Inheritance Pattern and Cross-Resistance Assessment of Flonicamid Resistance in the Biological Control Agent Chrysoperla carnea (Neuroptera: Chrysopidae)
DOI:
https://doi.org/10.25077/jrp.6.2.92-103.2025Keywords:
Autosomal inheritance, Chrysoperla carnea, cross-resistance, flonicamid, polygenicAbstract
A field-collected laboratory population of Chrysoperla carnea, a polyphagous predator important in integrated pest management, was subjected to flonicamid selection pressure for three generations using a micro-droplet topical bioassay. Following selection, the flonicamid-selected strain exhibited 6.83-fold resistance (LC50 = 260,730 ppm; 95% FL = 148,090–1,561,600 ppm) compared with the unselected strain (LC50 = 38,122 ppm; 95% FL = 23,259–138,440 ppm). Reciprocal crosses between resistant and susceptible parents produced overlapping 95% FLs, demonstrating autosomal inheritance with no detectable maternal or sex-linked effects. Dominance metrics indicated incomplete to partial dominance of resistance (DLC = 0.60 for F1; DLC = 0.55 for F2). Effective dominance estimates at four diagnostic doses (27,875; 62,500; 125,000; 272,000 ppm) yielded ED values of 0.53, 0.79, 0.91, and 0.88, respectively, showing increased dominance at higher doses. Chi-square goodness-of-fit tests rejected the null hypothesis of monogenic inheritance (p < 0.05), confirming a polygenic resistance model. Cross-resistance bioassays further revealed substantial co-selection effects, with resistance ratios of 24.35-fold for acetamiprid, 23.58-fold for triazophos, and 15.17-fold for deltamethrin, comparing initial and final LC50 values that showed non-overlapping 95% FLs. These results indicate that flonicamid resistance in C. carnea is a polygenic, autosomal, and incompletely to partially dominant trait. The findings provide genetic foresight for incorporating resistant predator populations into insecticide-compatible IPM programs and highlight the importance of mode-of-action-based chemical rotation to mitigate resistance co-selection in beneficial predator populations.
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References
Bourguet et al,2000. Insecticide resistance and dominance levels. Journal of Economic Entomology 93: 1588-1595. DOI: https://doi.org/10.1603/0022-0493-93.6.1588
Abbas, N., H. A. A. Khan, and S. A. Shad. 2014a. Resistance of the house fly Musca domestica (Diptera: Muscidae) to lambda-cyhalothrin: mode of inheritance, realized heritability, and cross-resistance to other insecticides. Ecotoxicology 23: 791–801. DOI: https://doi.org/10.1007/s10646-014-1217-7
Abbas, N., M. Abubakar, M. W. Hassan, S. A. Shad, & A. M. Hafez. (2021). Risk Assessment of Flonicamid Resistance in Musca domestica (Diptera: Muscidae): Resistance Monitoring, Inheritance, and Cross-Resistance Potential. Journal of Medical Entomology 58: 1779-1787. DOI: https://doi.org/10.1093/jme/tjab036
Abbas, N., M. Mansoor, S. Shad, A. Pathan, A. Waheed, M. Ejaz, M. Razaq, & M. Zulfiqar. (2014b). Fitness cost and realized heritability of resistance to spinosad in Chrysoperla carnea (Neuroptera: Chrysopidae). Bull. Entomol. Res. 104: 707–715. DOI: https://doi.org/10.1017/S0007485314000522
Abhay, M. N. S. (2018). ''SEASONAL ABUNDANCE AND EFFICACY OF INSECTICIDES. MAHATMA PHULE KRISHI VIDYAPEETH.
Abubakar, M., & S. A. Shad. (2024). Realized heritability, inheritance, and mechanism of chlorfenapyr resistance in biocontrol agent, Chrysoperla carnea (Stephens)(Neuroptera: Chrysopidae): A step towards sustainable pest management. Chemosphere 362: 142726. DOI: https://doi.org/10.1016/j.chemosphere.2024.142726
Abubakar, M., & S. A. Shad. (2025). Comparative biology of chlorantraniliprole selected and unselected Chrysoperla carnea (Stephens) populations: Stability of resistance, inheritance mode, and realized heritability—Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 289: 110125. DOI: https://doi.org/10.1016/j.cbpc.2025.110125
Afzal, M., & Khan, M. (1978). Life history and feeding behaviour of green lacewing, Chrysopa carnea Stephens (Neuroptera, Chrysopidae).
