Abstract:Structural deficiencies and functional abnormalities of heart valves represent an important cause of cardiovascular morbidity and mortality, and a number of diseases, such as aortic stenosis, have been recently associated with infectious agents. This study aimed to analyze oral bacteria in dental plaque, saliva, and cardiac valves of patients with cardiovascular disease. Samples of supragingival plaque, subgingival plaque, saliva, and cardiac valve tissue were collected from 42 patients with heart valve diseas… Show more
“…Dental plaque samples were obtained from the buccal and mesial surfaces of all teeth present using curettes and sterile absorbent paper cones. The samples were stored in a sterile vessel containing phosphate‐buffered saline (PBS) at −20°C for the molecular analysis …”
Section: Methodsmentioning
confidence: 99%
“…Aortic valve leaflets from five corpses submitted to autopsy were obtained aseptically up to 10 hours after death in the Forensic Expertise of the State of Ceará (PEFOCE). One part of the tissue sample was stored in a sterile Eppendorf tube containing PBS at −20°C for real‐time PCR analysis, and the other portion was maintained in 10% buffered formalin for the histological evaluations (hematoxylin and eosin‐HE staining), histochemistry (Giemsa staining), and immunohistochemistry (streptavidin‐biotin‐peroxidase).…”
Section: Methodsmentioning
confidence: 99%
“…The extracted DNA samples were submitted for real‐time PCR to evaluate the presence (+) or absence (−) of S mutans bacterial DNA . The primers and probes were commercially produced based on the 16S region of the bacterial ribosomal DNA (Life Technologies ® ).…”
Background
The present study aimed to investigate the presence or absence of Streptococcus mutans in oral cavity and valvular samples associating with the histomorphologic alterations of calcified aortic stenosis.
Methodology
Dental plaque and cardiac valve samples were collected from 10 patients with calcified aortic stenosis for molecular analysis of S mutans by real‐time polymerase chain reaction (PCR). Healthy valve tissue was also collected from five young cadavers and analyzed for S mutans. Moreover, fragments of all valvar specimens were submitted for histomorphological analysis and immunohistochemistry (anti‐S mutans and anti‐CD61).
Results
Streptococcus mutans was present in 100% of the oral cavity samples from the patients with calcified aortic stenosis in the molecular analysis. The analysis by real‐time PCR showed that S mutans presented the same proportion in healthy valves and those with calcified aortic stenosis (80%; P = 1.000). Conversely, the immunoexpression of S mutans was 37.40 (IC95% = 1.49‐937.00) times superior in samples of patients with cardiac disease (P = .007). The immunoexpression analysis showed that CD61 was present in seven (70%) calcified aortic stenosis samples, all of which were also immunopositive for S mutans.
Conclusions
Streptococcus mutans was found in the oral cavity, healthy valve tissue, and calcified aortic stenosis samples. However, the microorganism was visualized by immunohistochemistry only in the calcified aortic stenosis samples, which may suggest viability and an increased bacterial density in this condition. The association of the presence of S mutans and positive CD61 immunoexpression suggests a probable relationship with calcified aortic stenosis.
“…Dental plaque samples were obtained from the buccal and mesial surfaces of all teeth present using curettes and sterile absorbent paper cones. The samples were stored in a sterile vessel containing phosphate‐buffered saline (PBS) at −20°C for the molecular analysis …”
Section: Methodsmentioning
confidence: 99%
“…Aortic valve leaflets from five corpses submitted to autopsy were obtained aseptically up to 10 hours after death in the Forensic Expertise of the State of Ceará (PEFOCE). One part of the tissue sample was stored in a sterile Eppendorf tube containing PBS at −20°C for real‐time PCR analysis, and the other portion was maintained in 10% buffered formalin for the histological evaluations (hematoxylin and eosin‐HE staining), histochemistry (Giemsa staining), and immunohistochemistry (streptavidin‐biotin‐peroxidase).…”
Section: Methodsmentioning
confidence: 99%
“…The extracted DNA samples were submitted for real‐time PCR to evaluate the presence (+) or absence (−) of S mutans bacterial DNA . The primers and probes were commercially produced based on the 16S region of the bacterial ribosomal DNA (Life Technologies ® ).…”
Background
The present study aimed to investigate the presence or absence of Streptococcus mutans in oral cavity and valvular samples associating with the histomorphologic alterations of calcified aortic stenosis.
