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HUMAN Cytomegalovirus (HCMV) in Periodontitis: Clinical Implication and BIOLOGICAL Effects
J.E. BOTERO1, C.L. VIDAL1, B. PARRA2, A. CONTRERAS1, and A. JARAMILLO1, 1Universidad del Valle, Cali, Colombia, 2universidad del Valle, Cali, Colombia | Objective: the purpose of this study was first to correlate clinical
periodontal parameters in relation to HCMV infection and to analyze the
biological effects of HCMV infection in gingival fibroblasts. Methods: Subgingival plaque and
gingival crevicular fluid (GCF) samples were obtained from 44 periodontitis (37
ChP, 7 AgP) and 24 non-periodontitis individuals. Periodontopathic bacteria
were detected by culture while HCMV was detected by nested PCR and quantified
by real time PCR. Gingival fibroblasts (GF) were infected with the HCMV Towne
strain and the expression of mRNA for collagen I-III, IL1b and TNFa
was analyzed at 0, 24 and 72 hours. In addition, the production of IL1b
and TNFa was studied in the supernatant using an antibody protein array. Results: the prevalence of HCMV was
79.5% in periodontitis patients as compared to 25% in control subjects
(P<0.05). HCMV was cultured from GCF in one periodontitis patient. Probing
depth and clinical attachment level were increased at HCMV+ sites in periodontitis
subjects (P<0.05). Bleeding on probing was increased in HCMV+ subjects. The
mean number of HCMV copies was 605,3 c/mL in
periodontitis subjects vs. 6.45E-04 c/mL in control individuals. The
frequency detection (%) and levels (counts x 10E5) of P.gingivalis,
E.corrodens, Campylobacter
spp.,
P.intermedia / nigrescens and Enteric rods were elevated in HCMV+ periodontitis samples. HCMV
infection in GF resulted in a decrease in mRNA expression for collagen I and
III over time. mRNA expression for IL1b was increased at 72 hours was
comparable to supernatant levels. In contrast, TNFa mRNA expression was
increased at 24 hours while the highest production in supernatant was observed
at 72 hours. Conclusions: HCMV infection was
correlated to worse clinical parameter in HCMV + periodontitis subjects.
Alterations in GF biology by HCMV infection and in co-infection with
periodontopathic bacteria may help explain periodontal destruction.
| Seq #210 - Host-bacterial Interactions 2:00 PM-3:15 PM, Friday, July 4, 2008 Metro Toronto Convention Centre Exhibit Hall D-E |
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