Adaptive radiations in natural populations of prokaryotes: innovation is key

Author:

Vos Michiel12ORCID,Padfield Daniel12,Quince Christopher34,Vos Rutger56

Affiliation:

1. European Centre for Environment and Human Health, University of Exeter Medical School, Environment and Sustainability Institute , Treliever Road, Penryn Campus, Penryn, TR10 9FE , United Kingdom

2. Environment and Sustainability Institute, University of Exeter , Treliever Road, Penryn Campus, Penryn, TR10 9FE , United Kingdom

3. Organisms and Ecosystems, Earlham Institute , Norwich Research Park, Norwich NR4 7UZ , United Kingdom

4. Gut Microbes and Health, Quadram Institute , Norwich Research Park, Norwich NR4 7UQ , United Kingdom

5. Naturalis Biodiversity Center, Understanding Evolution , Darwinweg 2, Leiden 2333 CR , the Netherlands

6. Institute of Biology Leiden, Leiden University , Sylviusweg 72, Leiden 2333 BE , the Netherlands

Abstract

Abstract Prokaryote diversity makes up most of the tree of life and is crucial to the functioning of the biosphere and human health. However, the patterns and mechanisms of prokaryote diversification have received relatively little attention compared to animals and plants. Adaptive radiation, the rapid diversification of an ancestor species into multiple ecologically divergent species, is a fundamental process by which macrobiological diversity is generated. Here, we discuss whether ecological opportunity could lead to similar bursts of diversification in bacteria. We explore how adaptive radiations in prokaryotes can be kickstarted by horizontally acquired key innovations allowing lineages to invade new niche space that subsequently is partitioned among diversifying specialist descendants. We discuss how novel adaptive zones are colonized and exploited after the evolution of a key innovation and whether certain types of are more prone to adaptive radiation. Radiation into niche specialists does not necessarily lead to speciation in bacteria when barriers to recombination are absent. We propose that in this scenario, niche-specific genes could accumulate within a single lineage, leading to the evolution of an open pangenome.

Funder

NERC

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,Ecology,Microbiology

Reference80 articles.

1. Key evolutionary innovations;Alfaro,2014

2. Prokaryote genome fluidity is dependent on effective population size;Andreani;ISME J,2017

3. Structure and function of the global topsoil microbiome;Bahram;Nature,2018

4. Why are some microbes more ubiquitous than others? Predicting the habitat breadth of soil bacteria;Barberán,2014

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