Bee Health in the Central Black Sea Region and Surrounding Provinces: Regional Prevalence of American Foulbrood, Viral Diseases, Nosema, and Varroa
Abstract
Bacterial, fungal, viral, or parasitic agents found in bee farms play a significant role among the most important causes of colony losses observed in the honeybee (Apis mellifera L). Parasites and diseases affecting honey bees pose a significant threat to the sustainability and productivity of beekeeping in Türkiye. In this study, the presence of Paenibacillus larvae (P. larvae) the causative agent of American foulbrood, Acute Bee Paralysis Virus (ABPV), Black Queen Cell Virus (BQCV), Chronic Bee Paralysis Virus (CBPV), Deformed Wing Virus-A (DWV-A), Kashmir Bee Virus (KBV), Sacbrood Virus (SBV), Israeli Acute Bee Paralysis Virus (IAPV), Apis mellifera Filamentous Virus (AmFV), and Deformed Wing Virus-B (DWV-B formerly VDV-1), Nosema spp. and Varroa destructor (V. destructor) were investigated using microscopic, bacteriological, and molecular methods in suspected adult bee and larval samples collected from apiaries experiencing colony losses in Samsun, Sinop, Ordu, Amasya, and Tokat provinces during 2024 and 2025. According to the findings, mixed infections with two or more pathogens present together were detected in all colonies examined. At the end of the study, viral pathogens detected in samples from the Central Black Sea region and surrounding provinces were investigated. The prevalence rates were determined as follows: DWV-A 73.07%, BQCV 69.23%, SBV 67.3%, AmFV 65.38%, DWV-B 48.07%, ABPV 38.46%, CBPV 17.3%, IAPV 17.3%, and KBV 3.84%. In the samples examined, the prevalence of V. destructor was found to be 59.61%, Nosema ceranae 23.07%, and P. larvae, the causative agent of American Foulbrood, 28.84%. In conclusion, the results suggest that the cause of the losses observed in honey bee colonies is mixed infections. These multiple infections suppress the immune system and reduce colony resilience, thereby predisposing colonies to collapse and highlighting the necessity of multifactorial and holistic approaches for the maintenance of colony health.
Keywords
Apis mellifera L., Central Black Sea, Honey bee pathogens, Paenibacillus larvae, Viral Disease
Ethical Statement
References
- Abban, S., Smith, B., Corona, M., Cook, S. C., Evans, J. D., Chen, Y., & Alburaki, M. (2024). Prevalence and distribution of Varroa destructor and Nosema spp. in symptomatic honey bee colonies across the USA from 2015 to 2022. Scientific Reports, 14(1), 1726.
- Aglagane, A., Ravaioli, V., Er-Rguibi, O., Lavazza, A., Carra, E., Rabitti, A., Mouden, E. H. E., Aourir, M., & Frasnelli, M. (2024). Molecular investigation and infection patterns of seven viruses of honey bee (Apis mellifera L, 1758) populations from southeastern Morocco. Acta Tropica, 257, 107316.
- Akpinar, R., Bozdeveci, A., & Çelik, S. (2023). Diagnosis of American foulbrood in honey bees and honeycomb in the Central and Eastern Black Sea region. Fırat Üniversitesi Sağlık Bilimleri Veteriner Dergisi, 2023, 37(3), 245-250.
- Akpınar, R., Ozan, E., Celik, S., Bayram, Y., Akman, A., Kalayci, G., Cagirgan, A. A., Kadi, H., Kucukkalem, O. F., Oz, M. E., Yilmazer, R. E., Arif Bozdeveci, A., Kucukoglu, B., Guven, G., Yaldiz., & Karaoglu, S. A. (2024a). Prevalence and molecular analysis of some important viruses in honey bee colonies in Türkiye: the status of multiple infections. Archives of Virology, 169(9), 173.
- Akpınar, R. K., Gürler, A. T., Bölükbaş, C. S., Kaya, S., Arslan, S., Aydın, C., Türlek, Ş. Ö., Çelik, S. N., Beyazıt, A., Öncel, T., Erol, U., Çiftci, A. T., Bastem, Z., Ünal, H. H., Şenel, M., Bozdeveci, A., Karaoğlu, Ş. A., Yaldız, M., Güven, G., Küçükoğlu, B., & Kurt, M. (2024b). Prevalence and Phylogenetic Network Analysis of Nosema apis and +Nosema ceranae Isolates from Honeybee Colonies in Türkiye. Acta Parasitologica, 69(3), 1538-1546.
- Alburaki, M., Abban, S. K., Evans, J. D., & Chen, Y. P. (2024). Occurrence and distribution of two bacterial brood diseases (American and European foulbrood) in US honey bee colonies and resistance to antibiotics from 2015 to 2022. Journal of Apicultural Research, 63(4), 701–710.
- Alippi, A. M. (1995). Detection of Bacillus larvae spores in Argentinian honeys by using a semi-selective medium. Microbiologia SEM, 11, 343–350.
- Bahrami, M., Mohammadzadeh, D., Emami, S. J., Rabiee, M. H., & Bokaie, S. (2018). A survey on prevalence and risk factors of Varroasis in West Azerbaijan, Iran. International Journal of Acarology, 44(4–5), 185–188.
- Batan, N., Akpınar, R., İnan, C., Bıyık, S., Karaoglu, Ş. A., Bozdeveci, A., & Nisbet, C. (2025). Investigation of the Presence of Bacterial, Viral and Parasitic Agents in Honey Bee Enterprises in Samsun Region of Türkiye. Biology Bulletin, 52(5), 179.
- Bava, R., Castagna, F., Palma, E., Ceniti, C., Millea, M., Lupia, C., Britti, D., & Musella, V. (2023). Prevalence of Varroa destructor in Honeybee (Apis mellifera) Farms and Varroosis Control Practices in Southern Italy. Microorganisms, 11(5), 1228.