2007
DOI: 10.1038/ismej.2007.90
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Uncultured archaea in deep marine subsurface sediments: have we caught them all?

Abstract: Deep marine subsurface sediments represent a novel archaeal biosphere with unknown physiology; the sedimentary subsurface harbors numerous novel phylogenetic lineages of archaea that are at present uncultured. Archaeal 16S rRNA analyses of deep subsurface sediments demonstrate their global occurrence and wide habitat range, including deep subsurface sediments, methane seeps and organic-rich coastal sediments. These subsurface archaeal lineages were discovered by PCR of extracted environmental DNA; their detect… Show more

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Cited by 412 publications
(385 citation statements)
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“…PCR amplification of the V3 region of the 16S rRNA gene The total DNA in replicate samples was pooled together for PCR using the forward primer U341F (5 0 -CCTACGGGRSGCAGCAG-3 0 ) (Hansen et al, 1998) and reverse primer R685 (5 0 -ATCTACGC ATTTCACCGCTAC-3 0 ) for bacteria (Wang et al, 2004), and the forward primer A344F (5 0 -AYGGGGY GCASCAGGSG-3 0 ) and reverse primer A519R (5 0 -GG TDTTACCGCGGCKGCTG-3 0 ) for archaea (Teske and Sorensen, 2007) in separate reactions. A set of sixnucleotide (nt) barcodes was designed and added to the 5 0 end of U341F, R685, A344F and A519R for the multiplexing of samples in the pyrosequencing runs.…”
Section: Methodsmentioning
confidence: 99%
“…PCR amplification of the V3 region of the 16S rRNA gene The total DNA in replicate samples was pooled together for PCR using the forward primer U341F (5 0 -CCTACGGGRSGCAGCAG-3 0 ) (Hansen et al, 1998) and reverse primer R685 (5 0 -ATCTACGC ATTTCACCGCTAC-3 0 ) for bacteria (Wang et al, 2004), and the forward primer A344F (5 0 -AYGGGGY GCASCAGGSG-3 0 ) and reverse primer A519R (5 0 -GG TDTTACCGCGGCKGCTG-3 0 ) for archaea (Teske and Sorensen, 2007) in separate reactions. A set of sixnucleotide (nt) barcodes was designed and added to the 5 0 end of U341F, R685, A344F and A519R for the multiplexing of samples in the pyrosequencing runs.…”
Section: Methodsmentioning
confidence: 99%
“…DNA extracts of three samples (200, 700 and 1500 m) previously collected from the water column overlying Atlantis II Deep in central Red Sea (21120.76 0 N, 38104.68 0 E; October 2008; Ngugi and Stingl, 2012) were also included for phylogenetic community comparison with that of the BSI. Pyrotag sequencing was done using 16S rRNA gene primers for the V3-V6 (B343F/B1099rc; Liu et al, 2007) and V6-V9 (A934F/U1492R; Lane, 1991;Teske and Sorensen, 2008) regions for bacteria and archaea, respectively. Cell sorting and single-cell genomics were conducted at the Single Cell Genomics Center, Bigelow Laboratory for Ocean Sciences (East Boothbay, ME, USA) as described in Rinke et al (2014).…”
Section: Methodsmentioning
confidence: 99%
“…The archaeal 16S rRNA gene clone libraries for the cool, warm and hot AOM zones show significant differences ( Supplementary Figures S3-5). The cool and hot AOM zones are dominated by archaeal phylotypes of the uncultured Miscellaneous Crenarchaeotal Group archaea, one of the most frequently recovered archaeal lineages in marine subsurface sediments (Fry et al, 2008;Teske and Sørensen, 2008), by uncultured members of the Thermoproteales (Supplementary Figure S4), by ANME-1, and by relatives of thermophilic, mostly sulfate-and iron-reducing Archaeoglobales (Supplementary Figure S5). …”
Section: S Rrna Archaeal Diversitymentioning
confidence: 99%