Abstract

Many bacteria can exchange genetic material through horizontal gene transfer (HGT) mediated by plasmids and plasmid-borne transposable elements. Here, we study the population structure and dynamics of over 10,000 bacterial plasmids, by quantifying their genetic similarities and reconstructing a network based on their shared k-mer content. We use a community detection algorithm to assign plasmids into cliques, which correlate with plasmid gene content, bacterial host range, GC content, and existing classifications based on replicon and mobility (MOB) types. Further analysis of plasmid population structure allows us to uncover candidates for yet undescribed replicon genes, and to identify transposable elements as the main drivers of HGT at broad phylogenetic scales. Our work illustrates the potential of network-based analyses of the bacterial ‘mobilome’ and opens up the prospect of a natural, exhaustive classification framework for bacterial plasmids.

Highlights

  • Many bacteria can exchange genetic material through horizontal gene transfer (HGT) mediated by plasmids and plasmid-borne transposable elements

  • A dataset of complete bacterial plasmids was assembled comprising 10,696 sequences found in bacteria from 22 phyla and over 400 genera (Supplementary Data 1, Fig. 1a and Supplementary Fig. 1)

  • There are 3,328,916 bacterial genes available in the RefSeq database (NCBI Gene Statistics accessed on June 2019), meaning that roughly 1 in of the currently known bacterial genes are plasmid borne

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Summary

Introduction

Many bacteria can exchange genetic material through horizontal gene transfer (HGT) mediated by plasmids and plasmid-borne transposable elements. We study the population structure and dynamics of over 10,000 bacterial plasmids, by quantifying their genetic similarities and reconstructing a network based on their shared k-mer content. We use a community detection algorithm to assign plasmids into cliques, which correlate with plasmid gene content, bacterial host range, GC content, and existing classifications based on replicon and mobility (MOB) types. MOB-typing schemes generate fewer multiple assignments and can cover a potentially wider taxonomic range; they are not applicable to the classification of non-mobilizable plasmids. These two typing schemes have inspired several in silico classification tools, such as PlasmidFinder[12], the plasmid MultiLocus Sequence Typing database and MOB suite[15]. Our results illustrate the potential of network-based analyses of plasmid sequences and opens up the prospect of a natural, exhaustive classification framework for bacterial plasmids

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