Journal of Iranian Plant Protection Research

Journal of Iranian Plant Protection Research

Efficacy Comparison of Afidopyropen with Commonly Used Insecticides Against the green peach aphid (Myzus persicae Sulzer) (Hemiptera: Aphididae) Under Field Condition

Document Type : Research Article

Authors
1 Iranian Research Institute of Plant Protection, Agricultural Research, Education and Extension Organization (AREEO), Tehran, Iran
2 Charmahal & Bakhtiyari Agricultural and Natural Resources Research Center, Agricultural Research, Education and Extension Organization (AREEO), Shahrekord, Iran
3 Khorasan Razavi Agricultural and Natural Resources Research Center, Agricultural Research, Education and Extension Organization (AREEO), Mashhad, Iran
Abstract
Introduction
The green peach aphid, Myzus persicae Sulzer, a cosmopolitan aphid species, is one of the most important pests in Iran and worldwide, causing considerable damages through direct plant sap feeding and transmitting many plant viruses. It is a highly polyphagous, feeding on more than 50 plant families, causing losses to agro-industrial crops (including potato, sugar beet and tobacco), horticultural crops (including plants of Brassicaceae, Solanaceae and Cucurbitaceae families) and stone fruits (peach, apricot, and cherry, among others). A number of factors, such as its distribution, host range, mechanisms of plant damage, life cycle, capacity to disperse and ability to evolve resistance to insecticides, have enhanced the status of this species as a pest. For example, the life cycle is often anholocyclic meaning that it continues the parthenogenesis throughout the year, allowing populations to increase rapidly under favorable conditions and quickly reach damaging numbers. Currently, insecticide application is the primary and most effective option for controlling M. persicae. Indeed, since its damage is of great economic importance in Iran, several insecticide applications are performed against this pest during the cropping season. Biological characteristics, including short generation time and high reproductive capacity, has made this pest as one of the potential pests to develop resistance to insecticides. As a consequence, resistance to many insecticides has reported throughout the world. Globally, insect has shown high to extremely high levels of resistance to a wide range of conventional insecticides. The best Strategy for postpone the resistance evolution is to rotate Insecticides with different modes of action. Indeed, alternation of new mode of action groups have the potential to reduce the intensity of selection for new resistance mechanisms. In order to register new insecticides and diversify the insecticides basket, the present study was conducted to evaluate the field efficacy of Afidopyropen (Ventigra®) (DC 10%) in comparison with malathion (EC 57%) and pirimicarb (WP 50%). Afidopyropen (IRAC 9D) is a novel pyropene insecticide, derived from the fungus Aspergillus fumigatus, that inhibits the insect vanilloid-type transient receptor potential (TRPV) channels. It provides systemic protection in plants due to its high translaminar activity. Afidopyropen interacts with chordotonal stretch receptor neurons in various sap-feeding Hemiptera, which serve as mechanosensory functions by detecting articulatory movements, and causes insect death via starvation and desiccation. Afidopyropen also displays little risk to the environment and to humans. Afidopyropen has been registered for use on a broad range of crops, such as cotton, soybeans, wheat, citrus, pome fruit, stone fruit, tree nuts, leafy and fruiting vegetables, brassica, cucurbits, tuberous and corm vegetables as well as ornamental plants in many countries, such as USA, India, China and Australia.
 
Materials and Methods
The field trial was conducted in a randomized complete block design with five treatments and three replications in peach orchards of three provinces of Iran, Khorasan Razavi, Charmahal & Bakhtiyari and Qazvin, in 2022. To do this, at 3, 7 and 14 days after treatment, the aphid counts per branch were recorded on five shoots per tree, and efficay was calculated using the Henderson and Tilton's formula. The treatments consisted of Afidopyropen (0.1 ml L-1), Afidopyropen (0.075 ml L-1), malathion (2 ml L-1), pirimicarb (0.5 ml L-1) and control. Afidopyropen (DC 10%) was obtained from the representative of BASF Co., Ltd., Tehran, Iran. Other insecticides were purchased from Golsam Gorgan Chemical Co.
