Home Comparison of pathogens infection level in Ips typographus (Coleoptera: Curculionidae) beetles sampled in pheromone traps and at place of overwintering
Article
Licensed
Unlicensed Requires Authentication

Comparison of pathogens infection level in Ips typographus (Coleoptera: Curculionidae) beetles sampled in pheromone traps and at place of overwintering

  • Karolina Lukášová EMAIL logo and Jaroslav Holuša
Published/Copyright: June 16, 2015
Become an author with De Gruyter Brill

Abstract

The importance of pathogens in the population dynamics of Ips typographus remains a subject of ongoing debate. The main objective of our experiment was to compare the pathogen infection levels of individuals overwintering in bark with the levels of individuals from the same population captured with pheromone traps and thereby to determine primary answers as to whether it can be confirmed that pathogenic organisms affect the flight ability of bark beetles or their ability to leave their places of overwintering. A total of 402 I. typographus individuals were analyzed at a study location under limited management. Three pathogens were confirmed to be present: the gregarine Gregarina typographi, the virus ItEPV, and the microsporidium Nosema typographi. Infection levels of Gregarina typographi and ItEPV were the same in beetles collected at places of overwintering and in those beetles collected in pheromone traps within the immediate vicinity. As these pathogens infect the host’s intestine, the tendency to leave the places of overwintering is apparently not diminished. A similar analysis and comparison of pathogens located in the fat body might bring different results, as our study only detected N. typographi in a single dissected adult spruce bark beetle.

References

Burjanadze M., Goginashvili N. 2009. Occurrence of pathogens and nematodes in the spruce bark beetles, Ips typographus (Col., Scolytidae) in Borjomi Gorge. Bulletin of the Georgian National Academy of Sciences, 3, 145-150Search in Google Scholar

Christiansen E., Bakke A. 1988. The spruce bark beetle of Eurasia. In: (Ed. A.A. Berryman) Dynamics of forest insect populations. Plenum Publishing Corporation, New York, 480-50310.1007/978-1-4899-0789-9_23Search in Google Scholar

Duelli P., Zahradník P., Knížek M., Kalinová B. 1997. Migration in spruce bark beetles (Ips typographus L.) and the efficiency of pheromone traps. Journal of Applied Entomology, 121, 297-303. DOI: 10.1111/j.1439-0418.1997.tb01409.x 10.1111/j.1439-0418.1997.tb01409.xSearch in Google Scholar

Forster B. 1993. Development of the bark beetle situation in the Swiss storm-damage areas. Schweizerische Zeitschrift für Forstwesen, 144, 767-776Search in Google Scholar

Haidler B., Wegensteiner R., Weiser J. 2003. Occurrence of microsporidia and ther pathogens in associated living spruce bark beetles (Coleoptera, Scolytidae) in an Austrian forest. Insect Pathogens and Insect Parasitic Nematodes. IOBC wprs Bulletin, 26, 257-260Search in Google Scholar

Händel U., Wegensteiner R., Weiser J., Žižka Z. 2003. Occurrence of pathogens in associated living bark beetles (Col., Scolytidae) from different spruce stands in Austria. Journal of Pest Science, 76, 22-32. DOI: 10.1046/j.1439-0280.2003.03007.x 10.1046/j.1439-0280.2003.03007.xSearch in Google Scholar

Hlásny T., Turčáni M. 2013. Persisting bark beetle outbreak indicates the unsustainability of secondary Norway spruce forests: case study from Central Europe. Annals of Forest Science, 70, 481-491. DOI 10.1007/s13595-013-0279-710.1007/s13595-013-0279-7Search in Google Scholar

Holuša J., Lukášová K., Wegensteiner R., Grodzki W., Pernek M., Weiser J. 2013. Pathogens of the bark beetle Ips cembrae: microsporidia and gregarines known from other Ips species. Journal of Applied Entomology, 137, 181-187. DOI: 10.1111/ j.1439-0418.2012.01717.x Holuša J., Weiser J., Žižka Z. 2009. Pathogens of the spruce bark beetles Ips typographus and Ips duplicatus. Central European Journal of Biology, 4, 567-573. DOI: 10.2478/s11535-009-0044-y Lukášová K., Holuša J. 2011. Gregarina typographi (Eugregarinorida: Gregarinidae) in the bark beetle Ips typographus (Coleoptera: Curculionidae): changes in infection level in the breeding system. Acta Protozoologica, 50, 311-318. DOI: 10.4467/16890027AP.11.028.0065Search in Google Scholar

Lukášová K., Holuša J. 2012. Patogeny lýkožroutů rodu Ips (Coleoptera: Curculionidae: Scolytinae): review. Zprávy lesnického výzkumu, 3, 230-240Search in Google Scholar

Lukášová K., Holuša J., Turčáni M. 2013. Pathogens of Ips amitinus: new species and comparison with Ips typographus. Journal of Applied Entomology, 137, 188-196. DOI: 10.1111/jen.1200010.1111/jen.12000Search in Google Scholar

