Home / Current Issue / Paper 1713503
Studies on the Distribution of Bacillus Thuringiensis Isolated from Arable Soil in Keffi and Its Toxicity Against Mosquito Larvae
Subject area: Biological & Medical Sciences · Area of research: Environmental Microbiology
DOI: https://doi.org/10.64388/IREV9I7-1713503
Abstract
Plant pests and diseases affect 20%?40% of food production globally. Inadequate use of chemical pesticides to control pests has increased selection pressure, resulting in insect resistance and affects soil fertility. To resolve these issues, a new form of pest control is desperately needed. Most of the micro-organisms are capable of surviving in almost all sorts of environments. In the present scenario, development of diseases, resistanct varieties, and chemical pesticide resistance are a few major hurdles for insect pest management. Over the past two decades, biopesticides provide 1% of total plant protection worldwide; about 175 biopesticide compounds and 700 biopesticide products have already existed in the market globally. Entomotoxic microorganisms are becoming very effective as biocontrol agents of different pest and used as alternative to chemical pesticides. This study is aimed at distribution of Bacillus thuringiensis isolated from arable soil in Keffi and its toxicity against Mosquito larvae. Soil samples were collected using a clean spoon and inserted into sterile polythene bags from 30 different arable lands in Keffi. Isolation and identification of the bacteria was carried out using standard microbiological techniques. Light microscopy showed the presence of parasporal bodies produced by the isolates. Molecular identification was carried out using 16sRNA polymerase chain reaction method. Mosquito larvae were collected by allowing water containers filled with water to remain in an open space thereby facilitating laying of eggs by mosquitoes. The mean Standard deviation of the bacteria ranges from 1.2 ? 10 2 cfu/g to 11.2 ?103 cfu/g. The overall occurrence of Bacillus thuringiensis in this study was 40.0%. The highest isolates were isolated from arable soil collected from Nasarawa road while the lowest with occurrence of 17.0% was isolated from arable soil from Nasarawa State University (main campus). Arable soil where maize was grown had the highest number of isolates.The highest mean Standard deviation of the bacterial load was from Bacillus thuringiensis isolated from Nasarawa road and the lowest mean standard deviation was from Nasarawa state university (Main campus). Crystal proteins detected from Bacillus thuringiensis isolates were Cry 1, 2, 3, 4, 7, 9 and 11. Cry 1, Cry 2 and Cry 11 were the most abundantly detected crystal protein genes among the isolates. The detection of these cry genes was carried out using a PCR technique. All the 12 Bacillus thuringiensis isolates in the study were toxic to the larvae of mosquitoes and therefore could be adopted as a form of biopesticide and consequently used in controlling mosquito breeding and other pests of economic importance.
References
[1] Abo-Bakr, A., Mahmoud, E.F., Fatma, B., Ashraf, O.A. and Saad, M. (2020). Egyptian Journal of Biological Pest Control (2020) 30:54
[2] Adedayo, M.R. and Uthman, A.A. (2021). Bacillus thuringiensis Isolated from Flour Mill Soil and Its Toxicity against Culex and Aedes Larvae. Journal of Microbiology and Infectious Diseases. 11(4):224-232
[3] Aksoy, H.M.,Saruhan, I., Acka, I., Kaya, Y., Onder, H., Ozturk, M. and Aker, O. (2015). Isolation and Characterizatin of Bacillus thuringiensis Isolated from soil and their possible impact on Culex pipiens Larvae. Egyptian Journal of Biological pest control, 25(2):439-444
[4] Akwa, V.L., Bimbol, N.L., Samaila, K.L. and Marcus, N.D. (2007). Geography Perspective of Nasarawa State. Onaivi Printing and Publishing Company, Keffi, Nigeria, Pp: 3–5
[5] Ammouneh, H., Idris, M.E. and Makee, H. (2010). Isolation and characterization of native Bacillus thuringiensis isolates from Syrian soil and testing of their insecticidal activities against some insect pests. Turkish Journal of Agriculture. 35:421–431
[6] Boisvert, M. (2005). Utilization of Bacillus thuringiensis var. israelensis (Bti)-based formulation for the biological control of mosquito in Canada. Pp. 87-93
[7] Charles, J. F., and Barjac, H. (1982). Sporulation et cristallogénèse de Bacillus thuringiensis var. israelensis en microscopie électronique. Ann. Inst. Pasteur Mic. 133:425-442.
[8] Elleuch, J., Jaoua, S., Ginibre, C., Chandre, F., Tounsi, S., Zghal, R.Z., (2016). Toxin stability improvement and toxicity increase against dipteran and lepidopteran larvae of Bacillus thuringiensis crystal protein Cry2Aa. Pest Management Science. 72 (12), 2240–2246.
[9] Liang, H., Liu, Y., Zhu, J., Guan, P. and Li, S. (2011). Characterization of cry2-type genes of Bacillus thuringiensis strains from soil-isolated of Sichuan basin, China. Brazilian Journal of Microbiology 42, 140-146.
[10] Liu, J., Cui, X., Liu, Z., Guo, Z., Yu, Z., Yao, Q., Sui, Y., Jin, J., Liu, X. and Wang G (2019). The Diversity and Geographic Distribution of Cultivable Bacillus-Like Bacteria Across Black Soils of Northeast China. Frontiers in Microbiology, 10:1424.
[11] Melo, A.L., Soccol, V.T. and Soccol, C.R., (2016). Bacillus thuringiensis: mechanism of action, resistance, and new applications: a review. Critical Revised Biotechnology, 36 (2), 317–326.
