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Florez, L. V.

Publications and source records attributed to Florez, L. V..

2 recordsLinked to original sources

Cytoplasmic incompatibility between Old and New World populations of a tramp ant

As we enter the Anthropocene, the evolutionary dynamics of species will change drastically, and as yet unpredictably, due to human activity. Already today, increases in global human traffic have resulted in the rapid spread of species to new areas, leading to the formation of geographically isolated populations. These go on to evolve in allopatry, which can lead to reproductive isolation, and potentially, the formation of new species. Surprisingly, little is known about such eco-evolutionary processes in ants, even though numerous invasive ant species are globally distributed in geographically isolated populations. Here, we describe the first case of cytoplasmic incompatibility (CI) between populations of a cosmotropic distributed tramp ant with Asian roots, Cardiocondyla obscurior, which has acquired a novel Wolbachia strain in the New World. Our study uncovers the first symbiont-induced mechanism of reproductive isolation in ants, providing a novel perspective on the biology of globally distributed ants.

evolutionary biology

Horizontal gene transfer to a defensive symbiont with a reduced genome amongst a multipartite beetle microbiome

The loss of functions required for independent life when living within a host gives rise to reduced genomes in obligate bacterial symbionts. Although this phenomenon can be explained by existing evolutionary models, its initiation is not well understood. Here, we describe the microbiome associated with eggs of the beetle Lagria villosa, containing multiple bacterial symbionts related to Burkholderia gladioli including a reduced-genome symbiont thought to produce the defensive compound lagriamide. We find that the putative lagriamide producer is the only symbiont undergoing genome reduction, and that it has already lost most primary metabolism and DNA repair pathways. The horizontal acquisition of the lagriamide biosynthetic gene cluster likely preceded genome reduction, and unexpectedly we found that the symbiont accepted additional genes horizontally during genome reduction, even though it lacks the capacity for homologous recombination. These horizontal gene transfers suggest that absolute genetic isolation is not a requirement for genome reduction.

evolutionary biology