of house dust mites, Dermatophagoides spp. and Euroglyphus spp. Immunol Allergy Clin North Am 9:339–356

    Google Scholar 

  13. Oh MS, Yang JY, Lee HS (2012) Acaricidal toxicity of 2′-hydroxy- 4′-methylacetophenone isolated from Angelicae koreana roots and structure − activity relationships of its derivatives. J Agric Food Chem 60:3606–3611

    Article  CAS  Google Scholar 

  14. Choi YS, Hwang IS, Kang TJ, Lim JR, Choe KR (2011) Oviposition characteristics of Ricania sp. (Homoptera: Ricaniidae), a new fruit pest. Korean J Appl Entomol 50:367–372

    Article  Google Scholar 

  15. Choi DS, Kim DI, Ko SJ, Kang BR, Lee KS, Park JD, Choi KJ (2012) Occurrence ecology of Ricania sp. (Hemiptera: Ricaniidae) and selection of environmental friendly agricultural materials for control. Korean J Appl Entomol 51:141–148

    Article  Google Scholar 

  16. Yang JY, Lee HS (2012) Acaricidal activities of the active component of Lycopus lucidus oil and its derivatives against house dust and stored food mites (Arachnida: Acari). Pest Manage Sci 68:564–572

    Article  CAS  Google Scholar 

  17. Santos AOD, Ueda-Nakamura T, Dias Filho BP, Veiga Junior VF, Pinto AC, Nakamura CV (2008) Antimicrobial activity of Brazilian copaiba oils obtained from different species of the Copaifera genus. Mem Inst Oswaldo Cruz 103:277–281

    Article  Google Scholar 

  18. Kim HK, Kim JR, Ahn YJ (2004) Acaricidal activity of cinnamaldehyde and its congeners against Tyrophagus putrescentiae (Acari: Acaridae). J Stored Prod Res 40(1):55–63

    Article  CAS  Google Scholar 

  19. Wang Z, Kim HK, Tao W, Wang M, Ahn YJ (2011) Contact and fumigant toxicity of cinnamaldehyde and cinnamic acid and related compounds to Dermatophagoides farinae and Dermatophagoides pteronyssinus (Acari: Pyroglyphidae). J Med Entomol 48(2):366–371

    Article  CAS  Google Scholar 

  20. Bang KH, Lee DW, Park HM, Rhee YH (2000) Inhibition of fungal cell wall synthesizing enzymes by trans-cinnamaldehyde. Biosci Biotech Bioch 64(5):1061–1063

    Article  CAS  Google Scholar 

  21. Nagai H, Shimazawa T, Matsuura N (1982) Immunopharmacological studies of the aqueous extract of Cinnamomum cassia (CCAq) I. Anti-allergic Action. Jpn J Pharmacol 32(5):813–822

    Article  CAS  Google Scholar 

  22. Singh G, Maurya S, Catalan CA (2007) A comparison of chemical, antioxidant and antimicrobial studies of cinnamon leaf and bark volatile oils, oleoresins and their constituents. Food Chem Toxicol 45(9):1650–1661

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This work was carried out with the support of “Cooperative Research Program for Agriculture Science & Technology Development (Project title: Study on the ecology and development of management practice for an exotic and epidemic pest, Ricania sp., Project No. PJ0116902017)” Rural Development Administration, Korea.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hoi-Seon Lee.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Jeon, YJ., Lee, SG. & Lee, HS. Acaricidal and insecticidal activities of essential oils of Cinnamomum zeylanicum barks cultivated from France and India against Dermatophagoides spp., Tyrophagus putrescentiae and Ricania sp.. Appl Biol Chem 60, 259–264 (2017). https://doi.org/10.1007/s13765-017-0276-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13765-017-0276-x

Keywords