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To determine whether volatiles from bed bug eggs were similar to the defensive secretions from nymphs and adults, headspace volatiles from eggs of the common bed bug (Cimex lectularius L.) were collected by aeration, daily until hatch, and subsequently analyzed by gas chromatography-mass spectrometry. We now report that eucalyptol (1,8-epoxy-p-menthane) was identified from all egg samples. Blank control samples containing no eggs had no evidence of eucalyptol. Positive controls, containing nymphs, adults, and fecal deposits, showed the presence of the defensive secretions (E)-2-hexenal and (E)-2-octenal, but no eucalyptol. The lack of detectable (E)-2-hexenal and (E)-2-octenal in viable egg samples and the detection of eucalyptol are discussed in relation to canine detection of bed bugs.

Bed bugs Cimex lectularius L. were exposed to conidia (spores) of the entomopathogenic fungus Metarhizium anisopliae by feeding, aerosol spray, or contact with a treated surface. Feeding experiments demonstrated that bed bugs were innately susceptible to this fungus. However, only at 98% humidity were mortality rates high, regardless of whether bed bugs were sprayed with a fungal solution or contacted a treated surface. Mortality in treated bed bugs at ambient humidity did not increase when these bed bugs were kept in aggregation with other bed bugs that had recently blood fed to repletion. Based on these laboratory studies, we conclude that M. anisopliae is a poor pathogen for use in control of bed bugs, particularly at humidities that would likely be encountered under field conditions.

Bed bugs Cimex lectularius L. were exposed to conidia (spores) of the entomopathogenic fungus Metarhizium anisopliae by feeding, aerosol spray, or contact with a treated surface. Feeding experiments demonstrated that bed bugs were innately susceptible to this fungus. However, only at 98% humidity were mortality rates high, regardless of whether bed bugs were sprayed with a fungal solution or contacted a treated surface. Mortality in treated bed bugs at ambient humidity did not increase when these bed bugs were kept in aggregation with other bed bugs that had recently blood fed to repletion. Based on these laboratory studies, we conclude that M. anisopliae is a poor pathogen for use in control of bed bugs, particularly at humidities that would likely be encountered under field conditions.

Exposure of a pyrethroid-susceptible strain of bed bugs, Cimex lectularius L. (Hemiptera: Cimicidae) to varying concentrations of deltamethrin for 24 h indicated no significant difference in mortality between males, females, and nymphs at 24 nor at 168 h postexposure when bed bugs were removed to untreated surfaces at 24 h. In addition, many bed bugs classified as morbid or moribund at 24 h and removed to untreated surfaces at this time, recovered by 336 h (2 wk) and were capable of feeding when given the opportunity. Adult female bed bugs that survived were able to lay eggs and the resulting nymphs blood-fed. By contrast, all bed bugs classified as morbid or moribund at 24 h that remained on deltamethrin-treated surfaces for 336 h either died or were still classified as morbid or moribund at the end of this time. No bed bugs classified as morbid or moribund blood-fed when given the opportunity at 2 wk, regardless of whether they remained on the treated surfaces or were removed to untreated surfaces. A power analysis demonstrated we would have detected even moderate differences in mortality between males and females, had differences existed. Therefore, using males exclusively in efficacy assays is a suitable strategy to preserve females for laboratory colony purposes. Results also indicated there is little reason to assess efficacy beyond 1 wk, even when bed bugs are exposed for only 24 h.

Beekeepers apply various dusts to honey bee, Apis mellifera L., colonies to dislodge parasitic mites and control bacterial brood diseases. Anecdotal reports by beekeepers indicate that the antibiotic oxytetracycline (OTC) can be toxic when applied in powdered sugar to cells containing immature bee brood, but it was not known whether the purported toxicity is caused by the antibiotic or the sugar carrier. Additionally, the toxicity of various dusts, proposed for parasitic mite control, is poorly known. In the current studies, we tested OTC and two other antibiotics (tylosin and lincomycin, candidate compounds for use in honey bee colonies) in a powdered sugar carrier for larval toxicity. We also tested for larval toxicity, several dusts that have been proposed for mite control. OTC caused significant brood mortality of approximately 80% at the concentrations used in the hive (200 mg in 20 g sugar). In contrast, tylosin and lincomycin at the 200 mg dose were both similar to untreated controls, and only five times that concentration (1000 mg) caused significant brood mortality of approximately 65%. The addition of dusts, wheat flour, talc, and a commercially available protein supplement, BeePro, resulted in mortality levels between 65 and 80%, similar to that seen with OTC. The common antibiotic carrier, powered confectioners sugar, was nontoxic. The use of 100 unsealed brood cells was demonstrated to be a reliable means of assessing potential adverse affects of dry compounds on larval honey bees. Two new candidate antibiotics for use in honey bee colonies were less toxic to larval bees than the currently labeled antibiotic, OTC.