Impact of cultivation on characterisation of species composition of soil bacterial communities

被引:11
作者
McCaig, AE [1 ]
Grayston, SJ
Prosser, JI
Glover, LA
机构
[1] Univ Aberdeen, Inst Med Sci, Dept Mol & Cell Biol, Aberdeen AB25 2ZD, Scotland
[2] Macaulay Land Use Res Inst, Aberdeen AB15 8QH, Scotland
关键词
16S rDNA; molecular ecology; soil microbial diversity; Biolog;
D O I
10.1016/S0168-6496(00)00109-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The species composition of culturable bacteria in Scottish grassland soils was investigated using a combination of Biolog and 16S rDNA analysis for characterisation of isolates. The inclusion of a molecular approach allowed direct comparison of sequences from culturable bacteria with sequences obtained during analysis of DNA extracted directly from the same soil samples. Bacterial strains were isolated on Pseudomonas isolation agar (PIA), a selective medium, and on tryptone soya agar (TSA), a general laboratory medium. In total, 12 and 21 morphologically different bacterial cultures were isolated on PIA and TSA, respectively. Biolog and sequencing placed PIA isolates in the same taxonomic groups, the majority of cultures belonging to the Pseudomonas (sensu stricto) group. However, analysis of 165 rDNA sequences proved more efficient than Biolog for characterising TSA isolates due to limitations of the Microlog database for identifying environmental bacteria. In general, 165 rDNA sequences from TSA isolates showed high similarities to cultured species represented in sequence databases. although TSA-8 showed only 92.5% similarity to the nearest relative, Bacillus insolitus. In general, there was very little overlap between the culturable and uncultured bacterial communities, although two sequences, PIA-2 and TSA-13, showed >99% similarity to soil clones. A cloning step was included prior to sequence analysis of two isolates, TSA-5 and TSA-14, and analysis of several clones confirmed that these cultures comprised at least four and three sequence types. respectively. All isolate clones were most closely related to uncultured bacteria, with clone TSA-5.1 showing 99.8%;, similarity to a sequence amplified directly from the same soil sample. interestingly, one clone, TSA-5.4, clustered within a novel group comprising only uncultured sequences. This group, which is associated with the novel, deep-branching Acidobacterium capsulatum lineage, also included clones isolated during direct analysis of the same soil and from a wide range of other sample types studied elsewhere. The study demonstrates the value of fine-scale molecular analysis for identification of laboratory isolates and indicates the culturability of approximately 1% of the total population but under a restricted range of media and cultivation conditions. (C) 2001 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:37 / 48
页数:12
相关论文
共 49 条
[1]   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
[2]  
Barns SM, 1999, APPL ENVIRON MICROB, V65, P1731
[3]  
*BIOL, 1993, MAN ID BACT
[4]  
BOCHNER B, 1989, ASM NEWS, V55, P536
[5]   Molecular microbial diversity of an agricultural soil in Wisconsin [J].
Borneman, J ;
Skroch, PW ;
OSullivan, KM ;
Palus, JA ;
Rumjanek, NG ;
Jansen, JL ;
Nienhuis, J ;
Triplett, EW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (06) :1935-1943
[6]   Molecular microbial diversity in soils from eastern Amazonia: Evidence for unusual microorganisms and microbial population shifts associated with deforestation [J].
Borneman, J ;
Triplett, EW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (07) :2647-2653
[7]  
Dunbar J, 1999, APPL ENVIRON MICROB, V65, P1662
[8]   ISOLATION AND DIRECT COMPLETE NUCLEOTIDE DETERMINATION OF ENTIRE GENES - CHARACTERIZATION OF A GENE CODING FOR 16S-RIBOSOMAL RNA [J].
EDWARDS, U ;
ROGALL, T ;
BLOCKER, H ;
EMDE, M ;
BOTTGER, EC .
NUCLEIC ACIDS RESEARCH, 1989, 17 (19) :7843-7853
[9]   THE LINEAR PCR REACTION - A SIMPLE AND ROBUST METHOD FOR SEQUENCING AMPLIFIED RIBOSOMAL-RNA GENES [J].
EMBLEY, TM .
LETTERS IN APPLIED MICROBIOLOGY, 1991, 13 (03) :171-174
[10]  
EMBLEY TM, 1996, MOL APPROACHES ENV M, P39