posted on 2007-12-18, 15:45authored byNicholas H. Mann, Martha R.J. Clokie, Andrew Millard, Annabel Cook, William H. Wilson, Peter J. Wheatley, Audrey Letarov, H.M. Krisch
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.
History
Citation
Journal of Bacteriology, 2005, 187(9), pp.3188-3200