Abstract
SummaryPlasmids are important in microbial evolution and adaptation to new environments. Yet, carrying a plasmid can be costly, and long-term association of plasmids with their hosts is poorly understood. Here, we provide evidence that the Chlamydiae, a phylum of strictly host-associated intracellular bacteria, have coevolved with their plasmids since their last common ancestor. Current chlamydial plasmids are amalgamations of at least one ancestral plasmid and a bacteriophage. We show that the majority of plasmid genes are also found on chromosomes of extant chlamydiae. The most conserved plasmid gene families are predominantly vertically inherited, while accessory plasmid gene families show significantly increased mobility. We reconstructed the evolutionary history of plasmid gene content of an entire bacterial phylum over a period of around one billion years. Frequent horizontal gene transfer and chromosomal integration events illustrate the pronounced impact of coevolution with these extrachromosomal elements on bacterial genome dynamics in host-dependent microbes.
Highlights
Plasmids are extrachromosomal genetic elements encoding a wide range of genes that allow organisms from all domains of life to adapt to different stresses or niches.[1]
We present evidence for an ancient acquisition of the chlamydial plasmid and find that the evolutionary trajectory of plasmid genes is characterized by frequent chromosomal integration and horizontal gene transfer (HGT)
We compared the chlamydial plasmids in our dataset to known plasmids from other bacterial phyla and found that their size of 7.5– 145 kb falls into the range of described bacterial plasmids (Figure S2A)
Summary
Plasmids are extrachromosomal genetic elements encoding a wide range of genes that allow organisms from all domains of life to adapt to different stresses or niches.[1]. Plasmid-mediated transfer of antibiotic resistance is a key factor in the spread of antibiotic resistance and the increase in multi-resistant bacterial pathogens.[5]
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