An evaluation of 18S rDNA approaches for the study of fungal diversity in grassland soils

被引:77
作者
Hunt, J [1 ]
Boddy, L [1 ]
Randerson, PF [1 ]
Rogers, HJ [1 ]
机构
[1] Cardiff Univ, Cardiff Sch Biosci, Cardiff CF10 3TL, S Glam, Wales
关键词
D O I
10.1007/s00248-003-2018-3
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Fungal community structure and diversity in two types of agricultural grassland soil were investigated by amplified 18S ribosomal DNA restriction analysis (ARDRA) and 18S ribosomal DNA sequence analysis. These two grassland sites represent a species-rich old hay meadow and an agriculturally improved site with low floristic diversity. Two primer sets were used in combination to amplify approximately 550 bp of rDNA from three major fungal groups, the zygomycetes, basidiomycetes, and ascomycetes, and clone libraries were created for each site. 18S ARDRA was used to analyze 170 rDNA clones, and three diversity indices were calculated. A small-scale culturing analysis was also carried out and the most common isolates analyzed using ARDRA and sequence analysis. The soil fungal community revealed by the rDNA approaches was significantly different from that produced by this limited culture-based analysis. Twenty-eight soil-derived clones were sequenced, and many represented fungal taxa rarely reported in culture-based studies. The PCR-based techniques detected differences in diversity between the two fungal communities and changes in patterns of dominance that paralleled higher plant diversity. The results suggest that 18S rDNA-based approaches are a useful tool for initial screening of fungal communities, and that they represent a more comprehensive picture of the community than plate culturing.
引用
收藏
页码:385 / 395
页数:11
相关论文
共 49 条
[1]  
Allen M. F., 1992, The fungal community: its organization and role in the ecosystem., P455
[2]  
Anderson IC, 2003, ENVIRON MICROBIOL, V5, P36, DOI 10.1046/j.1462-2920.2003.00383.x
[3]   THE EFFECTS OF AGRICULTURAL MANAGEMENT ON THE SOIL BIOTA OF SOME UPLAND GRASSLANDS [J].
BARDGETT, RD ;
FRANKLAND, JC ;
WHITTAKER, JB .
AGRICULTURE ECOSYSTEMS & ENVIRONMENT, 1993, 45 (1-2) :25-45
[4]   PCR primers that amplify fungal rRNA genes from environmental samples [J].
Borneman, J ;
Hartin, RJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (10) :4356-4360
[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]   RAPID EXTRACTION OF FUNGAL DNA FOR PCR AMPLIFICATION [J].
CENIS, JL .
NUCLEIC ACIDS RESEARCH, 1992, 20 (09) :2380-2380
[7]  
Daniell TJ, 2001, FEMS MICROBIOL ECOL, V36, P203, DOI 10.1111/j.1574-6941.2001.tb00841.x
[8]   Rapid DNA extraction from ferns for PCR-based analyses [J].
Dempster, EL ;
Pryor, KV ;
Francis, D ;
Young, JE ;
Rogers, HJ .
BIOTECHNIQUES, 1999, 27 (01) :66-+
[9]  
Domsch K.H., 1980, COMPENDIUM SOIL FUNG
[10]   Management influences on soil microbial communities and their function in botanically diverse haymeadows of northern England and Wales [J].
Donnison, LM ;
Griffith, GS ;
Hedger, J ;
Hobbs, PJ ;
Bardgett, RD .
SOIL BIOLOGY & BIOCHEMISTRY, 2000, 32 (02) :253-263