AUTOGENY EXPRESSION IN CULEX PIPIENS COMPLEX POPULATIONS IN SERBIA

Main Article Content

Nađa Kukić
https://orcid.org/0009-0000-9949-6357
Tamara Popović
https://orcid.org/0009-0005-3137-689X
Dušan Petrić
Aleksandra Ignjatović Ćupina
https://orcid.org/0000-0001-7045-6896
Mihaela Kavran
https://orcid.org/0000-0001-5210-9727

Abstract

From a public health perspective, Culex pipiens (the house mosquito) is the most important mosquito species in Serbia. Its confirmed vector competence has enabled the sustained transmission of West Nile virus (WNV) to humans and animals in Serbia for over a decade. Despite this, the species’ biology and ecology remain underexplored: this study aims to help fill that knowledge gap.


This research examined autogeny in female mosquitoes and assessed whether the presence of males affects its expression. Larvae of the Cx. pipiens complex were collected from three ditches and two urban street catch basins and reared to adult stage. Experimental subjects included adults emerging from field collections and individuals originating from an autogenous laboratory colony. Female mosquitoes were maintained in cages either with or without males and fed solely on sugar solution (no blood meals), and left undisturbed for five to seven days to permit egg development. No oviposition site was provided. Subsequently, females were dissected and their ovarian development evaluated.


Results revealed that, under laboratory conditions, male presence did not affect autogeny expression. After 10-12 days, females contained no eggs in their abdomens, suggesting egg resorption due to the absence of an oviposition opportunity. In field-collected breeding sites, autogeny was rare: only two catch basins and one ditch yielded autogenous females. The highest rate observed was 45% (in a catch basin), while other positive sites recorded rates of 12.5% (catch basin) and 2.15% (ditch).


Given the documented coexistence of the pipiens and molestus biotypes within the same breeding sites, hybridization is likely to occur. Hybrids, feeding on both avian and mammalian hosts, are recognized for their role as bridge vectors in transmitting WNV to humans and other mammals, and thus hold considerable public health importance.

Article Details

How to Cite
Kukić, N., Popović, T., Petrić, D., Ignjatović Ćupina, A., & Kavran, M. (2025). AUTOGENY EXPRESSION IN CULEX PIPIENS COMPLEX POPULATIONS IN SERBIA. Acta Entomologica Serbica, 30(2). https://doi.org/10.5281/zenodo.17910625
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References

Becker, N., Jost, A., & Weitzel, T. (2012). The Culex pipiens complex in Europe. Journal of the American Mosquito Control Ass. 28, 53-67.

Becker, N., Jost, A., Weitzel, T., & Rettich, K. (1999). Exploiting the biology of urban mosquitoes for their control. In Proceedings of the 3rd International Conference on Urban Pests. Czech University of Agriculture, Prague, Czech Republic Vol. 19, 4259 pp.

Becker, N., Petrić, D., Zgomba, M., Boase, C., Madon, M., Dahl, C., Kaiser, A. (2010). Mosquitoes and their control: Second Edition. Springer Science & Business Media. https://doi.org/10.1007/978-3-540-92874-4

Bell, K. L., Noreuil, A., Molloy, E. K., & Fritz, M. L. (2024). Genetic and behavioral differences between above and below ground Culex pipiens bioforms. Heredity, 132(5), 221-231.

Blom, R., Krol, L., Langezaal, M., Schrama, M., Trimbos, K. B., Wassenaar, D., & Koenraadt, C. J. (2024). Blood-feeding patterns of Culex pipiens biotype pipiens and pipiens/molestus hybrids in relation to avian community composition in urban habitats. Parasites & Vectors, 17(1), 95.

Chapman, R.F. (2013). The insects: Structure and function. Cambridge University Press 978-0-521-11389-2

Ciota, A. T., Chin, P. A., & Kramer, L. D. (2013). The effect of hybridization of Culex pipiens complex mosquitoes on transmission of West Nile virus. Parasites & vectors, 6, 1-4.

Clements, A. (1992). The biology of mosquitoes: Development, Nutrition and Reproduction. Chapman and Hall, 2-6 Boundary Row, London

Cvjetković, I. H., Petrović, T., Petrić, D., Milošević, U., Radovanov, J., Kovačević, G., & Milošević, V. (2017). Usutu virus: an emerging flavivirus in Europe. Archives of Veterinary Medicine, 10(1), 25-35.

Detinova, T. S., Bertram, D. S., & World Health Organization. (1962). Age-grouping methods in Diptera of medical importance, with special reference to some vectors of malaria. World Health Organization.

Dimitrijević, D., Milinković, M., Grgić, B., & Ćosić, J. (2014). The current epidemiological situation of WNV in Serbia. In Proceedings of XVI Epizootiology days of Serbia

Fritz, M.L., Walker, E.D., Miller, J.R., Severson, D.W., & Dworkin, I. (2015). Divergent host preferences of above-and below-ground Culex pipiens mosquitoes and their hybrid offspring. Med Vet Entomol. 29(2):115–23.

Isoe, J., Riehle, M.A., & Miesfeld, R.L. (2024) Mosquito Egg Development and Eggshell Formation. Cold Spring Harb Protoc. 10, pdb.top107669. doi: 10.1101/pdb.top107669. PMID: 38190637.

Kassim, N. F. A., Webb, C. E., & Russell, R. C. (2012). Is the expression of autogeny by Culex molestus Forskal (Diptera: Culicidae) influenced by larval nutrition or by adult mating, sugar feeding, or blood feeding? Journal of Vector Ecology, 37(1), 162-171.

