Bacterial DNA detected on pathologically changed heart valves using 16S rRNA gene amplification

被引:14
|
作者
Chalupova, Miroslava [1 ,2 ,3 ]
Skalova, Anna [2 ,3 ,4 ]
Hajek, Tomas [5 ]
Geigerova, Lenka [2 ,4 ]
Kralova, Dana [2 ,3 ,4 ]
Liska, Pavel [6 ]
Hecova, Hana [1 ,2 ]
Molacek, Jiri [2 ,7 ]
Hrabak, Jaroslav [2 ,3 ,4 ]
机构
[1] Charles Univ Prague, Fac Med, Dept Stomatol, Alej Svobody 80, Plzen 30460, Czech Republic
[2] Charles Univ Prague, Univ Hosp Pilsen, Alej Svobody 80, Plzen 30460, Czech Republic
[3] Charles Univ Prague, Fac Med Pilsen, Biomed Ctr, Plzen, Czech Republic
[4] Charles Univ Prague, Fac Med, Dept Microbiol, Plzen, Czech Republic
[5] Charles Univ Prague, Univ Hosp Pilsen, Dept Cardiac Surg, Plzen, Czech Republic
[6] Czech Stat Off, Prague, Czech Republic
[7] Charles Univ Prague, Fac Med, Dept Surg, Plzen, Czech Republic
关键词
ATHEROSCLEROTIC VASCULAR-DISEASE; PROPIONIBACTERIUM-ACNES; CARDIOVASCULAR-DISEASES; ATHEROMATOUS PLAQUES; PERIODONTAL POCKETS; ENDOCARDITIS; BACTEREMIA;
D O I
10.1007/s12223-018-0611-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:707 / 711
页数:5
相关论文
共 50 条
  • [31] Functional profiling of bacterial communities in Lake Tuz using 16S rRNA gene sequences
    Oyewusi, Habeebat Adekilekun
    Abdul Wahab, Roswanira
    Edbeib, Mohamed Faraj
    Mohamad, Mohd Azrul Naim
    Abdul Hamid, Azzmer Azzar
    Kaya, Yilmaz
    Huyop, Fahrul
    BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT, 2021, 35 (01) : 1 - 10
  • [32] Non-specific amplification of human DNA is a major challenge for 16S rRNA gene sequence analysis
    Sidney P. Walker
    Maurice Barrett
    Glenn Hogan
    Yensi Flores Bueso
    Marcus J. Claesson
    Mark Tangney
    Scientific Reports, 10
  • [33] Non-specific amplification of human DNA is a major challenge for 16S rRNA gene sequence analysis
    Walker, Sidney P.
    Barrett, Maurice
    Hogan, Glenn
    Flores Bueso, Yensi
    Claesson, Marcus J.
    Tangney, Mark
    SCIENTIFIC REPORTS, 2020, 10 (01)
  • [34] Direct extraction of DNA from soil for amplification of 16S rRNA gene sequences by polymerase chain reaction
    Cho, JC
    Lee, DH
    Cho, YC
    Cho, JC
    Kim, SJ
    JOURNAL OF MICROBIOLOGY, 1996, 34 (03) : 229 - 235
  • [35] Comparative performance of the 16S rRNA gene in DNA barcoding of amphibians
    Vences M.
    Thomas M.
    Van Der Meijden A.
    Chiari Y.
    Vieites D.R.
    Frontiers in Zoology, 2 (1)
  • [36] Improved DNA Extraction and Amplification Strategy for 16S rRNA Gene Amplicon-Based Microbiome Studies
    Hong, Bo-Young
    Driscoll, Mark
    Gratalo, Dawn
    Jarvie, Thomas
    Weinstock, George M.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (05)
  • [37] Correction: Corrigendum: Intrinsic challenges in ancient microbiome reconstruction using 16S rRNA gene amplification
    Kirsten A. Ziesemer
    Allison E. Mann
    Krithivasan Sankaranarayanan
    Hannes Schroeder
    Andrew T. Ozga
    Bernd W. Brandt
    Egija Zaura
    Andrea Waters-Rist
    Menno Hoogland
    Domingo C. Salazar-García
    Mark Aldenderfer
    Camilla Speller
    Jessica Hendy
    Darlene A. Weston
    Sandy J. MacDonald
    Gavin H. Thomas
    Matthew J. Collins
    Cecil M. Lewis
    Corinne Hofman
    Christina Warinner
    Scientific Reports, 6
  • [38] Rapid bacterial identification by direct PCR amplification of 16S rRNA genes using the MinION nanopore sequencer
    Kai, Shinichi
    Matsuo, Yoshiyuki
    Nakagawa, So
    Kryukov, Kirill
    Matsukawa, Shino
    Tanaka, Hiromasa
    Iwai, Teppei
    Imanishi, Tadashi
    Hirota, Kiichi
    FEBS OPEN BIO, 2019, 9 (03): : 548 - 557
  • [39] 16S rRNA gene sequencing for bacterial pathogen identification in the clinical laboratory
    Patel J.B.
    Molecular Diagnosis, 2001, 6 (4) : 313 - 321
  • [40] Electrochemical detection of bacterial 16S rRNA gene using a biosensor based on poly-adenine tailed DNA probe
    Li, Lanying
    Li, Yan
    Wen, Yanli
    Wang, Lele
    Liang, Wen
    Yang, Xue
    Meng, Jiaoran
    Duan, Manlei
    Ding, Min
    Liu, Gang
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2018, 256