Olfactory Responses of the Greenhouse Whitefly Trialeurodes vaporariorum Westwood and Its Parasitoid Encarsia formosa Gahan to Volatile Compounds of Entomopatogenic Fungi of the Genus Lecanicillum

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Abstract

To assess the prospects for the joint use of entomopathogenic fungi (EPF) and entomophages in plant protection from greenhouse whitefly, the influence of volatile organic compounds (VOCs) of fungi on the behavior of the phytophage and its parasitoid encarsia in 2 types of olfactometers was studied. In the Y-shaped olfactometer, it was revealed that 3 out of 9 EPF strains had a significant effect on the behavior of the imago phytophagus. The mycelium of the Vl 72 strain of the L. muscarium species showed an attractive effect (AE = +16), and for the Vl 61 strain of the same species and the Vit 71 strain of the L. attenuatum has been found to have a repellent effect against the pest (AE = –28 and –20, respectively). Experiments in two-chamber olfactometers, where T. vaporariorum was tested not individually, but in groups (15 individuals each), showed that all the studied strains did not affect the reactions of the phytophage. The activity of VOCs fungi against encarsia was less pronounced compared to whitefly. In the Y-shaped olfactometer, it was shown that only Vit 71 (L. attenuatum) showed an attractive effect, the remaining strains did not cause reactions in the parasitoid or showed a tendency to attract it.

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G. V. Mitina

All-Russian Institute of Plant Protection

Author for correspondence.
Email: galmit@rambler.ru
Russian Federation, Shosse Podbel’skogo 3, St. Petersburg–Pushkin 196608

O. S. Kirillova

All-Russian Institute of Plant Protection

Email: galmit@rambler.ru
Russian Federation, Shosse Podbel’skogo 3, St. Petersburg–Pushkin 196608

A. A. Choglokova

All-Russian Institute of Plant Protection

Email: galmit@rambler.ru
Russian Federation, Shosse Podbel’skogo 3, St. Petersburg–Pushkin 196608

M. A. Cherepanova

All-Russian Institute of Plant Protection

Email: galmit@rambler.ru
Russian Federation, Shosse Podbel’skogo 3, St. Petersburg–Pushkin 196608

