Abstract

Bacteriophages typically infect a small set of related bacterial strains. The transfer of bacteriophages between more distant clades of bacteria has often been postulated, but remains mostly unaddressed. In this work we leverage the sequencing of a novel cluster of phages infecting Streptomyces bacteria and the availability of large numbers of complete phage genomes in public repositories to address this question. Using phylogenetic and comparative genomics methods, we show that several clusters of Actinobacteria-infecting phages are more closely related between them, and with a small group of Firmicutes phages, than with any other actinobacteriophage lineage. These data indicate that this heterogeneous group of phages shares a common ancestor with well-defined genome structure. Analysis of genomic %GC content and codon usage bias shows that these actinobacteriophages are poorly adapted to their Actinobacteria hosts, suggesting that this phage lineage could have originated in an ancestor of the Firmicutes, adapted to the low %GC content members of this phylum, and later migrated to the Actinobacteria, or that selective pressure for enhanced translational throughput is significantly lower for phages infecting Actinobacteria hosts.

Highlights

  • Referred to as phages, bacteriophages are viruses capable of infecting bacteria

  • Analysis of genomic %GC content and codon usage bias indicates that these actinobacteriophages are still undergoing amelioration, suggesting that selective pressure for translational optimization is weak, or that they could have originated as a result of an interphylum migration event from related Firmicutes phages

  • Genomic analysis indicated that these bacteriophages belong to the PhagesDB BI cluster, which encompasses bacteriophages isolated by other teams on different Streptomyces hosts, such as Streptomyces lividans JI1326 (Streptomyces phage Bing) or Streptomyces azureus NRRL B-2655 (Streptomyces phage Rima)

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Summary

Introduction

Referred to as phages, bacteriophages are viruses capable of infecting bacteria. In the last decade, decreasing sequencing costs have dramatically increased the number and diversity of bacteriophage genome sequences (Russell & Hatfull 2017). This influx of phage genomic data has reinforced the notion that phages are key players in geobiological processes, and the largest reservoirs of genetic diversity in the biosphere (Pedulla et al 2003). Studies of genetic diversity in over 600 mycobacteria-infecting phage genomes have revealed extensive mosaicism, and genetic exchange among relatively distant groups of mycobacteriophages. Analysis of genomic %GC content and codon usage bias indicates that these actinobacteriophages are still undergoing amelioration, suggesting that selective pressure for translational optimization is weak, or that they could have originated as a result of an interphylum migration event from related Firmicutes phages

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