[12] Osman, G., Already, R., Assaeedi, A., Organji, S., El-Ghareeb, D., Abulreesh, H. and Althubiani, A.(2015). Bioinsecticide Bacillus thuringiensis a comprehensive review. Egyptian Journal of. Biological Pest Control, 25 (1), 271.
[13] Pimentel, D. (2005). Environmental DNA economic costs of the application of pesticides primarily in the United States. Environment, Development and Sustainability, 7:229–252
[14] Praça, L.B., Batista, A.C. and Martins, E.S. (2004). Estirpes de Bacillus thuringiensise fetivas contra insetos das ordens Lepidoptera.Coleoptera e Diptera. Pesqui. Agropecu. Bras; 39 (5): 11-16.
[15] Rajendran, J. Subramanian, N. and Velu, R.K. (2018). Larvicidal Activity of Bacillus thuringiensis Isolated from Cotton Rhizosphere Soil against Anopheles Mosquito Larvae. Asian Journal of Pharmacology and Clinical Research 2; 11(9): 456-462.
[16] Rodríguez, P., Cerda, A., Font, X., Sánchez, A. and Artola, A. (2019). Valorisation of biowastedigestate through solid state fermentation to produce biopesticides from Bacillus thuringiensis. Waste Management, 93, 63–71.
[17] Sauka, D.H., Monella, R.H. and Benintende, G.B. (2010). Detection of the mosquitocidal toxin genes encoding Cry11 proteins from Bacillus thuringiensis using a novel PCR-RFLP method. Revised Argent Microbiology, 42:23–26
[18] Sayed, A.M. and Behle, R.W. (2017). Evaluating a dual microbial agent biopesticide with Bacillus thuringiensis var. kurstaki and Beauveria bassiana blastospores. Biocontrol Science and Technology, 27 (4), 461–474.
[19] Sridhara, P.B., Dharmashekara, C., Srinivasa, C., Shivamallu, C, Kollur, S.P. and Gopinath, S.M. (2021). Isolation, characterization, and optimization of protease-producing bacterium Bacillus thuringiensis from paddy field soil. Pharmacology Research; 13:89-95.
[20] Thomas, W., Claire, L.J., Karen, M. and Nicholas, J. (2014). Mosquito cell lines. Parasite and vectors, 7: 382.
[21] Valicente, F.H., Tuelher, E.S., Paiva, C.E.C., Gumaraes, M.R.F., Macedo, C.V. and Wolff, J.L.C. (2008). A new baculovirus isolate that does not cause the liquefaction of the integument in Spodoptera frugiperda dead larvae. Rev. Bras. de Milho e Sorgo 7(1):245-255.
How to cite this paper
@article{1713503,
author = {A. U. Suleiman , M. D. Makut, J. E. Owuna},
title = {Studies on the Distribution of Bacillus Thuringiensis Isolated from Arable Soil in Keffi and Its Toxicity Against Mosquito Larvae},
journal = {Iconic Research And Engineering Journals},
year = {2026},
volume = {9},
number = {7},
pages = {800-805},
issn = {2456-8880},
url = {https://www.irejournals.com/formatedpaper/1713503.pdf},
abstract = {Plant pests and diseases affect 20%?40% of food production globally. Inadequate use of chemical pesticides to control pests has increased selection pressure, resulting in insect resistance and affects soil fertility. To resolve these issues, a new form of pest control is desperately needed. Most of the micro-organisms are capable of surviving in almost all sorts of environments. In the present scenario, development of diseases, resistanct varieties, and chemical pesticide resistance are a few major hurdles for insect pest management. Over the past two decades, biopesticides provide 1% of total plant protection worldwide; about 175 biopesticide compounds and 700 biopesticide products have already existed in the market globally. Entomotoxic microorganisms are becoming very effective as biocontrol agents of different pest and used as alternative to chemical pesticides. This study is aimed at distribution of Bacillus thuringiensis isolated from arable soil in Keffi and its toxicity against Mosquito larvae. Soil samples were collected using a clean spoon and inserted into sterile polythene bags from 30 different arable lands in Keffi. Isolation and identification of the bacteria was carried out using standard microbiological techniques. Light microscopy showed the presence of parasporal bodies produced by the isolates. Molecular identification was carried out using 16sRNA polymerase chain reaction method. Mosquito larvae were collected by allowing water containers filled with water to remain in an open space thereby facilitating laying of eggs by mosquitoes. The mean Standard deviation of the bacteria ranges from 1.2 ? 10 2 cfu/g to 11.2 ?103 cfu/g. The overall occurrence of Bacillus thuringiensis in this study was 40.0%. The highest isolates were isolated from arable soil collected from Nasarawa road while the lowest with occurrence of 17.0% was isolated from arable soil from Nasarawa State University (main campus). Arable soil where maize was grown had the highest number of isolates.The highest mean Standard deviation of the bacterial load was from Bacillus thuringiensis isolated from Nasarawa road and the lowest mean standard deviation was from Nasarawa state university (Main campus). Crystal proteins detected from Bacillus thuringiensis isolates were Cry 1, 2, 3, 4, 7, 9 and 11. Cry 1, Cry 2 and Cry 11 were the most abundantly detected crystal protein genes among the isolates. The detection of these cry genes was carried out using a PCR technique. All the 12 Bacillus thuringiensis isolates in the study were toxic to the larvae of mosquitoes and therefore could be adopted as a form of biopesticide and consequently used in controlling mosquito breeding and other pests of economic importance.},
month = {January},
doi = {https://doi.org/10.64388/IREV9I7-1713503}
}