Detection of Insecticide Susceptibility Status and KDR Mutation in Field-Collected Aedes Aegypti from Different Districts of Punjab, India
Abstract
Background: As the state of Punjab has become endemic for dengue, this study was planned to determine the susceptibility status for two different classes of adulticides and the VGSC gene polymorphism in domain II of Aedes aegypti.
Methodology: Adult bioassays were performed with pyrethrum, deltamethrin and malathion as per the WHO protocol. AS-PCR and sequencing of VGSC gene were carried out to detect V1016G and Kdr (Knockdown resistance) mutations.
Results: Ae. aegypti from the districts of Ludhiana and Patiala were found to be resistant to pyrethrum. The V/ V genotype frequency was found to be higher in all districts. Three known polymorphisms in VGSC gene were not recorded but one synonymous and non-synonymous mutation was found. Group B intron was found in domain II of the VGSC gene. For deltamethrin and malathion, 100% susceptibility was recorded for all four districts.
Conclusion: Thus, the present findings indicate 100% susceptibility towards deltamethrin and malathion whereas, moderate resistance towards pyrethrum was recorded. Therefore, more studies should be planned to study polymorphisms in the various domains of the VGSC gene.
How to cite this article:
Kaura T, Devi S, Mewara A, Kaur J, Singh NI, Lovleen, Sharma SK, Ratho RK, Sehgal R, Grover GS. Detection of Insecticide Susceptibility Status and KDR Mutation in Field-Collected Aedes Aegypti from Different Districts of Punjab, India. J Commun Dis. 2022;54(4):21-28.
DOI: https://doi.org/10.24321/0019.5138.202298
References
Diouf K, Nour NM. Mosquito-borne diseases as a global health problem implications for pregnancy and travel. Obstet Gynecol Surv. 2017;72(5):309-18. [PubMed] [Google Scholar]
Omodior O, Luetke MC, Nelson EJ. Mosquito-borne infectious disease, risk-perceptions, and personal protective behavior among U.S. international travelers. Prev Med Rep. 2018;12:336-42. [PubMed] [Google Scholar]
Chakravarti A, Arora R, Luxemburger C. Fifty years of dengue in India. Trans R Soc Trop Med Hyg. 2012;106:273-82. [PubMed] [Google Scholar]
Bhatt S, Gething PW, Brady OJ, Messina JP, Farlow AW, Moyes CL, Drake JM, Brownstein JS, Hoen AG, Sankoh O, Myers MF, George DB, Jaenisch T, Wint GR, Simmons CP, Scott TW, Farrar JJ, Hay SI. The global distribution and burden of dengue. Nature. 2013;496:504-7. [PubMed] [Google Scholar]
Ganeshkumar P, Murhekar MV, Poornima V, Saravanakumar V, Sukumaran K, Anandaselvasankar A, John D, Mehendale SM. Dengue infection in India a systematic review and meta-analysis. PLoS Negl Trop Dis. 2018;12(7):e0006618. [PubMed] [Google Scholar]
Murray NE, Quam MB, Wilder-Smith A. Epidemiology of dengue past, present and future prospects. Clin Epidemiol. 2013;5:299-309. [PubMed] [Google Scholar]
Rather IA, Parray HA, Lone JB, Paek WK, Lim J, Bajpai VK, Park YH. Prevention and control strategies to counter dengue virus infection. Front Cell Infect Microbiol. 2017;7:336. [PubMed] [Google Scholar]
Johnson BJ, Ritchie SA, Fonseca DM. The state of the art of lethal oviposition trap-based mass interventions for arboviral control. Insects. 2017;8(1):5. [PubMed] [Google Scholar]
Amelia-Yap ZH, Chen CD, Sofian-Azirun M, Low VL. Pyrethroid resistance in the dengue vector Aedes aegypti in Southeast Asia present situation and prospects for management. Parasit Vectors. 2018;11:332. [PubMed] [Google Scholar]
Okia M, Hoel DF, Kirunda J, Rwakimari JB, Mpeka B, Ambayo D, Price A, Oguttu DW, Okui AP, Govere J. Insecticide resistance status of the malaria mosquitoes Anopheles gambiae and Anopheles funestus in eastern and northern Uganda. Malar J. 2018;17:157. [PubMed] [Google Scholar]
Oumbouke WA, Pignatelli P, Barreaux AM, Tia IZ, Koffi AA, Alou LP, Sternberg ED, Thomas MB, Weetman D, N’Guessan R. Fine scale spatial investigation of multiple insecticide resistance and underlying target-site and metabolic mechanisms in Anopheles gambiae in central Côte d’Ivoire. Sci Rep. 2020;10(1):15066. [PubMed] [Google Scholar]
Fang Y, Tambo E, Xue JB, Zhang Y, Zhou XN, Khater EI. Molecular analysis of targeted insecticide resistance gene mutations in field-caught mosquitoes of medical importance from Saudi Arabia. J Med Entomol. 2021;58:1839-48. [PubMed] [Google Scholar]
Kawada H, Higa Y, Komagata O, Kasai S, Tomita T, Yen NT, Loan LL, Sanchez RA, Takagi M. Widespread distribution of a newly found point mutation in voltage gated sodium channel in pyrethroid-resistant Aedes aegypti populations in Vietnam. PLoS Negl Trop Dis. 2009;3:e527. [PubMed] [Google Scholar]
Kushwah RB, Dykes CL, Kapoor N, Adak T, Singh OP. Pyrethroid-resistance and presence of two knockdown resistance (kdr) mutations, F1534C and a novel mutation T1520I, in Indian Aedes aegypti. PLoS Negl Trop Dis. 2015;9(1):e3332. [PubMed] [Google Scholar]
Chung HH, Cheng IC, Chen YC, Lin C, Tomita T, Teng HJ. Voltage-gated sodium channel intron polymorphism and four mutations comprise six haplotypes in an Aedes aegypti population in Taiwan. PLoS Negl Trop Dis. 2019;13(3):e0007291. [PubMed] [Google Scholar]
Devi S, Kaura T, Kaur J, Lovleen, Takkar J, Sharma SK, Grover GS. Prevalence of dengue vectors, larval breeding habitats, Stegomyia indices and their correlation with dengue cases in urban and rural areas of Punjab, India. JVector Borne Dis. 2020;57:176-81. [PubMed] [Google Scholar]
FAO/ IAEA. Guidelines for mass-rearing of Aedes mosquitoes. In Maiga H, Mamai W, Yamada H, Argilés R, Bouyer J, editors. Vienna, Austria Food and Agriculture Organization of the United Nations/ International Atomic Energy Agency. 2020;24.
