Mortality Responses of Spodoptera litura Following Feeding on BT- Sprayed Plants
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Keywords

 Crystals, Endospores, Hybrid vigor, Mortality, Recombinant bioinsecticides, survival.

How to Cite

Saad A. AlOtaibi. (2013). Mortality Responses of Spodoptera litura Following Feeding on BT- Sprayed Plants. Journal of Basic & Applied Sciences, 9, 195–215. https://doi.org/10.6000/1927-5129.2013.09.27

Abstract

Bacillus thuringiensis delta-endotoxins are safe biological insecticidal proteins whose usefulness has long been recognized. The first commercialized Bt insecticidal formulations were composed of spore-crystal preparations derived from wild-type strains. These products generally have a limited insecticidal host range and several genetically modified strains have, therefore, been constructed in this study using conjugation procedure. However, addition of a new plasmids to Bt strains already harboring other genes often resulted in broader - spectrum. Bacillus thuringiensis serovar Kurstaki, Bacillus subtilis and four of their transconjugants were used in this study as a biocontral agents against lepidopterous cotton pest. Bacterial transconjugants were evaluated for their hybrid vigor in relation to the mid parents and better parent. This evaluation was related to survival and mortality percentages induced in Spodoptera littoralis larvae. Two groups of bioinsecticides; crystals, crystals + endospores were used to be evaluated in this study. The results appeared that bioinsecticides containing crystals + endospores was more effective than crystals for increasing mortality percentage and reducing survival percentage. This effective was including reduction in the mean number of Spodoptera littoralis larvae feeding on leaves sprayed with crystals + endospores. Increasing mortality percentage of crystals + endospores was due to higher toxicological effects than that of crystals. This recommended bioinsecticide biologists to use crystals + endospores in all bioinsecticides formulations. Higher positive efficiency was appeared at 168 h of treatments. Recombinant Bacillus thuringiensis was more effective as biocontrol agents against lepidopteran pests at the early instars, because susceptibility was decreased with larval development. This indicated that the first instars were more susceptible to Bt sprayed plants than the later instar stages. The combined effects of crystals + endospores produced higher mortality. This factor was important to be considered in designing resistance management strategies.

https://doi.org/10.6000/1927-5129.2013.09.27
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References

Krattiger AF. Insect Resistance in Crops: A Case Study of Bacillus thuringiensis (Bt) and its Transfer to Developing Countries. ISAAA Briefs 2, A. F. 1998. The Importance of AgriBiotechnology to Global Prosperity. ISAAA Briefs 6 1997.

Oerke EC. Crop losses to pests. J Agric Sci 2006; 144: 31-43. http://dx.doi.org/10.1017/S0021859605005708

Srinivasan A, Giri A, Gupta V. Structural and functional diversities in lepidopteran serine proteases. Cell Mol Biol Lett 2006; 11: 132-54. http://dx.doi.org/10.2478/s11658-006-0012-8

Brooke E, Hines E. Viral biopesticides for Heliothine control-fact of fiction? Today's Life Sci 1999; 11: 38-45.

Haq SK, Atif SM, Khan RH. Protein proteinase inhibitor genes in combat against insects, pests, and pathogens: natural and engineered phytoprotection. Arch Biochem Biophys 2004; 431: 145-59. http://dx.doi.org/10.1016/j.abb.2004.07.022

Schnepf E, Crickmore N, Van Rie J, Lereclus D, Baum J, Feitelson J, et al. Bacillus thuringiensis and its pesticidal crystal proteins. Microbiol Mol Biol Rev 1998; 62: 775-806.

Angus TA. A bacterial toxin paralysing silkworm larvae. Nature 1954; 173: 54456. http://dx.doi.org/10.1038/173545a0

Lereclus D, Delecluse A, Lecadet MM. Diversity of Bacillus thuringiensis toxins and genes. In: Entwistle P, Cory JS, Bailey MJ, Higgs S. Eds. Diversity of Bacillus thuringiensis Toxins and Genes. Wiley, Chichester, UK 1993; pp. 37-69.

