Toxicity of Nerium oleander extracts against Pectinophora gossypiella (Saunders) (Lepidoptera: Gelechiidae)

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International Journal of Advanced Research in Biological Sciences ISSN: 2348-69 www.ijarbs.com DOI: 10.22192/ijarbs Coden: IJARQG(USA) Volume 5, Issue 3-2018 Research Article DOI: http://dx.doi.org/10.22192/ijarbs.2018.05.03.017 Toxicity of Nerium oleander extracts against Pectinophora gossypiella (Saunders) (Lepidoptera: Gelechiidae) Hemat Z. Moustafa (1), Heba Al Shater (2,3), and Heba Yousef (1,2) (1) Plant Protection Res. Institute, Agric. Res. Center, Giza, Egypt (2) Chemistry Department, Faculty of Sciences and Arts, University of Jeddah, Khulais, Jeddah, Saudi Arabia. (3) Forensic and Toxicology Department, El Menoufia University Hospital *Corresponding author: hemat.zakaria@gmail.com/hebayousef2004@yahoo.com Abstract Laboratory evaluation of 70% Hydroethanolic extracts of Nerium oleander (leaves, stems and flowers) against the 1 st instar larvae of Pectinophora gossypiella (Suanders). Stem extract was the most toxic on the tested insect. Leaves and stems prolonged the larval period while leaves and flowers prolonged the pupal period. The three extracts decrease the larval and pupal weight compared with the control weight. The contents of some heavy metals in the extracts were measured by ICP. The highest metal content of leaves was the Hg (16.27 mg/ 0.5g extract), but the highest metal content was Fe (0.689 mg/ 0.5g extract) in the steam and Ni (8.177 mg/ 0.5g extract) in the flowers. Keywords: Heavy metals, Nerium oleander, Pectinophora gossypiella, Toxicity. Introduction Nerium oleander is an evergreen shrub or small tree in the dogbane family Apocynaceae. It is known as oleander from its superficial resemblance to the unrelated plant Olive olea but has many other names like Nerium indicum Mill., and Nerium odorum Soland. The white and red flowered variety is equated with Nerium indicum (Chaudhary, et al., 2015). The pink bollworm (PBW), P. gossypiella (Saunders) (Lepidoptera: Gelechiidae) is considered a destructive and key pest of the bolls of cotton crop in Egypt and most cotton producing countries which causes great damage to the quality and quantity of cotton yield (El- Naggar, 2003). The metal which has a relatively high density and toxic at low quantity is referred as heavy metal, e.g., arsenic (As), lead (Pb), mercury (Hg), cadmium (Cd), chromium (Cr), thallium (Tl), etc. Some trace elements are also known as heavy metals, e.g., copper (Cu), selenium (Se) and zinc (Zn) ( Suganya et al., 2016). The present work aimed to investigate and find the relation between the content of some heavy metal elements (As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Zn) in 70% ethanolic extracts of Nerium oleander and the degree of toxicity against the Pink Bollworm, P. gossypiella. 163

Materials and Methods Plant material The plant N. oleander was collected from Khulias, Jeddah, Kingdom of Saudi Arabia. Preparation of extracts The fresh flowers, stems and leaves of N. oleander (50 g) were grounded separately and then macerated in 300 ml of 70% aqueous ethanol solution. After leaving the solutions 7days, they were filtered through Whatman No. 40 filter paper. The solvents were removed under reduced pressure using a rotary evaporator to obtain 3.47g extract for the flower, 2 g extract for the stems and 2.6g extract for leaves. Insect used The 1 st instar larvae of PBW, used in this study, was obtained from a standard laboratory colony, reared at Bollworm Department, Plant Protection Research Institute; Agriculture Research Centre (ARC), Giza, Egypt on an artificial diet for several generations away from any insecticidal contamination ( Rashad and Ammar, 1985). Toxicity assay Response of the newly hatched larvae of P. gossypiella was studied. Serial concentrations