TY - JOUR
T1 - Readapting to DCV infection without Wolbachia
T2 - frequency changes of Drosophila antiviral alleles can replace endosymbiont protection
AU - Faria, Vitor G.
AU - Martins, Nelson E.
AU - Schlötterer, Christian
AU - Sucena, Élio
N1 - Funding Information:
We would like to thank Viola Nolte and Tânia F. Paulo for help in experimental and analysis procedures, Sara Magalhães for critical comments and discussions that improved the manuscript. This work was supported by Instituto Gulbenkian de Ciência/Fundac¸ão Calouste Gulbenkian; FCT—Fundac¸ão para a Ciência e a Tecnologia (Portugal) (SFRH/BPD/62964/2009) to N.E.M. and (SFRH/BD/82299/2011 to V.G.F.); and Austrian Science Funds (FWF P27630) to C.S. CONGENTO, project LISBOA-01-0145-FEDER-022170, cofinanced by Lisboa Regional Operational Programme (Lisboa 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (ERDF), and Foundation for Science and Technology (Portugal).
Publisher Copyright:
© The Author(s) 2018.
PY - 2018/7/1
Y1 - 2018/7/1
N2 - There is now ample evidence that endosymbionts can contribute to host adaptation to environmental challenges. However, howendosymbiont presence affects the adaptive trajectory and outcome of the host is yet largely unexplored. InDrosophila, Wolbachia confers protection to RNAvirus infection, an effect that differs betweenWolbachia strains and can be targeted by selection. Adaptation to RNA virus infections is mediated by both Wolbachia and the host, raising the question of whether adaptive genetic changes in the host vary with the presence/absence of the endosymbiont. Here, we address this question using a polymorphic D.melanogaster population previously adapted to DCV infection for 35 generations in the presence of Wolbachia, from which we removed the endosymbiont and followed survival over the subsequent 20 generations of infection. After an initial severe drop, survival frequencies upon DCV selection increased significantly, as seen before in the presence of Wolbachia. Whole-genome sequencing, revealed that the major genes involved in the first selection experiment, pastrel and Ubc-E2H, continued to be selected in Wolbachia-free D. melanogaster, with the frequencies of protective alleles being closer to fixation in the absence of Wolbachia. Our results suggest that heterogeneity in Wolbachia infection status may be sufficient to maintain polymorphisms even in the absence of costs.
AB - There is now ample evidence that endosymbionts can contribute to host adaptation to environmental challenges. However, howendosymbiont presence affects the adaptive trajectory and outcome of the host is yet largely unexplored. InDrosophila, Wolbachia confers protection to RNAvirus infection, an effect that differs betweenWolbachia strains and can be targeted by selection. Adaptation to RNA virus infections is mediated by both Wolbachia and the host, raising the question of whether adaptive genetic changes in the host vary with the presence/absence of the endosymbiont. Here, we address this question using a polymorphic D.melanogaster population previously adapted to DCV infection for 35 generations in the presence of Wolbachia, from which we removed the endosymbiont and followed survival over the subsequent 20 generations of infection. After an initial severe drop, survival frequencies upon DCV selection increased significantly, as seen before in the presence of Wolbachia. Whole-genome sequencing, revealed that the major genes involved in the first selection experiment, pastrel and Ubc-E2H, continued to be selected in Wolbachia-free D. melanogaster, with the frequencies of protective alleles being closer to fixation in the absence of Wolbachia. Our results suggest that heterogeneity in Wolbachia infection status may be sufficient to maintain polymorphisms even in the absence of costs.
KW - DCV virus
KW - Defensive symbiosis
KW - Evolve and resequence
KW - Host-pathogen interactions
KW - Wolbachia
UR - http://www.scopus.com/inward/record.url?scp=85051691746&partnerID=8YFLogxK
U2 - 10.1093/gbe/evy137
DO - 10.1093/gbe/evy137
M3 - Article
C2 - 29947761
AN - SCOPUS:85051691746
SN - 1759-6653
VL - 10
SP - 1783
EP - 1791
JO - Genome Biology and Evolution
JF - Genome Biology and Evolution
IS - 7
ER -