Abstract

Carniolan honey bees (Apis mellifera carnica) are considered as an indigenous subspecies in Hungary adapted to most of the ecological and climatic conditions in this area. However, during the last decades Hungarian beekeepers have recognized morphological signs of the Italian honey bee (Apis mellifera ligustica). As the natural distribution of the honey bee subspecies can be affected by the importation of honey bee queens or by natural gene flow, we aimed at determining the genetic structure and characteristics of the local honey bee population using molecular markers. All together, 48 Hungarian and 84 foreign (Italian, Polish, Spanish, Liberian) pupae and/or workers were used for mitochondrial DNA analysis. Additionally, 53 sequences corresponding to 10 subspecies and the Buckfast hybrid were downloaded from GenBank. For the nuclear analysis, 236 Hungarian and 106 foreign honey bees were genotyped using nine microsatellites. Heterozygosity values, population‐specific alleles, FST values, principal coordinate analysis, assignment tests, structure analysis, and dendrograms were calculated. Haplotype and nucleotide diversity values showed moderate values. We found that one haplotype (H9) was dominant in Hungary. The presence of the black honey bee (Apis mellifera mellifera) was negligible, but a few individuals resembling other subspecies were identified. We proved that the Hungarian honey bee population is nearly homogeneous but also demonstrated introgression from the foreign subspecies. Both mitochondrial DNA and microsatellite analyses corroborated the observations of the beekeepers. Molecular analyses suggested that Carniolan honey bee in Hungary is slightly affected by Italian and black honey bee introgression. Genetic differences were detected between Polish and Hungarian Carniolan honey bee populations, suggesting the existence of at least two different gene pools within A. m. carnica.

Highlights

  • Honey bees provide an important pollination services in commercial crops and in many natural habitats worldwide (Klein et al 2007)

  • Additional populations located in Italy (A. m. ligustica), Liberia (A. m. adansonii), Spain (A. m. iberiensis), Poland (A. m. mellifera/carnica), and the Buckfast line from Hungary were used for comparison (Fig. 1)

  • The resulting sequences were compared to the reference sequence (Acc. no.: L06178.1, Apis mellifera ligustica complete mitochondrial genome)

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Summary

Introduction

Honey bees provide an important pollination services in commercial crops and in many natural habitats worldwide (Klein et al 2007). The evolutionary history of the species Apis mellifera (Linnaeus, 1758) was first determined based on morphometric parameters (Ruttner et al 1978). A. mellifera has up to 30 subspecies in different regions of the world (Ruttner 1988). These subspecies were classified into four main groups. One of them is the C lineage that includes north Mediterranean subspecies as A. m. The two major lineages of honey bee in Europe arose from two independent migration events from source populations in Africa (Whitfield et al 2006). The A group includes African subspecies, and the Oriental O group comprises subspecies mainly spread in the Mid-

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