McBride KE, Svab Z, Schaaf DJ, Hogan PS, Stalker DM, Maliga P. Amplification of a chimeric Bacillus gene in chloroplasts leads to an extraordinary level of an insecticidal protein in tobacco. BioTechnology 1995; 13: 362-65. http://dx.doi.org/10.1038/nbt0495-362

Behle RW, McGuire MR, Shasha BS. Effects of sunlight and simulated rain on residual activity of Bacillus thuringiensis formulations. J Econom Entomol 1997; 90: 1560-66.

Muhammad A, Young SY, McNew RW. Larval Mortality and Development of Pseudoplusia includens (Lepidoptera: Noctuidae) Reared on a Transgenic Bacillus thuringiensis-Cotton Cultivar Expressing CryIAc Insecticidal Protein. J Econom Entomol 2001; 94(5): 1053-58. http://dx.doi.org/10.1603/0022-0493-94.5.1053

Collins CH, Lyne PM. Microbiological Methods. 5th ed. Butterworths, London 1985; pp. 167-181.

Roth JR, Sonti RV. Role of gene duplications in the adaptation of Salmonella typhimurium to growth on limiting carbon sources. Genetics 1989; 123: 19-28.

Ames BN, Lee FD, Durston WE. An improved bacterial test system for the detection and classification of mutagens and carcinogens. Proc Natl Acad Sci USA 1973; 70: 782-86. http://dx.doi.org/10.1073/pnas.70.3.782

Lessl M, Balzer D, Weyrauch K, Lanka E. The mating pair formation system of plasmid RP4 defined by RSF 1010 mobilization and donor-specific phage propagation. J Bacteriol 1993; 175(20): 6415-25.

Karamanlidou G, Lambropoulos AF, Koliais SI, Manousis T, Ellar D. Toxicity of Bacillus thuringiensis to laboratory populations of the olive fruit fly (Dacus oleae). Appl Environ Microbiol 1991; 57: 2277-82.

Klanfon AR, De Barjac H. Screening of the insecticidal activity of Bacillus thuringiensis strains against the Egyptian cotton leafworm Spodoptera littoralis. Entomophaga 1985; 30: 177-86. http://dx.doi.org/10.1007/BF02372251

Ignoffo CM, Hostetter DL, Pinnell RE, Garcia C. Relative susceptibility of six soybean caterpillars to a standard preparation of Bacillus thuringiensis var. Kurstaki. J Econom Emtomol 1977; 70(1): 60-63.

Inagaki S, Miyasono M, Ishiguro T, Takeda R, Hayashi Y. Proteolytic processing of ?-endotoxin of Bacillus thuringiensis var. Kurstaki HD-1 in insensitive insect, Spodoptera litura: Unusual proteolysis in the presence of sodium dodecyl sulfate. J Invertebrate Pathol 1992; 60: 64-68. http://dx.doi.org/10.1016/0022-2011(92)90155-W

Bakker W. Enhanced hybrid vigor Benefits Breeder and Broiler. Cobb Focus Issue 2. 2006. http://www.cobbvantress. com/Publications/documents/Cobb_Focus_Two_2006.pdf.

Campbell NA, Reece JB. Biology 6th ed. Benjamin Cummings, Publ. San Francisco 2002.

Obonyo DN, Lovei GL, Songa JM, Oyieke FA, Mugo SN, Nyamasyo GHN. Developmental and mortality responses of Chilo partellus Swinhoe (Lepidoptera: Crambidae) and Sesamia calamistis Hampson (Lepidoptera: Noctuidae) following partial feeding on Bt-transgenic maize. J Appl Biosci 2008; 11: 554-63.

Schoenmaker A, Cusson M, Van Frankenhuyzen K. Interactions between Bacillus thuringiensis and parasitoids of late-instar larvae of the spruce budworm (Lepidoptera: Tortricidae). Can J Zool 2001; 79: 1697-703.

Dutton A, Romeis J, Bigler F. Effects of Bt maize expressing Cry1Ab and Bt spray on Spodoptera littoralis. Entomol Exper Appl 2005; 114: 161-69. http://dx.doi.org/10.1111/j.1570-7458.2005.00239.x

Moreau G, Bauce E. Lethal and sublethal effects of single and double applications of Bacillus thuringiensis variety kurstaki on Spruce Budworm (Lepidoptera: Tortricidae) larvae. J Econom Entomol 2003; 96: 280-86. http://dx.doi.org/10.1603/0022-0493-96.2.280

de Lara HM, Polanczyk RA, Alves SB, de Oliveira GM. Field persistence of Bacillus thuringiensis on maize leaves (Zea mays L.). Braz J Microbiol 2005; 36: 309-14.

