Insect Mortality Caused by Baculovirus: a Model of Second-Order Phase Transitions

V. G. Soukhovolsky; Суховольский В. Г.; D. K. Kurenschikov; Куренщиков Д. К.; Yu. D. Ivanova; Иванова Ю. Д.; A. V. Kovalev; Ковалев А. В.

doi:10.31857/S1026347022600595

Insect Mortality Caused by Baculovirus: a Model of Second-Order Phase Transitions

作者: Soukhovolsky V.¹, Kurenschikov D.², Ivanova Y.³, Kovalev A.⁴
隶属关系:
1. V.N. Sukachev Institute of Forest SB RAS, Russian Academy of Science, Siberian Branch
2. Institute of Water and Ecology Problems KFRC RAS, Far-Eastern Branch
3. Institute of Biophysics, Russian Academy of Science, Siberian Branch
4. Federal Research Center Krasnoyarsk Scientific Center, Russian Academy of Sciences, Siberian Branch
期: 编号 5 (2023)
页面: 557-567
栏目: ECOLOGY
URL: https://journals.rcsi.science/1026-3470/article/view/135561
DOI: https://doi.org/10.31857/S1026347022600595
EDN: https://elibrary.ru/WIYGJR
ID: 135561

如何引用文章

详细

Baculoviruses, especially prevalent in Lepidoptera, have attracted the most attention as biological insect control agents. Infection with baculoviruses is usually fatal and therefore can affect host population density, especially if virus transmission increases with host density. Lepidoptera larvae show a strong dose-dependent response to pathogens such as baculoviruses, so their response to various pathogen exposures was studied in the present work. Models of virus exposure to insect hosts are usually judged by whether or not they generate cyclical population dynamics of multiple host generations. However, the existing theoretical models based on systems of differential equations are of little use for practical application due to the large number of variables and free parameters. In this regard, the possibility of using a mathematical model for describing the epizootic Malacosoma neustria L. and Lymantria dispar L. under the influence of nuclear polyhedrosis virus is considered. To assess the sensitivity of insects to the effects of baculoviruses, laboratory experiments were carried out on the mortality of caterpillars under various infectious loads. In this paper, we consider the possibility of constructing a model for the lifetime of insects after exposure to baculoviruses as an analogue of a second-order phase transition in physical systems and give estimates of the model parameters for two insect species at different titers of baculoviruses and at different ages of caterpillars. The dependence of the parameters of the proposed model on nuclear polyhedrosis virus strains is shown. The importance of the applied parameters for the organization of forest protection measures is substantiated.

关键词

Second-order phase transitions, population dynamics, lackey moth, Malacosoma neustria, gypsy moth, Lymantria dispar, nuclear polyhedrosis virus

