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Review
. 2012;27(4):350-5.
doi: 10.1264/jsme2.me12037. Epub 2012 Oct 5.

Cyanophage infection in the bloom-forming cyanobacteria Microcystis aeruginosa in surface freshwater

Affiliations
Review

Cyanophage infection in the bloom-forming cyanobacteria Microcystis aeruginosa in surface freshwater

Yukari Yoshida-Takashima et al. Microbes Environ. 2012.

Abstract

Host-like genes are often found in viral genomes. To date, multiple host-like genes involved in photosynthesis and the pentose phosphate pathway have been found in phages of marine cyanobacteria Synechococcus and Prochlorococcus. These gene products are predicted to redirect host metabolism to deoxynucleotide biosynthesis for phage replication while maintaining photosynthesis. A cyanophage, Ma-LMM01, infecting the toxic cyanobacterium Microcystis aeruginosa, was isolated from a eutrophic freshwater lake and assigned as a member of a new lineage of the Myoviridae family. The genome encodes a host-like NblA. Cyanobacterial NblA is known to be involved in the degradation of the major light harvesting complex, the phycobilisomes. Ma-LMM01 nblA gene showed an early expression pattern and was highly transcribed during phage infection. We speculate that the co-option of nblA into Microcystis phages provides a significant fitness advantage to phages by preventing photoinhibition during infection and possibly represents an important part of the co-evolutionary interactions between cyanobacteria and their phages.

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Figures

Fig. 1
Fig. 1
Microcystis aeruginosa and its cyanophage Ma-LMM01. (A) Optical micrograph of Microcystis aeruginosa; (B) transmission electron micrograph of negatively stained cyanophage Ma-LMM01.
Fig. 2
Fig. 2
Expression profiles of phage and host genes. Transcript levels of phage- and host-encoded genes were determined using real-time RT-PCR during infection of Microcystis aeruginosa NIES-298 to Ma-LMM01. The rnpB gene encoding RNase P RNA of M. aeruginosa was used as an internal standard to normalize the transcription levels. Mean and standard deviation of three replicates are shown. (A) nrdA and g91, (B) host-nblA and phage-nblA, and (C) cpcA. Only the expression profiles from 0 to 9 h pi are shown since the host cells were lysed at 12 h pi.
Fig. 3
Fig. 3
Schematic summarizing the potential strategy of cyanophage possessing nblA during infection of Microcystis aeruginosa. M. aeruginosa is commonly found in surface waters due to the buoyancy provided by the gas vesicles, and is intensively and frequently exposed to extensive light. Therefore, phage NblA might function to prevent photoinhibition caused by the absorption of excess light energy upon phage infection. In addition, the phage might use degraded phycobilisomes as an important source of amino acids for phage structural protein synthesis.

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