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. 2007 May 15;104(20):8374-8.
doi: 10.1073/pnas.0702813104. Epub 2007 May 4.

Multitrophic interaction facilitates parasite-host relationship between an invasive beetle and the honey bee

Affiliations

Multitrophic interaction facilitates parasite-host relationship between an invasive beetle and the honey bee

Baldwyn Torto et al. Proc Natl Acad Sci U S A. .

Abstract

Colony defense by honey bees, Apis mellifera, is associated with stinging and mass attack, fueled by the release of alarm pheromones. Thus, alarm pheromones are critically important to survival of honey bee colonies. Here we report that in the parasitic relationship between the European honey bee and the small hive beetle, Aethina tumida, the honey bee's alarm pheromones serve a negative function because they are potent attractants for the beetle. Furthermore, we discovered that the beetles from both Africa and the United States vector a strain of Kodamaea ohmeri yeast, which produces these same honey bee alarm pheromones when grown on pollen in hives. The beetle is not a pest of African honey bees because African bees have evolved effective methods to mitigate beetle infestation. However, European honey bees, faced with disease and pest management stresses different from those experienced by African bees, are unable to effectively inhibit beetle infestation. Therefore, the environment of the European honey bee colony provides optimal conditions to promote the unique bee-beetle-yeast-pollen multitrophic interaction that facilitates effective infestation of hives at the expense of the European honey bee.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Fig. 1.
Fig. 1.
Representative GC-EAD profiles using male antennae of A. tumida and guard bee antennae responding to compounds in the Super Q extract of volatiles collected at the entrance of the honey bee colony for 48 h: for honey bee alarm pheromone IPA (1), along with 2-heptanone (2), styrene (3), and heptanal (4) were detected strongly by antennae of both male and female SHB, whereas only 4 was detected by antenna of the honey bee.
Fig. 2.
Fig. 2.
Wind tunnel responses of a mixed sex of A. tumida (4–8 weeks old) to volatiles released from a combination of worker bees and a brood comb, brood comb alone, and SHB-infested brood comb without worker bees. For each test, there were three replicates. n = 25 beetles per replicate. Bars with the same letter were not significantly different (P < 0.05, LSD test).
Fig. 3.
Fig. 3.
Representative total ion chromatograms of Super Q volatile extracts of brood comb covered with worker bees (Top), brood comb alone (Middle), and SHB-infested brood comb without worker bees (Bottom). Arrow indicates peak for isopentyl acetate. IS, butyl butyrate the internal standard.
Fig. 4.
Fig. 4.
Wind tunnel responses of A. tumida males and females (4–8 weeks old) to volatiles released from different media inoculated with (filled bars) or without (open bars) the Kodamaea strain isolate from beetle larvae sterilized bee collected pollen (a), sterilized commercial pollen substitute (Bee Pro) (b); and sterilized bee collected pollen (c) (filled bars) compared with SDAY (open bars), both inoculated with the yeast isolate. There were three replicates in each test. n = 25 beetles per replicate. Bars with the same letter were not significantly different (P < 0.05, LSD test).
Fig. 5.
Fig. 5.
Amount of 3-methyl-butanol (honey bee alarm pheromone precursor) and IPA (honey bee alarm pheromone) released by sterilized bee-collected pollen inoculated for 7 days with the yeast K. ohmeri, isolated from Aethina tumida obtained from honey bee colonies in Florida and Kenya (mean of three replicates, error bars represent standard error). Bars with the same letter are not significantly different (Student's t test, P < 0.05).

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