Brogdon WG, Chan A. Guideline for evaluating insecticide resistance in vectors using the CDC bottle bioassay. CDC Atlanta USA: CDC Technical Report. 2010;28.
Tyagi BK, Munirathinam A, Krishnamoorthi R, Venkatesh A. A field-based handbook of identification keys to mosquitoes of public health importance in India. India, Madurai Centre for Research in Medical Entomology. 2012;25-7.
World Health Organization. Test procedures for insecticide resistance monitoring in malaria vector mosquitoes. 2nd ed. Geneva, Switzerland. World Health Organization. 2016;48.
Abramides GC, Roiz D, Guitart R, Quintana S, Guerrero I, Giménez N. Effectiveness of a multiple intervention strategy for the control of the tiger mosquito (Aedes albopictus) in Spain. Trans R Soc Trop Med Hyg. 2011;105:281-8. [PubMed] [Google Scholar]
Paredes-Esquivel C, Lenhart A, del Rio R, Leza MM, Estrugo M, Chalco E, Casanova W, Miranda MA. The impact of indoor residual spraying of deltamethrin on dengue vector populations in the Peruvian Amazon. Acta Trop. 2016;154:139-44. [PubMed] [Google Scholar]
Reiter P, Nathan MB. Guidelines for assessing the efficacy of insecticidal space sprays for control of dengue vector Aedes aegypti. WHO/CDS/CPE/PVC/2001.1. World Health Organization. 2001. [Google Scholar]
World Health Organization. Standard operating procedure for testing insecticide susceptibility of adult mosquitoes in WHO bottle bioassays. WHO Bottlebioassay/ 01/2022;14.
Soni M, Bhattacharya C, Sharma J, Dutta P. Bioassay and molecular study for detection of insecticide resistance dengue causing mosquito vectors. Indian J Med Microbiol. 2018;36(3):435-8. [PubMed] [Google Scholar]
Excoffier L, Lischer HE. Arlequin suite ver 3.5 a new series of programs to perform population genetics analyses under Linux and Windows. Mol Eco Resource. 2010;10:564-7. [PubMed] [Google Scholar]
Campos KB, Martins AJ, Rodovalho CM, Bellinato DF, Dias LS, Macoris ML, Andrighetti MT, Lima JB, Obara MT. Assessment of the susceptibility status of Aedes aegypti (Diptera Culicidae) populations to pyriproxyfen and malathion in a nation-wide monitoring of insecticide resistance performed in Brazil from 2017 to 2018. Parasit Vectors. 2020;13:531. [PubMed] [Google Scholar]
Orsborne J, Banks SD, Hendy A, Gezan SA, Kaur H, Wilder-Smith A, Lindsay SW, Loan JG. Personal protection of permethrin-treated clothing against Aedes aegypti, the vector of dengue and Zika virus, in the laboratory. PLoS One. 2016;11:e0152805. [PubMed] [Google Scholar]
Wylie BJ, Hauptman M, Woolf AD, Goldman RH. Insect repellents during pregnancy in the era of the Zika virus. Obstet Gynecol. 2016;128:1111-5. [PubMed] [Google Scholar]
Chatterjee M, Ballav S, Maji AK, Basu N, Sarkar BC, Saha P. Polymorphisms in voltage-gated sodium channel gene and susceptibility of Aedes albopictus to insecticides in three districts of northern West Bengal, India. PLoS Nel Trop Dis. 2018;12(1):e0006192. [PubMed] [Google Scholar]
Hamid PH, Ninditya VI, Prastowo J, Haryanto A, Taubert A, Hermosilla C. Current status of Aedes aegypti insecticide resistance development from Banjarmasin, Kalimantan, Indonesia. Biomed Res Int. 2018;2018:1735358. [PubMed] [Google Scholar]
Pinto J, Palomino M, Mendoza-Uribe L, Sinti C, Liebman KA, Lenhart A. Susceptibility to insecticides and resistance mechanisms in three populations of Aedes aegypti from Peru. Parasit Vectors. 2019;12:494. [PubMed] [Google Scholar]
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