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High sample throughput genotyping for estimating C-lineage introgression in the dark honeybee: an accurate and cost-effective SNP-based tool

Citation

Henriques, D., Browne, K.A., Barnett, M.W. et al. High sample throughput genotyping for estimating C-lineage introgression in the dark honeybee: an accurate and cost-effective SNP-based tool. Sci Rep 8, 8552 (2018). https://doi.org/10.1038/s41598-018-26932-1

Abstract

The natural distribution of the honeybee (Apis mellifera L.) has been changed by humans in recent decades to such an extent that the formerly widest-spread European subspecies, Apis mellifera mellifera, is threatened by extinction through introgression from highly divergent commercial strains in large tracts of its range. Conservation efforts for A. m. mellifera are underway in multiple European countries requiring reliable and cost-efficient molecular tools to identify purebred colonies. Here, we developed four ancestry-informative SNP assays for high sample throughput genotyping using the iPLEX Mass Array system. Our customized assays were tested on DNA from individual and pooled, haploid and diploid honeybee samples extracted from different tissues using a diverse range of protocols. The assays had a high genotyping success rate and yielded accurate genotypes. Performance assessed against whole-genome data showed that individual assays behaved well, although the most accurate introgression estimates were obtained for the four assays combined (117 SNPs). The best compromise between accuracy and genotyping costs was achieved when combining two assays (62 SNPs). We provide a ready-to-use cost-effective tool for accurate molecular identification and estimation of introgression levels to more effectively monitor and manage A. m. mellifera conservatories.

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José Rufino provided computational resources at the Polytechnic Institute of Bragança, Portugal. DH was supported by a PhD scholarship (SFRH/BD/84195/2012) from the Portuguese Science Foundation (FCT). KAB receives a PhD fellowship from the Irish Research Council. MP was supported by the Swiss Federal Office for Agriculture FOAG and the Fondation Sur-la-Croix, Basel. IM was supported by Saavedra Fajardo fellowship from the Fundación Séneca (20036/SF/16). MAP is a member of and receives support from the COST Action FA1307 (SUPER-B). Funding for genotyping of Irish honeybees was gratefully received from the Eva Crane Trust, the Native Irish Honeybee Society and the Department of Agriculture, Food and the Marine (16/GR/09). MB and TCF are funded by an Institute Strategic Grant from the Biotechnology and Biological Sciences Research Council (BBSRC) (BB/JO1446X/1). Financial support for this research was provided to MAP and LG by 2013–2014 BiodivERsA/FACCE-JPI joint call for research proposals, with the national funders FCT (Portugal), “Agence Nationale de la Recherche” (France), and “Ministério de Economia y Competividade” (Spain).

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