Abstract
AbstractThe gut microbiota features important genetic diversity, and the specific spatial features of the gut may shape evolution within this environment. We investigate the fixation probability of neutral bacterial mutants within a minimal model of the gut that includes hydrodynamic flow and resulting gradients of food and bacterial concentrations. We find that this fixation probability is substantially increased compared to an equivalent well-mixed system, in the regime where the profiles of food and bacterial concentration are strongly spatially-dependent. Fixation probability then becomes independent of total population size. We show that our results can be rationalized by introducing an active population, which consists of those bacteria that are actively consuming food and dividing. The active population size yields an effective population size for neutral mutant fixation probability in the gut.Significance statementThe human body harbors numerous and diverse bacteria, the vast majority of which are located in the gut. These bacteria can mutate and evolve within the gut, which is their natural environment. This can have important public health implications, e.g. when gut bacteria evolve antibiotic resistance. The gut features specific characteristics, including hydrodynamic flow and resulting gradients of food and bacterial concentrations. How do these characteristics impact the evolution and diversity of gut bacteria? We demonstrate that they can substantially increase the probability that neutral mutants reach high proportions and eventually take over the population. This is because only a fraction of gut bacteria is actively dividing. Thus, the specific environment of the gut enhances neutral bacterial diversity.
Publisher
Cold Spring Harbor Laboratory
Cited by
3 articles.
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