An improved fluorescence in situ hybridization protocol for the identification of bacteria and archaea in marine sediments

In situ identification of prokaryotic cells in subsurface sediments is hampered by the low cellular rRNA contents of the target organisms. Fluorescence in situ hybridization with catalyzed reporter deposition (CARD-FISH) has the potential to overcome this limitation, and was therefore optimized for...

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Main Authors: Ishii, K., Mussmann, M., MacGregor, B., Amann, R.
Format: Article in Journal/Newspaper
Language:English
Published: 2004
Subjects:
Online Access:http://hdl.handle.net/21.11116/0000-0001-D0EC-A
http://hdl.handle.net/21.11116/0000-0007-8FCD-2
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spelling ftpubman:oai:pure.mpg.de:item_2485828 2023-08-20T04:07:58+02:00 An improved fluorescence in situ hybridization protocol for the identification of bacteria and archaea in marine sediments Ishii, K. Mussmann, M. MacGregor, B. Amann, R. 2004-11-22 application/pdf http://hdl.handle.net/21.11116/0000-0001-D0EC-A http://hdl.handle.net/21.11116/0000-0007-8FCD-2 eng eng http://hdl.handle.net/21.11116/0000-0001-D0EC-A http://hdl.handle.net/21.11116/0000-0007-8FCD-2 info:eu-repo/semantics/openAccess FEMS Microbiology Ecology info:eu-repo/semantics/article 2004 ftpubman 2023-08-01T23:11:51Z In situ identification of prokaryotic cells in subsurface sediments is hampered by the low cellular rRNA contents of the target organisms. Fluorescence in situ hybridization with catalyzed reporter deposition (CARD-FISH) has the potential to overcome this limitation, and was therefore optimized for a 40 cm deep sediment core sampled from a tidal sandy flat of the German Wadden Sea. Treatment with methanol and H(2)O(2) inactivated endogenous peroxidases and effectively reduced the background signal. Percentage of DAPI stained cells detected with the probe combination EUB(I-III), targeting nearly all the Bacteria, were comparable for CARD-FISH with a horseradish peroxidase (HRP)-labeled probe and FISH with a fluorescently monolabeled probe in the 2-3 cm depth interval (92% and 82%, respectively), but significantly higher with the HRP-labeled probe at 35-40 cm, the deepest layer sampled (63% with HRP vs. 26% with monolabeled probe). With CARD-FISH Alphaproteobacteria and the Desulfobulbaceae group of sulfate-reducing bacteria were detected only in the upper layers. In contrast, Desulfosarcinales, the Bacteroidetes group, Planctomycetes, Betaproteobacteria, and Gammaproteobacteria were found at all depths. Archaea were detectable with ARCH915-HRP after achromopeptidase treatment. Surprisingly, aggregates of Bacteria and Archaea were found, below 12 cm depth, that strongly resemble consortia involved in anoxic oxidation of methane that have previously been found in sediments near methane hydrate deposits. With the optimized CARD-FISH protocol, microbial populations could also be detected in deeper sediment horizons. Furthermore, the intensity of the CARD-FISH signals improved detection of rare organisms such as Archaea. Article in Journal/Newspaper Methane hydrate Max Planck Society: MPG.PuRe
institution Open Polar
collection Max Planck Society: MPG.PuRe
op_collection_id ftpubman
language English
description In situ identification of prokaryotic cells in subsurface sediments is hampered by the low cellular rRNA contents of the target organisms. Fluorescence in situ hybridization with catalyzed reporter deposition (CARD-FISH) has the potential to overcome this limitation, and was therefore optimized for a 40 cm deep sediment core sampled from a tidal sandy flat of the German Wadden Sea. Treatment with methanol and H(2)O(2) inactivated endogenous peroxidases and effectively reduced the background signal. Percentage of DAPI stained cells detected with the probe combination EUB(I-III), targeting nearly all the Bacteria, were comparable for CARD-FISH with a horseradish peroxidase (HRP)-labeled probe and FISH with a fluorescently monolabeled probe in the 2-3 cm depth interval (92% and 82%, respectively), but significantly higher with the HRP-labeled probe at 35-40 cm, the deepest layer sampled (63% with HRP vs. 26% with monolabeled probe). With CARD-FISH Alphaproteobacteria and the Desulfobulbaceae group of sulfate-reducing bacteria were detected only in the upper layers. In contrast, Desulfosarcinales, the Bacteroidetes group, Planctomycetes, Betaproteobacteria, and Gammaproteobacteria were found at all depths. Archaea were detectable with ARCH915-HRP after achromopeptidase treatment. Surprisingly, aggregates of Bacteria and Archaea were found, below 12 cm depth, that strongly resemble consortia involved in anoxic oxidation of methane that have previously been found in sediments near methane hydrate deposits. With the optimized CARD-FISH protocol, microbial populations could also be detected in deeper sediment horizons. Furthermore, the intensity of the CARD-FISH signals improved detection of rare organisms such as Archaea.
format Article in Journal/Newspaper
author Ishii, K.
Mussmann, M.
MacGregor, B.
Amann, R.
spellingShingle Ishii, K.
Mussmann, M.
MacGregor, B.
Amann, R.
An improved fluorescence in situ hybridization protocol for the identification of bacteria and archaea in marine sediments
author_facet Ishii, K.
Mussmann, M.
MacGregor, B.
Amann, R.
author_sort Ishii, K.
title An improved fluorescence in situ hybridization protocol for the identification of bacteria and archaea in marine sediments
title_short An improved fluorescence in situ hybridization protocol for the identification of bacteria and archaea in marine sediments
title_full An improved fluorescence in situ hybridization protocol for the identification of bacteria and archaea in marine sediments
title_fullStr An improved fluorescence in situ hybridization protocol for the identification of bacteria and archaea in marine sediments
title_full_unstemmed An improved fluorescence in situ hybridization protocol for the identification of bacteria and archaea in marine sediments
title_sort improved fluorescence in situ hybridization protocol for the identification of bacteria and archaea in marine sediments
publishDate 2004
url http://hdl.handle.net/21.11116/0000-0001-D0EC-A
http://hdl.handle.net/21.11116/0000-0007-8FCD-2
genre Methane hydrate
genre_facet Methane hydrate
op_source FEMS Microbiology Ecology
op_relation http://hdl.handle.net/21.11116/0000-0001-D0EC-A
http://hdl.handle.net/21.11116/0000-0007-8FCD-2
op_rights info:eu-repo/semantics/openAccess
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