eISSN: 2221-6197 DOI: 10.31301/2221-6197

Activities of detoxifying enzymes in adults of houseflies Musca domestica L. selected with chlorfenapyr

Year: 2020

Pages: 492-503

Number: Volume 12, issue 4

Summary:

In insects, biochemical mechanisms of insecticide resistance base on increasing of activities of main detoxyfying enzymes – monooxygenases, nonspesific esterases, and glutathion-S-transferases. Currently, the progress of resistance development and the degree of contributing enzymes to resistance in insects have been studied for certain insecticides. The goal of this study was to assess activities of monooxygenase, carboxylesterase, glutathione-S-transferase, and alkaline phosphatase in females and males housefly Musca domestica in the second, fourth, sixth, eighth and tenth generations of the chlorfenapyr-selected strain. Evaluation of chlorfenapyr susceptibility showed that adults M. domestica in tenth generations was tolerating to chlorfenapyr as the resistance ration value was 3.6. In certain generations of chlorfenapyr-selected strain M. domestica, monooxygenase activities in males and females were 1.4-2.1 times more, and alkaline phosphatase activities in females were 2.3-2.7 times more than that in control insects. Glutathione-S-transferase activities had no significant differences in adults M. domestica of control and chlorfenapyr-selected strains. For chlorfenapyr-selected strain M. domestica, activities of monooxygenase, carboxylesterase, and alkaline phosphatase differed in males and females of same generations that suggests that mode and pattern of resistance development might be sex-specific in this specie.

Keywords:

P450 monooxygenase, carboxylesterase, glutathione-S-transferase, mode of insecticide resistance

References:

  1. Abbas N., Shad S.A., Ismail M. Resistance to Conventional and New Insecticides in House Flies (Diptera: Muscidae) From Poultry Facilities in Punjab, Pakistan. Journal of Economic Entomology. 2015. V.108 (2). P.826-833. doi: 10.1093/jee/tou057
  2. Ahmad M., Hollingworth R.M. Synergism of insecticides provides evidence of metabolic mechanisms of resistance in the obliquebanded leafroller Choristoneura rosaceana (Lepidoptera: Tortricidae). Pest Manag Sci. 2004. V.60(5). P.465-473. doi: 10.1002/ps.829
  3. Ameen A., Kaakeh W., Bennett G.W. Integration of chlorfenapyr into a management program for German cockroach (Dictyoptera: Blattellidae) // J. Agric. Urban Entomol. 2000. V.17. P. 135-142.
  4. Amelia-Yap Z.H., Sofian-Azirun M., Chen C.D., Suana I.W., Lau K.W., Elia-Amira N.M.R., HaziqahRashid A., Tan T.K., Lim Y.A.L., Low V.L. Pyrethroids Use: Threats on Metabolic-Mediated Resistance Mechanisms in the Primary Dengue Vector Aedes aegypti (Diptera: Culicidae). Journal of Medical Entomology. 2019. V.56(3). P.811–816. doi: 10.1093/jme/tjz007
  5. Aponte A., Penilla R.P., Rodríguez A.D., Ocampo C.B. Mechanisms of pyrethroid resistance in Aedes (Stegomyia) aegypti from Colombia. Acta Tropica. 2019. V.191. P. 146-154. doi: 10.1016/j.actatropica.2018.12.021
  6. Buczkowski G., Scharf M. E., Ratliff C. R., Bennett G. W. Efficacy of simulated barrier treatments against laboratory colonies of Pharaoh ant. J. Econ. Entomol. 2005. V. 98. P. 485-492. doi: 10.1093/jee/98.2.485
  7. Byford R.L., Craig M.E., Crosby B.L. A review of ectoparasites and their effect on cattle production. J Anim Sci. 1992. V.70(2). P. 597-602. doi: 10.2527/1992.702597x
  8. Dremova V.P., Putintseva L.S., Khodakov P.E. Meditsinskaya dezinsektsiya: Osnovnye printsipy, sredstva i metody. Ekaterinburg: Vitar-Putived', 1999. 320 s (In Russian)
  9. Emtithal A.E.-S., Thanaa A.El-B. Efficacy of some insecticides on field populations of Culex pipiens (Linnaeus) from Egypt. J.Basic Appl. Zool. 2012. V. 65. P. 62-73. doi: 10.1016/j.jobaz.2012.07.005
  10. Eremina O. Chlorfenapyr - perspective pyrrole insecticide for combating resistant synanthropic insects. Pest-Management . 2017. V.1(101). S. 41-49. (In Russian)
  11. Eremina O. Sinergisty kak instrument entomotoksikologicheskikh issledovaniy: issledovanie fermentnykh sistem komnatnykh mukh Musca domestica L. Soobshchenie 1. Prikladnaya entomologiya. 2011. V.1. S. 27-37. (In Russian)
  12. Farooq M., Freed S. Mortality, Biological, and Biochemical Response of Musca domestica (Diptera: Muscidae) to Selected Insecticides // J. Entomol. Sci. 2018. V. 53. P. 27-45. doi: 10.18474/jes17-22.1
  13. Förster M., Klimpel S., Mehlhorn H., Sievert K., Messler S., Pfeffer K. Pilot study on synanthropic flies (e.g. Musca, Sarcophaga, Calliphora, Fannia, Lucilia, Stomoxys) as vectors of pathogenic microorganisms. Parasitology Research. 2007. V.101. P.243–246. doi: 10.1007/s00436-007-0522-y
  14. Glantz S.A. Primer of Biostatistics. McGrawHill, Inc. Translation from English. Moscow, Practica Publ., 1999. 459 p.
  15. Guglielmone A.A., Volpogni M.M., Scherling N., Cobeñas M.M., Mangold A. J., Anziani O. S., loppolo M., Doscher M. Chlorfenapyr ear tags to control Haematobia irritans (L.) (Diptera: Muscidae) on cattle. Vet. Parasitol. 2000. V.93(1). P. 77-82. doi: 10.1016/s0304-4017(00)00335-6
  16. Hodgson E. The significance of cytochrome P450 in insects. Insert Biochem. 1983. V.13.(3). P 237- 251. doi: 10.1016/0020-1790(83)90044-6
  17. Ibragimkhalilova, I.V., Eremina O.Yu.. Development of method for assessing toxic baits and the comparison of the contact and peroral effects of insecticides on house fly (Musca domesticaL.). Agricul. Chem. 2007. V.12. S. 56-62 (in Russian)