 
Results and Discussion
The combined analysis of variance confirmed that interaction of treatment × place was not significant, meaning that the experimental treatments had the same responses at different locations. Therefore, the data were statistically analyzed based on this, without considering the locations. The results showed that in all days of post treatment, Afidopyropen (0.1 ml L-1) had the highest efficacy (93-92%), whereas malathion showed the lowest (79-86 %). The reduced dose of Afidopyropen (0.075 ml L-1), also exhibited good efficacy (%87) at all days of post treatments and there was no significant statistical difference with Afidopyropen with 0.1 ml/L field rate. Additionally, pirimicarb did not show significant statistical difference with malathion at all days of post treatments.
 
Conclusion
In conclusion, our results showed that Afidopyropen exhibited acceptable efficacy against Myzus persicae, required for registration in Iran. However, since the both Afidopyropen concentrations (0.075 and 0.1 ml L-1) had the same efficiency and considering the low-input of pesticides to the environment and as the economic view, it is recommended to use the application rate of 0.075 ml L-1 against this pest.   
Keywords
Subjects

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Anonymous. (2023). Agricultural Statistical Yearbook, (Volume 3, Greenhouse and Horticultural Crops) Center for Statistics, Information and Communication Technology. Ministry of Agriculture of Iran. (In Persian)
Angelella, G. M., & Waters, T. D. (2023). Afidopyropen as a potential tool for potato leafroll virus management in post-neonicotinoid potato production. Journal of Economic Entomology, 116(3), 713-718. https://doi.org/10.1093/jee/toad042
Bass, C., Puinean, A. M., Zimmer, C. T., Denholm, I., Field, L. M., Foster, S. P., & Williamson, M. S. (2014). The evolution of insecticide resistance in the peach potato aphid, Myzus persicae. Insect Biochemistry and Molecular Biology, 51, 41-51. https://doi.org/10.1016/j.ibmb.2014.05.003
Bavithra, C. M. M. L., Murugan, M., Balasubramani, V., Harish, S., & Prakash, K. (2024). Baseline susceptibility of an A1 quarantine pest-the South American tomato pinworm Tuta absoluta (Lepidoptera: Gelechiidae) to insecticides: past incidents and future probabilities in line to implementing successful pest management. Frontiers in Plant Science, 15, 1404250.  https://doi.org/10.3389/fpls.2024.1404250
Behdad, E. (1996) Encyclopedia of Iranian Plant Protection, Plant Pests, Diseases and Weeds. Yadbod Press. Isfahan, Iran. (In Persian)
Belabess, Z., Tahiri, A., & Lahlali, R. (2025). From symptoms to solutions: A deep dive into potato leaf roll virus pathology. Journal of Crop Health, 77(1), 1-18.  https://doi.org/10.1007/s10343-024-01096-3
Bing-Mei, S. O. N. G., Yan, J. I. A. N. G., Xin, C. H. E. N., Wan-Nan, C. H. E. N. G., Yu, Z. H. A. N. G., & Hong-Sheng, P. A. N. (2023). Effectiveness of different pesticides on Aphis gossypii and a safety evaluation of Hippodamia variegata. Chinese Journal of Applied Entomology, 60(5). https://doi.org/10.7679/j.issn.2095-1353.2023.147.
Blackman, R. L., & Eastop, V. F. (2008). Aphids on the World's Herbaceous Plants and Shrubs, 2 Volume Set. John Wiley & Sons.
