This is a preview and has not been published.

Molecular Responses of Varroa destructor to Thyme Essential Oil Exposure

Authors

Keywords:

Chemosensing gene (Varroa PRTF-like gene)‎, Chemoreceptor gene (Ionotropic glutamate receptors – IR25a-like gene)‎, Neurotransmitter gene (GABA-activated RDL receptor)‎, Thyme Essential Oil (Origanum onites L.)‎, Varroa mite (Varroa destructor)‎

Abstract

Varroa mites (Varroa destructor) continue to pose a serious threat to honey bee (Apis mellifera spp.) health, exhibiting significant resistance development to synthetic acaricides. This study investigated the efficacy of thyme (Origanum onites L.) essential oil (TEOV) as botanical alternative, focusing on mite survival across different feeding contexts and the underlying molecular responses. Adult mites were exposed to three TEOV doses (0.1, 1, and 10 ppm), across different feeding contexts (GA;larvae, GB;fat body, and GC;live honey bee). Mortality exhibited dose and time dependency, particularly at 24 h post-exposure to TEOV. The most responsive host tissue was found to be the mites feeding on larvae and fat body tissue. Interestingly, the susceptibility of the mites was found to be influenced by the context of feeding, which suggests that nutrition affects the susceptibility of TEOV. At the molecular level, TEOV elicited delayed but dose-dependent transcriptional responses: pheromone receptor transcription factor-like (PRTF-like) was strongly upregulated at higher doses after 24h, consistent with activation of stress- or detoxification pathways, additionally Ionotropic glutamate receptors (IGRs)- Ionotropic Receptor 25a-like (IR25a-like) exhibited a general, significant elevation in response to TEOV exposure, suggesting an effort to activate an adaptive chemosensory response. In contrast, the expression of GABA-activated RDL (Dieldrine Resistance) receptor (GABA-RDL) was not generally affected at any dose or time of observation. The result reveals that the neurotoxic action of TEOV is not through transcription-regulated pathway via this receptor. No activity of the mite genes was detected in the control group indicating that any gene activity changes are attributable to treatment with thyme. The selectivity ratio (SR) was calculated as 17.0. The materials have shown their mortality rates, gene expression and physiology by two mechanisms: a fast action as neurotoxicants and long-term stress for TEOV. All results demonstrate its potential as a plant-derived acaricide.

Author Biographies

Tuğçe Olgun, Apicultural Research Center

Apicultural Research Center, Aegean Agricultural Research Institute, Izmir, Türkiye

Metin Erdoğan, The Faculty of Veterinary Medicine.

  Afyon Kocatepe University, Afyonkarahisar, Türkiye.

Miray Dayıoğlu, Apicultural Research Center.

Miray Dayıoğlu, Aegean Agricultural Research Institute, Izmir, Türkiye

Ünal Karik, Department of Medicinal and Aromatic Plants.

Ünal Karik, Aegean Agricultural Research Institute, Izmir, Türkiye

References

Ramsey SD, Ochoa R, Bauchan G, Gulbronson C, Mowery JD, Cohen A, Lim D, Joklik J, Cicero JM, Ellis JD, Hawthorne D, VanEngelsdorp D. Varroa destructor feeds primarily on honey bee fat body tissue and not hemolymph. Proceedings of the National Academy of Sciences.2019;116(5):1792–1801.DOI: 10.1073/pnas.1818371116.

McGruddy RA, Bulgarella M, Felden A, Baty JW, Haywood J, Stahlmann-Brown P, Lester PJ. Are increasing honey bee colony losses attributed to Varroa destructor in New Zealand driven by miticide resistance? Journal of Apicultural Research. 2024;63(4):648–659.

Celikkol E, Doğac E. The status of pyrethroid resistance mutation frequencies in Varroa destructor populations in the most important beekeeping areas of Türkiye. Experimental and Applied Acarology. 2025;94(2):32. DOI: 10.1007/s10493-025-01002-0.

Bahreini R, González-Cabrera J, Hernández-Rodríguez CS, Moreno-Martí S, Muirhead S, et al. Arising amitraz and pyrethroids resistance mutations in the ectoparasitic Varroa destructor mite in Canada. Scientific Reports. 2025;15:1587. DOI: 10.1038/s41598-025-85279-6.

O'Connell DP, Healy K, Wilton J, Botías C, Jones JC. A systematic meta-analysis of the efficacy of treatments for a global honey bee pathogen—the Varroa mite. Science of The Total Environment. 2025;178228.

Ramzi H, Ismaili MR, Aberchane M, Zaanoun S. Chemical characterization and acaricidal activity of Thymus satureioides C. & B. and Origanum elongatum E. & M. (Lamiaceae) essential oils against Varroa destructor Anderson & Trueman (Acari: Varroidae). Industrial Crops and Products. 2017;108:201–207.

Hybl M, Bohatá A, Rádsetoulalová I, Kopecký M, Hoštičková I, Vaníčková A, Mráz P. Evaluating the efficacy of 30 different essential oils against Varroa destructor and honey bee workers (Apis mellifera). Insects. 2021;12(11):1045. DOI: 10.3390/insects12111045.

Bava R, Castagna F, Palma E, Marrelli M, Conforti F, Musolino V, Carresi C, Lupia C, Ceniti C, Tilocca B, Roncada P, Britti D, Musella V. Essential oils for a sustainable control of honeybee varroosis. Veterinary Sciences. 2023;10(5):308. DOI: 10.3390/vetsci10050308.

