A freshwater cyanophage whose genome indicates close relationships to photosynthetic marine cyanomyophages

Summary Bacteriophage S‐CRM01 has been isolated from a freshwater strain of Synechococcus and shown to be present in the upper Klamath River valley in northern California and Oregon. The genome of this lytic T4‐like phage has a 178 563 bp circular genetic map with 297 predicted protein‐coding genes...

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Veröffentlicht in:Environmental microbiology 2011-07, Vol.13 (7), p.1858-1874
Hauptverfasser: Dreher, Theo W., Brown, Nathan, Bozarth, Connie S., Schwartz, Andrew D., Riscoe, Erin, Thrash, Cameron, Bennett, Samuel E., Tzeng, Shin-Cheng, Maier, Claudia S.
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Sprache:eng
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Zusammenfassung:Summary Bacteriophage S‐CRM01 has been isolated from a freshwater strain of Synechococcus and shown to be present in the upper Klamath River valley in northern California and Oregon. The genome of this lytic T4‐like phage has a 178 563 bp circular genetic map with 297 predicted protein‐coding genes and 33 tRNA genes that represent all 20‐amino‐acid specificities. Analyses based on gene sequence and gene content indicate a close phylogenetic relationship to the ‘photosynthetic’ marine cyanomyophages infecting Synechococcus and Prochlorococcus. Such relatedness suggests that freshwater and marine phages can draw on a common gene pool. The genome can be considered as being comprised of three regions. Region 1 is populated predominantly with structural genes, recognized as such by homology to other T4‐like phages and by identification in a proteomic analysis of purified virions. Region 2 contains most of the genes with roles in replication, recombination, nucleotide metabolism and regulation of gene expression, as well as 5 of the 6 signature genes of the photosynthetic cyanomyophages (hli03, hsp20, mazG, phoH and psbA; cobS is present in Region 3). Much of Regions 1 and 2 are syntenic with marine cyanomyophage genomes, except that a segment encompassing Region 2 is inverted. Region 3 contains a high proportion (85%) of genes that are unique to S‐CRM01, as well as most of the tRNA genes. Regions 1 and 2 contain many predicted late promoters, with a combination of CTAAATA and ATAAATA core sequences. Two predicted genes that are unusual in phage genomes are homologues of cellular spoT and nusG.
ISSN:1462-2912
1462-2920
DOI:10.1111/j.1462-2920.2011.02502.x