Division of Hygiene and Medical Microbiology, Innsbruck Medical University, Innsbruck, Austria.
J Clin Microbiol. 2012 Jul;50(7):2250-4. doi: 10.1128/JCM.00362-12. Epub 2012 May 2.
A new commercially available universal 16S and 18S rRNA gene PCR test, which is followed by sequence analysis of amplicons (SepsiTest), was evaluated for rapid identification of pathogens in the diagnosis of bone and joint infections. Eighty-three orthopedic samples and 21 specimens from other normally sterile body sites collected from 84 patients were analyzed in parallel by culture and PCR for detection of bacteria and fungi. Compared to culture, the diagnostic sensitivity and specificity of PCR were 88.5% and 83.5%, respectively. The detection rate of PCR (34.6%) was higher than that of bacterial culture (25.0%) as a consequence of the presence of fastidious and noncultivable species in samples and antibiotic treatment of patients. Thirteen culture-negative infections were identified by PCR, and PCR was able to detect culture-proven polymicrobial infections. On the other hand, three samples were culture positive but PCR negative. SepsiTest was demonstrated to be a valuable supplemental tool in the rapid detection of bacteria, especially for fastidious and noncultivable organisms, allowing earlier initiation of pathogen-adapted therapy in patients with bone and joint infections.
一种新的商业化通用 16S 和 18S rRNA 基因 PCR 检测方法,随后对扩增子进行序列分析(SepsiTest),用于快速鉴定骨和关节感染中的病原体。对 84 名患者的 83 个骨科样本和 21 个来自其他正常无菌体部位的标本进行了平行的培养和 PCR 检测,以检测细菌和真菌。与培养相比,PCR 的诊断敏感性和特异性分别为 88.5%和 83.5%。由于样品中存在难培养和不能培养的物种以及患者的抗生素治疗,PCR 的检测率(34.6%)高于细菌培养(25.0%)。PCR 鉴定出了 13 例培养阴性感染,并且 PCR 能够检测出培养证实的混合感染。另一方面,有三个样本培养阳性而 PCR 阴性。SepsiTest 被证明是一种快速检测细菌的有价值的辅助工具,特别是对于难培养和不能培养的生物,允许对骨和关节感染患者尽早开始针对病原体的治疗。