Manjarres-Suarez, A. & Olivero-Verbel, J. Chemical control of Aedes aegypti: A historical perspective. Revista Costarricense de Salud Pública. 22(1), 68–75 (2013).
Mossa, A. T., Mohafrash, S. M. & Chandrasekaran, N. Safety of natural insecticides: Toxic effects on experimental animals. BioMed. Res. Int. https://doi.org/10.1155/2018/4308054 (2018).
Hamdan, H., Sofian-Azirun, M., Nazni, W. A. & Lee, H. L. Insecticide resistance development in Culex quinquefasciatus (Say), Aedes aegypti (L.) and Aedes albopictus (Skuse) larvae against malathion, permethrin and temephos. Trop. Biomed. 22(1), 45–52 (2005).
Xu, Q., Liu, H., Zhang, L. & Liu, N. Resistance in the mosquito, Culex quinquefasciatus, and possible mechanisms for resistance. Pest Manage Sci. 61(11), 1096–1102 (2005).
Hidayati, H., Nazni, W. A., Lee, H. L. & Sofian-Azirun, M. Insecticide resistance development in Aedes aegypti upon selection pressure with malathion. Trop. Biomed. 28(2), 425–437 (2011).
Bedini, S. et al. Essential oils sensory quality and their bioactivity against the mosquito Aedes albopictus. Sci. Rep. 8(1), 1 (2018).
Vannette, R. L. & Fukami, T. Nectar microbes can reduce secondary metabolites in nectar and alter effects on nectar consumption by pollinators. Ecology 97(6), 1410–1419 (2016).
Tetali, S. D. Terpenes and isoprenoids: A wealth of compounds for global use. Planta 249(1), 1–8 (2019).
Ryan, M. F. & Byrne, O. Plant-insect coevolution and inhibition of acetylcholineesterase. J. Chem. Ecol. 14, 1965e1975 (1988).
Bloomquist, J. R. et al. Mode of action of the plant-derived silphinenes on insect and mammalian GABAA receptor/chloride channel complex. Pestic Biochem. Physiol. 91(1), 17e23 (2008).
Khambay, B. P., Batty, D., Jewess, P. J., Bateman, G. L. & Hollomon, D. W. Mode of action and pesticidal activity of the natural product dunnione and of some analogues. Pest Manage Sci. 59(2), 174e182 (2003).
Enan, E. Insecticidal activity of essential oils: Octopaminergic sites of action. Comp. Biochem. Physiol. C Toxicol. Pharmacol. 130(3), 325–337 (2001).
Rattan, R. S. Mechanism of action of insecticidal secondary metabolites of plant origin. Crop. Prot. 29(9), 913–920 (2010).
Pugazhvendan, S. R., Ross, P. R. & Elumalai, K. 2012) Insecticidal and repellant activities of four indigenous medicinal plants against stored grain pest, Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae. Asian Pac. J. Trop. Dis. 2, S16-20 (2012).
Obeng-Ofori, D. & Reichmuth, C. H. Bioactivity of eugenol, a major component of essential oil of Ocimum suave (Wild.) against four species of stored-product coleoptera. Int. J. Pest Manage. 43(1), 89–94 (1997).
Scalvenzi, L. et al. Larvicidal activity of Ocimum campechianum, Ocotea quixos and Piper aduncum essential oils against Aedes aegypti. Parasite 26, 23 (2019).
Huang, Y., Lin, M., Jia, M., Hu, J. & Zhu, L. Chemical composition and larvicidal activity against Aedes mosquitoes of essential oils from Arisaema fargesii. Pest Manag Sci. https://doi.org/10.1002/ps.5542 (2019).
Koch, T. et al. Temporary zinc oxide–eugenol cement: Eugenol quantity in dentin and bond strength of resin composite. Eur. J. Oral Sci. 121(4), 363–369 (2013).
Jaganathan, S. K. & Supriyanto, E. Antiproliferative and molecular mechanism of eugenol-induced apoptosis in cancer cells. Molecules 17(6), 6290–6304 (2012).
Ali, S. et al. Antimicrobial activities of Eugenol and Cinnamaldehyde against the human gastric pathogen Helicobacter pylori. Ann. Clin. Microbiol. Antimicrob. 4(1), 20 (2005).
Nam, H. & Kim, M. M. Eugenol with antioxidant activity inhibits MMP-9 related to metastasis in human fibrosarcoma cells. Food Chem. Toxicol. 55, 106–112 (2013).
Strode, C., Donegan, S., Garner, P., Enayati, A. A. & Hemingway, J. The impact of pyrethroid resistance on the efficacy of insecticide-treated bed nets against African anopheline mosquitoes: Systematic review and meta-analysis. PLOS Med. 11(3), e1001619 (2014).
