Mechanisms of <i>Trichodesmium</i> demise within the New Caledonian lagoon during the VAHINE mesocosm experiment
The globally important marine diazotrophic cyanobacterium <i>Trichodesmium</i> is abundant in the New Caledonian lagoon (southwestern Pacific Ocean) during austral spring/summer. We investigated the cellular processes mediating <i>Trichodesmium</i> mortality from large surfac...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Copernicus Publications
2016-07-01
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Series: | Biogeosciences |
Online Access: | http://www.biogeosciences.net/13/4187/2016/bg-13-4187-2016.pdf |
Summary: | The globally important marine diazotrophic cyanobacterium
<i>Trichodesmium</i> is abundant in the New Caledonian lagoon (southwestern
Pacific Ocean) during austral spring/summer. We investigated the cellular
processes mediating <i>Trichodesmium</i> mortality from large surface
accumulations (blooms) in the lagoon. <i>Trichodesmium</i> cells (and
associated microbiota) were collected at the time of surface accumulation,
enclosed under simulated ambient conditions, and sampled over time to
elucidate the stressors and subcellular underpinning of rapid biomass demise
(> 90 % biomass crashed within ∼ 24 h).
Metatranscriptomic profiling of <i>Trichodesmium</i> biomass, 0, 8 and
22 h after incubations of surface accumulations, demonstrated upregulated
expression of genes required to increase phosphorus (P) and iron (Fe)
availability and transport, while genes responsible for nutrient storage were
downregulated. Total viral abundance oscillated throughout the experiment and
showed no significant relationship with the development or demise of the
<i>Trichodesmium</i> biomass. Enhanced caspase-specific activity and
upregulated expression of a suite of metacaspase genes, as the
<i>Trichodesmium</i> biomass crashed, implied autocatalytic programmed cell
death (PCD) as the mechanistic cause. Concurrently, genes associated with
buoyancy and gas vesicle production were strongly downregulated concomitant
with increased production and high concentrations of transparent exopolymeric
particles (TEP). The rapid, PCD-mediated, decline of the
<i>Trichodesmium</i> biomass, as we observed from our incubations,
parallels mortality rates reported from <i>Trichodesmium</i> blooms in
situ. Our results suggest that, whatever the ultimate factor, PCD-mediated
death in <i>Trichodesmium</i> can rapidly terminate blooms, facilitate
aggregation, and expedite vertical flux to depth. |
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ISSN: | 1726-4170 1726-4189 |