Evaluation of the denaturing gradient gel electrophoresis-apparatus as a parameter influencing soil microbial community fingerprinting

被引:17
作者
Ascher, J. [1 ]
Ceccherini, M. T. [1 ]
Chronakova, A. [2 ,3 ]
Jirout, J. [2 ,3 ]
Borgogni, F. [1 ]
Elhottova, D. [2 ,3 ]
Simek, M. [2 ,3 ]
Pietramellara, G. [1 ]
机构
[1] Univ Firenze, Dipartimento Sci Suolo & Nutr Pianta, I-50144 Florence, Italy
[2] Univ S Bohemia, Inst Soil Biol, Biol Ctr AS CR, VVI, Ceske Budejovice 37005, Czech Republic
[3] Univ S Bohemia, Fac Sci, Ceske Budejovice 37005, Czech Republic
关键词
Cattle impact; DGGE; DGGE interfering factors; Soil microbial community fingerprinting; DNA EXTRACTION METHOD; BACTERIAL COMMUNITIES; METHANOGENIC ARCHAEA; DIVERSITY ANALYSIS; CATTLE HUSBANDRY; RIBOSOMAL-RNA; PRIMERS; DGGE; BIOMASS; IMPACT;
D O I
10.1007/s11274-010-0349-z
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
We compared two denaturing gradient gel electrophoresis (DGGE) systems-DCode (Biorad, Hercules, CA, USA) and PhorU (Ingeny, Leiden, NL), performing community level 16S and 18S rRNA gene fragment-PCR-DGGE with total DNA extracted from upland pasture soil used for outdoor cattle husbandry. The methodological evaluation of the DGGE apparatus as parameter influencing DGGE fingerprinting, based on cluster analysis of soil bacterial and fungal community fingerprints, was made in terms of the resulting information about microbial community structures and their response to different degrees of cattle impact. Although the comparative DGGE analysis with different DGGE systems provided similar clustering of microbial community structures in correlation with the degree of cattle impact, our results suggest the DGGE system to be a factor influencing DGGE analysis. To our knowledge this is the first attempt to investigate the hypothetical impact of the DGGE system due to different technical characteristics, recommending the use of one and the same DGGE apparatus throughout an experiment, if the monitoring of microbial community structures requires multiple gel-to-gel analysis.
引用
收藏
页码:1721 / 1726
页数:6
相关论文
共 39 条
[11]  
Green S.J., 2006, A guide to denaturing gradient gel electrophoresis
[12]   Disturbing Impact of Outdoor Cattle Husbandry on Community of Arbuscular Mycorrhizal Fungi in Upland Pasture Soil [J].
Jirout, Jiri ;
Triska, Jan ;
Ruzickova, Kamila ;
Elhottova, Dana .
COMMUNICATIONS IN SOIL SCIENCE AND PLANT ANALYSIS, 2009, 40 (1-6) :736-745
[13]   KJELDAHL METHOD FOR TOTAL NITROGEN [J].
KIRK, PL .
ANALYTICAL CHEMISTRY, 1950, 22 (02) :354-358
[14]  
Kowalchuk GA, 2006, SOIL BIOL, V8, P159
[15]   Application of polymerase chain reaction-denaturing gradient gel electrophoresis for comparison of direct and indirect extraction methods of soil DNA used for microbial community fingerprinting [J].
Kozdrój, J ;
van Elsas, JD .
BIOLOGY AND FERTILITY OF SOILS, 2000, 31 (05) :372-378
[16]   Evaluation of different primers for PCR-DGGE analysis of cheese-associated enterococci [J].
Lorbeg, Petra Mohar ;
Majhenic, Andreja Canzek ;
Rogelj, Irena .
JOURNAL OF DAIRY RESEARCH, 2009, 76 (03) :265-271
[17]   Microbial diversity in soil: ecological theories, the contribution of molecular techniques and the impact of transgenic plants and transgenic microorganisms [J].
Lynch, JM ;
Benedetti, A ;
Insam, H ;
Nuti, MP ;
Smalla, K ;
Torsvik, V ;
Nannipieri, P .
BIOLOGY AND FERTILITY OF SOILS, 2004, 40 (06) :363-385
[18]   Extractable dsDNA and product formation as measures of microbial growth in soil upon substrate addition [J].
Marstorp, H ;
Witter, E .
SOIL BIOLOGY & BIOCHEMISTRY, 1999, 31 (10) :1443-1453
[19]   DNA extraction from soils: Old bias for new microbial diversity analysis methods [J].
Martin-Laurent, F ;
Philippot, L ;
Hallet, S ;
Chaussod, R ;
Germon, JC ;
Soulas, G ;
Catroux, G .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (05) :2354-2359
[20]   How to get more out of molecular fingerprints: practical tools for microbial ecology [J].
Marzorati, Massimo ;
Wittebolle, Lieven ;
Boon, Nico ;
Daffonchio, Daniele ;
Verstraete, Willy .
ENVIRONMENTAL MICROBIOLOGY, 2008, 10 (06) :1571-1581