Comparison between a Broad-Range Real-Time and a Broad-Range End-Point PCR Assays for the Detection of Bacterial 16S rRNA in Clinical Samples

被引:0
作者
Meddeb, Mariam [1 ]
Koebel, Christelle [1 ]
Jaulhac, Benoit [1 ]
Schramm, Frederic [1 ]
机构
[1] Univ Strasbourg, Fac Med, Strasbourg, France
关键词
16S rRNA; real-time PCR; broad-range PCR; molecular diagnosis; POLYMERASE-CHAIN-REACTION; BACILLUS-CEREUS MENINGITIS; HELCOCOCCUS-KUNZII; INFECTIVE ENDOCARDITIS; SEQUENCE-ANALYSIS; WHIPPLES-DISEASE; RDNA PCR; IDENTIFICATION; DNA; DIAGNOSIS;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Broad range PCR targeting the 16S rRNA gene is widely used to test clinical samples for the presence of bacterial DNA. End-point 16S PCR is both time-consuming and at high risk of cross-contamination. Prior to the replacement of the 16S end-point PCR assay routinely used in our clinical laboratory by a new 16S real-time PCR assay, we aimed to compare the performances of both techniques for the direct diagnosis of bacterial infections in clinical samples. In this prospective study, 129 clinical samples were included for direct comparison of both techniques. The sensitivity of 16S real-time PCR assay (76%) was significantly higher than that of end-point 16S PCR assay (41%) (p<0.01). Specificities of both PCR assays did not differ significantly (p=0.43). The 16S real-time PCR assay yielded an etiological diagnosis in 19% of culture-negative samples. It constitutes a reliable and complementary diagnostic tool to the bacterial culture.
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页码:18 / 25
页数:8
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