Cargando…

Microbial community structure and function on sinking particles in the North Pacific Subtropical Gyre

Sinking particles mediate the transport of carbon and energy to the deep-sea, yet the specific microbes associated with sedimenting particles in the ocean's interior remain largely uncharacterized. In this study, we used particle interceptor traps (PITs) to assess the nature of particle-associa...

Descripción completa

Detalles Bibliográficos
Autores principales: Fontanez, Kristina M., Eppley, John M., Samo, Ty J., Karl, David M., DeLong, Edward F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436931/
https://www.ncbi.nlm.nih.gov/pubmed/26042105
http://dx.doi.org/10.3389/fmicb.2015.00469
_version_ 1782372157543677952
author Fontanez, Kristina M.
Eppley, John M.
Samo, Ty J.
Karl, David M.
DeLong, Edward F.
author_facet Fontanez, Kristina M.
Eppley, John M.
Samo, Ty J.
Karl, David M.
DeLong, Edward F.
author_sort Fontanez, Kristina M.
collection PubMed
description Sinking particles mediate the transport of carbon and energy to the deep-sea, yet the specific microbes associated with sedimenting particles in the ocean's interior remain largely uncharacterized. In this study, we used particle interceptor traps (PITs) to assess the nature of particle-associated microbial communities collected at a variety of depths in the North Pacific Subtropical Gyre. Comparative metagenomics was used to assess differences in microbial taxa and functional gene repertoires in PITs containing a preservative (poisoned traps) compared to preservative-free traps where growth was allowed to continue in situ (live traps). Live trap microbial communities shared taxonomic and functional similarities with bacteria previously reported to be enriched in dissolved organic matter (DOM) microcosms (e.g., Alteromonas and Methylophaga), in addition to other particle and eukaryote-associated bacteria (e.g., Flavobacteriales and Pseudoalteromonas). Poisoned trap microbial assemblages were enriched in Vibrio and Campylobacterales likely associated with eukaryotic surfaces and intestinal tracts as symbionts, pathogens, or saprophytes. The functional gene content of microbial assemblages in poisoned traps included a variety of genes involved in virulence, anaerobic metabolism, attachment to chitinaceaous surfaces, and chitin degradation. The presence of chitinaceaous surfaces was also accompanied by the co-existence of bacteria which encoded the capacity to attach to, transport and metabolize chitin and its derivatives. Distinctly different microbial assemblages predominated in live traps, which were largely represented by copiotrophs and eukaryote-associated bacterial communities. Predominant sediment trap-assocaited eukaryotic phyla included Dinoflagellata, Metazoa (mostly copepods), Protalveolata, Retaria, and Stramenopiles. These data indicate the central role of eukaryotic taxa in structuring sinking particle microbial assemblages, as well as the rapid responses of indigenous microbial species in the degradation of marine particulate organic matter (POM) in situ in the ocean's interior.
format Online
Article
Text
id pubmed-4436931
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-44369312015-06-03 Microbial community structure and function on sinking particles in the North Pacific Subtropical Gyre Fontanez, Kristina M. Eppley, John M. Samo, Ty J. Karl, David M. DeLong, Edward F. Front Microbiol Microbiology Sinking particles mediate the transport of carbon and energy to the deep-sea, yet the specific microbes associated with sedimenting particles in the ocean's interior remain largely uncharacterized. In this study, we used particle interceptor traps (PITs) to assess the nature of particle-associated microbial communities collected at a variety of depths in the North Pacific Subtropical Gyre. Comparative metagenomics was used to assess differences in microbial taxa and functional gene repertoires in PITs containing a preservative (poisoned traps) compared to preservative-free traps where growth was allowed to continue in situ (live traps). Live trap microbial communities shared taxonomic and functional similarities with bacteria previously reported to be enriched in dissolved organic matter (DOM) microcosms (e.g., Alteromonas and Methylophaga), in addition to other particle and eukaryote-associated bacteria (e.g., Flavobacteriales and Pseudoalteromonas). Poisoned trap microbial assemblages were enriched in Vibrio and Campylobacterales likely associated with eukaryotic surfaces and intestinal tracts as symbionts, pathogens, or saprophytes. The functional gene content of microbial assemblages in poisoned traps included a variety of genes involved in virulence, anaerobic metabolism, attachment to chitinaceaous surfaces, and chitin degradation. The presence of chitinaceaous surfaces was also accompanied by the co-existence of bacteria which encoded the capacity to attach to, transport and metabolize chitin and its derivatives. Distinctly different microbial assemblages predominated in live traps, which were largely represented by copiotrophs and eukaryote-associated bacterial communities. Predominant sediment trap-assocaited eukaryotic phyla included Dinoflagellata, Metazoa (mostly copepods), Protalveolata, Retaria, and Stramenopiles. These data indicate the central role of eukaryotic taxa in structuring sinking particle microbial assemblages, as well as the rapid responses of indigenous microbial species in the degradation of marine particulate organic matter (POM) in situ in the ocean's interior. Frontiers Media S.A. 2015-05-19 /pmc/articles/PMC4436931/ /pubmed/26042105 http://dx.doi.org/10.3389/fmicb.2015.00469 Text en Copyright © 2015 Fontanez, Eppley, Samo, Karl and DeLong. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Fontanez, Kristina M.
Eppley, John M.
Samo, Ty J.
Karl, David M.
DeLong, Edward F.
Microbial community structure and function on sinking particles in the North Pacific Subtropical Gyre
title Microbial community structure and function on sinking particles in the North Pacific Subtropical Gyre
title_full Microbial community structure and function on sinking particles in the North Pacific Subtropical Gyre
title_fullStr Microbial community structure and function on sinking particles in the North Pacific Subtropical Gyre
title_full_unstemmed Microbial community structure and function on sinking particles in the North Pacific Subtropical Gyre
title_short Microbial community structure and function on sinking particles in the North Pacific Subtropical Gyre
title_sort microbial community structure and function on sinking particles in the north pacific subtropical gyre
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436931/
https://www.ncbi.nlm.nih.gov/pubmed/26042105
http://dx.doi.org/10.3389/fmicb.2015.00469
work_keys_str_mv AT fontanezkristinam microbialcommunitystructureandfunctiononsinkingparticlesinthenorthpacificsubtropicalgyre
AT eppleyjohnm microbialcommunitystructureandfunctiononsinkingparticlesinthenorthpacificsubtropicalgyre
AT samotyj microbialcommunitystructureandfunctiononsinkingparticlesinthenorthpacificsubtropicalgyre
AT karldavidm microbialcommunitystructureandfunctiononsinkingparticlesinthenorthpacificsubtropicalgyre
AT delongedwardf microbialcommunitystructureandfunctiononsinkingparticlesinthenorthpacificsubtropicalgyre