Shen, B. et al. Cytochrome P450 genes expressed in the deltamethrin-susceptible and-resistant strains of Culex pipiens pallens. Pestic Biochem. Physiol. 75(1–2), 19–26 (2003).
Zhu, Y. C., Snodgrass, G. L. & Chen, M. S. Enhanced esterase gene expression and activity in a malathion-resistant strain of the tarnished plant bug, Lygus lineolaris. Insect Biochem. Mol. Bio. 34(11), 1175–1186 (2004).
Che-Mendoza, A., Penilla, R. P. & Rodríguez, D. A. Insecticide resistance and glutathione S-transferases in mosquitoes: A review. Afr. J. Biotechnol. 8(8) (2009).
Liu, N., Xu, Q., Zhu, F. & Zhang, L. E. Pyrethroid resistance in mosquitoes. Insect. Science 13(3), 159–166 (2006).
Bisset, J. A. et al. Temephos resistance and esterase activity in the mosquito Aedes aegypti in Havana, Cuba increased dramatically between 2006 and 2008. Med. Vet. Entomol. 25(3), 233–239 (2011).
Tak, J. H., Jovel, E. & Isman, M. B. Effects of rosemary, thyme and lemongrass oils and their major constituents on detoxifying enzyme activity and insecticidal activity in Trichoplusia ni. Pestic Biochem. Physiol. 140, 9–16 (2017).
Diniz, D. F. et al. Fitness cost in field and laboratory Aedes aegypti populations associated with resistance to the insecticide temephos. Parasit. Vectors 8(1), 1–5 (2015).
Promsiri, S., Naksathit, A., Kruatrachue, M. & Thavara, U. Evaluations of larvicidal activity of medicinal plant extracts to Aedes aegypti (Diptera: Culicidae) and other effects on a non-target fish. Insect Sci. 13(3), 179–188 (2006).
Morlan, H. B., Hayes, R. O. & Schoof, H. F. Methods for mass rearing of Aedes aegypti (L.). Public Health Rep. 78(8), 711 (1963).
Ethiopian Public Health Institute (EPHI). Bacterial, Parasitic and Zoonotic Diseases Research Directorate Public Health Entomology Research Team (PHERT), Anopheles mosquito rearing and insectary handling guidelines 2017. https://www.ephi.gov.et/images/pictures/download2009/Anopheles-mosquito-rearing-and-insectary-handling-guideline.pdf
WHO. Who guidelines for laboratory and field testing of mosquito larvicides, who/cds/whopes/gcdpp/2005, 13 (2005)
Abbott, W. S. A method of computing the effectiveness of an insecticide. J. Econ. Entomol. 18(2), 265–267 (1925).
Finney, D. J. Probit analysis. (ed. Hewlett, P. S.). Cambridge University Press, Cambridge, England. xv+ 333 pp (1971).
Safi, N. H. et al. Evidence of metabolic mechanisms playing a role in multiple insecticides resistance in Anopheles stephensi populations from Afghanistan. Malar J. 16(1), 100 (2017).
Lowry, O. H., Rosebrough, N. J., Farr, A. L. & Randall, R. J. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193, 265–275 (1951).
Navikaite-Snipaitiene, V. et al. Development of antioxidant food packaging materials containing eugenol for extending display life of fresh beef. Meat Sci. 145, 9–15 (2018).
Hu, Q., Zhou, M. & Wei, S. Progress on the antimicrobial activity research of clove oil and eugenol in the food antisepsis field. J. Food Sci. 83(6), 1476–1483 (2018).
Ghosh, V., Mukherjee, A. & Chandrasekaran, N. Eugenol-loaded antimicrobial nanoemulsion preserves fruit juice against, microbial spoilage. Colloids Surf., B 114, 392–397 (2014).
Baker, B. P. & Grant, J. A. Eugenol profile. https://ecommons.cornell.edu/bitstream/handle/1813/56125/eugenol-MRP-NYSIPM.pdf?sequence=1. Barceloux D. 2008. M (2018).
Sarma, R., Adhikari, K., Mahanta, S. & Khanikor, B. Combinations of plant essential oil based terpene compounds as larvicidal and adulticidal agent against Aedes aegypti (Diptera: Culicidae). Sci. Rep. 9(1), 1–2 (2019).
Govindarajan, M., Rajeswary, M., Hoti, S. L., Bhattacharyya, A. & Benelli, G. Eugenol, α-pinene and β-caryophyllene from Plectranthus barbatus essential oil as eco-friendly larvicides against malaria, dengue and Japanese encephalitis mosquito vectors. Parasitol. Res. 115(2), 807–815 (2016).