Bordini, I., Naranjo, S. E., Fournier, A., & Ellsworth, P. C. (2025). Determining selectivity of isocycloseram and afidopyropen and their compatibility with conservation biological control in Arizona cotton. Pest Management Science, 81(2), 639-653.   https://doi.org/10.1002/ps.8460
Chen, X. D., Ashfaq, M., & Stelinski, L. L. (2018). Susceptibility of Asian citrus psyllid, Diaphorina citri (Hemiptera: Liviidae), to the insecticide afidopyropen: A new and potent modulator of insect transient receptor potential channels. Applied Entomology and Zoology, 53(4), 453-461. https://doi.org/10.1007/s13355-018-0574-8
da Silva Queiroz, O., Nyoike, T. W., & Koch, R. L. (2020). Baseline susceptibility to afidopyropen of soybean aphid (Hemiptera: Aphididae) from the north central United States. Crop Protection, 129, 105020. https://doi.org/10.1016/j.cropro.2019.105020
Dimase, M., Rossitto De Marchi, B., Barreto da Silva, F., Lahiri, S., Beuzelin, J., Hutton, S., & Smith, H. A. (2024). Monitoring the susceptibility of Bemisia tabaci Middle East-Asia Minor 1 (Hemiptera: Aleyrodidae) to afidopyropen, cyantraniliprole, dinotefuran, and flupyradifurone in south Florida vegetable fields. Journal of Economic Entomology, 117(4), 1606-1615. https://doi.org/10.1093/jee/toae104
Ding, W., Xu, T., Zhu, G., Chu, P., Liu, S., & Xue, M. (2024). Lethal and sublethal effects of afidopyropen and flonicamid on life parameters and physiological responses of the tobacco whitefly, Bemisia tabaci MEAM1. Agronomy, 14(8), 1774. https://doi.org/10.3390/agronomy14081774
Gavkare, O. M. K. A. R., Kumar, S., Sharma, N. I. K. H. I. L., & Sharma, P. L. (2013). Evaluation of some novel insecticides against Myzus persicae (Sulzer). The Bioscan, 8(3), 1119-1121.
Gill, G. S., & Chong, J. H. (2021). Efficacy of selected insecticides as replacement for neonicotinoids in managing sweetpotato whitefly on poinsettia. HortTechnology, 31(6), 745-752. https://doi.org/10.21273/horttech04853-21
Goto, K., Horikoshi, R., Mitomi, M., Oyama, K., Hirose, T., Sunazuka, T., & Ōmura, S. (2019). Synthesis and insecticidal efficacy of pyripyropene derivatives. Part II—Invention of afidopyropen. The Journal of Antibiotics, 72(9), 661-681. https://doi.org/10.1038/s41429-019-0193-9
Horikoshi, R., Goto, K., Mitomi, M., Sunazuka, T., & Ōmura, S. (2025). Research and development of an insecticide, afidopyropen. Journal of Pesticide Science, 50(1), 14. https://doi.org/10.1584/jpestics.j25-01 
Horikoshi, R., Goto, K., Mitomi, M., Oyama, K., Hirose, T., Sunazuka, T., & Ōmura, S. (2022). Afidopyropen, a novel insecticide originating from microbial secondary extracts. Scientific Reports, 12(1), 1-10. https://doi.org/10.1038/s41598-022-06729-z
IRAC. (2025). Insecticide Resistance Action Committee. https://www.irac-online.org. Mode of Action Classification Scheme, Version 11.3, January 2025.
