CHU de Bordeaux, Hopital Pellegrin, Laboratoire de Bactériologie, Bordeaux, France.
J Clin Microbiol. 2011 Apr;49(4):1245-50. doi: 10.1128/JCM.01657-10. Epub 2011 Jan 19.
Kingella kingae is an emerging osteoarticular pathogen in young children. Its isolation by traditional culture methods remains difficult, underscoring the need to implement other diagnostic methods for its detection and identification, such as nucleic acid amplification tests. Although the genome of this bacterium has not yet been sequenced, a toxin named RTX has been identified. The goal of this study was to develop sensitive, specific, and rapid molecular methods based on the rtxA toxin gene sequence to diagnose this infection. Two real-time PCR assays (SYBR green and TaqMan chemistries) targeting this gene are reported. Sensitivity and specificity were first evaluated successfully with 67 strains: 31 Kingella kingae isolates and 36 strains from other bacterial species. Then, 52 clinical specimens positive or negative by culture and/or PCR (16S rRNA and cpn60 genes) were tested with these assays. A nested PCR assay with subsequent sequencing was also developed to confirm the presence of Kingella kingae isolates in these clinical specimens. The results obtained demonstrate that these assays are accurate for the diagnosis of Kingella kingae infection.
金氏金菌是一种新兴的儿童骨关节炎病原体。其传统培养方法的分离仍然很困难,这突显了需要实施其他诊断方法来检测和鉴定它,如核酸扩增试验。尽管该细菌的基因组尚未测序,但已经鉴定出一种名为 RTX 的毒素。本研究的目的是基于 rtxA 毒素基因序列开发敏感、特异和快速的分子方法来诊断这种感染。本文报道了两种针对该基因的实时 PCR 检测方法(SYBR 绿色和 TaqMan 化学)。首先成功地用 67 株菌株评估了敏感性和特异性:31 株金氏金菌分离株和 36 株来自其他细菌物种的菌株。然后,用这些检测方法检测了 52 份临床标本,这些标本通过培养和/或 PCR(16S rRNA 和 cpn60 基因)检测为阳性或阴性。还开发了一种巢式 PCR 检测方法,随后进行测序,以确认这些临床标本中是否存在金氏金菌分离株。获得的结果表明,这些检测方法可准确诊断金氏金菌感染。