Farrell John J, Larson Joshua A, Akeson Jeffrey W, Lowery Kristin S, Rounds Megan A, Sampath Rangarajan, Bonomo Robert A, Patel Robin
University of Illinois School of Medicine, Department of Medicine, Peoria, Illinois, USA
Division of Laboratory Medicine, St. Francis Medical Center, Peoria, Illinois, USA.
J Clin Microbiol. 2014 Jun;52(6):2248-50. doi: 10.1128/JCM.00432-14. Epub 2014 Mar 26.
We describe the first reported case of Ureaplasma parvum prosthetic joint infection (PJI) detected by PCR. Ureaplasma species do not possess a cell wall and are usually associated with colonization and infection of mucosal surfaces (not prosthetic material). U. parvum is a relatively new species name for certain serovars of Ureaplasma urealyticum, and PCR is useful for species determination. Our patient presented with late infection of his right total knee arthroplasty. Intraoperative fluid and tissue cultures and pre- and postoperative synovial fluid cultures were all negative. To discern the pathogen, we employed PCR coupled with electrospray ionization mass spectrometry (PCR/ESI-MS). Our patient's failure to respond to empirical antimicrobial treatment and our previous experience with PCR/ESI-MS in culture-negative cases of infection prompted us to use this approach over other diagnostic modalities. PCR/ESI-MS detected U. parvum in all samples. U. parvum-specific PCR testing was performed on all synovial fluid samples to confirm the U. parvum detection.
我们描述了首例通过聚合酶链反应(PCR)检测到微小脲原体人工关节感染(PJI)的病例报告。脲原体属没有细胞壁,通常与粘膜表面(而非假体材料)的定植和感染有关。微小脲原体是解脲脲原体某些血清型的一个相对较新的物种名称,PCR有助于物种鉴定。我们的患者出现了右全膝关节置换术后的晚期感染。术中液体和组织培养以及术前和术后滑液培养均为阴性。为了识别病原体,我们采用了PCR结合电喷雾电离质谱(PCR/ESI-MS)的方法。我们的患者对经验性抗菌治疗无反应,以及我们之前在培养阴性的感染病例中使用PCR/ESI-MS的经验促使我们选择这种方法而非其他诊断方式。PCR/ESI-MS在所有样本中均检测到微小脲原体。对所有滑液样本进行了微小脲原体特异性PCR检测,以确认微小脲原体的检测结果。