Ahmad, S. F., S. Ahmed, R. R. Khan, & M. K. Nadeem. (2010). Evaluation of insecticide resistance in two strains of fruit fly, Bactrocera zonata (Saunders)(Tephritidae: Diptera), with the fruit dip method. Pakistan Entomologist 32: 163–167.
Aktar, M. W., D. Sengupta, & A. Chowdhury. (2009). Impact of pesticide use in agriculture: their benefits and hazards. Interdisciplinary toxicology 2: 1. DOI: https://doi.org/10.2478/v10102-009-0001-7
Ansari, M. S., M. A. Moraiet, & S. Ahmad. (2013). Insecticides: impact on the environment and human health, pp. 99–123, Environmental deterioration and human health: natural and anthropogenic determinants. Springer. DOI: https://doi.org/10.1007/978-94-007-7890-0_6
Baker, J., P. J. Mendoza, R. Beeman, & J. Throne. (1998). Fitness of a malathion-resistant strain of the parasitoid Anisopteromalus calandrae (Hymenoptera: Pteromalidae). Journal of Economic Entomology 91: 50–55. DOI: https://doi.org/10.1093/jee/91.1.50
Balasubramani, V., & M. Swamiappan. (1994). Development and Feeding Potential of the Green Lacewing Chrysoperla carnea (Steph.)(Neur. Chrysopidae) on different insect pests of cotton. Anzeiger für Schädlingskunde, Pflanzenschutz, Umweltschutz 67: 165-167. DOI: https://doi.org/10.1007/BF01905539
Batool, A., K. Abdullah, M. Mamoon-ur-Rashid, M. K. Khattak, & S. S. Abbas. (2014). Effect of prey density on biology and functional response of Chrysoperla carnea (Stephens)(Neuroptera: Chrysopidae). Pak. J. Zool. 46.
Carrière, Y. 2003. Haplodiploidy, sex, and the Evolution of pesticide resistance. Journal of Economic Entomology 96: 1626-1640. DOI: https://doi.org/10.1603/0022-0493-96.6.1626
Croft, B., & A. Brown. (1975). Responses of Arthropod Natural Enemies to Insecticides. Annu. Rev. Entomol. 20: 285–335. DOI: https://doi.org/10.1146/annurev.en.20.010175.001441
Desneux, N., A. Decourtye, & J.-M. Delpuech. (2007). The sublethal effects of pesticides on beneficial arthropods. Annu. Rev. Entomol. 52: 81–106. DOI: https://doi.org/10.1146/annurev.ento.52.110405.091440
Devine, G. J., & M. J. Furlong. (2007). Insecticide use: Contexts and ecological consequences. Agriculture and Human Values 24: 281–306. DOI: https://doi.org/10.1007/s10460-007-9067-z
Hameed, Y., M. Rizwan, M. Shahzaib, M. Sarmad, M. F. Hamid, S. M. Zaka, K. Abbas, & M. Zakria. (2022). Functional Response of Chrysoperla carnea (Stephens)(Neuroptera: Chrysopidae) to Lipaphis erysimi (Kaltenbach) and Diuraphis noxia (Kurdjumov). Pakistan J Zool 55: 1-5. DOI: https://doi.org/10.17582/journal.pjz/20190705190700
Hancock, H. Year. Published. Field performance of flonicamid (F1785) in cotton, pp. 1629-1636. In Proc Beltwide Cotton Conf, 2003.
Henry, C. S., S. J. Brooks, P. Duelli, & J. B. Johnson. (2006). Courtship song of the South African lacewing Chrysoperla zastrowi (Esben‐Petersen)(Neuroptera: Chrysopidae): evidence for a trans‐equatorial geographic range? Journal of Natural History 40: 2173-2195. DOI: https://doi.org/10.1080/00222930601088107
Hoy, M. A. 1976. Genetic improvement of insects: fact or fantasy. Environ. Entomol. 5: 833-839. DOI: https://doi.org/10.1093/ee/5.5.833
Hoy, M. A. 1990. Pesticide resistance in arthropod natural enemies: variability and selection responses, pp. 203-236, Pesticide resistance in arthropods. Springer. DOI: https://doi.org/10.1007/978-1-4684-6429-0_8
IRAC. (2025). Insecticide Resistance Action Committee.
