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Molecular and Biochemical Detection of Insecticide Resistance in the Leishmania Vector, Phlebotomus Papatasi (Diptera: Psychodidae) to Dichlorodiphenyltrichloroethane and Pyrethroids, in Central Iran Publisher Pubmed



Shiranibidabadi L1, 2 ; Oshaghi MA3 ; Enayati AA4 ; Akhavan AA3, 5 ; Zahraeiramazani AR3 ; Yaghoobiershadi MR3 ; Rassi Y3 ; Aghaeiafshar A2, 6 ; Koosha M3 ; Arandian MH7 ; Ghanei M7 ; Ghassemi M3 ; Vatandoost H3, 5
Authors
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Authors Affiliations
  1. 1. Department Of Vector Biology And Control, Faculty Of Public Health, Kerman University Of Medical Sciences, Kerman, Iran
  2. 2. Research Center Of Tropical And Infectious Diseases, Kerman University Of Medical Sciences, Kerman, Iran
  3. 3. Department Of Medical Entomology And Vector Control, School Of Public Health, Tehran University Of Medical Sciences, Tehran, Iran
  4. 4. Department Of Medical Entomology And Vector Control, School Of Public Health, Mazandaran University Of Medical Sciences, Sari, Iran
  5. 5. Institute For Environmental Research, Tehran University Of Medical Sciences, Tehran, Iran
  6. 6. Leishmaniasis Research Center, Kerman University Of Medical Sciences, Kerman, Iran
  7. 7. Esfahan Health Research Station, National Institute Of Health Research, Tehran University Of Medical Sciences, Tehran, Iran

Source: Journal of Medical Entomology Published:2022


Abstract

The aim of the present study was to explore resistance markers and possible biochemical resistance mechanisms in the Phlebotomine sand fly Phlebotomus papatasi in Esfahan Province, central Iran. Homogenous resistant strains of sand flies were obtained by exposing P. papatasi collected from Esfahan to a single diagnostic dose of DDT. The adults from the colony were tested with papers impregnated with four pyrethroid insecticides: Permethrin 0.75%, Deltamethrin 0.05%, Cyfluthrin 0.15%, and Lambdacyhalothrin 0.05% to determine levels of cross-resistance. To discover the presence of mutations, a 440 base pair fragment of the voltage gated sodium channel (VGSC) gene was amplified and sequenced in both directions for the susceptible and resistant colonies. We also assayed the amount of four enzymes that play a key role in insecticide detoxification in the resistant colonies. A resistance ratio (RR) of 2.52 folds was achieved during the selection of resistant strains. Sequence analysis revealed no knockdown resistance (kdr) mutations in the VGSC gene. Enzyme activity ratio of the resistant candidate and susceptible colonies were calculated for α-esterases (3.78), β-esterases (3.72), mixed function oxidases (MFO) (3.21), and glutathione-S-transferases (GST) (1.59). No cross-resistance to the four pyrethroids insecticides was observed in the DDT resistant colony. The absence of kdr mutations in the VGSC gene suggests that alterations in esterase and MFO enzymes are responsible for the resistant of P. papatasi to DDT in central Iran. This information could have significant predictive utility in managing insecticide resistant in this Leishmania vector. © 2022 The Author(s). Published by Oxford University Press on behalf of Entomological Society of America. All rights reserved.
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