Development and Evaluation of a New Effective Tool and Method for Assessing Varroadestructor (Acari: Varroidae) Mite Populations in Honey Bee Colonies.

A new device for assessing Varroa destructor (Anderson−Truman) mite infestations in honey bee colonies was designed, tested, and evaluated against the sugar roll method, a widely used method by beekeepers. The Varroa Shaker Device (VSD) is constructed of polyvinyl chloride (PVC) pipe that separates into three parts. Inside the shaker there are two mesh sizes; the larger mesh separates the bees from the mites, and the smaller mesh captures the mites. The VSD can be used by shaking bees with only water as the wash solution. The recovery of mites using the VSD is >90%, which is such as that recorded for using the sugar roll method. Our tests demonstrated that the VSD accurately assessed mite loads when fewer than 250 bees were sampled and shaken with 250 mL of water for one minute. To assure accurate mite counts are achieved with any sampling device, honey bees should be taken from frames with an open and/or capped brood where the mites are more likely located. The VSD can be used in both laboratory and field settings to accurately assess honey bee colonies for levels of mite infestation or for collecting live mites for research purposes.

Multiclass determination and confirmation of antibiotic residues in honey using LC-MS/MS.

A multiclass method has been developed for the determination and confirmation in honey of tetracyclines (chlortetracycline, doxycycline, oxytetracycline, and tetracycline), fluoroquinolones (ciprofloxacin, danofloxacin, difloxacin, enrofloxacin, and sarafloxacin), macrolides (tylosin), lincosamides (lincomycin), aminoglycosides (streptomycin), sulfonamides (sulfathiazole), phenicols (chloramphenicol), and fumagillin residues using liquid chromatography tandem mass spectrometry (LC-MS/MS). Erythromycin (a macrolide) and monensin (an ionophore) can be detected and confirmed but not quantitated. Honey samples (approximately 2 g) are dissolved in 10 mL of water and centrifuged. An aliquot of the supernatant is used to determine streptomycin. The remaining supernatant is filtered through a fine-mesh nylon fabric and cleaned up by solid phase extraction. After solvent evaporation and sample reconstitution, 15 antibiotics are assayed by LC-MS/MS using electrospray ionization (ESI) in positive ion mode. Afterward, chloramphenicol is assayed using ESI in negative ion mode. The method has been validated at the low part per billion levels for most of the drugs with accuracies between 65 and 104% and coefficients of variation less than 17%. The evaluation of matrix effects caused by honey of different floral origin is presented.