Huang F, Leonard BR, Gable RH. Comparative susceptibility of European Corn Borer, Southwestern Corn Borer, and Sugarcane Borer (Lepidoptera: Crambidae) to Cry1Ab protein in a commercial Bacillus thuringiensis corn hybrid. J Econom Entomol 2006; 99: 194-202. http://dx.doi.org/10.1603/0022-0493(2006)099[0194:CSOECB

Horner TA, Dively GP, Herbert DA. Development, survival and fitness performance of Helicoverpa zeae (Lepidoptera: Noctuidae) in MON810 Bt field corn. J Econom Entomol 2003; 96: 914-24. http://dx.doi.org/10.1603/0022-0493-96.3.914

Dively GP, Rose R, Sears MK, Hellmich RL, Stanley-Horn DE, Calvin DD, et al. Effects on Monarch Butterfly Larvae (Lepidoptera: Danaidae) after continuous exposure to Cry1Ab-expressing corn during anthesis. Environ Entomol 2004; 33: 1116-25. http://dx.doi.org/10.1603/0046-225X-33.4.1116

Haggag KHE, Abou Yousef HM. Differentiation among Egyptian Bacillus thuringiensis Strains at Sporulation by Whole Cellular Protein Profiles. World J Agric Sci 2010; 6(2): 224-33.

Zhu1 S, Jianwei S, Xianghui L, Li D, Erdal NY, Feng G. Development and Reproduction of Propylaea japonica (Coleoptera: Coccinellidae) Raised on Aphis gossypii (Homoptera: Aphididae) Fed Transgenic Cotton. Zoological Studies 2006; 45(1): 98-103.

Dutton A, Klein H, Romeis J, Bigler F. Prey-mediated effects of Bacillus thuringiensis spray on the predator Chrysoperla carnea in maize. Biol Control 2002; 26: 209-15. http://dx.doi.org/10.1016/S1049-9644(02)00127-5

Gelernter WD. Targeting insecticide - resistant market: new development in microbial based products. In: Green MB, Moberg WK, LeBaron H, Eds. Targeting insecticide-resistant market: new development in microbial based products. American Chemical Society, Washington, DC, 1990; pp. 105-117.

McGaughey WH. Effects of larval age on the susceptibility of almond moths and Indianmeal moths to Bacillus thuringiensis. J Econom Entomol 1978; 71: 923-25.

Huang F, Buschman LL, Higgins RA. Susceptibility of different instars of European Corn Borer (Lepidoptera: Crambidae) to diet containing Bacillus thuringiensis. J Econom Entomol 1999; 92: 547-50.

Eizaguirre M, Tort S, Lopez C, Albajes R. Effects of sublethal concentrations of Bacillus thuringiensis on larval development of Sesamia nonagroides. J Econom Entomol 2005; 98: 464-70. http://dx.doi.org/10.1603/0022-0493-98.2.464

Tettamanti G, Grimaldi A, Casartelli M, Ambrosetti E, Ponti B, Congiu T, et al. Programmed cell death and stem cell differentiation are responsible for midgut replacement in Heliothis virescens during prepupal instar. Cell Tissue Res 2007; 330: 345-59. http://dx.doi.org/10.1007/s00441-007-0449-8

Huang F, Buschman LL, Higgins RA. Susceptibility of different instars of European Corn Borer (Lepidoptera: Crambidae) to diet containing Bacillus thuringiensis. J Econom Entomol 1999; 92: 547-50.

Khan ZR, Chiliswa P, Ampong-Nyarkpo K, Smart LE, Polaszek A, Wandera J, et al. Utilisation of wild gramineous plants from management of cereal stem borers in Africa. Insect Sci Appl 1997; 17: 143-50.

Mulaa MA, Bergvinson D, Mugo S, Ngeny J. Developing Insect Resistance Management Strategies for Bt Maize in Kenya. African Crop Science Conference Proceedings. Minia University, Egypt 2007; vol. 8: 1067-70.

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Copyright (c) 2013 Saad A. AlOtaibi