Xu Yijuan, Rudkjøbing Vibeke Børsholt, Simonsen Ole, Pedersen Christian, Lorenzen Jan, Schønheyder Henrik Carl, Nielsen Per Halkjaer, Thomsen Trine Rolighed
Department of Biotechnology, Chemistry and Environmental Engineering, Aalborg University, Aalborg, Denmark.
FEMS Immunol Med Microbiol. 2012 Jul;65(2):291-304. doi: 10.1111/j.1574-695X.2012.00949.x. Epub 2012 Mar 22.
Formation of biofilm is a prominent feature of prosthetic joint infections (PJIs) and constitutes a challenge to current sampling procedures and culture practices. Molecular techniques have a potential for improving diagnosis of biofilm-adapted, slow-growing and non-culturable bacteria. In this exploratory study we investigated the bacterial diversity in specimens from 22 patients clinically suspected of having PJIs. Bacteriological cultures were performed according to standard practice. A total of 55 specimens from 25 procedures ('specimen sets') were submitted to broad range 16S rRNA gene PCR, cloning, sequencing and phylogenetic analysis. More than 40 bacterial taxa within six phyla were identified in 14 specimen sets originating from 11 patients. Direct observation of biofilm was made in selected specimens by fluorescence in situ hydridization. 16S rRNA gene analysis and bacteriological cultures were concordant for 15/25 specimen sets (60%; five positive, 10 negative); additional taxa were detected in four sets by gene analysis, and discrepant results were obtained for six sets, five of which were negative on culture. Polymicrobial communities were revealed in 9/14 sets by gene analysis and 1/10 sets by culture (P < 0.05). Although our study was not conclusive, these findings are consistent with a primary role of biofilm formation in PJIs.
生物膜的形成是人工关节感染(PJI)的一个显著特征,对当前的采样程序和培养方法构成了挑战。分子技术有可能改善对适应生物膜生长、生长缓慢且不可培养细菌的诊断。在这项探索性研究中,我们调查了22例临床疑似患有PJI患者标本中的细菌多样性。按照标准操作进行细菌培养。对来自25个手术(“标本组”)的总共55份标本进行了广泛的16S rRNA基因PCR、克隆、测序和系统发育分析。在来自11名患者的14个标本组中鉴定出了六个门内的40多个细菌分类群。通过荧光原位杂交对选定标本进行生物膜的直接观察。16S rRNA基因分析和细菌培养在15/25个标本组中结果一致(60%;5个阳性,10个阴性);基因分析在4个标本组中检测到了额外的分类群,6个标本组得到了不一致的结果,其中5个在培养时为阴性。基因分析在9/14个标本组中揭示了多微生物群落,培养在1/10个标本组中揭示了多微生物群落(P < 0.05)。尽管我们的研究尚无定论,但这些发现与生物膜形成在PJI中的主要作用是一致的。