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dc.contributor.author
Freund, Lisa
dc.contributor.author
Vasse, Marie
dc.contributor.author
Velicer, Gregory J.
dc.date.accessioned
2021-01-25T08:45:10Z
dc.date.available
2021-01-25T06:39:40Z
dc.date.available
2021-01-25T08:45:10Z
dc.date.issued
2020
dc.identifier.other
10.1101/2020.12.23.424158
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/465073
dc.identifier.doi
10.3929/ethz-b-000465073
dc.description.abstract
Evolutionary diversification can occur in allopatry or sympatry, can be unselected or driven by selection, and can be phenotypically manifested immediately or remain phenotypically latent until later manifestation in a newly encountered environment. Diversification of host-parasite interactions is frequently studied in the context of intrinsically selective coevolution, but the potential for host-parasite interaction phenotypes to diversify latently during parasite-blind evolution is rarely considered. Here we use a social bacterium experimentally adapted to several environments in the absence of phage to analyse allopatric diversification of latent host quality - the degree to which a host population supports a viral epidemic. Phage-blind evolution reduced host quality overall, with some bacteria becoming completely resistant to growth suppression by phage. Selective-environment differences generated only mild divergence in host-quality. However, selective environments nonetheless played a major role in shaping evolution by determining the degree of stochastic diversification among replicate populations within treatments. Ancestral motility genotype was also found to strongly shape patterns of latent hostquality evolution and diversification. These outcomes show that adaptive landscapes can differ in how they constrain stochastic diversification of a latent phenotype and that major effects of selection on biological diversification can be missed by focusing on trait means. Collectively, our findings suggest that latent-phenotype evolution (LPE) should inform host-parasite evolution theory and that diversification should be conceived broadly to include latent phenotypes.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Cold Spring Harbor Laboratory
en_US
dc.rights.uri
http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
adaptive landscape
en_US
dc.subject
bacteriophages
en_US
dc.subject
byproduct evolution
en_US
dc.subject
cryptic genetic variation
en_US
dc.subject
MyxoEE
en_US
dc.subject
phenotypic plasticity
en_US
dc.subject
pleiotropy
en_US
dc.title
Hidden paths to endless forms most wonderful: Parasite-blind diversification of host quality
en_US
dc.type
Working Paper
dc.rights.license
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
dc.date.published
2020-12-23
ethz.journal.title
bioRxiv
ethz.size
11 p.
en_US
ethz.publication.place
Cold Spring Harbor, NY
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02350 - Dep. Umweltsystemwissenschaften / Dep. of Environmental Systems Science::02720 - Institut für Integrative Biologie / Institute of Integrative Biology::03939 - Velicer, Gregory J. / Velicer, Gregory J.
en_US
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02350 - Dep. Umweltsystemwissenschaften / Dep. of Environmental Systems Science::02720 - Institut für Integrative Biologie / Institute of Integrative Biology::03939 - Velicer, Gregory J. / Velicer, Gregory J.
en_US
ethz.date.deposited
2021-01-25T06:39:47Z
ethz.source
FORM
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2021-01-25T08:45:22Z
ethz.rosetta.lastUpdated
2022-03-29T04:56:59Z
ethz.rosetta.versionExported
true
ethz.COinS
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