References

  1. Avilla J., Albajes R., Alomar O., Castañe C., Gabarra R. Biological control of whiteflies on vegetable crops // Biocontrol in protected culture / Еds. Heinz K.M., Van Driesche R.G. and Parrella M.P. Batavia, IL: Ball Publishing, 2004. P. 171−184.
  2. Zhang G.F., Lövei G.L., Hu M., Wan F.H. Asymmetric consequences of host plant occupation on the competition between the whiteflies Bemisia tabaci cryptic species MEAM1 and Trialeurodes vaporariorum (Hemiptera: Aleyrodidae) // Pest Manag. Sci. 2014. V. 70. P. 1797−1807.
  3. Jones D.R. Plant viruses transmitted by whiteflies // Eur. J. Plant Pathol. 2003. V. 109. P. 195−219.
  4. Яркулов Ф.Я. Методы учета и биологическое подавление тепличной белокрылки в защищенном грунте // Дальневост. аграрн. вестн. 2011. T. 1. № 17. С. 16−21.
  5. De Vis R.M.J., Van Lenteren J.C. Biological control of Trialeurodes vaporariorum by Encarsia formosa on tomato in unheated greenhouses in the high altitude tropics // Bul. Insectol. 2008. V. 61. P. 43–57.
  6. Liu T.-X., Stansly P.A., Gerling D. Whitefly parasitoids: distribution, life history, bionomics, and utilization // Annu Rev. Entomol. 2015. V. 60. P. 1–15.
  7. Чалков А.А. Биологическая борьба с вредителями овощных культур защищенного грунта. М.: Россельхозиздат, 1986. 94 с.
  8. Hoddle M., van Driesche R., Sanderson J. Biology and use of the whitefly parasitoid Encarsia Formosa // Annu Rev. Entomol. 1998. V. 43. P. 645–669.
  9. Hall R.A. The fungus Verticillium lecanii as a microbial insecticide against aphids and scales // Microbial control of pests and plant diseases 1970–1980. London: Academic Press, 1981. P. 483–498.
  10. Goettel M.S., Koike M., Kim J.J., Aiuchi D., Shinya R., Brodeur J. Potential of Lecanicillium spp. for management of insects, nematodes and plant diseases // J. Invertebr. Pathol. 2008. V. 98. P. 25.
  11. Faria M.R., Wraight S.P. Mycoinsecticides and mycoacaricides: a comprehensive list with worldwide coverage and international classification of formulation types // Biol. Control. 2007. V. 43. № 3. P. 237–256.
  12. Ren S.X., Ali S., Huang Z., Wu J.H. Lecanicillium muscarium as microbial insecticide against whitefly and its interaction with other natural enemies // Current research, technology and education topics in applied microbiology and microbial biotechnology. 2010. V. 1. P. 339−348.
  13. Reddy S.G.E. Lecanicillium spp. for the management of aphids, whiteflies, thrips, scales and mealy bugs // Arthropods-Are They Beneficial for Mankind? 2020. IntechOpen, 20 p.
  14. Roy H.E., Pell J.K. Interactions between entomopathogenic fungi and other natural enemies: implications for biological control // Biocontrol Sci. Tech. 2000. V. 10. P. 737−752.
  15. Fransen J.J., van Lenteren J.C. Host selection and survival of the parasitoid Encarsia formosa after treatment of parasitized greenhouse whitefly, Trialeurodes vaporariorium, in the presence of hosts infected with the fungus Ashersonia alyerodis // Entomol. Exp. Appl. 1993. V. 69. P. 239–249.
  16. Oreste M., Bubici G., Poliseno M., Tarasco E. Effect of Beauveria bassiana and Metarhizium anisopliae on the Trialeurodes vaporariorum – Encarsia formosa system // J. Pest. Sci. 2016. V. 89. P. 153−160.
  17. Pazyuk I.M., Choglokova A.A., Mitina G.V. Effect of entomopathogenic fungi of the genus Lecanicillium on behavioral reactions and average per-day fecundity of the predatory bug Orius laevigatus Fieber (Heteroptera, Anthocoridae) // BIO Web of Conf. 2022. V. 43. 02003.
  18. Митина Г.В., Степанычева Е.А., Чоглокова А.А. Влияние энтомопатогенных грибов Akanthomyces и Lecanicillium на поведенческие реакции и жизнеспособность оранжерейной белокрылки Trialeurodes vaporariorum // Вестн. защиты раст. 2020. Т. 103. № 4. С. 265−268.
  19. Митина Г.В., Степанычева Е.А., Чоглокова А.А., Черепанова М.А. Сравнительные реакции сосущих фитофагов на летучие вещества спор энтомопатогенных грибов // Защита раст. от вредных организмов. Мат-лы X Международ. научн.-практ. конф., посвящ. 100-летию КубанГАУ. Краснодар, 2021. С. 239−241.
  20. Закладной Г.А. Защита зерна и продуктов его переработки от вредителей. М.: Колос, 1983. 215 с.
  21. Pascual-Villalobos M.J., Robledo A. Screening for antiinsect activity in mediterranean plants // Ind. Crops Prod. 1998. V. 8. P. 183–194.
  22. Kanmiya K. Mating behaviour and vibratory signals in whiteflies (Hemiptera: Aleyrodidae) // Insect Sounds and Communication / Eds. Drosopoulos S., Claridge M.F. Taylor & Francis, 2006. P. 365–379.
  23. Fattoruso V., Anfora G., Mazzoni V. Vibrational communication and mating behavior of the greenhouse whitefly Trialeurodes vaporariorum Westwood (Hemiptera: Aleyrodidae) // Sci. Rep. 2021. V. 11. № 1. P. 1−11.
  24. Berardo A., Fattoruso V., Mazzoni V., Pugno N.M. Coupling computational vibrational models and experimental biotremology to develop a green pest control strategy against the greenhouse whitefly Trialeurodes vaporariorum // J. R. Soc. Interface. 2022. V. 19. № 195. 20220311.
  25. Nyasembe V.O., Teal E.A.P., Mukabana W.R., Tumlinson J.H., Torto B. Behavioural response of the malaria vector Anopheles gambiae to host plant volatiles and synthetic blends // Parasites Vectors. 2012. V. 5. P. 234.
  26. Deletre E., Schatz B., Bourguet D., Changre F., Williams L., Ratnadass A., Martin T. Prospects for repellent in pest control: current developments and future challenges // Chemoecology. 2016. V. 26. P. 127–142.
  27. Webster B. The role of olfaction in aphid host location // Physiol. Entomol. 2012. V. 37. P. 10–18.
  28. Diabate S., Deletre E., Murungi L.K., Fiaboe K.K., Subramanian S., Wesonga J., Martin T. Behavioural responses of bean flower thrips (Megalurothrips sjostedti) to vegetative and floral volatiles from different cowpea cultivars // Chemoecology. 2019. V. 29. № 2. P. 73−88.
  29. Fazeli-Dinan M., Talaei-Hassanloui R., Allahyari H. Host preference of Encarsia formosa (Hym.: Aphelinidae) towards untreated and Lecanicillium longisporum-treated Trialeurodes vaporariorum (Hem.: Aleyrodidae) // J. Asia-Pacific Entomol. 2016. V. 19. № 4. P. 1145−1150.
  30. Fazeli-Dinan M., Talaei-Hassanloui R., Goettel M. Virulence of the entomopathogenic fungus Lecanicillium longisporum against the greenhouse whitefly, Trialeurodes vaporariorum and its parasitoid Encarsia formosa // Inter. J. Pest. Manag. 2016. V. 62. № 3. P. 251−260.
  31. Baverstock J., Alderson P.G., Pell J.K. Influence of the aphid pathogen Pandora neoaphidis on the foraging behaviour of the aphid parasitoid Aphidius ervi // Ecol. Entomol. 2005. V. 30. № 6. P. 665−672.
  32. Кузьмин А.Г., Титов Ю.А., Митина Г.В., Чоглокова А.А. Масс-спектрометрические исследования состава летучих органических соединений, выделяемых различными видами грибов рода Lecanicillium // Науч. приборостроение. 2021. Т. 31. № 4. С. 71−78.
  33. Митина Г.В., Степанычева Е.А., Чоглокова А.А., Черепанова М. А. Влияние летучих органических соединений энтомопатогенных грибов рода Lecanicillium и их компонента, уксусной кислоты, на поведение самок западного цветочного трипса Frankliniella occidentalis (Pergande) (Thysanoptera, Thripidae) // Энтомол. oбозр-е. 2023. Т. 102. № 2. С. 249−259.

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2. Fig. 1. Scheme for assessing the olfactory reactions of insects to VOCs of entomopathogenic fungi: (a) – in a Y-shaped olfactometer, (b) – in a two-chamber olfactometer; 1 – block with mycelium, 2 – agar block, 3 – chamber for releasing test insects.

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