Jayasekharan, B. S., Sreedhar, U., Venkateswarlu, V., & Naik, S. B. (2022). Efficacy of afidopyropen against tobacco aphid, Myzus persicae nicotianae (Blackman) and impact on natural enemies in tobacco. Tobacco Research, 48(1), 51-54. https://doi.org/10.1079/cabicompendium.35639
Kandasamy, R., London, D., Stam, L., von Deyn, W., Zhao, X., Salgado, V. L., & Nesterov, A. (2017). Afidopyropen: New and potent modulator of insect transient receptor potential channels. Insect Biochemistry and Molecular Biology, 84, 32-39. https://doi.org/10.1016/j.ibmb.2017.03.005
Kang-Sheng, M. A, Tang, Q. L., Liang, P. Z., Li, J. H., & Gao, X. W. (2022). A sublethal concentration of afidopyropen suppresses the population growth of the cotton aphid, Aphis gossypii Glover (Hemiptera: Aphididae). Journal of Integrative Agriculture, 21(7), 2055-2064. https://doi.org/10.1016/s2095-3119(21)63714-0
Kirkland, L. S., Babineau, M., Ward, S. E., Van Rooyen, A. R., Chirgwin, E., Mata, L., & Umina, P. A. (2024). Assessing the risk of resistance to flonicamid and afidopyropen in green peach aphid (Hemiptera: Myzus persicae) via in-vivo selection. Crop Protection, 184, 106783. https://doi.org/10.1016/j.cropro.2024.106783
Koch, R. L., da Silva Queiroz, O., Aita, R. C., Hodgson, E. W., Potter, B. D., Nyoike, T., & Ellers‐Kirk, C. D. (2020). Efficacy of afidopyropen against soybean aphid (Hemiptera: Aphididae) and toxicity to natural enemies. Pest Management Science, 76(1), 375-383. https://doi.org/10.1002/ps.5525
Kumar, V., McKenzie, C. L., & Osborne, L. S. (2018). Effect of foliar application of afidopyropen on Bemisia tabaci and Amblyseius swirskii, 2018. Arthropod Management Tests, 43(1), tsy071. https://doi.org/10.1093/amt/tsx054
Leichter, C. A., Thompson, N., Johnson, B. R., & Scott, J. G. (2013). The high potency of ME-5343 to aphids is due to a unique mechanism of action. Pesticide Biochemistry and Physiology, 107(2), 169-176. https://doi.org/10.1016/j.pestbp.2013.06.009
Li, R., Cheng, S., Liang, P., Chen, Z., Zhang, Y., Liang, P., & Gao, X. (2022). Status of the resistance of Aphis gossypii Glover, (Hemiptera: Aphididae) to afidopyropen originating from microbial secondary metabolites in China. Toxins, 14(11), 750. https://doi.org/10.3390/toxins14110750
Liu, X., Fu, Z., Zhu, Y., Gao, X., Liu, T. X., & Liang, P. (2022). Sublethal and transgenerational effects of afidopyropen on biological traits of the green peach aphid Myzus persicae (Sluzer). Pesticide Biochemistry and Physiology, 180, 104981. https://doi.org/10.1016/j.pestbp.2021.104981
Liu, X., Ban, N., Fu, Z., Gao, X., Liu, T. X., & Liang, P. (2023). Persistent toxicity and dissipation dynamics of afidopyropen against the green peach aphid Myzus persicae (Sulzer) in cabbage and chili. Ecotoxicology and Environmental Safety, 252, 114584. https://doi.org/10.1016/j.ecoenv.2023.114584
Liu, X., Wang, Q., Liu, X., Xiao, D., Liu, T. X., & Liang, P. (2024). Molecular mechanisms for selective action of afidopyropen to Myzus persicae and Coccinella septempunctata. Pest Management Science, 80(8), 3893-3900. https://doi.org/10.1002/ps.8092
Mahalanobish, D., Dutta, S., Roy, D., Biswas, A., Sarkar, S., Mondal, D., & Sarkar, P. K. (2022). Field-evolved resistance and mechanisms in Bemisia tabaci Asia I to a novel pyropene insecticide, afidopyropen, in India. Crop Protection, 162, 106078. https://doi.org/10.1016/j.cropro.2022.106078
Noorbakhsh, S. (editor), (2025) List of Important Pests, Diseases and Weeds of Major Agricultural Crops, Pesticides and Recommended Methods to Control Them. Iranian Plant Protection Organization Publication. Tehran, Iran. 224 pp. (In Persian)
Paschapur, A. U., Manoj, M. S., Pavan, J. S., & Subramanian, S. (2025). Exploiting TRP channel diversity in insects: A pathway to next-generation pest management. Archives of Toxicology, 99(6), 2277-2297. https://doi.org/10.1007/s00204-025-04012-4
Peck, S. L., & McQuate, G. T. (2000). Field tests of environmentally friendly malathion replacements to suppress wild Mediterranean fruit fly (Diptera: Tephritidae) populations. Journal of Economic Entomology, 93(2), 280-289. https://doi.org/10.1603/0022-0493-93.2.280
Raisch, T., & Raunser, S. (2023). The modes of action of ion-channel-targeting neurotoxic insecticides: Lessons from structural biology. Nature Structural & Molecular Biology, 30(10), 1411-1427. https://doi.org/10.1038/s41594-023-01113-5
Sparks, T. C., Storer, N., Porter, A., Slater, R., & Nauen, R. (2021). Insecticide resistance management and industry: The origins and evolution of the I nsecticide R esistance A ction C ommittee (IRAC) and the mode of action classification scheme. Pest Management Science, 77(6), 2609-2619. https://doi.org/10.1002/ps.6254
Sparks, T. C., Crossthwaite, A. J., Nauen, R., Banba, S., Cordova, D., Earley, F., & Wessels, F. J. (2020). Insecticides, biologics and nematicides: Updates to IRAC’s mode of action classification-a tool for resistance management. Pesticide Biochemistry and Physiology, 167, 104587.
