Nosema ceranae DNA in honey bee haemolymph and honey bee mite Varroa destructor
2014
Glavinić, Uroš (Faculty of Veterinary Medicine, Belgrade (Serbia). Department of Biology) | Stevanović, Jevrosima (Faculty of Veterinary Medicine, Belgrade (Serbia). Department of Biology) | Gajić, Bojan (Faculty of Veterinary Medicine, Belgrade (Serbia). Department of Parasitology) | Simeunović, Predrag (Faculty of Veterinary Medicine, Belgrade (Serbia). Department of Biology) | Durić, Spomenka (Faculty of Veterinary Medicine, Belgrade (Serbia). Department of Biology) | Vejnović, Branislav (Faculty of Veterinary Medicine, Belgrade (Serbia). Department of Biology) | Stanimirović, Zoran (Faculty of Veterinary Medicine, Belgrade (Serbia). Department of Biology)
Honey bee mite Varroa destructor and microsporidium Nosema ceranae are currently considered the most important threats to honey bees and beekeeping. It has been believed that both N. apis and N. ceranae invade exclusively epithelial cells of the honey bee ventriculus. However, some fi ndings suggest that these microsporidia may infect other tissues of honey bees. There are indications that these pathogens could be found in honey bee haemolymph, as the medium for its distribution to anatomically distant tissues. Knowing that V. destructor being an ectoparasitic mite feeds on the honey bee’s haemolymph, the aim of this study was to investigate if DNA of Nosema spp. microsporidia could be found in honey bee haemolymph and in V. destructor. The study was conducted on bee haemolymph and V. destructor mites from 44 Apis mellifera colonies. From each hive fi ve mite individuals and 10 μL of haemolymph (from 4-5 bees) were used as samples for DNA isolation and PCR detection of Nosema spp. The DNA of N. ceranae was confi rmed in 61.36% of V. destructor mites and 68.18% of haemolymph samples. This is the fi rst report of N. ceranae DNA in honey bee haemolymph and in V. destructor mites. The fi nding of DNA of N. ceranae in V. destructor could be interpreted as the result of mite feeding on N. ceranae infected bee haemolymph. However, for a full confi rmation of the vector role of V. destructor in spreading of nosemosis, further microscopy investigations are required for the detection of spores in both investigated matrices (haemolymph and V. destructor internal tissues).
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