Molecular diagnosis of bloodstream infections: planning to (physically) reach the bedside

被引:44
作者
Leggieri, N. [1 ]
Rida, A. [2 ]
Francois, P. [3 ]
Schrenzel, Jacques [1 ,3 ]
机构
[1] Univ Hosp Geneva, Bacteriol Lab, Infect Dis Serv, CH-1211 Geneva 14, Switzerland
[2] PSE C, Spinomix SA, Lausanne, Switzerland
[3] Univ Hosp Geneva, Genom Res Lab, Infect Dis Serv, CH-1211 Geneva 14, Switzerland
基金
瑞士国家科学基金会;
关键词
broad-range PCR; molecular identification; PCR whole blood; rapid identification; real-time PCR; DESORPTION IONIZATION-TIME; POLYMERASE-CHAIN-REACTION; FLIGHT MASS-SPECTROMETRY; ROUTINE IDENTIFICATION; STAPHYLOCOCCUS-AUREUS; ANTIMICROBIAL THERAPY; METHICILLIN-RESISTANT; RAPID IDENTIFICATION; MULTIPLEX PCR; BACTERIA;
D O I
10.1097/QCO.0b013e32833bfc44
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose of review Faster identification of infecting microorganisms and treatment options is a first-ranking priority in the infectious disease area, in order to prevent inappropriate treatment and overuse of broad-spectrum antibiotics. Standard bacterial identification is intrinsically time-consuming, and very recently there has been a burst in the number of commercially available nonphenotype-based techniques and in the documentation of a possible clinical impact of these techniques. Recent findings Matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) is now a standard diagnostic procedure on cultures and hold promises on spiked blood. Meanwhile, commercial PCR-based techniques have improved with the use of bacterial DNA enrichment methods, the diversity of amplicon analysis techniques (melting curve analysis, microarrays, gel electrophoresis, sequencing and analysis by mass spectrometry) leading to the ability to challenge bacterial culture as the gold standard for providing earlier diagnosis with a better 'clinical' sensitivity and additional prognostic information. Summary Laboratory practice has already changed with MALDI-TOF MS, but a change in clinical practice, driven by emergent nucleic acid-based techniques, will need the demonstration of real-life applicability as well as robust clinical-impact-oriented studies.
引用
收藏
页码:311 / 319
页数:9
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