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Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
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Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
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Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
Journal Article

Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection

2019
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Overview
Phytoplankton and associated microbial communities provide organic carbon to oceanic food webs and drive ecosystem dynamics. However, capturing those dynamics is challenging. Here, an in situ, semi-Lagrangian, robotic sampler profiled pelagic microbes at 4 h intervals over ~2.6 days in North Pacific high-nutrient, low-chlorophyll waters. We report on the community structure and transcriptional dynamics of microbes in an operationally large size class (>5 μm) predominantly populated by dinoflagellates, ciliates, haptophytes, pelagophytes, diatoms, cyanobacteria (chiefly Synechococcus) , prasinophytes (chiefly Ostreococcus) , fungi, archaea, and proteobacteria. Apart from fungi and archaea, all groups exhibited 24-h periodicity in some transcripts, but larger portions of the transcriptome oscillated in phototrophs. Periodic photosynthesis-related transcripts exhibited a temporal cascade across the morning hours, conserved across diverse phototrophic lineages. Pronounced silica:nitrate drawdown, a high flavodoxin to ferredoxin transcript ratio, and elevated expression of other Fe-stress markers indicated Fe-limitation. Fe-stress markers peaked during a photoperiodically adaptive time window that could modulate phytoplankton response to seasonal Fe-limitation. Remarkably, we observed viruses that infect the majority of abundant taxa, often with total transcriptional activity synchronized with putative hosts. Taken together, these data reveal a microbial plankton community that is shaped by recycled production and tightly controlled by Fe-limitation and viral activity.
Publisher
Nature Publishing Group UK,Oxford University Press,Nature Publishing Group
Subject

45

/ 631/326/171/1878

/ 704/158/2446/2447

/ 704/47

/ Archaea

/ Biomedical and Life Sciences

/ California

/ Chlorophyll

/ Ciliates

/ Ciliophora - genetics

/ Ciliophora - metabolism

/ Ciliophora - radiation effects

/ Ciliophora - virology

/ Communities

/ Community structure

/ Cyanobacteria

/ Diatoms - genetics

/ Diatoms - metabolism

/ Diatoms - radiation effects

/ Diatoms - virology

/ Dinoflagellates

/ Dinoflagellida - genetics

/ Dinoflagellida - metabolism

/ Dinoflagellida - radiation effects

/ Dinoflagellida - virology

/ Drawdown

/ Ecology

/ Ecosystem dynamics

/ Environmental Sciences & Ecology

/ Evolutionary Biology

/ Ferredoxin

/ Flavodoxin

/ Food Chain

/ Food chains

/ Food webs

/ Fungi

/ Gene expression

/ Haptophyta - genetics

/ Haptophyta - metabolism

/ Haptophyta - radiation effects

/ Haptophyta - virology

/ Iron

/ Iron - metabolism

/ Life Sciences

/ Light effects

/ Marine ecosystems

/ Marine microorganisms

/ Markers

/ Microbial activity

/ Microbial Ecology

/ Microbial Genetics and Genomics

/ Microbiology

/ Microbiomes

/ Microbiota

/ Microorganisms

/ Nutrient dynamics

/ Oceans and Seas

/ Organic carbon

/ Periodicity

/ Photosynthesis

/ Phytoplankton

/ Phytoplankton - genetics

/ Phytoplankton - metabolism

/ Phytoplankton - radiation effects

/ Phytoplankton - virology

/ Plankton

/ Plankton - genetics

/ Plankton - metabolism

/ Plankton - radiation effects

/ Plankton - virology

/ Silica

/ Silicon dioxide

/ Transcription

/ Transcription, Genetic

/ Transcriptomes

/ Virus Physiological Phenomena

/ Viruses - genetics

/ Windows (intervals)