NICHOLAS SCHOOL FACULTY
division of Marine Science & Conservation
Publications [#163289] of Cindy L Van Dover
search PubMed.Papers Published
- Andrew J. Reed, Ruth Dorn, Cindy L. Van Dover, Richard A. Lutz, Costantino Vetriani, Phylogenetic diversity of methanogenic, sulfate-reducing and methanotrophic prokaryotes from deep-sea hydrothermal vents and cold seeps,
Deep-Sea Research II
(2009) (56:1665-1674.)
(last updated on 2009/09/12)
Abstract: Microbial communities of methanogenic, sulfate-reducing and methanotrophic prokaryotes from deepsea
environments were investigated by molecular phylogenetic analysis of the deduced amino acid
sequences of the genes encoding for the methyl coenzyme M reductase (mcrA), dissimilatory sulfite
reductase (dsrAB) and particulate methane monoxygenase (pmoA), respectively. Clone libraries of PCR
amplified genes were constructed using DNA extracted from deep-sea vent chimneys (Rainbow and
Logatchev hydrothermal vent fields, Mid-Atlantic Ridge, Atlantic Ocean; 91N East Pacific Rise, Pacific
Ocean) and from vertically subsampled sediment cores from cold-seep areas (Blake Ridge, western
Atlantic Ocean; Florida Escarpment, Gulf of Mexico). Recombinant clones were screened by RFLP and
representative dsrAB, mcrA and pmoA genes were sequenced. The dsrAB sequences grouped primarily
within the orders Desulfobacterales, Syntrophobacterales and the Gram-positive order Clostridales. Coldseep
mcrA sequences were distributed among the ANME-2c, -2d and -2e groups, which were previously
shown to be associated with the anaerobic oxidation of methane. This study also reports the first mcrA
sequences from a high-temperature, black smoker chimney (Logatchev) to group within the ANME-2e
subgroup. The majority of the remaining hydrothermal vent mcrA sequences were primarily related to
thermophilic members of the anaerobic, methanogenic order Methanococcales. A shift in the dominant
ANME-2 group with depth in the sediment for both Florida Escarpment and Blake Ridge mcrA libraries
was detected. ANME-2d related clones were detected in the top zones of both cores, with the frequency
of ANME-2e related clones increasing with depth. All pmoA sequences retrieved from the cold-seep sites
were found to be related to Type I methanotrophic members of the g-proteobacteria, and were primarily
distributed among three major clusters of sequences. No Type II pmoA sequences related to
methanotrophic members of the a-proteobacteria were detected, suggesting that the methanotrophic
communities in these cold-seep areas are dominated by Type I g-proteobacteria.
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c.vandover@duke.edu
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