of 20, 10, 5 and 2.5 (g extract/ 100g diet) were prepared. Fourty newly hatched larvae were transferred individually to the surface of the treated diet, the live larvae transferred after 6 hours on untreated diet and kept in glass tubes (2 x 7.5 cm). The same procedure was done against the newly hatched larvae with untreated diet and used as control. All tubes were capped with cotton stopper and incubated at 26±2 ºc and 70-85% RH and inspected daily until pupation. Mortality was recorded at intervals after 1, 5 and 7 days after larval feeding. Mortalities percentages were corrected according to Abbott formula in each case (Abbott, 1925). The LC 50 concentration was used to investigate the effect of Nerium oleander extracts on the development stages of P. gossypiella larval and pupal duration, weight, and their reduction in weight were calculated as follow: Weight reduction = (weight of control weight of treatment / weight of control) X 100. Digestion of Plant extract and Analysis of Heavy Metals In brief, 0.5 gm of the extract was digested by using 5 ml of concentrated HNO3. The sample was digested until the clear solution was obtained. The digested solution was diluted to the final volume of 100 ml with distilled water and then heated with continuous shaking for 30 min. The sample solution was then filtered through membrane (0.45micron) filter. Finally, the digested samples were used for metal analysis using Inductively Coupled Plasma Mass Spectrometry (Optima 8300 ICP-OES). Results and Discussion The insecticidal activity of the leave extract against the 1 st instar larvae of P. gossypiella was recorded in table (1). The results showed that the toxic effect of the extract against the insect increased with the increase of concentration. The highest percentage of mortality was (g extract / 100g diet) at the concentration 20 (g extract/ 100g diet). Table (1): Toxic effect of N. oleander leave extract against the 1 st instar larvae of P. gossypiella Corrected Mortality % Conc. After 1day After 5 days 7 days 20 10 70 5 55 2.5 25 25 25 control LC 50 5.47 5.16 4. Slope 1.55±0.99 1.52±0.92 1.61±0.94 Values in the same column with different letters were significantly different (ANOVA, Duncan s multiple range test P < 0.05). 164

Data in table (2) describe the toxicity of stems extract against the 1 st instar larvae of P. gossypiella. The concentration 20% was the most effective against the tested insect. Table (2): toxic effect of N. oleander stems extract against the 1 st instar larvae of P. gossypiella Corrected Mortality Conc. After 1day After 5 days 7 days 20 10 5 40 55 55 2.5 30 45 50 control LC 50 5.61 3.71 3.33 Slope 1.96±0.92 1.56±0.96 1.40±0.91 Values in the with different letters were significantly different (ANOVA, Duncan s multiple range test P < 0.05) same column Table (3) explains the toxic effect of N. oleander flower extract against the 1 st instar larvae of P. gossypiella. The extract was effective at all concentrations used. The toxic effect increased with the increasing of concentration. Table (3): toxic effect of N. oleander flower extract against the 1 st instar larvae of P. gossypiella Conc. 20 10 5 2.5 control LC 50 Corrected Mortality After 1day After 5 days 90 63.33 16.67 26.67 4.90 4.14 7 days 63.33 26.67 4.14 Slope 2.44±0.94 1.94±0. 