Viruses Inhibit CO2 Fixation in the Most Abundant Phototrophs on Earth

Marine picocyanobacteria of the genera Prochlorococcus and Synechococcus are the most numerous photosynthetic organisms on our planet [1, 2]. With a global population size of 3.6 × 1027 [3], they are responsible for approximately 10% of global primary production [3, 4]. Viruses that infect Prochloro...

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Veröffentlicht in:Current biology 2016-06, Vol.26 (12), p.1585-1589
Hauptverfasser: Puxty, Richard J., Millard, Andrew D., Evans, David J., Scanlan, David J.
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Sprache:eng
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Zusammenfassung:Marine picocyanobacteria of the genera Prochlorococcus and Synechococcus are the most numerous photosynthetic organisms on our planet [1, 2]. With a global population size of 3.6 × 1027 [3], they are responsible for approximately 10% of global primary production [3, 4]. Viruses that infect Prochlorococcus and Synechococcus (cyanophages) can be readily isolated from ocean waters [5–7] and frequently outnumber their cyanobacterial hosts [8]. Ultimately, cyanophage-induced lysis of infected cells results in the release of fixed carbon into the dissolved organic matter pool [9]. What is less well known is the functioning of photosynthesis during the relatively long latent periods of many cyanophages [10, 11]. Remarkably, the genomes of many cyanophage isolates contain genes involved in photosynthetic electron transport (PET) [12–18] as well as central carbon metabolism [14, 15, 19, 20], suggesting that cyanophages may play an active role in photosynthesis. However, cyanophage-encoded gene products are hypothesized to maintain or even supplement PET for energy generation while sacrificing wasteful CO2 fixation during infection [17, 18, 20]. Yet this paradigm has not been rigorously tested. Here, we measured the ability of viral-infected Synechococcus cells to fix CO2 as well as maintain PET. We compared two cyanophage isolates that share different complements of PET and central carbon metabolism genes. We demonstrate cyanophage-dependent inhibition of CO2 fixation early in the infection cycle. In contrast, PET is maintained throughout infection. Our data suggest a generalized strategy among marine cyanophages to redirect photosynthesis to support phage development, which has important implications for estimates of global primary production. •Viruses of abundant marine cyanobacteria shut down CO2 fixation during infection•The strength of the shutdown is dependent on the viral gene content•Viruses encoding genes that actively shut down CO2 fixation are less productive Puxty et al. show that marine cyanobacterial viruses modify host photosynthesis to maximize energy production but inhibit CO2 fixation. These phototrophs are responsible for ∼10% of global CO2 fixation, and up to 60% of cells are infected at any time. Therefore, this phenomenon has implications for the assessment of primary production of the biosphere.
ISSN:0960-9822
1879-0445
DOI:10.1016/j.cub.2016.04.036