Brogdon, W. G. & Barber, A. M. Fenitrothion-deltamethrin cross-resistance conferred by esterases in Guatemalan Anopheles albimanus. Pestic Biochem. Physiol. 37(2), 130–139 (1990).
Fischer, I. U., Von Unruh, G. E. & Dengler, H. J. The metabolism of eugenol in man. Xenobiotica 20(2), 209–222 (1990).
Koodalingam, A., Mullainadhan, P. & Arumugam, M. Effects of extract of soapnut Sapindus emarginatus on esterases and phosphatases of the vector mosquito, Aedes aegypti (Diptera: Culicidae). Acta Trop. 118(1), 27–36 (2011).
Cao, C. W., Zhang, J., Gao, X. W., Liang, P. & Guo, H. L. Overexpression of carboxylesterase gene associated with organophosphorous insecticide resistance in cotton aphids, Aphis gossypii (Glover). Pestic Biochem. Physiol. 90(3), 175–180 (2008).
Hemingway, J., Hawkes, N. J., McCarroll, L. & Ranson, H. The molecular basis of insecticide resistance in mosquitoes. Insect Biochem. Mol. Biol. 34(7), 653–665 (2004).
Devonshire, A. L. & Moores, G. D. A carboxylesterase with broad substrate specificity causes organophosphorus, carbamate and pyrethroid resistance in peach-potato aphids (Myzus persicae). Pestic Biochem. Physiol. 18(2), 235–246 (1982).
Rompelberg, C. J. et al. Inhibition of rat, mouse, and human glutathione-s-transferase by eugenol and its oxidation products. Chem-Biol. Interact. 99(1–3), 85–97 (1996).
Qin, W., Huang, S., Li, C., Chen, S. & Peng, Z. Biological activity of the essential oil from the leaves of Piper sarmentosum Roxb.(Piperaceae) and its chemical constituents on Brontispa longissima (Gestro)(Coleoptera: Hispidae). Pestic Biochem. Physiol. 96(3), 132–139 (2010).
Muthusamy, R. & Shivakumar, M. S. Resistance selection and molecular mechanisms of cypermethrin resistance in red hairy caterpillar (Amsacta albistriga Walker). Pestic Biochem. Physiol. 117, 54–61 (2015).
Muthusamy, R., Vishnupriya, M. & Shivakumar, M. S. Biochemical mechanism of chlorantraniliprole resistance in Spodoptera litura (Fab) (Lepidoptera: Noctuidae). J. Asia-Pacific Entomol. 17(4), 865–869 (2014).
Rachokarn, S., Piyasaengthong, N. & Bullangpoti, V. Impact of botanical extracts derived from leaf extracts Melia azedarach L. (Meliaceae) and Amaranthus viridis L. (Amaranthaceae) on populations of Spodoptera exigua (Hübner)(Lepidoptera: Noctuidae) and detoxification enzyme activities. Commun. Agric. Appl. Biol. Sci. 73(3), 451–457 (2008).
Tang, F., Zhang, X., Liu, Y., Gao, X. & Liu, N. In vitro inhibition of glutathione S-transferases by several insecticides and allelochemicals in two moth species. Int. J. Pest Manage. 60(1), 33–38 (2014).
Paeporn, P. et al. Biochemical detection of pyrethroid resistance mechanism in Aedes aegypti in Ratchaburi province, Thailand. Trop. Biomed. 21(2), 145–151 (2004).
Bullangpoti, V., Wajnberg, E., Audant, P. & Feyereisen, R. Antifeedant activity of Jatropha gossypifolia and Melia azedarach senescent leaf extracts on Spodoptera frugiperda (Lepidoptera: Noctuidae) and their potential use as synergists. Pest Manage Sci. 68(9), 1255–1264 (2012).
Koou, S. Y., Chong, C. S., Vythilingam, I., Ng, L. C. & Lee, C. Y. Pyrethroid resistance in Aedes aegypti larvae (Diptera: Culicidae) from Singapore. J. Med. Entomol. 51(1), 170–181 (2014).
Yougang, A. P. et al. Nationwide profiling of insecticide resistance in Aedes albopictus (Diptera: Culicidae) in Cameroon. PLoS ONE 15(6), e0234572 (2020).
Nebert, D. W. et al. Genetic mechanisms controlling the induction of polysubstrate monooxygenase (P-450) activities. Ann. Rev. Pharmacol. Toxicol. 21(1), 431–462 (1981).
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