Stochasticity, determinism, and contingency shape genome evolution of endosymbiotic bacteria

Bret M. Boyd (), Ian James, Kevin P. Johnson, Robert B. Weiss, Sarah E. Bush, Dale H. Clayton and Colin Dale
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Bret M. Boyd: Virginia Commonwealth University
Ian James: University of Utah
Kevin P. Johnson: University of Illinois
Robert B. Weiss: University of Utah
Sarah E. Bush: University of Utah
Dale H. Clayton: University of Utah
Colin Dale: University of Utah

Nature Communications, 2024, vol. 15, issue 1, 1-14

Abstract: Abstract Evolution results from the interaction of stochastic and deterministic processes that create a web of historical contingency, shaping gene content and organismal function. To understand the scope of this interaction, we examine the relative contributions of stochasticity, determinism, and contingency in shaping gene inactivation in 34 lineages of endosymbiotic bacteria, Sodalis, found in parasitic lice, Columbicola, that are independently undergoing genome degeneration. Here we show that the process of genome degeneration in this system is largely deterministic: genes involved in amino acid biosynthesis are lost while those involved in providing B-vitamins to the host are retained. In contrast, many genes encoding redundant functions, including components of the respiratory chain and DNA repair pathways, are subject to stochastic loss, yielding historical contingencies that constrain subsequent losses. Thus, while selection results in functional convergence between symbiont lineages, stochastic mutations initiate distinct evolutionary trajectories, generating diverse gene inventories that lack the functional redundancy typically found in free-living relatives.

Date: 2024
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DOI: 10.1038/s41467-024-48784-2

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