Michalková V., Krascsenitsová E., Kozánek M. 2011. On the pathogens of the spruce bark beetle Ips typographus (Coleoptera: Scolytinae) in the Western Carpathians. Biologia, 67, 217-221. DOI: 10.2478/s11756-011-0154-710.2478/s11756-011-0154-7Search in Google Scholar

Nemec V., Zumr V., Stary P. 1993. Studies on the nutritional state and the response to aggregation pheromones in the bark beetle, Ips typographus (L.) (Col., Scolytidae). Journal of Applied Entomology, 116, 358-363. DOI: 10.1111/j.1439-0418.1993.tb01208.x 10.1111/j.1439-0418.1993.tb01208.xSearch in Google Scholar

Plašil P., Cudlín P. 2005. Population dynamics of eight-toothed spruce bark beetle (Ips typographus [L.]) in the area of National Nature Reserve Praděd in 1998-2001. Journal of Forest Science, 51, 359-370 10.17221/4571-JFSSearch in Google Scholar

Takov D., Pilarska D.,Wegensteiner R. 2010. List of protozoan and microsporidian pathogens of economically important bark beetle species (Coleoptera: Curculionidae: Scolytinae) in Europe. Acta Zoologica Bulgarica, 62, 201-209Search in Google Scholar

Wegensteiner R. 2004. Pathogens in bark beetles. In: (Eds. F. Lieutier, K.R. Day A. Battisti J.-C. Grégoire H.F. Evans) Bark and wood boring insects in living trees in Europe, Asynthesis. Kluwer Academic Publishers, Dordrecht, 291-31310.1007/978-1-4020-2241-8_12Search in Google Scholar

Wegensteiner R., Dedryver C.-A., Pierre J.-S. 2010. The comparative prevalence and demographic impact of two pathogens in swarming Ips typographus adults: a quantitative analysis of long term trapping data. Agricultural and Forest Entomology, 12, 49-57. DOI: 10.1111/j.1461-9563.2009.00449.x 10.1111/j.1461-9563.2009.00449.xSearch in Google Scholar

Wegensteiner R., Stradner A., Händel U. 2014. Occurrence of pathogens in Ips typographus (Coleoptera: Curculionidae) and in other spruce bark beetles from the wilderness reserve Dürrenstein (Lower Austria). Biologia, 69, 92-100. DOI:10.2478/s11756-013-0286-z10.2478/s11756-013-0286-zSearch in Google Scholar

Wegensteiner R., Weiser J. 1996. Untersuchungen zum Auftreten von Pathogen by Ips typographus (Coleoptera: Scolytidae) aus einem Naturschutzgebiet in Schwartzwald (Baden-Württemberg). Anzeiger für Schädlingskunde, Pflanzenschutz, Umweltschutz, 69, 162-167. DOI: 10.1007/BF0190680810.1007/BF01906808Search in Google Scholar

Wegensteiner R., Weiser J. 2004. Annual variation of pathogen occurrence and pathogen prevalence in Ips typographus L. (Col, Scolytidae) from the BOKU University Forest Demonstration Centre. Journal of Pest Science, 77, 221-228. DOI: 10.1007/s10340-004-0056-310.1007/s10340-004-0056-3Search in Google Scholar

Weiser J., Pultar O., Žižka Z. 2000. Biological protection of forest against bark beetle outbreaks with poxvirus and other pathogens. IUAPPA, Section B, 12, 168-172Search in Google Scholar

Wermelinger B. 2004. Ecology and management of the spruce bark beetle Ips typographus - a review of recent research. Forest Ecology and Management, 202, 67-82. DOI: 10.1016/ j.foreco.2004.07.01810.1016/j.foreco.2004.07.018Search in Google Scholar

Weslien J., Lindelöw A. 1990. Recapture of marked spruce bark beetles (Ips typographus) in pheromone traps using area-wide mass trapping. Canadian Journal of Forest Research, 20, 1786-1790. DOI: 10.1139/x90-23810.1139/x90-238Search in Google Scholar

Wichmann L., Ravn H.P. 2001. The spread of Ips typographus (L.) (Coleoptera, Scolytidae) attacks following heavy windthrow in Denmark, analysed using GIS. Forest Ecology and Management, 148, 31-39. DOI:10.1016/S0378-1127(00)00477-110.1016/S0378-1127(00)00477-1Search in Google Scholar

Yaman M., Baki H. 2010. The first record of Gregarina typographi Fuchs (Protista: Apicomplexa: Gregarinidae) from the European spruce bark beetle, Ips typographus (Linnaeus) (Coleoptera: Curculionidae, Scolytinae) in Turkey. Turkish Journal of Parasitology, 34, 179-82. DOI: 10.5152/tpd. 2010.08Search in Google Scholar