  18. Khan H.A.A., Akram W., Iqbal J., Naeem-Ullah U. Thiamethoxam Resistance in the House Fly, Musca domestica L.: Current Status, Resistance Selection, Cross-Resistance Potential and Possible Biochemical Mechanisms. PLoS ONE. 2015. V.10(5): e0125850. doi: 10.1371/journal.pone.0125850
  19. Khrunin A.V. Biokhimicheskie i molekulyarnye aspekty metabolicheskoy ustoychivosti nasekomykh k insektitsidam // Agrokhimiya. 2001. V. 7. S. 72 – 85. (In Russian)
  20. Kristensen M. Glutathione S-transferase and insecticide resistance in laboratory strains and field populations of Musca domestica. Journal of Economic Entomology. 2005. V. 98(4). P. 1341-1348. doi: 10.1603/0022-0493-98.4.1341
  21. Levchenko M. A., Silivanova E. A. Effektivnost' insektitsidnykh primanochnykh sostavov dlya bor'by s mukhami. Vestnik veterinarii. 2015. V. 2 (73). S. 23–26. [The effectiveness of insecticidal bait compositions for houseflies control] (In Russian)
  22. Li J., Wang Q., Zhang L., Gao X Characterization of imidacloprid resistance in the housefly Musca domestica (Diptera:Muscidae). Pesticide Biochemistry and Physiology. 2012. V.102. P. 109-114. doi: 10.1016/j.pestbp.2011.10.012
  23. Li Q., Huang J., Yuan J. Status and preliminary mechanism of resistance to insecticides in a field strain of housefly (Musca domestica, L.). Revista Brasileira de Entomologia. 2018. Vol.62. P.311–314. doi: 10.1016/j.rbe.2018.09.003
  24. Li R., Wang K., Xia X. Resistance selection by meilingmycin and chlorfenapyr and activity changes of detoxicated enzymes in Tetranychus urticae // Acta Phytophylacica Sinica. 2005. V. 32(3). P.309-313.
  25. Li X., Schuler M.A., Berenbaum M.R. Molecular mechanisms of metabolic resistance to synthetic and natural xenobiotics. Annual Review of Entomology. 2007. V.52. P.231–253. doi: 10.1146/annurev.ento.51.110104.151104
  26. Liu N., Yue X. Insecticide resistance and crossresistance in house fly (Diptera: Muscidae). J. Econ. Entomol. 2000. V 93. № 4. Р 1269- 1275. doi: 10.1603/0022-0493-93.4.1269
  27. Lopatina Yu.V., Eremina O.Yu. Mekhanizmy rezistentnosti chlenistonogikh k pestitsidam: snizhenie pronitsaemosti kutikuly i rol' AVS-transporterov // Meditsinskaya parazitologiya i parazitarnye bolezni. 2018. V.4. S. 42-52. [Mechanisms of insecticide resistance in arthropods: reduced сuticle penetration and ABC transporters] (In Russian) doi: 10.33092/0025- 8326mp2018.4.42-52
  28. Low V.L., Chen C.D., Lee H.L., Tan T.K., Chen C.F., Leong C.S., et al. Enzymatic Characterization of Insecticide Resistance Mechanisms in Field Populations of Malaysian Culex quinquefasciatus Say (Diptera: Culicidae). .PLoS ONE. 2013. V.8(11): e79928. doi: 10.1371/journal.pone.0079928
  29. Lowry O.H., Rosebrough N.J., Farr A.L., Randall R.J. Protein measurement with Folin phenol reagent. J. Biol. Chem. 1951. V. 193 (1). P. 265-275.
  30. Markussen M.D.K., Kristensen M. Cytochrome P450 monooxygenase-mediated neonicotinoid resistance in the house fly Musca domestica L. Pesticide Biochemistry and Physiology. 2010. V.98 (1). P.50-58. doi: 10.1016/j.pestbp.2010.04.012
  31. Markussen M.D.K., Kristensen M. Spinosad resistance in female Musca domestica L. from a field derived population. Pest. Manag. Sci. 2012. V. 68. P. 75- 82. doi: 10.1002/ps.2223
  32. Ministry of Health of Brazil. Quantification methodology for enzyme activity related to insecticide resistance in Aedes aegypti. Ministry of Health of Brazil, Fundação Oswaldo Cruz. Brasília: Ministério da Saúde. 2006. 128 p.
  33. N'Guessan R., Boko P., Odjo A., Akogbeto M., Yates A., Rowland M. Chlorfenapyr: a pyrrole insecticide for the control of pyrethroid or DDT resistant Anopheles gambiae (Diptera: Culicidae) mosquitoes. Acta Tropica. 2007. V.102. P.69-78. doi: 10.1016/j.actatropica.2007.03.003
