Acknowledgement
This research was funded by the Cooperative Research Program supported by the Rural Development Administration (RS-2025-02692988), and by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Republic of Korea (NRF-2021R1A6A1A03044242).
References
- Balding, P.R., Porro, C.S., McLean, K.J., Sutcliffe, M.J., Marechal, J.-D., Munro, A.W., Visser, S.P.D., 2008. How do azoles inhibit cytochrome P450 enzymes? A density functional study. J. Phys. Chem. A 112, 12911-12918. https://doi.org/10.1021/jp802087w
- Cho, S.-R., Kyung, Y., Shin, S., Kang, W.-J., Jung, D.H., Lee, S.-J., Park, G.-H., Kim, S.I., Cho, S.W., Kim, H.K., 2018. Susceptibility of field populations of Plutella xylostella and Spodoptera exigua to four diamide insecticides. Korean J. Appl. Entomol. 57, 43-50.
- Dalhoff, K., Gottardi, M., Kretschmann, A., Cedergreen, N., 2016. What causes the difference in synergistic potentials of propiconazole and prochloraz toward pyrethroids in Daphnia magna? Aquat. Toxicol. 172, 95-102. https://doi.org/10.1016/j.aquatox.2015.12.007
- Feyereisen, R., 2012. Insect CYP genes and P450 enzymes. in: Gilbert, L.I. (Ed.), Insect molecular biology and biochemistry. Elsevier, Amsterdam, pp. 236-316.
- Gottardi, M., Cedergreen, N., 2019. The synergistic potential of azole fungicides does not directly correlate to the inhibition of cytochrome P450 activity in aquatic invertebrates. Aquat. Toxicol. 207, 187-196. https://doi.org/10.1016/j.aquatox.2018.12.010
- Haas, J., Glaubitz, J., Koenig, U., Nauen, R., 2022. A mechanismbased approach unveils metabolic routes potentially mediating chlorantraniliprole synergism in honey bees, Apis mellifera L., by azole fungicides. Pest Manag. Sci. 78, 965-973. https://doi.org/10.1002/ps.v78.3
- Haas, J., Nauen, R., 2021. Pesticide risk assessment at the molecular level using honey bee cytochrome P450 enzymes: a complementary approach. Environ. Int. 147, 106372. https://doi.org/10.1016/j.envint.2020.106372
- Han, C., Rahman, M.-M., Kim, J., Lueke, B., Nauen, R., 2024. Genome-wide analysis of detoxification genes conferring diamide insecticide resistance in Spodoptera exigua identifies CYP9A40. Chemosphere 367, 143623. https://doi.org/10.1016/j.chemosphere.2024.143623
- Han, C., Rahman, M.-M., Shin, J., Kim, J.H., Lee, S.H., Kwon, M., Timm, A.E., Ramasamy, S., Lee, Y., Kang, S., 2023. Exaptation of I4760M mutation in ryanodine receptor of Spodoptera exigua (Lepidoptera: Noctuidae): Lessons from museum and field samples. Pestic. Biochem. Physiol. 195, 105579. https://doi.org/10.1016/j.pestbp.2023.105579
- Huang, J.-M., Zhao, Y.-X., Sun, H., Ni, H., Liu, C., Wang, X., Gao, C.-F., Wu, S.-F., 2021. Monitoring and mechanisms of insecticide resistance in Spodoptera exigua (Lepidoptera: Noctuidae), with special reference to diamides. Pestic. Biochem. Physiol. 174, 104831. https://doi.org/10.1016/j.pestbp.2021.104831
- Jan, S., Liu, S., Hafeez, M., Zhang, X., Dawar, F.U., Guo, J., Gao, C., Wang, M., 2017. Isolation and functional identification of three cuticle protein genes during metamorphosis of the beet armyworm, Spodoptera exigua. Sci. Rep. 7, 16061. https://doi.org/10.1038/s41598-017-16435-w