参考

Исаев А.С., Хлебопрос Р.Г., Недорезов Л.В., Кондаков Ю.П., Киселев В.В., Суховольский В.Г. Популяционная динамика лесных насекомых. М.: Наука, 2001. 374 с.
Ландау Л.Д., Лифшиц Е.М. Теоретическая физика Статистическая физика. Ч. I. М.: Наука, 1976. 584 с.
Anderson R.M., May R.M. Infectious diseases and population cycles of forest insects // Science. 1980. V. 210. P. 658–661.
Bailey D., Chandler W.P., Grant J., Greaves G., Prince M. Tatchell. Biopesticides: Pest Management and Regulation. CABI International, Wallingford. 2010. 232 p.
Bonsall M., Godfray H.C.J., Briggs C., Hassell M.P. Does host self-regulation increase the likelihood of insect-pathogen population cycles? // Am. Nat. 1999. V. 153. P. 228–235.
Boots M., Norman R. Sublethal infection and the population dynamics of host-microparasite interactions // J. Anim. Ecol. 2000. V. 69. P. 517–524.
Bowers R., Begon M., Hodgkinson D. Host-pathogen population cycles in forest insects? Lessons from simple models reconsidered // Oikos. 1993. V. 67. P. 529–538.
Briggs C.J., Godfray H.C.J. The dynamics of insect-pathogen interactions in seasonal environments // Theor. Popul. Biol. 1996. V. 50. P. 149–177.
Bruce A.D., Cowley R.A. Structural phase transitions. L.: Taylor & Francis, 1981. 326 p.
Copping L.G., Menn J.J. Biopesticides: a review of their actions, applications and efficacy// Pest Manage Sci. 2000. V. 56. P. 651–676.
Cory J.S., Clarke E.E., Brown M.L., Hails R.S., O’Reilly D.R. Microparasite manipulation of an insect: the influence of the egt gene on the interaction between a baculovirus and its lepidopteran host // Funct. Ecol. 2004. V. 18. P. 443–450.
Cory J.S., Myers J.H. The ecology and evolution of insect baculoviruses // Ann. Rev. Ecol. Evol. Syst. 2003. V. 34. P. 239–272.
Cox D.R., Oakes D. Analysis of survival data. CRC Press, Boca Raton, 1984. 208 p.
Dwyer G., Dushoff J., Elkinton J.S., Levin S.A. Pathogen-driven outbreaks in forest defoliators revisited: building models from experimental data // Am. Nat. 2000. V. 156. P. 105–120.
Dwyer G., Elkinton J.S., Buonaccorsi J.P. Host heterogeneity in susceptibility and disease dynamics: tests of a mathematical model // Am. Nat. 1997. V. 150. P. 685–707.
Elam P., Vail P.V., Schreiber F. Infectivity of Autographa californica nuclear polyhedrosis virus extracted with digestive fluids of Heliothis zea, Estigmene acrea, and carbonate solutions // J. Invertebr. Pathol. 1990. V. 55. P. 278–283.
Elkinton J.S. Gypsy Moth. In Encyclopedia of Insects; Resh V.H., Cardé R.T. Eds.; Academic Press: San Diego, CA, USA, 2009. P. 435–439.
Engelhard E.K., Volkman L.E. Developmental resistance in fourth instar Trichoplusia ni orally inoculated with Autographa californica M nuclear polyhedrosis virus // Virology. 1995. V. 209. P. 384–389.
Getz W., Pickering J. Epidemic models: thresholds and population regulation // Am. Nat. 1983. V. 121. P. 893–898.
Goldberg A.V., Romanowski V., Federici B.A., Sciocco de Cap A. Effect of the epap granulovirus on its host, Epinotia aporema (Lepidoptera: Tortricida) // J. Invertebr. Pathol. 2002. V. 80. P. 148–159.
Han Y., van Houte S., Drees G.F., van Oers M.M., Ros V.I.D. Parasitic manipulation of host behaviour: baculovirus SeMNPV EGT facilitates tree-top disease in Spodoptera exigua larvae by extending the time to death // Insects. 2015. V. 6. P. 716–731.
Harrison R.L., Keena M.A., Rowley D.L. Classification, genetic variation and pathogenicity of Lymantria dispar nucleopolyhedrovirus isolates from Asia, Europe, and North America // J. Invertebr. Pathol. 2013. V. 116. P. 27–35.
Hochberg M. Nonlinear transmission rates and the dynamics of infectious diseases // J. Theor. Biol. 1991. V. 153. P. 301–321.
