Bacterial DNA detected on pathologically changed heart valves using 16S rRNA gene amplification
Language English Country United States Media print-electronic
Document type Journal Article
Grant support
LO1503
Ministerstvo Školství, Mládeže a Tělovýchovy
Q39
Lékařská Fakulta v Plzni, Univerzita Karlova
00669806
Univeristy Hospital in Pilsen
15-32727A
Agentura Pro Zdravotnický Výzkum České Republiky
PubMed
29786766
DOI
10.1007/s12223-018-0611-6
PII: 10.1007/s12223-018-0611-6
Knihovny.cz E-resources
- MeSH
- Gene Amplification * MeSH
- Bacteria classification genetics MeSH
- Endocarditis, Bacterial microbiology mortality pathology therapy MeSH
- Heart Valve Prosthesis Implantation methods MeSH
- DNA, Bacterial * MeSH
- Middle Aged MeSH
- Humans MeSH
- Polymerase Chain Reaction MeSH
- RNA, Ribosomal, 16S * MeSH
- Sequence Analysis, DNA MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Heart Valves microbiology pathology MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- DNA, Bacterial * MeSH
- RNA, Ribosomal, 16S * MeSH
Nowadays, dental diseases are one of the most common illnesses in the world. Some of them can lead to translocation of oral bacteria to the bloodstream causing intermittent bacteraemia. Therefore, a potential association between oral infection and cardiovascular diseases has been discussed in recent years as a result of adhesion of oral microbes to the heart valves. The aim of this study was to detect oral bacteria on pathologically changed heart valves not caused by infective endocarditis. In the study, patients with pathologically changed heart valves were involved. Samples of heart valves removed during heart valve replacement surgery were cut into two parts. One aliquot was cultivated aerobically and anaerobically. Bacterial DNA was extracted using Ultra-Deep Microbiome Prep (Molzym GmbH, Bremen, Germany) followed by a 16S rRNA gene PCR amplification using Mastermix 16S Complete kit (Molzym GmbH, Bremen, Germany). Positive PCR products were sequenced and the sequences were analyzed using BLAST database ( http://www.ncbi.nlm.nih/BLAST ). During the study period, 41 samples were processed. Bacterial DNA of the following bacteria was detected in 21 samples: Cutibacterium acnes (formerly Propionibacterium acnes) (n = 11; 52.38% of patients with positive bacterial DNA detection), Staphylococcus sp. (n = 9; 42.86%), Streptococcus sp. (n = 1; 4.76%), Streptococcus sanguinis (n = 4; 19.05%), Streptococcus oralis (n = 1; 4.76%), Carnobacterium sp. (n = 1; 4.76%), Bacillus sp. (n = 2; 9.52%), and Bergeyella sp. (n = 1; 4.76%). In nine samples, multiple bacteria were found. Our results showed significant appearance of bacteria on pathologically changed heart valves in patients with no symptoms of infective endocarditis.
Biomedical Center Faculty of Medicine in Pilsen Charles University Plzen Czech Republic
Czech Statistical Office Prague Czech Republic
Department of Cardiac Surgery University Hospital in Pilsen Charles University Plzen Czech Republic
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