Selection for outbreeding in Varroa parasitising resistant honey bee (Apis mellifera) colonies

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Selection for outbreeding in Varroa parasitising resistant honey bee (Apis mellifera) colonies. / Conlon, Benjamin H.; Kastally, Chedly; Kardell, Marina; Kefuss, John; Moritz, Robin F. A.; Routtu, Jarkko.

I: Ecology and Evolution, Bind 10, Nr. 14, 2020, s. 7806-7811.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Conlon, BH, Kastally, C, Kardell, M, Kefuss, J, Moritz, RFA & Routtu, J 2020, 'Selection for outbreeding in Varroa parasitising resistant honey bee (Apis mellifera) colonies', Ecology and Evolution, bind 10, nr. 14, s. 7806-7811. https://doi.org/10.1002/ece3.6506

APA

Conlon, B. H., Kastally, C., Kardell, M., Kefuss, J., Moritz, R. F. A., & Routtu, J. (2020). Selection for outbreeding in Varroa parasitising resistant honey bee (Apis mellifera) colonies. Ecology and Evolution, 10(14), 7806-7811. https://doi.org/10.1002/ece3.6506

Vancouver

Conlon BH, Kastally C, Kardell M, Kefuss J, Moritz RFA, Routtu J. Selection for outbreeding in Varroa parasitising resistant honey bee (Apis mellifera) colonies. Ecology and Evolution. 2020;10(14):7806-7811. https://doi.org/10.1002/ece3.6506

Author

Conlon, Benjamin H. ; Kastally, Chedly ; Kardell, Marina ; Kefuss, John ; Moritz, Robin F. A. ; Routtu, Jarkko. / Selection for outbreeding in Varroa parasitising resistant honey bee (Apis mellifera) colonies. I: Ecology and Evolution. 2020 ; Bind 10, Nr. 14. s. 7806-7811.

Bibtex

@article{2e7df1b9cf4f40e283cd1aae519d8b26,
title = "Selection for outbreeding in Varroa parasitising resistant honey bee (Apis mellifera) colonies",
abstract = "Parasitism is expected to select for counter-adaptations in the host: driving a coevolutionary arms race. However, human interference between honey bees (Apis mellifera) andVarroamites removes the effect of natural selection and restricts the evolution of host counter-adaptations. With full-sibling mating common amongVarroa, this can rapidly select for virulent, highly inbred,Varroapopulations. We investigated how the evolution of host resistance could affect the infesting population ofVarroamites. We screened aVarroa-resistant honey bee population near Toulouse, France, for aVarroaresistance trait: the inhibition ofVarroa'sreproduction in drone pupae. We then genotypedVarroawhich had co-infested a cell using microsatellites. Across all resistant honey bee colonies,Varroa'sreproductive success was significantly higher in co-infested cells but the distribution ofVarroabetween singly and multiply infested cells was not different from random. While there was a trend for increased reproductive success whenVarroaof differing haplotypes co-infested a cell, this was not significant. This suggests local mate competition, through the presence of anotherVarroafoundress in a pupal cell, may be enough to helpVarroaovercome host resistance traits; with a critical mass of infestingVarroaoverwhelming host resistance. However, the fitness trade-offs associated with preferentially co-infesting cells may be too high forVarroato evolve a mechanism to identify already-infested cells. The increased reproductive success ofVarroawhen co-infesting resistant pupal cells may act as a release valve on the selective pressure for the evolution of counter resistance traits: helping to maintain a stable host-parasite relationship.",
keywords = "co-evolution, genetics, local mate competition, optimality, reproduction, Varroadestructor, VARROA-DESTRUCTOR, REPRODUCTION, CELLS, RECOMBINATION",
author = "Conlon, {Benjamin H.} and Chedly Kastally and Marina Kardell and John Kefuss and Moritz, {Robin F. A.} and Jarkko Routtu",
year = "2020",
doi = "10.1002/ece3.6506",
language = "English",
volume = "10",
pages = "7806--7811",
journal = "Ecology and Evolution",
issn = "2045-7758",
publisher = "Wiley",
number = "14",

}

RIS

TY - JOUR

T1 - Selection for outbreeding in Varroa parasitising resistant honey bee (Apis mellifera) colonies

AU - Conlon, Benjamin H.

