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Biology subjects

Athreya, G.

Publications and source records attributed to Athreya, G..

2 recordsLinked to original sources

On the structure of an evolutionary transition: dependence and cohesion in incipient endosymbioses

Eukaryogenesis is the prototypical example of an egalitarian evolutionary transition in individuality, and endosymbiosis, more generally, is central to the origins of many complex biological systems. Why do only some symbioses undergo such a transition, and how does the host-symbiont relationship change during this process? Here, we characterise endosymbiosis by two emergent collective-level properties: host and symbiont survival as a collective ("mutual dependence") and the level of synchronised reproduction ("reproductive cohesion"). Using adaptive dynamics, we study the evolution of the traits underlying these properties. First, by adding a carrying capacity for the collective population - a realism omitted in previous models - we find novel reasons why complete dependence or cohesion might not evolve, thus providing further theoretical support for the rarity of transitions in individuality. Second, our model suggests that asymmetries in evolutionary outcomes of hosts and symbionts can be explained by a difference in their population growth parameters, coupled with their shared fate when in a collective. Lastly, we show that during the early stages of an endosymbiosis, even if investments in dependence and cohesion are uncorrelated, mutual dependence arises faster than reproductive cohesion. Our results hence shed light on three aspects of endosymbiosis: coevolution between the host and symbiont, coevolution between dependence and cohesion, and ultimately on the opportunity of undergoing an evolutionary transition. Connecting to ecological factors, this work uncovers fundamental properties of endosymbioses, providing a clear way forward for theoretical and empirical investigations.

evolutionary biology↗

Antibiotic-mediated interactions underlying microbial diversity

The immense diversity observed in natural microbial communities is surprising in light of the numerous weapons microbes have evolved to inhibit each others growth. It is thus imperative to understand which interaction patterns can sustain a biodiverse community when individual species antagonistically affect one another. In this study, we leverage potent methods from theoretical ecology to show how antibiotic-mediated interactions between microbes drive biological diversity. Building on previous experimental and theoretical results, we analyse the dynamics induced by various interaction graphs involving antibiotic production, resistance, and degradation. Previous work has recognised the importance of a particular producer-sensitive-degrader (PSD) motif in the interaction graph. We study this motif in detail and elucidate the mechanistic reason for this importance. Concretely, we give exact rules for coexistence in some simple cases where exhaustive enumeration of the interaction graphs is feasible. More generally, our results suggest that the PSD motif, in combination with a cyclic interaction structure, is sufficient for stable coexistence in well-mixed populations. Using individual-based simulations, we then study the importance of the PSD motif in spatially structured populations. We show that community coexistence is robust for an extensive range of antibiotic and degrader diffusivities. Together, these findings illuminate the interaction patterns that give rise to diversity in complex microbial communities, stressing that antagonism does not imply a lack of diversity and suggesting clear approaches for culturing synthetic microbial consortia.

microbiology↗