2.49±0.98 In this respect, Lokesh et al., (2010) found that the leaf extract of N. oleander contains larvicidal activity for the most available genera in the survey. In addition, Ali et al., (2008) found that T. granarium larvae showed 10% mortality after 72 hours at 100mg dose level of N. oleander leaf extract. Also, Hussain et al., (1996 ) reported that treated Spodoptera littoralis with N. oleander extract induced remarkably increase mortality. And, N. oleander ethanolic extracts showed insecticidal activity against rice weevil, Sitophilus oryzae infesting stored wheat and rice (Satpathi et al., 1992). Fouad et al. (2015) concluded that the larvicidal activity of hydroethanolic extract of N. oleander on C. pipiens could be due to the major 1 components. This would include the flavonoids, the sterols, and the terpenes. And, Trease and Evans (2002); Tiwari and Singh (2004 ) found that the leaves of N. oleander contain a mixture of very toxic cardiac glycosides of cardenolides like oleandrin, oleandrigenin, digoxin, digitonin, digitoxigenin, nerizoside, neritaloside, and odoroside. Semiz, (2017), indicated that N. oleander leaves extract can be used as a commercial insecticide against Thaumetopoea wilkinsoni. The duration and weight of larvae and pupae of newly hatched larvae, treated with the LC 50 concentrations of N. oleander extracts are shown in table (4). The average of larval duration for the larvae treated with N. oleander stems, leaves and flowers extracts was 27.15,

26.69 and 17.14 days, respectively, while the control recorded 16.01 days. The average of pupal duration for the larvae treated with N. oleander leaves and flowers was significantly differs than control. All the extracts recorded a significantly reduction in larval and pupal weight when compared with the control weight. Table (4): Effect of LC 50 of N. oleander on the developmental parameters of P. gossypiella under laboratory conditions Larvae duration Pupal period Treatments Duration days Weight (g) W.R % Pupal duration (days) Weight (g) W.R% Stems 27.15 a ±0.23 0.027 c ±05 42.55 8.25 c ±0.20 0.021 c ±3 42.55 Leaves 26.69 b ±0.35 0.022 d ±3 53.19 12.62 a ±0.27 0.0203 c ±4 44.04 Flowers 17.14 c ±0.21 0.039 b ±4 17.02 11.90 b ±0.37 0.0256 b ±2 32.77 Control 16.01 d ±0.58 0.047 a ±5 7.97 c ±0.23 0.041 a ±42 F value 6968.26*** 568.46*** 232.34*** 696.94*** LSD 0.23 15 0.51 12 Values in the same column with different letters were significantly different (ANOVA, Duncan s multiple range test P < 0.05) The data in table (5) represents the heavy metal contents in ethanolic extract of N. oleander different parts. The metals (As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Zn) contents were measured by ICP instrument. The highest metal content of leaves was Hg16.27 (mg/ 0.5gm extract), but the highest metal content was Fe 0.689 (mg / 0.5gm extract) in the steam and Ni was 8.177 (mg/ 0.5gm extract) in the flowers. Table (5): The heavy metal contents in ethanolic extracts of N. oleander Element As Cd Co Cr Cu Fe Hg Mn Ni Pb Zn Concentration (mg/ 0.5gm extract) Leaves Stems Flowers 0.492 0.301 0.048 0.098 0.012 0.027 0.110 0.458 0.099 0.8 1.111 0.689 3.356 16.27 0.102 5.475 0.338 0.090 0.127 0.187 0.019 8.177 0.746 0.250 166

Heavy metals received major attention because of their persistent toxic effect ( Lagrana et al., 2011). The toxic effect of some heavy metals against insects was previously reported by Suganya et al., (2016) ; Baghban (2014); El-Sheikh et al., (2010) and Kitvatanachai (2005). Lagrana et al., 2011, reported the toxic effect of Cu, Cd and Pb against chironomids. Yousef et al., 2016 reported the toxic effect of some heavy metals present in Calotropis procera and Ocimum sanctum against Pectinophora gossypiella (Saunds.). Conclusion In conclusion, the results of the present study provide new data focusing on insecticidal efficacy of N. oleander extracts on P. gossypiella. Such findings may encourage a further research to test N. oleander extracts effects against non-target organisms in the environment. References Abbott, W. S. A. (1925). Method for computing the effectiveness of an insecticide. J. Econ. Entomol., 18: 2. Ali, S.S. Ali,S. Munir, S. and Riaz, T. (2008). Insecticidal and bactericidal effects of ethanolic leaf extract of common oleander Nerium oleander. Punjab Univ. J. Zool., 23: (1-2) pp. Baghban, A. Sendi, J. J. Zibaee, A. and Khosravi, R. (2014). Effect of heavy metals (Cd, Cu, and Zn) on feeding indices and energy reserves of the cotton boll worm Helicoverpa armigera Hübner (Lepidoptera: Noctuidae). Journal of plant protection research. 