Johnson, M. W., & B. E. Tabashnik. (2018). Laboratory selection for pesticide resistance in natural enemies. Applications of genetics to arthropods of biological control significance: 91-106. DOI: https://doi.org/10.1201/9781351069762-5
Khan Pathan, A., A. H. Sayyed, M. Aslam, M. Razaq, G. Jilani, & M. A. Saleem. (2008). Evidence of field-evolved resistance to organophosphates and pyrethroids in Chrysoperla carnea (Neuroptera: Chrysopidae). Journal of Economic Entomology 101: 1676-1684. DOI: https://doi.org/10.1093/jee/101.5.1676
Khulbe, P., P. Ravi, R. P. Maurya, & M. Khan. (2005). Biology of Chrysoperla carnea (Stephens) on different host insects. Annals of Plant Protection Sciences 13: 351-354.
Li, L., H. Cheng, J. Gai, & D. Yu. (2007). Genome-wide identification and characterization of putative cytochrome P450 genes in the model legume Medicago truncatula. Planta 226: 109-123. DOI: https://doi.org/10.1007/s00425-006-0473-z
Lira, R., D. Nascimento, J. Torres, and H. Siqueira. 2019. Predation on diamondback moth larvae and aphid by resistant and susceptible lady beetle, Eriopis connexa. Neotrop. Entomol. 48: 909-918. DOI: https://doi.org/10.1007/s13744-019-00702-8
Lourenço, P., C. Brito, T. Backeljau, D. Thierry, & M. Ventura. (2006). Molecular systematics of the Chrysoperla carnea group (Neuroptera: Chrysopidae) in Europe. Journal of Zoological Systematics and Evolutionary Research 44: 180–184. DOI: https://doi.org/10.1111/j.1439-0469.2006.00352.x
Mahzoum, A. M., M. Villa, J. Benhadi-Marín, & J. A. Pereira. (2020). Functional response of Chrysoperla carnea (Neuroptera: Chrysopidae) larvae on Saissetia oleae (Olivier)(Hemiptera: Coccidae): Implications for biological control. Agronomy 10: 1511. DOI: https://doi.org/10.3390/agronomy10101511
Maia, J. B., G. A. Carvalho, P. Medina, A. Garzón, P. d. C. Gontijo, and E. Vinuela. (2016). Lethal and sublethal effects of pesticides on Chrysoperla carnea larvae (Neuroptera: Chrysopidae) and the influence of rainfastness in their degradation pattern over time. Ecotoxicology 25: 845-855. DOI: https://doi.org/10.1007/s10646-016-1641-y
Mansoor, M. M., and S. A. Shad. (2019). Resistance of green lacewing, Chrysoperla carnea (Stephens), to buprofezin: Cross resistance patterns, preliminary mechanism, and realized heritability. Biol. Control 129: 123-127. DOI: https://doi.org/10.1016/j.biocontrol.2018.10.008
Mansoor, M. M., and S. A. Shad. (2020). Genetics, cross-resistance, and realized heritability of resistance to acetamiprid in the generalist predator, Chrysoperla carnea (Steph.)(Neuroptera: Chrysopidae). Egyptian Journal of Biological Pest Control 30: 23. DOI: https://doi.org/10.1186/s41938-020-0213-x
Mansoor, M. M., and S. A. Shad. (2022). Methoxyfenozide tolerance in Chrysoperla carnea: inheritance, dominance, and preliminary detoxification mechanisms. Plos one 17: e0265304. DOI: https://doi.org/10.1371/journal.pone.0265304
Mansoor, M. M., A. B. M. Raza, N. Abbas, M. A. Aqueel, & M. Afzal. (2017). Resistance of green lacewing, Chrysoperla carnea Stephens, to nitenpyram: cross-resistance patterns, mechanism, stability, and realized heritability. Pestic. Biochem. Physiol. 135: 59-63. DOI: https://doi.org/10.1016/j.pestbp.2016.06.004
Relyea, R. A. (2005). The impact of insecticides and herbicides on the biodiversity and productivity of aquatic communities. Ecol. Appl. 15: 618-627. DOI: https://doi.org/10.1890/03-5342
Roush, R. T., and J. A. McKenzie. (1987). Ecological genetics of insecticide and acaricide resistance. DOI: https://doi.org/10.1146/annurev.en.32.010187.002045
Sayyed, A. H., D. Omar, and D. J. Wright. (2004). Genetics of spinosad resistance in a multi‐resistant field‐selected population of Plutella xylostella. Pest Management Science: formerly Pesticide Science 60: 827-832. DOI: https://doi.org/10.1002/ps.869
Sayyed, A. H., A. K. Pathan, & U. Faheem. (2010). Cross-resistance, genetics, and stability of resistance to deltamethrin in a population of Chrysoperla carnea from Multan, Pakistan. Pestic. Biochem. Physiol. 98: 325-332. DOI: https://doi.org/10.1016/j.pestbp.2010.07.004
Shaukat, M. (2018). Feeding behaviour and life durations of Chrysoperla carnea (Stephens)(Neuroptera: Chrysopidae) feeding on a variety of hosts. Journal of Entomology and Zoology Studies 6: 691-697.