Kim, S., Trocke, S., & Sim, C. (2018). Comparative studies of stenogamous behaviour in the mosquito Culex pipiens complex. Medical and Veterinary Entomology, 32(4), 427–435. https://doi.org/10.1111/mve.12309

Klowden, M. J., & Chambers, G. M. (1991). Male accessory gland substances activate egg development in nutritionally stressed Aedes aegypti mosquitoes. Journal of insect physiology, 37(10), 721-726.

McLaughlin, J.M., & Bratu, D.P. (2015). Drosophila melanogaster oogenesis: An overview. Methods Mol Biol 1328:1–20. doi: 10.1007/978-1-4939-2851-4_1

Mclean, R. G., Ubico, S. R., Docherty, D. E., Hansen, W. R., Sileo, L., & McNamara, T. S. (2001). West Nile Virus Transmission and Ecology in Birds. Annals of the New York Academy of Sciences, 951(1), 54-57. https://doi.org/10.1111/j.1749-6632.2001.tb02684.x

O'meara, G. F., & Evans, D. G. (1977). Autogeny in saltmarsh mosquitoes induced by a substance from the male accessory gland. Nature, 267(5609), 342-344.

O'Meara, G. F., & Petersen, J. L. (1985). Effects of mating and sugar feeding on the expression of autogeny in crabhole mosquitoes of the genus Deinocerites (Diptera: Culicidae). Journal of medical entomology, 22(5), 485-490.

Petrić, D., Petrović, T., Cvjetković, I. H., Zgomba, M., Milošević, V., Lazić, G. & Petrić, M. (2017). West Nile virus ‘circulation’ in Vojvodina, Serbia: Mosquito, bird, horse and human surveillance. Molecular and cellular probes, 31, 28-36.

Petrović, T., Šekler, M., Petrić, D., Lazić, S., Debeljak, Z., Vidanović, D., Ignjatović Ćupina, A., Lazić, G., Lupulović, D., Kolarević, M. & Plavšić, B. (2018). Methodology and results of integrated WNV surveillance programmes in Serbia. PLoS One, 13(4), p.e0195439.

Petrović, T., Šekler, M., Petrić, D., Vidanović, D., Debeljak, Z., Lazić, G., Lupulović, D., Kavran, M., Samojlović, M., Ignjatović Ćupina, A., & Tešović, B. (2021). Intensive West Nile virus circulation in Serbia in 2018—results of integrated surveillance program. Pathogens, 10(10), p.1294.

Reusken, C. B. E. M., De Vries, A., Buijs, J., Braks, M. A. H., Den Hartog, W., & Scholte, E.J. (2010). Scientific Note First evidence for presence of Culex pipiens biotype molestus in the Netherlands, and of hybrid biotype pipiens and molestus in northern Europe. Journal of Vector Ecology, 35(1), 210-212.

Rosay, B. (1969). Anatomical indicators for assessing age of mosquitoes: changes in ovarian follicles. Annals of the Entomological Society of America, 62(3), 605-611.

Roy, S., Saha, T.T., Zou, Z., & Raikhel, A.S. (2018) Regulatory pathways controlling female insect reproduction. Annu Rev Entomol 63:489–511. doi: 10.1146/annurev-ento-020117-043258

Šiljegović, S., Mouillaud, T., Jiolle, D., Petrić, D., Ignjatović-Ćupina, A., Vasić, A., & Kavran, M. (2024). Dirofilaria sp. and blood meal analysis in mosquitoes collected in Vojvodina and Mačva, and the first report of Setaria tundra (Issaitshikoff & Rajewskaya, 1928) in Serbia. Animals, 14(9), 1255.

Šolaja, S., Goletić, Š., Veljović, L. & Glišić, D. (2024). Complex patterns of WNV evolution: a focus on the Western Balkans and Central Europe. Frontiers in veterinary science, 11, p.1494746.

Su, T., & Mulla, M. S. (1997). Nutritional reserves, body weight, and starvation tolerance of autogenous and anautogenous strains of Culex tarsalis (Diptera: Culicidae). Journal of medical entomology, 34(1), 68-73.

Turell, M. J. (2012). Members of the Culex pipiens Complex as Vectors of Viruses1. Journal of the American Mosquito Control Association, 28(4s), 123-126.

Vereecken, S., Vanslembrouck, A., Kramer, I. M., & Müller, R. (2022). Phenotypic insecticide resistance status of the Culex pipiens complex: a European perspective. Parasites & Vectors, 15(1), 423.

Vogels, C. B. F., Van De Peppel, L. J. J., Van Vliet, A. J. H., Westenberg, M., Ibañez-Justicia, A., Stroo, A., Buijs, J. A., Visser, T. M., & Koenraadt, C. J. M. (2015). Winter activity and aboveground hybridization between the two biotypes of the West Nile virus vector Culex pipiens. Vector-Borne and Zoonotic Diseases, 15(10), 619–626. https://doi.org/10.1089/vbz.2015.1820

Vogels, C. B., Fros, J. J., Göertz, G. P., Pijlman, G. P., & Koenraadt, C. J. (2016). Vector competence of northern European Culex pipiens biotypes and hybrids for West Nile virus is differentially affected by temperature. Parasites & vectors, 9(1), 393.

Vujić, A., Stefanović, A., Dragičević, I., Matijević, T., Pejčić, L., Knežević, M. & Veselić, S. (2010). Species composition and seasonal dynamics of mosquitoes (Diptera: Culicidae) in flooded areas of Vojvodina, Serbia. Archives of Biological Sciences, 62(4), 1193-1206.