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Characterization of Microbial Population Shifts during Sample Storage
The objective of this study was to determine shifts in the microbial community structure and potential function based on standard Integrated Ocean Drilling Program (IODP) storage procedures for sediment cores. Standard long-term storage protocols maintain sediment temperature at 4°C for mineralogy,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281211/ https://www.ncbi.nlm.nih.gov/pubmed/22363327 http://dx.doi.org/10.3389/fmicb.2012.00049 |
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author | Mills, Heath J. Reese, Brandi Kiel Peter, Cruz St. |
author_facet | Mills, Heath J. Reese, Brandi Kiel Peter, Cruz St. |
author_sort | Mills, Heath J. |
collection | PubMed |
description | The objective of this study was to determine shifts in the microbial community structure and potential function based on standard Integrated Ocean Drilling Program (IODP) storage procedures for sediment cores. Standard long-term storage protocols maintain sediment temperature at 4°C for mineralogy, geochemical, and/or geotechnical analysis whereas standard microbiological sampling immediately preserves sediments at −80°C. Storage at 4°C does not take into account populations may remain active over geologic time scales at temperatures similar to storage conditions. Identification of active populations within the stored core would suggest geochemical and geophysical conditions within the core change over time. To test this potential, the metabolically active fraction of the total microbial community was characterized from IODP Expedition 325 Great Barrier Reef sediment cores prior to and following a 3-month storage period. Total RNA was extracted from complementary 2, 20, and 40 m below sea floor sediment samples, reverse transcribed to complementary DNA and then sequenced using 454 FLX sequencing technology, yielding over 14,800 sequences from the six samples. Interestingly, 97.3% of the sequences detected were associated with lineages that changed in detection frequency during the storage period including key biogeochemically relevant lineages associated with nitrogen, iron, and sulfur cycling. These lineages have the potential to permanently alter the physical and chemical characteristics of the sediment promoting misleading conclusions about the in situ biogeochemical environment. In addition, the detection of new lineages after storage increases the potential for a wider range of viable lineages within the subsurface that may be underestimated during standard community characterizations. |
format | Online Article Text |
id | pubmed-3281211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32812112012-02-23 Characterization of Microbial Population Shifts during Sample Storage Mills, Heath J. Reese, Brandi Kiel Peter, Cruz St. Front Microbiol Microbiology The objective of this study was to determine shifts in the microbial community structure and potential function based on standard Integrated Ocean Drilling Program (IODP) storage procedures for sediment cores. Standard long-term storage protocols maintain sediment temperature at 4°C for mineralogy, geochemical, and/or geotechnical analysis whereas standard microbiological sampling immediately preserves sediments at −80°C. Storage at 4°C does not take into account populations may remain active over geologic time scales at temperatures similar to storage conditions. Identification of active populations within the stored core would suggest geochemical and geophysical conditions within the core change over time. To test this potential, the metabolically active fraction of the total microbial community was characterized from IODP Expedition 325 Great Barrier Reef sediment cores prior to and following a 3-month storage period. Total RNA was extracted from complementary 2, 20, and 40 m below sea floor sediment samples, reverse transcribed to complementary DNA and then sequenced using 454 FLX sequencing technology, yielding over 14,800 sequences from the six samples. Interestingly, 97.3% of the sequences detected were associated with lineages that changed in detection frequency during the storage period including key biogeochemically relevant lineages associated with nitrogen, iron, and sulfur cycling. These lineages have the potential to permanently alter the physical and chemical characteristics of the sediment promoting misleading conclusions about the in situ biogeochemical environment. In addition, the detection of new lineages after storage increases the potential for a wider range of viable lineages within the subsurface that may be underestimated during standard community characterizations. Frontiers Research Foundation 2012-02-17 /pmc/articles/PMC3281211/ /pubmed/22363327 http://dx.doi.org/10.3389/fmicb.2012.00049 Text en Copyright © 2012 Mills, Reese and Peter. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Microbiology Mills, Heath J. Reese, Brandi Kiel Peter, Cruz St. Characterization of Microbial Population Shifts during Sample Storage |
title | Characterization of Microbial Population Shifts during Sample Storage |
title_full | Characterization of Microbial Population Shifts during Sample Storage |
title_fullStr | Characterization of Microbial Population Shifts during Sample Storage |
title_full_unstemmed | Characterization of Microbial Population Shifts during Sample Storage |
title_short | Characterization of Microbial Population Shifts during Sample Storage |
title_sort | characterization of microbial population shifts during sample storage |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281211/ https://www.ncbi.nlm.nih.gov/pubmed/22363327 http://dx.doi.org/10.3389/fmicb.2012.00049 |
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