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Journal of Clinical Microbiology, January 1998, p. 157-160, Vol. 36, No. 1
Research Laboratory,
Received 24 April 1997/Returned for modification 16 July
1997/Accepted 1 October 1997
Simple sample-processing methods for PCR detection of
Porphyromonas gingivalis, a major pathogen causing adult
periodontitis, from saliva were studied. The ability to detect P. gingivalis from 118 salivary samples by PCR after boiling and
Chelex 100 processing was compared with bacterial culture. P. gingivalis was detected three times more often by PCR than by
culture. Chelex 100 processing of saliva proved to be effective in
preventing PCR inhibition and was applied to determine the occurrence
of P. gingivalis in saliva samples from 263 Finnish
subjects between 5 and 80 years of age. The occurrence of P. gingivalis increased with age, and it was detected by PCR in the
saliva of 5.0% of subjects between 5 and 10 years of age, 13.8% of
subjects between 11 and 20 years of age, 13.4% of subjects between 21 and 30 years of age, and 63.3% of subjects between 31 and 80 years of
age. The results indicate that P. gingivalis is a rare
finding in saliva from periodontally healthy children and young adults
but a frequent one in saliva from adult periodontitis patients.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Detection of Porphyromonas gingivalis
from Saliva by PCR by Using a Simple Sample-Processing Method
*
Corresponding author. Mailing address: Institute of
Dentistry, Research Laboratory, P.O. Box 41, FIN-00014 University of
Helsinki, Finland. Phone: 358-9-19127316. Fax: 358-9-19127519.
Journal of Clinical Microbiology, January 1998, p. 157-160, Vol. 36, No. 1
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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