Price KL, Lummis SCR. An atypical residue in the pore of Varroa destructor GABA-activated RDL receptors affects picrotoxin block and thymol modulation. Insect Biochemistry and Molecular Biology. 2014;55:19–25. DOI: 10.1016/j.ibmb.2014.10.002.

Price KL, Lummis SCR. Characterisation of thymol effects on RDL receptors from the bee parasite Varroa destructor. Pesticide Biochemistry and Physiology. 2022;183:105064.

Benton R, Vannice KS, Gomez-Diaz C, Vosshall LB. Variant ionotropic glutamate receptors as chemosensory receptors in Drosophila. Cell. 2009;136(1):149–162. DOI: 10.1016/j.cell.2008.12.001.

Rytz R, Croset V, Benton R. Ionotropic receptors (IRs): Chemosensory ionotropic glutamate receptors in Drosophila and beyond. Insect Biochemistry and Molecular Biology. 2013;43(9):888–897. DOI: 10.1016/j.ibmb.2013.02.007.

Singh NK, Eliash N, Stein I, Kamer Y, Ilia Z, Rafaeli A, Soroker V. Identification and gene-silencing of a putative odorant receptor transcription factor in Varroa destructor: possible role in olfaction. Insect Molecular Biology. 2016;25(2):181–190.

Eliash N, Singh NK, Thangarajan S, Sela N, Leshkowitz D, Kamer Y, et al. Chemosensing of honeybee parasite, Varroa destructor: Transcriptomic analysis. Scientific Reports. 2017;7(1):13091.

Soroker V, Singh NK, Eliash N, Plettner E. Olfaction as a target for control of honeybee parasite mite Varroa destructor. In: Olfactory Concepts of Insect Control—Alternative to Insecticides. Volume 1. Cham: Springer International Publishing; 2019. p. 117–134.

Imdorf A, Bogdanov S, Ochoa RI, Calderone NW. Use of essential oils for the control of Varroa jacobsoni in honey bee colonies. Apidologie. 1999;30(2–3):209–228.

Alsaadi M, Keshlaf MM, Mirwan HB. Some essential oils as potential control agents for Varroa destructor in infected honey bees (Apis mellifera). Open Veterinary Journal. 2024;14(2):692–698.

Gashout HA, Guzmán-Novoa E. Acute exposure to thymol and coumaphos causes gene expression changes associated with stress responses in honey bees (Apis mellifera L.). Journal of Apicultural Research. 2017;56(3):264–270.

Boncristiani H, Underwood R, Schwarz R, Evans JD, Pettis J, et al. Direct effect of acaricides on pathogen loads and gene expression levels in honey bees (Apis mellifera L.). Apidologie. 2012;43(5):514–520.

Gashout HA, Goodwin PH, Guzman-Novoa E. Lethality of synthetic and natural acaricides to worker honey bees (Apis mellifera) and their impact on the expression of health and detoxification-related genes. Environmental Science and Pollution Research. 2018;25:34730–34739. DOI: 10.1007/s11356-018-3205-6.

Anonymous. TSE EN ISO 6571—Baharatlar, Çeşniler ve Tıbbi Bitkiler: Uçucu Yağ Muhtevasının Tayini (hidrodistilasyon yöntemi). Türk Standartları Enstitüsü. 2011.

Chapuy C, Ribbens L, Renou M, Dacher M, Armengaud C. Thymol affects congruency between olfactory and gustatory stimuli in bees. Scientific Reports. 2019;9(1):7752.

Williams GR, Alaux C, Costa C, Csaki T, Doublet V, Eisenhardt D, et al. Standard methods for maintaining adult Apis mellifera in cages under in vitro laboratory conditions. Journal of Apicultural Research. 2013;52(1):1–36.

Kalendar R, Lee D, Schulman AH. FastPCR software for PCR primer and probe design and repeat search. Genes, Genomes and Genomics. 2009;3(1):1–14.

Pfaffl MW. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Research. 2001;29(9):e45.

Sabahi Q, Morfin N, Emsen B, Gashout HA, Kelly PG, Otto S, Guzmán-Novoa E. Evaluation of dry and wet formulations of oxalic acid, thymol, and oregano oil for Varroa mite (Acari: Varroidae) control in honey bee (Hymenoptera: Apidae) colonies. Journal of Economic Entomology. 2020;113(6):2588–2594.

Castagna F, Bava R, Piras C, Carresi C, Musolino V, Lupia C, Marrelli M, Conforti F, Palma E, Britti D, Musella V. Green veterinary pharmacology for honey bee welfare and health: Origanum heracleoticum L. (Lamiaceae) essential oil for the control of Apis mellifera varroatosis. Veterinary Sciences. 2022;9(3):124. DOI: 10.3390/vetsci9030124.

Ait Hamou Mohamedd ZG. Exploring the chemical and acaricidal diversity of Algerian Origanum essential oils against Varroa destructor: A comparative study. Periodico di Mineralogia. 2023;92(5). DOI: 10.37896/pd92.5/92514.

Alparslan B, Taşlı H, Erkan C. Effective control of Varroa destructor mites with Juniperus excelsa, Juglans regia, Origanum onites, and Mentha spicata leaf extracts: A study of honey bee colonies. Journal of Apicultural Research. 2024;1–12.

Downloads

Published

2026-04-09

Issue

Section

Articles

How to Cite

Olgun, T., Erdoğan, M., Dayıoğlu, M., & Karik, Ünal. (2026). Molecular Responses of Varroa destructor to Thyme Essential Oil Exposure. The Iraqi Journal of Veterinary Medicine. https://doi.org/10.30539/tbzcty13

Publication Dates