Yaman M., Baki H. 2011. First record of Entomopoxvirus of Ips typographus (Linnaeus) (Coleoptera: Curculionidae, Scolytinae) for Turkey. Acta Zoologica Bulgarica, 63, 199-202Search in Google Scholar

Received: 2014-11-10
Revised: 2015-2-9
Accepted: 2015-3-18
Published Online: 2015-6-16
Published in Print: 2015-9-1

© W. Stefański Institute of Parasitology, PAS

Articles in the same Issue

  1. A new species of Entobdella Blainville in Lamarck, 1818 (Monogenea: Capsalidae: Entobdellinae) from the Greenland halibut, Reinhardtius hippoglossoides
  2. Redescription and phylogenetic relationships of the rare Lyperosomum sarothrurae Baer, 1959 (Digenea: Dicrocoeliidae)
  3. Molecular epidemiology, risk factors and hematochemical alterations induced by Theileria annulata in bovines of Punjab (India)
  4. Molecular characterization of Setaria digitata from Mithun (Bos frontalis)
  5. Redescription and genetic characterization of Philometra lagocephali Moravec et Justine 2008 (Nematoda: Philometridae) from Lagocephalus lunaris (Bloch and Schneider) (Tetraodontiformes: Tetradontidae) in the South China Sea
  6. A new Cosmocercoides species (Nematoda: Cosmocercidae), C. tonkinensis n. sp., in the scale-bellied tree lizard (Acanthosaura lepidogaster) from Vietnam
  7. Ophthalmology hospital wards contamination to pathogenic free living Amoebae in Iran
  8. Eye fluke infection status in Baltic cod, Gadus morhua, after three decades and their use as ecological indicators
  9. Aplectana dubrajpuri sp. nov. (Nematoda: Cosmocercidae) in Hoplobatrachus tigerinus (Anura: Dicroglossidae) from Dubrajpur, Birbhum, West Bengal, India
  10. Trypanosoma cruzi DTU TcII presents higher blood parasitism than DTU TcI in an experimental model of mixed infection
  11. Molecular phylogeny and ultrastructure of Myxobolus cf. cuneus, a parasite of patinga hybrid and Henneguya pseudoplatystoma, a parasite of pintado hybrid
  12. Supplementary data of Henneguya leporinicola (Myxozoa, Myxosporea) a parasite of Leporinus macrocephalus from fish farms in the state of São Paulo, Brazil
  13. Prevalence and genotype of Giardia duodenalis in dairy cattle from Northern and Northeastern part of Thailand
  14. Comparison of pathogens infection level in Ips typographus (Coleoptera: Curculionidae) beetles sampled in pheromone traps and at place of overwintering
  15. A new species of Isospora (Apicomplexa: Eimeriidae) from eastern coachwhip, Coluber flagellum flagellum (Reptilia: Ophidia) from Oklahoma
  16. The first report of Trichinella pseudospiralis presence in domestic swine and T. britovi in wild boar in Bosnia and Herzegovina
  17. Metazoan parasite infracommunities of Mycteroperca bonaci (Poey, 1960) (Pisces: Epinephelidae) in reef and coastal environments off the coast of Yucatán, México
  18. Dirofilariasis – an emergent human parasitosis in Romania
  19. Two new picobiin mite species (Acari: Cheyletoidea: Syringophilidae) parasitizing passerine birds in Guyana
  20. New species of Prosotocus (Digenea; Pleurogenidae) and other helminths in Euphlyctis cyanophlyctis (Anura: Dicroglossidae) from Punjab, India
  21. Chimeric DNA vaccines encoding Eimeria acervulina macrophage migration inhibitory factor (E.MIF) induce partial protection against experimental Eimeria infection
  22. Variations in cercarial production and the level of in vitro activation of metacercariae of two different isolates of Fasciola hepatica
  23. Effect of body size on the abundance of ectoparasitic mites on the wild rodent Oligoryzomys nigripes
  24. Evaluation of reactivity to Echinococcus spp. among rural inhabitants in Poland
  25. Wild boars meat as a potential source of human trichinellosis in Poland: current data
  26. Liver fluke (Fasciola hepatica) naturally infecting introduced European brown hare (Lepus europaeus) in northern Patagonia: phenotype, prevalence and potential risk
  27. Molecular characterization of Fascioloides magna (Trematoda: Fasciolidae) from south-western Poland based on mitochondrial markers
  28. Fatal Paratanaisia bragai (Digenea: Eucotylidae) infection in scarlet macaws (Ara macao) in Costa Rica
  29. First Molecular Characterization of Aspiculuris tetraptera (Nematoda: Heteroxynematidae) from Mus musculus (Rodentia: Muridae) in India
  30. Molecular characterization of muscle-parasitizing didymozoid from a chub mackerel, Scomber japonicus
  31. Diagnosis and therapy of Capillaria plica infection: report and literature review
Downloaded on 10.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/ap-2015-0064/html
Scroll to top button