Phylum- and class-specific PCR primers for general microbial community analysis

被引:96
作者
Blackwood, CB [1 ]
Oaks, A [1 ]
Buyers, JS [1 ]
机构
[1] USDA ARS, Beltsville Agr Res Ctr, Sustainable Agr Syst Lab, Beltsville, MD 20705 USA
关键词
D O I
10.1128/AEM.71.10.6193-6198.2005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Amplification of a particular DNA fragment from a mixture of organisms by PCR is a common first step in methods of examining microbial community structure. The use of group-specific primers in community DNA profiling applications can provide enhanced sensitivity and phylogenetic detail compared to domain-specific primers. Other uses for group-specific primers include quantitative PCR and library screening. The purpose of the present study was to develop several primer sets targeting commonly occurring and important groups. Primers specific for the 16S ribosomal sequences of Alphaproteobacteria, Betaproteobacteria, Bacilli, Actinobacteria, and Planctomycetes and for parts of both the 18S ribosomal sequence and the internal transcribed spacer region of Basidiomycota were examined. Primers were tested by comparison to sequences in the ARB 2003 database, and chosen primers were further tested by cloning and sequencing from soil community DNA. Eighty-five to 100% of the sequences obtained from clone libraries were found to be placed with the groups intended as targets, demonstrating the specificity of the primers under field conditions. It will be important to reevaluate primers over time because of the continual growth of sequence databases and revision of microbial taxonomy.
引用
收藏
页码:6193 / 6198
页数:6
相关论文
共 42 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   PHYLOGENETIC IDENTIFICATION AND IN-SITU DETECTION OF INDIVIDUAL MICROBIAL-CELLS WITHOUT CULTIVATION [J].
AMANN, RI ;
LUDWIG, W ;
SCHLEIFER, KH .
MICROBIOLOGICAL REVIEWS, 1995, 59 (01) :143-169
[3]  
Anderson IC, 2003, ENVIRON MICROBIOL, V5, P36, DOI 10.1046/j.1462-2920.2003.00383.x
[4]   Review and re-analysis of domain-specific 16S primers [J].
Baker, GC ;
Smith, JJ ;
Cowan, DA .
JOURNAL OF MICROBIOLOGICAL METHODS, 2003, 55 (03) :541-555
[5]   Eubacterial community structure and population size within the soil light fraction, rhizosphere, and heavy fraction of several agricultural systems [J].
Blackwood, CB ;
Paul, EA .
SOIL BIOLOGY & BIOCHEMISTRY, 2003, 35 (09) :1245-1255
[6]   Diversity and community structure within anoxic sediment from marine salinity meromictic lakes and a coastal meromictic marine basin, Vestfold Hills, Eastern Antarctica [J].
Bowman, JP ;
Rea, SM ;
McCammon, SA ;
McMeekin, TA .
ENVIRONMENTAL MICROBIOLOGY, 2000, 2 (02) :227-237
[7]   The Ribosomal Database Project (RDP-II): previewing a new autoaligner that allows regular updates and the new prokaryotic taxonomy [J].
Cole, JR ;
Chai, B ;
Marsh, TL ;
Farris, RJ ;
Wang, Q ;
Kulam, SA ;
Chandra, S ;
McGarrell, DM ;
Schmidt, TM ;
Garrity, GM ;
Tiedje, JM .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :442-443
[8]   Molecular community analysis of microbial diversity [J].
Dahllöf, I .
CURRENT OPINION IN BIOTECHNOLOGY, 2002, 13 (03) :213-217
[9]   The domain-specific probe EUB338 is insufficient for the detection of all Bacteria:: Development and evaluation of a more comprehensive probe set [J].
Daims, H ;
Brühl, A ;
Amann, R ;
Schleifer, KH ;
Wagner, M .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 1999, 22 (03) :434-444
[10]   Novel bacterial lineages at the (sub)division level as detected by signature nucleotide-targeted recovery of 16S rRNA genes from bulk soil and rice roots of flooded rice microcosms [J].
Derakshani, M ;
Lukow, T ;
Liesack, W .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (02) :623-631