AU - Kastally, Chedly

AU - Kardell, Marina

AU - Kefuss, John

AU - Moritz, Robin F. A.

AU - Routtu, Jarkko

PY - 2020

Y1 - 2020

N2 - Parasitism is expected to select for counter-adaptations in the host: driving a coevolutionary arms race. However, human interference between honey bees (Apis mellifera) andVarroamites removes the effect of natural selection and restricts the evolution of host counter-adaptations. With full-sibling mating common amongVarroa, this can rapidly select for virulent, highly inbred,Varroapopulations. We investigated how the evolution of host resistance could affect the infesting population ofVarroamites. We screened aVarroa-resistant honey bee population near Toulouse, France, for aVarroaresistance trait: the inhibition ofVarroa'sreproduction in drone pupae. We then genotypedVarroawhich had co-infested a cell using microsatellites. Across all resistant honey bee colonies,Varroa'sreproductive success was significantly higher in co-infested cells but the distribution ofVarroabetween singly and multiply infested cells was not different from random. While there was a trend for increased reproductive success whenVarroaof differing haplotypes co-infested a cell, this was not significant. This suggests local mate competition, through the presence of anotherVarroafoundress in a pupal cell, may be enough to helpVarroaovercome host resistance traits; with a critical mass of infestingVarroaoverwhelming host resistance. However, the fitness trade-offs associated with preferentially co-infesting cells may be too high forVarroato evolve a mechanism to identify already-infested cells. The increased reproductive success ofVarroawhen co-infesting resistant pupal cells may act as a release valve on the selective pressure for the evolution of counter resistance traits: helping to maintain a stable host-parasite relationship.

AB - Parasitism is expected to select for counter-adaptations in the host: driving a coevolutionary arms race. However, human interference between honey bees (Apis mellifera) andVarroamites removes the effect of natural selection and restricts the evolution of host counter-adaptations. With full-sibling mating common amongVarroa, this can rapidly select for virulent, highly inbred,Varroapopulations. We investigated how the evolution of host resistance could affect the infesting population ofVarroamites. We screened aVarroa-resistant honey bee population near Toulouse, France, for aVarroaresistance trait: the inhibition ofVarroa'sreproduction in drone pupae. We then genotypedVarroawhich had co-infested a cell using microsatellites. Across all resistant honey bee colonies,Varroa'sreproductive success was significantly higher in co-infested cells but the distribution ofVarroabetween singly and multiply infested cells was not different from random. While there was a trend for increased reproductive success whenVarroaof differing haplotypes co-infested a cell, this was not significant. This suggests local mate competition, through the presence of anotherVarroafoundress in a pupal cell, may be enough to helpVarroaovercome host resistance traits; with a critical mass of infestingVarroaoverwhelming host resistance. However, the fitness trade-offs associated with preferentially co-infesting cells may be too high forVarroato evolve a mechanism to identify already-infested cells. The increased reproductive success ofVarroawhen co-infesting resistant pupal cells may act as a release valve on the selective pressure for the evolution of counter resistance traits: helping to maintain a stable host-parasite relationship.

KW - co-evolution

KW - genetics

KW - local mate competition

KW - optimality

KW - reproduction

KW - Varroadestructor

KW - VARROA-DESTRUCTOR

KW - REPRODUCTION

KW - CELLS

KW - RECOMBINATION

U2 - 10.1002/ece3.6506

DO - 10.1002/ece3.6506

M3 - Journal article

VL - 10

SP - 7806

EP - 7811

JO - Ecology and Evolution

JF - Ecology and Evolution

SN - 2045-7758

IS - 14

ER -

ID: 246826552