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Applied and Environmental Microbiology, December 2002, p. 6077-6086, Vol. 68, No. 12
0099-2240/02/$04.00+0     DOI: 10.1128/AEM.68.12.6077-6086.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Sequencing-Independent Method To Generate Oligonucleotide Probes Targeting a Variable Region in Bacterial 16S rRNA by PCR with Detachable Primers

Stefan Bertilsson,^1, Colleen M. Cavanaugh,² and Martin F. Polz^1*

Department of Civil and Environmental Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139,¹ Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts 02138²

Received 1 April 2002/ Accepted 29 August 2002

Oligonucleotide probes targeting the small-subunit rRNA are commonly used to detect and quantify bacteria in natural environments. We developed a PCR-based approach that allows synthesis of oligonucleotide probes targeting a variable region in the 16S rRNA without prior knowledge of the target sequence. Analysis of all 16S rRNA gene sequences in the Ribosomal Database Project database revealed two universal primer regions bracketing a variable, population-specific region. The probe synthesis is based on a two-step PCR amplification of this variable region in the 16S rRNA gene by using three universal bacterial primers. First, a double-stranded product is generated, which then serves as template in a linear amplification. After each of these steps, products are bound to magnetic beads and the primers are detached through hydrolysis of a ribonucleotide at the 3' end of the primers. This ultimately produces a single-stranded oligonucleotide of about 30 bases corresponding to the target. As probes, the oligonucleotides are highly specific and could discriminate between nucleic acids from closely and distantly related bacterial strains, including different species of Vibrio. The method will facilitate rapid generation of oligonucleotide probes for large-scale hybridization assays such as screening of clone libraries or strain collections, ribotyping microarrays, and in situ hybridization. An additional advantage of the method is that fluorescently or radioactively labeled nucleotides can be incorporated during the second amplification, yielding intensely labeled probes.

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* Corresponding author. Mailing address: The Ralph M. Parsons Laboratory, Department of Civil and Environmental Engineering, Massachusetts Institute of Technology, 15 Vassar St., Cambridge, MA 02139. Phone: (617) 253-7128. Fax: (617) 253-7475. E-mail: mpolz{at}mit.edu.

Present address: Department of Evolutionary Biology, Limnology, Uppsala University, SE-75236 Uppsala, Sweden.

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Applied and Environmental Microbiology, December 2002, p. 6077-6086, Vol. 68, No. 12
0099-2240/02/$04.00+0     DOI: 10.1128/AEM.68.12.6077-6086.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

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