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Applied and Environmental Microbiology, January 1999, p. 6-10, Vol. 65, No. 1
Rowett Research Institute,
Received 6 July 1998/Accepted 14 October 1998
Competitive PCR was used to monitor the survival of a 520-bp DNA
target sequence from a recombinant plasmid, pVACMC1, after admixture of
the plasmid with freshly sampled human saliva. The fraction of the
target remaining amplifiable ranged from 40 to 65% after 10 min of
exposure to saliva samples from five subjects and from 6 to 25% after 60 min of exposure. pVACMC1 plasmid DNA that had been
exposed to degradation by fresh saliva was capable of transforming
naturally competent Streptococcus gordonii DL1 to
erythromycin resistance, although transforming activity decreased rapidly, with a half-life of approximately 50 s. S. gordonii DL1 transformants were obtained in the presence of
filter-sterilized saliva and a 1-µg/ml final concentration of pVACMC1
DNA. Addition of filter-sterilized saliva instead of heat-inactivated
horse serum to S. gordonii DL1 cells induced competence,
although with slightly lower efficiency. These findings indicate that
DNA released from bacteria or food sources within the mouth has the
potential to transform naturally competent oral bacteria. However,
further investigations are needed to establish whether transformation of oral bacteria can occur at significant frequencies in vivo.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Fate of Free DNA and Transformation of the Oral
Bacterium Streptococcus gordonii DL1 by Plasmid DNA in
Human Saliva
*
Corresponding author. Mailing address: Rowett
Research Institute, Greenburn Road, Bucksburn, Aberdeen AB21 9SB,
Great Britain. Phone: 44 (0) 1224 712751. Fax: 44 (0) 1224 716687. E-mail: d.mercer{at}rri.sari.ac.uk.
Applied and Environmental Microbiology, January 1999, p. 6-10, Vol. 65, No. 1
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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