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A molecular tool to detect genetic introgression from Spermatheca content

dc.contributor.authorHenriques, Dora
dc.contributor.authorSmith, Stephen
dc.contributor.authorLopes, Ana
dc.contributor.authorWegener, Jakob
dc.contributor.authorMusin, Eduard
dc.contributor.authorHoppe, Andreas
dc.contributor.authorParejo, Melanie
dc.contributor.authorMcCormack, Grace P.
dc.contributor.authorPinto, M. Alice
dc.date.accessioned2022-10-21T15:01:44Z
dc.date.available2022-10-21T15:01:44Z
dc.date.issued2022
dc.description.abstractThe genetic integrity of Apis mellifera mellifera is threatened by introgression in many places of its native distribution, after recurrent importations of commercial queens typically belonging to the divergent C-lineage. A growing interest in keeping and protecting A. m. mellifera has motivated the development of conservation programs in many places of Europe. As part of the conservation efforts, isolated mating stations are set to avoid unwanted crosses, but these are not always effective as matings with unwanted drones are frequently reported. An interesting method to monitor the degree of isolation of mating stations could be through genetic analysis of the queen spermatheca contents. While this method implies that queens selected for monitoring are sacrificed, it can be a powerful way of assessing the effectiveness of mating stations because it would allow easy detection of unwanted alleles. Here, we developed an SNP-based tool suited to the analysis of DNA extracted from spermatheca or from pooled DNA of varying sources. To that end, we first designed an SNP panel from whole-genome sequence data generated from 228 drones, of which 148 belonged to the M-lineage (117 A. m. iberiensis and 31 A. m. mellifera) and 80 to the C-lineage (46 A. m. carnica and 34 A. m. ligustica). A total of 5,007 highly differentiated SNPs was found. Based on different criteria, 130 SNPs were selected to be included in the genotyping tool. This tool is based on the NEBNext Direct Genotyping Solution that allows high-throughput, sequence-based target genotyping of single-individual or pooled DNA. To assess the tool’s sensitivity and accuracy, 142 samples (DNA extracted from spermatheca and tissue, as well as known DNA mixtures) were genotyped. After removing the problematic SNPs, 81 were retained and these were able to provide an estimate of the pool introgression level with great accuracy. This tool represents a significant advance in the genetic analysis of honey bee colonies with a variety of applications, including breeding and conservation of A. m. mellifera.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationHenriques, Dora; Smith, Stephen; Lopes, Ana Rita; Wegener, Jakob; Musin, Eduard; Hoppe, Andreas; Parejo, Melanie; McCormack, Grace P.; Pinto, M. Alice (2022). A molecular tool to detect genetic introgression from Spermatheca content. In Eurbee 9: 9th European Conference of Apidology. Belgradept_PT
dc.identifier.urihttp://hdl.handle.net/10198/26039
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherEstonian University of Life Sciencept_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectSNPspt_PT
dc.subjectPoolspt_PT
dc.subjectSpermatheca contentpt_PT
dc.titleA molecular tool to detect genetic introgression from Spermatheca contentpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceBelgradept_PT
oaire.citation.endPage52pt_PT
oaire.citation.startPage52pt_PT
oaire.citation.titleEurbee 9: 9th European Conference of Apidologypt_PT
person.familyNameHenriques
person.familyNameLopes
person.familyNamePinto
person.givenNameDora
person.givenNameAna
person.givenNameM. Alice
person.identifier.ciencia-id291F-986F-07DA
person.identifier.ciencia-idF014-6835-054D
person.identifier.ciencia-idF814-A1D0-8318
person.identifier.orcid0000-0001-7530-682X
person.identifier.orcid0000-0002-1888-2262
person.identifier.orcid0000-0001-9663-8399
person.identifier.scopus-author-id55761737300
person.identifier.scopus-author-id8085507800
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublicationd2abd09f-a90c-4cfb-9a60-7fc32f56184d
relation.isAuthorOfPublication5c8dc714-e63c-4ac6-882e-92deafa4bbe8
relation.isAuthorOfPublication0667fe04-7078-483d-9198-56d167b19bc5
relation.isAuthorOfPublication.latestForDiscovery5c8dc714-e63c-4ac6-882e-92deafa4bbe8

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