54: 367-673. Chaudhary, K. Prasad, D.N. and Sandhu, B.S. (2015). Preliminary pharmacognostic and phytochemical studies on Nerium oleander Linn. (White cultivar). Journal of Pharmacognosy and Phytochemistry. 4(1): 185-188. Fouad, E.A.; Raja G. Yassine; E. Z. and Abdelhakim E. L. (2015). Larvicidal Activity of Nerium oleander against Larvae West Nile Vector Mosquito Culex pipiens (Diptera: Culicidae). Journal of Parasitology Research. Volume 2015, Article ID 9430, 5 pages. http://dx.doi.org/10.1155/2015/9430. El-Naggar, A. Z. A. (2003). Evaluation of Certain New Approaches of Control Measures in an Integrated Pest Management Program of Cotton Bollworms.Ph. D. Thesis, Faculty of Agriculture (Saba-Bacha), Alexandria University, Egypt, 164pp. El-Sheikh, T. M. Y. Fouda, M. A. Hassan M. I. Abd- Elghaphar A. and Hasaballah A. I. (2010). Toxicological Effects of Some Heavy Metal Ions on Culex pipiens L. (Diptera: Culicidae) Egypt. Acad. J. biolog. Sci. 2 (1):63-76. Hussain, A.M., Makkar, A.W., Sokkar, A.L., Allam, A.M. and Mostafa, S.A. (1996). The bioactivity of certain benzoylphenylureas on the cotton leaf worm Spodoptera littoralis (Boisd) moth s survival, longevity and fecundity ann. Agric. Sci. Moshtohor., 34: 1263-1276. Kitvatanachai, S. Apiwathnasorn, C. Leemingsawat, S. Wongwit, W. and Tornee, S. (2005). Determination of lead toxicity in culex quinquefasciatus mosquitoes in the laboratory. Southeast asian j trop med public health. 36: 862-874. Lagrana, C. C. Apodaca, D. C. David, C. P. (2011). Toxicity of Cu2+, Cd2+ and Pb2+ Metal Ions in Chironomids and Factors that Affect Metal Accumulation. International Conference on Environment Science and Engineering IPCBEE. 8: 9-13. Lokesh, R. Leonard Barnabas, E. Madhuri, P. and Saurav, K. (2010). Larvicidal Activity of Trigonella foenum and Nerium oleander Leaves Against Mosquito Larvae Found in Vellore City, India. Sundar Current Research Journal of Biological Sciences 2(3): 154-1 Rashad, A. M. and E. D. Ammer (1985). Mass-rearing of spiny bollworm, Earias insulana (Boisd.) on semi-artificial diet. Bull. Soc. ent. Egypt. :239-244. Satpathi, C. R., Ghatak, S. S. and Bhusan, T. K., (1992). Insecticidal properties of some plant extracts against rice weevil, Sitophilus oryzae L. (Cuclionidae: Coleoptera). Environ. Ecol., 10: 79-100. Semiz, G. (2017). Larvicidal activity of Nerium oleander L. leaf extract against Pine Processionary Moth (Thaumetopoea wilkinsoni Tams.). Journal of Entomology and Zoology Studies, 5(6): 79-81. Suganya, M. Karthi, S and Shivakumar, M. S. (2016). Effect of Cadmium and Lead Exposure on Tissue Specific Antioxidant Response in Spodoptera litura. Free Radicals and Antioxidants. 6(1): 90-100. Tiwari, S. and Singh, A. (2004). Toxic and sub-lethal effects of oleandrin on biochemical parameters of fresh water air breathing murrel, Channa punctatus (Bloch.), Indian Journal of Experimental. Biology, 42(4): 413 418. 167

Trease, G. E. and Evans W. C. (2002). Pharmacognosy, W.B. Saunders, Edinburg, Tex, USA, 15th edition. Yousef H., El-Shater H., and Moustafa H. Z. (2016). Efficacy of two Ethanolic Plant Extracts against the Pink Bollworm Pectinophora gossypiella (Saunders) (Lepidoptera: Gelechiidae). Egypt. J. Biol. Pest Control, 26(2):241-244. Int. J. Adv. Res. Biol. Sci. (2018). 5(3): 163-168 Access this Article in Online Website: www.ijarbs.com Subject: Agricultural Quick Response Sciences Code DOI:10.22192/ijarbs.2018.05.03.017 How to cite this article: Hemat Z. Moustafa, Heba Al Shater, and Heba Yousef. (2018). Toxicity of Nerium oleander extracts against Pectinophora gossypiella (Saunders) (Lepidoptera: Gelechiidae). Int. J. Adv. Res. Biol. Sci. 5(3): 163-168. DOI: http://dx.doi.org/10.22192/ijarbs.2018.05.03.017 168