Methodology
Dental plaque and cardiac valve samples were collected from 10 patients with calcified aortic stenosis for molecular analysis of S mutans by real‐time polymerase chain reaction (PCR). Healthy valve tissue was also collected from five young cadavers and analyzed for S mutans. Moreover, fragments of all valvar specimens were submitted for histomorphological analysis and immunohistochemistry (anti‐S mutans and anti‐CD61).
Results
Streptococcus mutans was present in 100% of the oral cavity samples from the patients with calcified aortic stenosis in the molecular analysis. The analysis by real‐time PCR showed that S mutans presented the same proportion in healthy valves and those with calcified aortic stenosis (80%; P = 1.000). Conversely, the immunoexpression of S mutans was 37.40 (IC95% = 1.49‐937.00) times superior in samples of patients with cardiac disease (P = .007). The immunoexpression analysis showed that CD61 was present in seven (70%) calcified aortic stenosis samples, all of which were also immunopositive for S mutans.
Conclusions
Streptococcus mutans was found in the oral cavity, healthy valve tissue, and calcified aortic stenosis samples. However, the microorganism was visualized by immunohistochemistry only in the calcified aortic stenosis samples, which may suggest viability and an increased bacterial density in this condition. The association of the presence of S mutans and positive CD61 immunoexpression suggests a probable relationship with calcified aortic stenosis.
“…Using polymerase chain reaction (PCR), oral bacteria Streptococcus mutans, Prevotella intermedia, Porphyromonas gingivalis, Treponema denticola and Aggregatibacter actinomycetemcomitans have all been detected on cardiac valve samples [5,6]. Antibodies to oral gram-negative (gm−) bacteria have been detected in the synovial fluid of patients with rheumatoid arthritis (RA) and it has been found that patients with RA are more likely to develop periodontitis despite age and smoking history; even further, patients with periodontal infections are less responsive to RA treatments [4].…”
Introduction
Periodontal diseases are polymicrobial inflammatory disorders of the tissue, ligament, and bone structures supporting teeth. Periodontitis (inflammation with corresponding loss of attachment) affects 40–50% of adults. Recently, members of the Triggering Receptor on Myeloid Cell (TREM) family have been studied to determine their relationship to these diseases.
Areas covered
TREM-1 is a receptor expressed on the surface of PMNs, monocytes, macrophages, dendritic cells, vascular smooth muscle cells, and keratinocytes upregulated in the presence of periodontal inflammation. TREM-1 expression can be upregulated by oral bacterium Porphyromonas gingivalis that can be abrogated by a sub-antimicrobial dose of doxycycline. When cleaved from the cell surface, a soluble form of TREM-1 (sTREM-1) can be used as a biomarker of inflammation and might also provide a link between oral and systemic inflammation. While less understood, TREM-2 has a role in osteoclastogenesis which could contribute to the alveolar bone destruction seen in more advanced periodontitis.
Expert Commentary
Additional studies to simulate biofilm microenvironment in TREM research are warranted. Longitudinal studies determining TREM-1, sTREM-1, and TREM-2 levels in tissues over time and progression of periodontal diseases would provide valuable information in the role of TREM receptors as indicators of or contributors to the disease process.
“…The incidence of bacteremia and related systemic diseases due to oral anaerobic bacteria following different procedures such as: endodontic treatment, tooth extraction, periodontal surgery, tongue scraping and root scaling has been well documented [10][11][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27] and anaerobe periodontal bacteria are isolated more frequently than facultative anaerobic bacteria, such as Streptococcus spp. [28].…”
Section: Oral Surgery and Risk For Bacteremiamentioning
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