  34. N’Guessan R., Boko P., Odjo A., Knols B., Akogbeto M., Rowland M. Control of pyrethroid resistant Anopheles gambiae and Culex quinquefasciatus mosquitoes with chlorfenapyr in Benin. Tropical Medicine & International Health. 2009. V.14. P. 389- 395. doi: 10.1111/j.1365-3156.2009.02245.x
  35. Qayyum M.A., Wakil W., Arif M.J., Sahi S.T., Saeed N.A., Russell D.A. Multiple Resistances Against Formulated Organophosphates, Pyrethroids, and NewerChemistry Insecticides in Populations of Helicoverpa armigera (Lepidoptera: Noctuidae) from Pakistan. Journal of Economic Entomology. 2015. V.108 (1). P. 286–293. doi: 10.1093/jee/tou037
  36. Romero A., Potter M.F., Haynes K.F. Evaluation of chlorfenapyr for control of the bed bug, Cimex lectularius L. Pest Manag. Sci. 2010. V.66. P. 1243- 1248. doi: 10.1002/ps.2002
  37. Rust M.K., Saran R.K. Toxicity, repellency, and transfer of chlorfenapyr against western subterranean termites (Isoptera: Rhinotermitidae). J. Econ. Entomol. 2006. V.99 (3). P. 864-872. doi: 10.1093/jee/99.3.864
  38. Sarkar M., Bhattacharyya I.K., Borkotoki A., Goswami D., Rabha B., Baruah I., Srivastava R.B. Insecticide resistance and detoxifying enzyme activity in the principal bancroftian filariasis vector, Culex quinquefasciatus, in northeastern India. Medical and Veterinary Entomology. 2009. V. 23(2). V. 122-131. doi: 10.1111/j.1365-2915.2009.00805.x
  39. Scott J., Warren W.C., Beukeboom L.W., Bopp D., Clark A.G. et al. Genome of the house fly, Musca domestica L., a global vector of diseases with adaptations to a septic environment. Genome Biology. 2014. V.15. P.466. doi: 10.1186/s13059-014-0466-3
  40. Serebrov V.V., Gerber O.N., Malyarchuk A.A., Martemyanov V.V., Alekseev A.A., Glupov V.V. Effect of Entomopathogenic Fungi on Detoxification Enzyme Activity in Greater Wax Moth Galleria mellonella L. (Lepidoptera, Pyralidae) and Role of Detoxification Enzymes in Development of Insect Resistance to Entomopathogenic Fungi. Biology Bulletin. 2006. V. 33 (6). P. 581-586. doi: 10.1134/s1062359006060082
  41. Sokolyanskaya M.P. Formirovanie rezistentnosti k piretroidam u lichinok komnatnoy mukhi Musca domestica. Agrokhimiya. 2014. V.3. S. 54-59. [Development of pyrethroid resistance in larvae of housefly Musca domestica] (In Russian)
  42. Sokolyanskaya M.P. Toksikologicheskaya i biokhimicheskaya kharakteristika protsessa formirovaniya rezistentnosti u komnatnoy mukhi (Musca domestica L.) k sovremennym insektitsidam. Avtoref. diss. na soiskanie uchenoy stepeni kandidata biologicheskikh nauk. Vserossiyskiy nauchnoissledovatel'skiy institut zashchity rasteniy rossiyskoy akademii sel'skokhozyaystvennykh nauk. SanktPeterburg, 2007. (In Russian)
  43. Sokolyanskaya M.P., Amirkhanov D.V. Fiziologo-biokhimicheskie mekhanizmy rezistentnosti v populyatsiyakh chlenistonogikh. Agrokhimiya. 2010. V.11. S. 87. [Physiological and biochemical mechanisms of resistance in arthropod populations] (In Russian)
  44. Sokolyanskaya M.P., Gayfullina L.R., Saltykova E.S., Nikolenko A.G. Biokhimicheskie i kletochnye mekhanizmy ustoychivosti komnatnoy mukhi (Musca domestica L.) k bitoksibatsillinu. Agrokhimiya. 2016. V.1. S. 52-58. [The biochemical and cellular mechanisms of the resistance of the house fly (Musca domestica L.) to bitoxibacillin] (In Russian)
  45. Sparks T.C., Crossthwaite A.J., Nauen R., Banba S., Cordova D., Earley F., Ebbinghaus-Kintscher U., Fujioka S., Hirao A., Karmon D., Kennedy R., Nakao T., Popham H.J.R., Salgado V., Watson G.B., Wedel B.J., Wessels F.J. Insecticides, biologics and nematicides: Updates to IRAC’s mode of action classification - a tool for resistance management. Pesticide Biochemistry and Physiology. 2020. V. 167:104587. doi: 10.1016/j.pestbp.2020.104587