Stone, B. (1968). A formula for determining the degree of dominance in cases of monofactorial inheritance of resistance to chemicals. Bulletin of the World Health Organization 38: 325.
Tabashnik, B. E., J. M. Schwartz, N. Finson, and M. W. Johnson. (1992). Inheritance of resistance to Bacillus thuringiensis in diamondback moth (Lepidoptera: Plutellidae). Journal of Economic Entomology 85: 1046-1055. DOI: https://doi.org/10.1093/jee/85.4.1046
Tauber, C. A. (1974). Systematics of North American chrysopid larvae: Chrysopa carnea group (Neuroptera). The Canadian Entomologist 106: 1133-1153. DOI: https://doi.org/10.4039/Ent1061133-11
Ullah, I., S. Wazir, N. Abbas, M. Naeem, K. Abdullah, Z. Mahmood, M.-u. Rashid, and A. M. Hafez. 2021. Monitoring of field-evolved resistance to flonicamid, neonicotinoid, and conventional insecticides in the Oxycarenus hyalinipennis costa. Environmental Monitoring and Assessment 193: 382. DOI: https://doi.org/10.1007/s10661-021-09158-z
Villa, M., I. Somavilla, S. A. Santos, J. A. López-Sáez, and J. A. Pereira. 2019. Pollen feeding habits of Chrysoperla carnea (adults) in the olive grove agroecosystem. Agriculture, Ecosystems & Environment 283: 106573. DOI: https://doi.org/10.1016/j.agee.2019.106573
Wilkes, A. (1942). The influence of selection on the preferendum of a chalcid (Microplectron fuscipennis Zett.) and its significance in the biological control of an insect pest. Proceedings of the Royal Society of London. Series B-Biological Sciences 130: 400-415. DOI: https://doi.org/10.1098/rspb.1942.0009
Wolf, J. B., and M. J. Wade. (2009). What are maternal effects (and what are they not)? Philosophical Transactions of the Royal Society B: Biological Sciences 364: 1107-1115. DOI: https://doi.org/10.1098/rstb.2008.0238
Wu, G., S. Jiang, and T. Miyata. (2004). Seasonal changes of methamidophos susceptibility and biochemical properties in Plutella xylostella (Lepidoptera: Yponomeutidae) and its parasitoid Cotesia plutellae (Hymenoptera: Braconidae). Journal of Economic Entomology 97: 1689-1698. DOI: https://doi.org/10.1603/0022-0493-97.5.1689
Xu, F., G. Du, D. Xu, L. Chen, X. Zha, and Z. Guo. 2021. Residual behavior and dietary intake risk assessment of flonicamid, dinotefuran, and its metabolites on peach trees. J. Sci. Food Agric. 101: 5842-5850. DOI: https://doi.org/10.1002/jsfa.11236
Zang, L.-S., Z. R. Akhtar, A. Ali, K. Tariq, & M. R. Campos. (2022). Flubendiamide resistance and its mode of inheritance in tomato pinworm Tuta absoluta (Meyrick)(Lepidoptera: Gelechiidae). Insects 13: 1023. DOI: https://doi.org/10.3390/insects13111023
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