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Updated: Aug 18, 2026

Environmental Sampling of Photosynthetic Microbes and Their Viruses: From Field to Lab
Published on: July 3, 2025
The genome of S-PM2, a "photosynthetic" T4-type bacteriophage that infects marine Synechococcus strains
Nicholas H Mann1, Martha R J Clokie, Andrew Millard
1Department of Biological Sciences, University of Warwick, Coventry CV4 7AL, UK. N.H.Mann@warwick.ac.uk
Abstract:
Bacteriophage S-PM2 infects several strains of the abundant and ecologically important marine cyanobacterium Synechococcus. A large lytic phage with an isometric icosahedral head, S-PM2 has a contractile tail and by this criterion is classified as a myovirus (1). The linear, circularly permuted, 196,280-bp double-stranded DNA genome of S-PM2 contains 37.8% G+C residues. It encodes 239 open reading frames (ORFs) and 25 tRNAs. Of these ORFs, 19 appear to encode proteins associated with the cell envelope, including a putative S-layer-associated protein. Twenty additional S-PM2 ORFs have homologues in the genomes of their cyanobacterial hosts. There is a group I self-splicing intron within the gene encoding the D1 protein. A total of 40 ORFs, organized into discrete clusters, encode homologues of T4 proteins involved in virion morphogenesis, nucleotide metabolism, gene regulation, and DNA replication and repair. The S-PM2 genome encodes a few surprisingly large (e.g., 3,779 amino acids) ORFs of unknown function. Our analysis of the S-PM2 genome suggests that many of the unknown S-PM2 functions may be involved in the adaptation of the metabolism of the host cell to the requirements of phage infection. This hypothesis originates from the identification of multiple phage-mediated modifications of the host's photosynthetic apparatus that appear to be essential for maintaining energy production during the lytic cycle.
Insights
Marine cyanophage S-PM2 infects Synechococcus, impacting its energy production. Its genome reveals novel functions potentially adapting host metabolism for phage replication during infection.
Area of Science:
- Microbiology
- Virology
- Marine Biology
Background:
- Bacteriophage S-PM2 is a myovirus that infects marine cyanobacteria, particularly Synechococcus.
- Cyanobacteria are ecologically significant in marine environments.
- Understanding phage-host interactions is crucial for marine ecosystem dynamics.
Purpose of the Study:
- To analyze the genome of bacteriophage S-PM2.
- To identify genes and functions related to phage replication and host interaction.
- To investigate phage-mediated modifications of host metabolism.
Main Methods:
- Genome sequencing and analysis of bacteriophage S-PM2.
- Identification and characterization of open reading frames (ORFs).
- Comparative genomics to identify homologous genes in cyanobacterial hosts and other phages.
Main Results:
- The S-PM2 genome is 196,280 bp with 37.8% G+C content, encoding 239 ORFs and 25 tRNAs.
- 40 ORFs show homology to T4 phage proteins involved in various functions, including morphogenesis and DNA metabolism.
- Multiple S-PM2 ORFs are linked to host cell envelope and metabolism, including modifications to the photosynthetic apparatus.
Conclusions:
- The S-PM2 genome encodes numerous proteins with unknown functions, potentially involved in adapting host metabolism for phage replication.
- Phage-induced modifications of the host's photosynthetic apparatus are likely essential for energy production during the lytic cycle.
- S-PM2 represents a significant model for studying phage-cyanobacteria interactions and their impact on marine microbial ecosystems.
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