Improvement of phylum- and class-specific primers for real-time PCR quantification of bacterial taxa

被引:351
作者
De Gregoris, Tristano Bacchetti [2 ]
Aldred, Nick [2 ]
Clare, Anthony S. [2 ]
Burgess, J. Grant [1 ]
机构
[1] Newcastle Univ, Dove Marine Lab, N Shields NE30 4PZ, Tyne & Wear, England
[2] Newcastle Univ, Sch Marine Sci & Technol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
基金
英国自然环境研究理事会;
关键词
qPCR; Bacteria; Broad taxonomic unit; SYBR green; 16S RIBOSOMAL-RNA; GEL-ELECTROPHORESIS ANALYSIS; OLIGONUCLEOTIDE PROBES; MICROBIAL COMMUNITIES; CLASS ACTINOBACTERIA; RT-PCR; MARINE; GENES; SOIL; DIVERSITY;
D O I
10.1016/j.mimet.2011.06.010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mapping the distribution of phylogenetically distinct bacteria in natural environments is of primary importance to an understanding of ecological dynamics. Here we present a quantitative PCR (qPCR) assay for the analysis of higher taxa composition in natural communities that advances previously available methods by allowing quantification of several taxa during the same qPCR run. Existing primers targeting the 16S rRNA gene specific for Firmicutes, Actinobacteria, Bacteroidetes and for the alpha and gamma subdivisions of the Proteobacteria were improved by largely increasing the coverage of the taxon they target without diminishing their specificity. The qPCR assay was validated in vitro testing artificial mixtures of 16S rRNA sequences and used to characterise the composition of natural communities developing in young marine biofilms. The possible contribution of the proposed technique in revealing ecological dynamics affecting higher bacterial taxa is discussed. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:351 / 356
页数:6
相关论文
共 46 条
[1]   Single-cell identification in microbial communities by improved fluorescence in situ hybridization techniques [J].
Amann, Rudolf ;
Fuchs, Bernhard M. .
NATURE REVIEWS MICROBIOLOGY, 2008, 6 (05) :339-348
[2]   PRIMROSE: a computer program for generating and estimating the phylogenetic range of 16S rRNA oligonucleotide probes and primers in conjunction with the RDP-II database [J].
Ashelford, KE ;
Weightman, AJ ;
Fry, JC .
NUCLEIC ACIDS RESEARCH, 2002, 30 (15) :3481-3489
[3]   PCR bias in ecological analysis:: A case study for quantitative Taq nuclease assays in analyses of microbial communities [J].
Becker, S ;
Böger, P ;
Oehlmann, R ;
Ernst, A .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (11) :4945-+
[4]   Phylum- and class-specific PCR primers for general microbial community analysis [J].
Blackwood, CB ;
Oaks, A ;
Buyers, JS .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (10) :6193-6198
[5]   Quantitative real-time RT-PCR - a perspective [J].
Bustin, SA ;
Benes, V ;
Nolan, T ;
Pfaffl, MW .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2005, 34 (03) :597-601
[6]  
Bustin Stephen A, 2004, J Biomol Tech, V15, P155
[7]   Development and evaluation of specific 16S rDNA primers for marine Cytophaga-Flavobacteria cluster [J].
Chen, Xihan ;
Zeng, Yonghui ;
Jiao, Nianzhi .
MOLECULAR ECOLOGY NOTES, 2006, 6 (04) :1278-1281
[8]   Bacterial primary colonization and early succession on surfaces in marine waters as determined by amplified rRNA gene restriction analysis and sequence analysis of 16S rRNA genes [J].
Dang, HY ;
Lovell, CR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (02) :467-475
[9]   Base-calling of automated sequencer traces using phred.: I.: Accuracy assessment [J].
Ewing, B ;
Hillier, L ;
Wendl, MC ;
Green, P .
GENOME RESEARCH, 1998, 8 (03) :175-185
[10]   Assessment of soil microbial community structure by use of taxon-specific quantitative PCR assays [J].
Fierer, N ;
Jackson, JA ;
Vilgalys, R ;
Jackson, RB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (07) :4117-4120