Real-time PCR quantification and diversity analysis of the functional genes aprA and dsrA of sulfate-reducing prokaryotes in marine sediments of the Peru continental margin and the Black Sea

被引:44
作者
Blazejak, Anna [1 ]
Schippers, Axel [1 ,2 ]
机构
[1] Fed Inst Geosci & Nat Resources BGR, D-30655 Hannover, Germany
[2] Leibniz Univ Hannover, Fac Nat Sci, D-30167 Hannover, Germany
来源
FRONTIERS IN MICROBIOLOGY | 2011年 / 2卷
基金
美国国家科学基金会;
关键词
deep biosphere; real-time PCR; subsurface; ODP; sulfate-reducing prokaryotes; aprA; dsrA; MICROBIAL COMMUNITIES; REDUCTASE GENES; MOLECULAR CHARACTERIZATION; FLOOR BIOSPHERE; NEAR-SURFACE; TIDAL FLAT; AARHUS BAY; DEEP; BACTERIA; OXIDATION;
D O I
10.3389/fmicb.2011.00253
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sulfate-reducing prokaryotes (SRP) are ubiquitous and quantitatively important members in many ecosystems, especially in marine sediments. However their abundance and diversity in subsurface marine sediments is poorly understood. In this study, the abundance and diversity of the functional genes for the enzymes adenosine 5'-phosphosulfate reductase (aprA) and dissimilatory sulfite reductase (dsrA) of SRP in marine sediments of the Peru continental margin and the Black Sea were analyzed, including samples from the deep biosphere (ODP site 1227). For aprA quantification a Q-PCR assay was designed and evaluated. Depth profiles of the aprA and dsrA copy numbers were almost equal for all sites. Gene copy numbers decreased concomitantly with depth from around 10(8)/g sediment close to the sediment surface to less than 10(5)/g sediment at 5 mbsf. The 16S rRNA gene copy numbers of total bacteria were much higher than those of the functional genes at all sediment depths and used to calculate the proportion of SRP to the total Bacteria. The aprA and dsrA copy numbers comprised in average 0.5-1% of the 16S rRNA gene copy numbers of total bacteria in the sediments up to a depth of ca. 40 mbsf. In the zone without detectable sulfate in the pore water from about 40-121 mbsf (Peru margin ODP site 1227), only dsrA (but not aprA) was detected with copy numbers of less than 10(4)/g sediment, comprising ca. 14% of the 16S rRNA gene copy numbers of total bacteria. In this zone, sulfate might be provided for SRP by anaerobic sulfide oxidation. Clone libraries of aprA showed that all isolated sequences originate from SRP showing a close relationship to aprA of characterized species or form a new cluster with only distant relation to aprA of isolated SRP. For dsrA a high diversity was detected, even up to 121 m sediment depth in the deep biosphere.
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页数:11
相关论文
共 68 条
[1]   Rapid detection and quantification of bisulfite reductase genes in oil field samples using real-time PCR [J].
Agrawal, Akhil ;
Lal, Banwari .
FEMS MICROBIOLOGY ECOLOGY, 2009, 69 (02) :301-312
[2]   Molecular characterization of sulfate-reducing bacteria in a New England salt marsh [J].
Bahr, M ;
Crump, BC ;
Klepac-Ceraj, V ;
Teske, A ;
Sogin, ML ;
Hobbie, JE .
ENVIRONMENTAL MICROBIOLOGY, 2005, 7 (08) :1175-1185
[3]   Quantification of sulfate-reducing bacteria in industrial wastewater, by real-time polymerase chain reaction (PCR) using dsrA and apsA genes [J].
Ben-Dov, Eitan ;
Brenner, Asher ;
Kushmaro, Ariel .
MICROBIAL ECOLOGY, 2007, 54 (03) :439-451
[4]   Coexistence of bacterial sulfide oxidizers, sulfate reducers, and spirochetes in a gutless worm (Oligochaeta) from the Peru margin [J].
Blazejak, A ;
Erséus, C ;
Amann, R ;
Dubilier, N .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (03) :1553-1561
[5]   High abundance of JS']JS-1-and Chloroflexi-related Bacteria in deeply buried marine sediments revealed by quantitative, real-time PCR [J].
Blazejak, Anna ;
Schippers, Axel .
FEMS MICROBIOLOGY ECOLOGY, 2010, 72 (02) :198-207
[6]   Geochemistry of Peruvian near-surface sediments [J].
Böning, P ;
Brumsack, HJ ;
Böttcher, ME ;
Schnetger, B ;
Kriete, C ;
Kallmeyer, J ;
Borchers, SL .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2004, 68 (21) :4429-4451
[7]  
Bottrell SH, 2008, GEOCHIM COSMOCHIM AC, V72, pA102
[8]   Isotopic evidence for anoxic pyrite oxidation and stimulation of bacterial sulphate reduction in marine sediments [J].
Bottrell, SH ;
Parkes, RJ ;
Cragg, BA ;
Raiswell, R .
JOURNAL OF THE GEOLOGICAL SOCIETY, 2000, 157 :711-714
[9]   The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments [J].
Bustin, Stephen A. ;
Benes, Vladimir ;
Garson, Jeremy A. ;
Hellemans, Jan ;
Huggett, Jim ;
Kubista, Mikael ;
Mueller, Reinhold ;
Nolan, Tania ;
Pfaffl, Michael W. ;
Shipley, Gregory L. ;
Vandesompele, Jo ;
Wittwer, Carl T. .
CLINICAL CHEMISTRY, 2009, 55 (04) :611-622
[10]   Respiratory chains in the last common ancestor of living organisms [J].
Castresana, J ;
Moreira, D .
JOURNAL OF MOLECULAR EVOLUTION, 1999, 49 (04) :453-460