Use of quantitative PCR and culture methods to characterize ecological flux in bacterial biofilms
- PMID: 17596351
- PMCID: PMC2045240
- DOI: 10.1128/JCM.01131-07
Use of quantitative PCR and culture methods to characterize ecological flux in bacterial biofilms
Abstract
An in vitro model of supragingival plaque associated with gingivitis was characterized by traditional culture techniques, comparative 16S rRNA gene sequencing of isolates, and quantitative PCR (QPCR). Actinomyces naeslundii, Prevotella spp., and Porphyromonas gingivalis increased under conditions emulating gingivitis. Gram-negative species and total bacteria were dramatically underestimated by culture compared to the estimates obtained by QPCR.
Figures
References
-
- Boutaga, K., P. H. Savelkoul, E. G. Winkel, and A. J. van Winkelhoff. 2007. Comparison of subgingival bacterial sampling with oral lavage for detection and quantification of periodontal pathogens by real-time polymerase chain reaction. J. Periodontol. 78:79-86. - PubMed
-
- Evans, D. J., D. G. Allison, M. R. Brown, and P. Gilbert. 1990. Effect of growth-rate on resistance of gram-negative biofilms to cetrimide. J. Antimicrob. Chemother. 26:473-478. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous
