Two-step bacterial broad-range polymerase chain reaction analysis of heart valve tissue improves bacteriological diagnosis of infective endocarditis

被引:17
作者
Boussier, Remi [1 ]
Rogez, Sylvie [1 ]
Francois, Bruno [2 ]
Denes, Eric [3 ]
Ploy, Marie-Cecile [1 ]
Garnier, Fabien [1 ]
机构
[1] CHU Limoges, Lab Bacteriol Virol Hyg, F-87800 Limoges, France
[2] CHU Limoges, Serv Reanimat Polyvalente, F-87800 Limoges, France
[3] CHU Limoges, Serv Malad Infect, F-87800 Limoges, France
关键词
Infective endocarditis; Molecular diagnostic; Two-step broad-range PCR; Real-time PCR; Heart valve; CULTURE-NEGATIVE ENDOCARDITIS; MOLECULAR DIAGNOSIS; PCR AMPLIFICATION; DNA;
D O I
10.1016/j.diagmicrobio.2012.11.013
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Positive heart valve (HV) culture is a major Duke's criterion for the diagnosis of infective endocarditis but is poorly sensitive. Two broad-range 16S rDNA polymerase chain reaction (PCR) methods were applied to 31 HV samples: first, a real-time method, then conventional end-point PCR was applied to HV samples on which the first PCR was negative. Five specific real-time PCR procedures were also used in order to identify Bartonella spp., Tropheryma whipplei, Chlamydophila pneumoniae, Mycoplasma pneumonia, and Coxiella burnetii. A strategy combining the 2-step broad-range PCR methods improved the sensitivity of the molecular method from 38.7% to 58%. Specific PCR identified 1 T. whipplei, which was also identified by conventional end-point PCR. These results confirm that blood culture is the gold standard for the diagnosis of infective endocarditis, shows that molecular methods applied to HV can be useful when blood culture is negative, and that 2-step broad-range PCR approach seems to be more sensitive. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:240 / 244
页数:5
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