Ilyinykh A., Kurenschikov D., Ilyinykh Ph., Imranova E., Polenogova O., Baburin A. Sensitivity of gypsy moth Lymantria dispar larvae from geographically removed populations to nucleopolyhedrovirus // SHILAP Revta. lepid. 2013. V. 41. P. 349–356.
Kalbfleisch J., Prentice R. The Statistical Analysis of Failure Time Data. N.Y.: J. Wiley, 2002. 462 p.
Kleinbaum D.G., Klein M. Survival analysis: a self-learning text. Springer-Verlag N.Y. Inc., 2012. 700 p.
Marrone P.G. Barriers to adoption of biological control agents and biological pesticides// CAB Reviews: Perspectives in Agriculture, Veterinary Science, Nutrition and Natural Resources. 2007. V. 2. № 051. 12 p.
Martemyanov V.V., Dubovskiy I.M., Rantala M.J., Salminen J.-P., Belousova I.A., Pavlushin S.V., Bakhvalov S.A., Glupov V.V. The Effects of Defoliation-Induced Delayed Changes in Silver Birch Foliar Chemistry on Gypsy Moth Fitness, Immune Response, and Resistance to Baculovirus Infection // J. Chem. Ecol. 2012. V. 38. P. 295–305.
Matthews H.J., Smith I., Edwards J.P. Lethal and sublethal effects of a granulovirus on the tomato moth Lacanobia oleracea // J. Invertebr. Pathol. 2001. V. 80. P. 73–80.
Milks M.L., Myers J.M., Leptich M.K. Costs and stability of cabbage looper resistance to a nucleopolyhedrovirus // Evol. Ecol. 2002. V. 16. P. 369–385.
Moscardi F. Assessment of the application of baculoviruses for control of Lepidoptera // Ann. Rev. Entomol. 1999. V. 44. P. 257–289.
Myers J.H. Population fluctuations of the western tent caterpillar in southwestern British Columbia. // Popul. Ecol. 2000. V. 42. P. 231–241.
Myers J., Malakar H.R., Cory J.S. Syblethal nucleopolyhedrovirus infection effects on female pupal weight, egg mass size, and vertical transmission in gypsy moth (Lepidoptera: Lymantriidae) // Environ. Entomol. 2000. V. 29. P. 1268–1272.
Podgwaite J.D. Gypchek: Biological Insecticide for the Gypsy Moth // J. For. 1999. V. 97. P. 16–19.
Regniere J. Vertical transmission of diseases and population dynamics of insects with discrete generations: a model // J. Theor. Biol. 1984. V. 107. P. 287–301.
Rohrmann G.R. Baculovirus molecular biology. 3rd ed. Bethesda (MD): Nat. Center Biotechnol. Inform. (US), 2013. 347 p.
Saxena A., Byram P.K., Singh S.K., Chakraborty J., Murhammer D., Giri L.J. A structured review of baculovirus infection process: integration of mathematical models and biomolecular information on cell-virus interaction // General Virology. 2018. V. 99. P. 1151–1171.
Shrestha S., Elderd B.D., Dukic V. Bayesian-based survival analysis: inferring time to death in host-pathogen interactions // Environmental and Ecological Statistics. 2019. V. 26. P. 17–45.
Szewcyk B., Hoyos-Carvajal L., Paluszek M., Skrzecz I., Lobo de Souza M. Baculovirusesre-emerging biopesticides // Biotechnol. Adv. 2006. V. 24. P. 143–160.
Thakore Y. The biopesticide market for global agricultural use // Ind. Biotechnol. 2006. V. 2(3). P. 194–208.
Ulrich Y., Schmid-Hempel P. Host modulation of parasite competition in multiple infections // Proc. R. Soc. Lond. B: Biol. Sci. 2012. V. 279. P. 2982–2989.
Vezina A., Peterman R. Tests of the role of nuclear polyhedrosis virus in the population dynamics of its host, Douglas-fir tussock moth, Orgyia pseudotsugata (Lepidpotera: Lymantriidae) // Oecologia. 1985. V. 67. P. 260–266.
White A., Bowers R., Begon M. Host-pathogen cycles in self-regulated forest insect systems: resolving conflicting predictions // Am. Nat. 1996. V. 148. P. 220–225.
Woods S.A., Elkinton J.S. Bimodal patterns of mortality from nuclear polyhedrosis virus in gypsy moth Lymantria dispar populations // J. Invertebr. Pathol. 1987. V. 50. P. 151–157.