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Applied and Environmental Microbiology, November 2000, p. 4605-4614, Vol. 66, No. 11
Monterey Bay Aquarium Research Institute,
Moss Landing, California 95039
Received 15 July 2000/Accepted 14 August 2000
Few techniques are currently available for quantifying specific
prokaryotic taxa in environmental samples. Quantification of specific
genotypes has relied mainly on oligonucleotide hybridization to
extracted rRNA or intact rRNA in whole cells. However, low abundance
and cellular rRNA content limit the application of these techniques in
aquatic environments. In this study, we applied a newly developed
quantitative PCR assay (5'-nuclease assay, also known as
TaqMan) to quantify specific small-subunit (SSU) rRNA genes (rDNAs)
from uncultivated planktonic prokaryotes in Monterey Bay. Primer and
probe combinations for quantification of SSU rDNAs at the domain and
group levels were developed and tested for specificity and
quantitative reliability. We examined the spatial and temporal variations of SSU rDNAs from Synechococcus plus
Prochlorococcus and marine Archaea and compared
the results of the quantitative PCR assays to those obtained by
alternative methods. The 5'-nuclease assays reliably quantified rDNAs
over at least 4 orders of magnitude and accurately measured the
proportions of genes in artificial mixtures. The spatial and temporal
distributions of planktonic microbial groups measured by the
5'-nuclease assays were similar to the distributions estimated by
quantitative oligonucleotide probe hybridization, whole-cell
hybridization assays, and flow cytometry.
0099-2240/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Quantitative Analysis of Small-Subunit rRNA Genes
in Mixed Microbial Populations via 5'-Nuclease Assays
*
Corresponding author. Mailing address: Monterey Bay
Aquarium Research Institute, 7700 Sandholdt Rd., P.O. Box 628, Moss
Landing, CA 95039. Phone: (831) 775-1843. Fax: (831) 775-1645. E-mail: delong{at}mbari.org.
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