Talepour, F., & Rashki Shivani, A. (2016). Survey of interaction among entomopathogen fungus, Metarhizium anisopliae, the aphid, Myzus persicae and its host plant canola. Journal of Applied Research in Plant Protection, 5(1), 209-216.
Ōmura, S., Tomoda, H., Kim, Y. K., & Nishida, H. (1993). Pyripyropenes, highly potent inhibitors of acyl-CoA: Cholesterol acyltransferase produced by Aspergillus fumigatus. The Journal of Antibiotics. 46, 1168-1169. https://doi.org/10.7164/antibiotics.46.1168
Panini, M., Dradi, D., Marani, G., Butturini, A., & Mazzoni, E. (2013). Detecting the presence of target-site resistance to neonicotinoids and pyrethroids in Italian populations of Myzus persicae. Pest Management Science, 70, 931e938. https://doi.org/10.1002/ps.3630
Puinean, A. M., Foster, S. P., Oliphant, L., Denholm, I., Field, L. M., Millar, N. S., & Bass, C. (2010). Amplification of a cytochrome P450 gene is associated with resistance to neonicotinoid insecticides in the aphid Myzus persicae. Plos Genetics, 6(6), e1000999. https://doi.org/10.1371/journal.pgen.1000999
Shi, D., Liang, P., Zhang, L., Lv, H., Gao, X., You, H., & Ma, K. (2022). Susceptibility baseline of Aphis gossypii Glover (Hemiptera: Aphididae) to the novel insecticide afidopyropen in China. Crop Protection, 151, 105834. https://doi.org/10.1016/j.cropro.2021.105834
Spalthoff, C., Salgado, V. L., Balu, N., David, M. D., Hehlert, P., Huang, H., & Göpfert, M. C. (2023). The novel pyridazine pyrazolecarboxamide insecticide dimpropyridaz inhibits chordotonal organ function upstream of TRPV channels. Pest Management Science, 79(5), 1635-1649. https://doi.org/10.1002/ps.7352
Van Edmen, H. F., & Harrington, R., (2017). Aphids on the World's Crops, an Identification and Information Guide, second ed. John Wiley & Sons Ltd, Chichester, UK, 716 pp.
Wang, R., Gao, B., Che, W., Qu, C., Zhou, X., & Luo, C. (2022). First report of field resistance to Afidopyropen, the novel Pyropene insecticide, on Bemisia tabaci Mediterranean (Q Biotype) from China. Agronomy, 12(3), 724. https://doi.org/10.3390/agronomy12030724
Xie, J., Zheng, Y., Liu, X., Dong, F., Xu, J., Wu, X., & Zheng, Y. (2019). Human health safety studies of a new insecticide: Dissipation kinetics and dietary risk assessment of afidopyropen and one of its metabolites in cucumber and nectarine. Regulatory Toxicology and Pharmacology, 103, 150-157. https://doi.org/10.1016/j.yrtph.2019.01.025
Zhang, Z., Shi, H., Xu, W., Liu, J., Geng, Z., Chu, D., & Guo, L. (2021). Pymetrozine-resistant whitefly Bemisia tabaci (Gennadius) populations in China remain susceptible to afidopyropen. Crop Protection, 149, 105757. https://doi.org/10.1016/j.cropro.2021.105757
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