  46. Ullah S., Shah RM, Shad SA. Genetics, realized heritability and possible mechanism of chlorfenapyr resistance in Oxycarenus hyalinipennis (Lygaeidae: Hemiptera). Pesticide Biochemistry and Physiology. 2016. V. 133. P. 91-96. doi: 10.1016/j.pestbp.2016.02.007
  47. United States Environmental Protection Agency. Fact Sheets on New Active Ingredients. Pesticide Fact Sheet: Chlorfenapyr [pdf]. 2001. Available at: https://www3.epa.gov/pesticides/chem_search/reg_actio ns/registration/fs_PC-129093_01-Jan-01.pdf (accessed 10 August 2020).
  48. Van Leeuwen T., Stillatus V., Tirry L. Genetic analysis and cross-resistance spectrum of a laboratoryselected chlorfenapyr resistant strain of two-spotted spider mite (Acari: Tetranychidae). Exp Appl Acarol. 2004. V.32(4). P. 249-261. doi: 10.1023/b:appa.0000023240.01937.6d
  49. Van Leeuwen T., Van Pottelberge S., Tirry L. Comparative acaricide susceptibility and detoxifying enzyme activities in field-collected resistant and susceptible strains of Tetranychus urticae. Pest Manag Sci. 2005. V.61(5). V.499-507. doi: 10.1002/ps.1001
  50. Wang X., Wang J., Cao X et al. Long-term monitoring and characterization of resistance to chlorfenapyr in Plutella xylostella (Lepidoptera: Plutellidae) from China. Pest Manag Sci. 2019. V.75(3). P. 591-597. doi: 10.1002/ps.5222
  51. Wang Z., Liu S., Yang B., Liu Z. Characterization of soluble and membrane-bound alkaline phosphatase in Nilaparvata lugens and their potential relation to development and insecticide resistance. Arch. Insect Biochem. Physiol. 2011. V. 78. P. 30-45. doi: 10.1002/arch.20437
  52. Wen Z., Scott J.G. Cross-resistance to imidacloprid in strains of German cockroach (Blattella germanica) and house fly (Musca domestica). Pestic. Sci. 1997. V 49. P. 367-371. doi: 10.1002/(sici)1096- 9063(199704)49:4<_x0033_67:_x003a_aid-ps542>3.0.co;2-l
  53. Zhang L., Gao X., Liang P. Beta-cypermethrin resistance associated with high carboxylesterase activities in a strain of house fly, Musca domestica (Diptera: Muscidae). Pesticide Biochemistry and Physiology. 2007. V. 89(1). P. 65-72. doi: 10.1016/j.pestbp.2007.03.001
  54. Zhang S., Zhang X., Shen J., Mao K., You H., Li J. Susceptibility of field populations of the diamondback moth, Plutella xylostella, to a selection of insecticides in Central China. Pesticide Biochemistry and Physiology. 2016. V.132. P. 38-46, doi: 10.1016/j.pestbp.2016.01.007
  55. Zhang Y., Wang Y., Ma Z., Zhai D., Gao X., Shi X. Cytochrome P450 monooxygenases-mediated sexdifferential spinosad resistance in house flies Musca domestica (Diptera: Muscidae). Pesticide Biochemistry and Physiology. 2019. V.157. P. 178-185. doi: 10.1016/j.pestbp.2019.03.024
  56. Zhang, Y., Guo, M., Ma, Z. et al. Esterasemediated spinosad resistance in house flies Musca domestica (Diptera: Muscidae). Ecotoxicology. 2020. V.29. P. 35–44. doi:10.1007/s10646-019-02125-y
  57. Zhao Y., Wang Q., Ding J., Wang Y., Zhang Z., Liu F., Mu W. Sublethal effects of chlorfenapyr on the life table parameters, nutritional physiology and enzymatic properties of Bradysia odoriphaga (Diptera: Sciaridae). Pesticide Biochemistry and Physiology. 2018. V. 148. P. 93-102. doi: 10.1016/j.pestbp.2018.04.003
  58. Zhu F., Lavine L., O'Neal S., Lavine M., Foss C., Walsh D. Insecticide Resistance and Management Strategies in Urban Ecosystems. Insects. 2016. V.7: 2. doi: 10.3390/insects7010002
  59.  
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eISSN: 2221-6197 DOI: 10.31301/2221-6197