Bacterial diversity in the bulk soil and rhizosphere fractions of Lolium perenne and Trifolium repens as revealed by PCR restriction analysis of 16S rDNA

被引:125
作者
Marilley, L [1 ]
Vogt, G [1 ]
Blanc, M [1 ]
Aragno, M [1 ]
机构
[1] Univ Neuchatel, Microbiol Lab, CH-2007 Neuchatel, Switzerland
关键词
microbial molecular ecology; rhizobacteria; rhizosphere; soil bacterial diversity; 16S rDNA;
D O I
10.1023/A:1004309008799
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
The rhizosphere of Trifolium repens and Lolium perenne was divided into three fractions: the bulk soil, the soil adhering to the roots and the washed roots (rhizoplane and endorhizosphere). After isolation and purification of DNA from these fractions, 16S rDNA was amplified by PCR and cloned to obtain a collection of 16S rRNA genes representative of the bacterial communities of these three fractions. The genes were then characterized by PCR restriction analysis. Each different profile was used to define an operational taxonomic unit (OTU). The numbers of OTUs and the numbers of clones among these OTUs allowed to calculate a diversity index. The number of OTUs decreased as root proximity increased and a few OTUs became dominant, resulting in a lower diversity index. In the root fraction of T. repens, the restriction profile of the dominant OTU matched the theoretical profile of the 16S rRNA gene of Rhizobium leguminosarum. This study showed that plant roots create a selective environment for microbial populations.
引用
收藏
页码:219 / 224
页数:6
相关论文
共 32 条
[11]   RECOGNITION OF CHIMERIC SMALL-SUBUNIT RIBOSOMAL DNAS COMPOSED OF GENES FROM UNCULTIVATED MICROORGANISMS [J].
KOPCZYNSKI, ED ;
BATESON, MM ;
WARD, DM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1994, 60 (02) :746-748
[12]   RAPID IDENTIFICATION OF RHIZOBIA BY RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS OF PCR-AMPLIFIED 16S RIBOSOMAL-RNA GENES [J].
LAGUERRE, G ;
ALLARD, MR ;
REVOY, F ;
AMARGER, N .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1994, 60 (01) :56-63
[13]   Estimation of the abundance of an uncultured soil bacterial strain by a competitive quantitative PCR method [J].
Lee, SY ;
Bollinger, J ;
Bezdicek, D ;
Ogram, A .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (10) :3787-3793
[14]   POTENTIAL RISKS OF GENE AMPLIFICATION BY PCR AS DETERMINED BY 16S RDNA ANALYSIS OF A MIXED-CULTURE OF STRICT BAROPHILIC BACTERIA [J].
LIESACK, W ;
WEYLAND, H ;
STACKEBRANDT, E .
MICROBIAL ECOLOGY, 1991, 21 (03) :191-198
[15]   OCCURRENCE OF NOVEL GROUPS OF THE DOMAIN BACTERIA AS REVEALED BY ANALYSIS OF GENETIC MATERIAL ISOLATED FROM AN AUSTRALIAN TERRESTRIAL ENVIRONMENT [J].
LIESACK, W ;
STACKEBRANDT, E .
JOURNAL OF BACTERIOLOGY, 1992, 174 (15) :5072-5078
[16]  
Lynch J. M., 1990, The rhizosphere., P1
[17]   THE RIBOSOMAL DATABASE PROJECT [J].
MAIDAK, BL ;
LARSEN, N ;
MCCAUGHEY, MJ ;
OVERBEEK, R ;
OLSEN, GJ ;
FOGEL, K ;
BLANDY, J ;
WOESE, CR .
NUCLEIC ACIDS RESEARCH, 1994, 22 (17) :3485-3487
[18]   A computer-simulated restriction fragment length polymorphism analysis of bacterial small-subunit rRNA genes: Efficacy of selected tetrameric restriction enzymes for studies of microbial diversity in nature? [J].
Moyer, CL ;
Tiedje, JM ;
Dobbs, FC ;
Karl, DM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (07) :2501-2507
[19]   ESTIMATION OF DIVERSITY AND COMMUNITY STRUCTURE THROUGH RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM DISTRIBUTION ANALYSIS OF BACTERIAL 16S RIBOSOMAL-RNA GENES FROM A MICROBIAL MAT AT AN ACTIVE, HYDROTHERMAL VENT SYSTEM, LOIHI SEAMOUNT, HAWAII [J].
MOYER, CL ;
DOBBS, FC ;
KARL, DM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1994, 60 (03) :871-879
[20]  
Sambrook J., 2002, MOL CLONING LAB MANU