- Johnson, R.M., Dahlgren, L., Siegfried, B.D., Ellis, M.D., 2013. Acaricide, fungicide and drug interactions in honey bees (Apis mellifera). PLoS One 8, e54092. https://doi.org/10.1371/journal.pone.0054092
- Joußen, N., Agnolet, S., Lorenz, S., Schöne, S.E., Ellinger, R., Schneider, B., Heckel, D.G., 2012. Resistance of Australian Helicoverpa armigera to fenvalerate is due to the chimeric P450 enzyme CYP337B3. Proc. Natl. Acad. Sci. U.S.A. 109, 15206-15211. https://doi.org/10.1073/pnas.1202047109
- Kim, J., Khan, M., Lee, S.H., Nauen, R., 2025. Understanding and managing diamide insecticide resistance in lepidopteran pests: insights into RyR mutations and metabolic mechanisms. Pestic. Biochem. Physiol. 215, 106629. https://doi.org/10.1016/j.pestbp.2025.106629
- Kim, J., Nam, H.Y., Kwon, M., Choi, J.H., Cho, S.R., Kim, G.-H., 2021. Novel diamide resistance-linked mutation in Korean Spodoptera exigua and a LAMP assay based on a mutationassociated intronic InDel. J. Pest Sci. 94, 1017-1029. https://doi.org/10.1007/s10340-020-01314-7
- Kwon, K., 2025. Elucidation of deltamethrin resistance mechanisms mediated by CNS-specific cytochrome P450s in Helicoverpa armigera. M.S. Thesis, Seoul National University, Seoul.
- Lai, T., Su, J., 2011. Assessment of resistance risk in Spodoptera exigua (Hübner) (Lepidoptera: Noctuidae) to chlorantraniliprole. Pest Manag. Sci. 67, 1468-1472. https://doi.org/10.1002/ps.v67.11
- Lewis, K.A., Tzilivakis, J., Warner, D.J., Green, A., 2016. An international database for pesticide risk assessments and management. Hum. Ecol. Risk Assess. 22, 1050-1064. https://doi.org/10.1080/10807039.2015.1133242
- Nishimoto, R., 2019. Global trends in the crop protection industry. J. Pestic. Sci. 44, 141-147. https://doi.org/10.1584/jpestics.D19-101
- Park, D., Choi, M., Noh, M., Kim, J., Khan, M., 2025. Synergistic effects of azole fungicides with diamide in Spodoptera exigua. Proc. 2025 Fall Int. Conf. Korean Soc. Appl. Entomol. p. 80.
- Park, H., Cho, S., Jeon, J., Kang, W., Kim, H., Koo, H., Park, B., Kim, G., 2021. Insecticide management programs for diamideresistant beet armyworm, Spodoptera exigua (Lepidoptera: Noctuidae). Korean J. Pestic. Sci. 25, 128-137. https://doi.org/10.7585/kjps.2021.25.2.128
- Sparks, T.C., 2013. Insecticide discovery: an evaluation and analysis. Pestic. Biochem. Physiol. 107, 8-17. https://doi.org/10.1016/j.pestbp.2013.05.012
- Walsh, T.K., Joussen, N., Tian, K., McGaughran, A., Anderson, C.J., Qiu, X., Ahn, S.-J., Bird, L., Pavlidi, N., Vontas, J., 2018. Multiple recombination events between two cytochrome P450 loci contribute to global pyrethroid resistance in Helicoverpa armigera. PLoS One 13, e0197760. https://doi.org/10.1371/journal.pone.0197760
- Xu, L., Li, D., Qin, J., Zhao, W., Qiu, L., 2016. Over-expression of multiple cytochrome P450 genes in fenvalerate-resistant field strains of Helicoverpa armigera from north of China. Pestic. Biochem. Physiol. 132, 53-58. https://doi.org/10.1016/j.pestbp.2016.01.003