|
Sign In to gain access to subscriptions and/or personal tools.
|
Subgingival and Tongue Microbiota during Early Periodontitis
A.C.R. Tanner1,*,
B.J. Paster1,
S.C. Lu1,
E. Kanasi1,
R. Kent, Jr.2,
T. Van Dyke3 and
S.T. Sonis4
1 Department of Molecular Genetics and
2 Department of Biostatistics, The Forsyth Institute, 140 The Fenway, Boston, MA 02115, USA;
3 Clinical Research Center at Boston University School of Dental Medicine; and
4 Division of Oral Medicine, Brigham and Womens Hospital, Boston
Correspondence: * corresponding author, annetanner{at}forsyth.org
Periodontal infections have a microbial etiology. Association of species with early disease would be useful in determining which microbes initiate periodontitis. We hypothesized that the microbiota of subgingival and tongue samples would differ between early periodontitis and health. A cross-sectional evaluation of 141 healthy and early periodontitis adults was performed with the use of oligonucleotide probes and PCR. Most species differed in associations with sample sites; most subgingival species were associated with subgingival samples. Few species were detected more frequently in early periodontitis by DNA probes. Porphyromonas gingivalis and Tannerella forsythia (Tannerella forsythensis) were associated with early periodontitis by direct PCR. In conclusion, the microbiota of tongue samples was less sensitive than that of subgingival samples in detecting periodontal species, and there was overlap in species detected in health and early periodontitis. Detection of periodontal pathogens in early periodontitis suggests an etiology similar to that of more advanced disease.
Key Words: microbiology tongue subgingival health early periodontitis
Journal of Dental Research, Vol. 85, No. 4,
318-323 (2006)
DOI: 10.1177/154405910608500407

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
M. A. Nadkarni, K.-L. Chhour, G. Browne, N. A. Jacques, and N. Hunter
Lysine Gingipain (kgp) Biovars of Porphyromonas gingivalis Exhibit Differential Distribution on Oral Mucosal Sites
J. Clin. Microbiol.,
October 1, 2009;
47(10):
3350 - 3352.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H. Kurata, S. Awano, A. Yoshida, T. Ansai, and T. Takehara
The prevalence of periodontopathogenic bacteria in saliva is linked to periodontal health status and oral malodour
J. Med. Microbiol.,
May 1, 2008;
57(5):
636 - 642.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. R. Cortelli, D. R. Aquino, S. C. Cortelli, C. B. Fernandes, J. de Carvalho-Filho, G. C. N. Franco, F. O. Costa, and T. Kawai
Etiological Analysis of Initial Colonization of Periodontal Pathogens in Oral Cavity
J. Clin. Microbiol.,
April 1, 2008;
46(4):
1322 - 1329.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Onishi, K. Honma, S. Liang, P. Stathopoulou, D. Kinane, G. Hajishengallis, and A. Sharma
Toll-Like Receptor 2-Mediated Interleukin-8 Expression in Gingival Epithelial Cells by the Tannerella forsythia Leucine-Rich Repeat Protein BspA
Infect. Immun.,
January 1, 2008;
76(1):
198 - 205.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. L. Barnett
The rationale for the daily use of an antimicrobial mouthrinse
J Am Dent Assoc,
November 1, 2006;
137(suppl_3):
16S - 21S.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|