Cargando…

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

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kolody, B. C., McCrow, J. P., Allen, L. Zeigler, Aylward, F. O., Fontanez, K. M., Moustafa, A., Moniruzzaman, M., Chavez, F. P., Scholin, C. A., Allen, E. E., Worden, A. Z., Delong, E. F., Allen, A. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794264/
https://www.ncbi.nlm.nih.gov/pubmed/31320727
http://dx.doi.org/10.1038/s41396-019-0472-2
_version_ 1783459252259520512
author Kolody, B. C.
McCrow, J. P.
Allen, L. Zeigler
Aylward, F. O.
Fontanez, K. M.
Moustafa, A.
Moniruzzaman, M.
Chavez, F. P.
Scholin, C. A.
Allen, E. E.
Worden, A. Z.
Delong, E. F.
Allen, A. E.
author_facet Kolody, B. C.
McCrow, J. P.
Allen, L. Zeigler
Aylward, F. O.
Fontanez, K. M.
Moustafa, A.
Moniruzzaman, M.
Chavez, F. P.
Scholin, C. A.
Allen, E. E.
Worden, A. Z.
Delong, E. F.
Allen, A. E.
author_sort Kolody, B. C.
collection PubMed
description 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.
format Online
Article
Text
id pubmed-6794264
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-67942642019-10-17 Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection Kolody, B. C. McCrow, J. P. Allen, L. Zeigler Aylward, F. O. Fontanez, K. M. Moustafa, A. Moniruzzaman, M. Chavez, F. P. Scholin, C. A. Allen, E. E. Worden, A. Z. Delong, E. F. Allen, A. E. ISME J Article 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. Nature Publishing Group UK 2019-07-18 2019-11 /pmc/articles/PMC6794264/ /pubmed/31320727 http://dx.doi.org/10.1038/s41396-019-0472-2 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kolody, B. C.
McCrow, J. P.
Allen, L. Zeigler
Aylward, F. O.
Fontanez, K. M.
Moustafa, A.
Moniruzzaman, M.
Chavez, F. P.
Scholin, C. A.
Allen, E. E.
Worden, A. Z.
Delong, E. F.
Allen, A. E.
Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
title Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
title_full Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
title_fullStr Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
title_full_unstemmed Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
title_short Diel transcriptional response of a California Current plankton microbiome to light, low iron, and enduring viral infection
title_sort diel transcriptional response of a california current plankton microbiome to light, low iron, and enduring viral infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794264/
https://www.ncbi.nlm.nih.gov/pubmed/31320727
http://dx.doi.org/10.1038/s41396-019-0472-2
work_keys_str_mv AT kolodybc dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT mccrowjp dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT allenlzeigler dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT aylwardfo dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT fontanezkm dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT moustafaa dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT moniruzzamanm dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT chavezfp dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT scholinca dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT allenee dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT wordenaz dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT delongef dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection
AT allenae dieltranscriptionalresponseofacaliforniacurrentplanktonmicrobiometolightlowironandenduringviralinfection