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Applied and Environmental Microbiology, July 1999, p. 2994-3000, Vol. 65, No. 7
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Comparative Diversity of Ammonia Oxidizer 16S rRNA
Gene Sequences in Native, Tilled, and Successional Soils
Mary Ann
Bruns,1,*
John R.
Stephen,2,3,
George A.
Kowalchuk,3
James I.
Prosser,2 and
Eldor A.
Paul1
National Science Foundation Center for
Microbial Ecology and Department of Crop and Soil Sciences, Michigan
State University, East Lansing, Michigan 488241;
Department of Molecular and Cell Biology, Institute of Medical
Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD,
Scotland2; and Netherlands Institute of
Ecology, 6666 ZG Heteren, The Netherlands3
Received 22 December 1998/Accepted 25 April 1999
Autotrophic ammonia oxidizer (AAO) populations in soils from
native, tilled, and successional treatments at the Kellogg Biological Station Long-Term Ecological Research site in southwestern Michigan were compared to assess effects of disturbance on these bacteria. N
fertilization effects on AAO populations were also evaluated with soils
from fertilized microplots within the successional treatments.
Population structures were characterized by PCR amplification of
microbial community DNA with group-specific 16S rRNA gene (rDNA) primers, cloning of PCR products and clone hybridizations with group-specific probes, phylogenetic analysis of partial 16S rDNA sequences, and denaturing gradient gel electrophoresis (DGGE) analysis.
Population sizes were estimated by using most-probable-number (MPN)
media containing varied concentrations of ammonium sulfate. Tilled
soils contained higher numbers than did native soils of culturable AAOs
that were less sensitive to different ammonium concentrations in MPN
media. Compared to sequences from native soils, partial 16S rDNA
sequences from tilled soils were less diverse and grouped exclusively
within Nitrosospira cluster 3. Native soils yielded
sequences representing three different AAO clusters. Probes for
Nitrosospira cluster 3 hybridized with DGGE blots from
tilled and fertilized successional soils but not with blots from native
or unfertilized successional soils. Hybridization results thus
suggested a positive association between the Nitrosospira cluster 3 subgroup and soils amended with inorganic N. DGGE patterns for soils sampled from replicated plots of each treatment were nearly
identical for tilled and native soils in both sampling years,
indicating spatial and temporal reproducibility based on treatment.
*
Corresponding author. Present address: Department of
Land, Air and Water Resources, University of California, Davis, CA
95616-8627. Phone: (530) 752-0146. Fax: (530) 752-1552. E-mail:
mvbruns{at}ucdavis.edu.

Present address: Center for Environmental Biotechnology, University
of Tennessee, Knoxville, TN 37932-2575.
Applied and Environmental Microbiology, July 1999, p. 2994-3000, Vol. 65, No. 7
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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