Division of Infectious Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
J Clin Microbiol. 2012 Nov;50(11):3501-8. doi: 10.1128/JCM.00834-12. Epub 2012 Aug 15.
Periprosthetic tissue and/or synovial fluid PCR has been previously studied for prosthetic joint infection (PJI) diagnosis; however, few studies have assessed the utility of PCR on biofilms dislodged from the surface of explanted arthroplasties using vortexing and sonication (i.e., sonicate fluid PCR). We compared sonicate fluid 16S rRNA gene real-time PCR and sequencing to culture of synovial fluid, tissue, and sonicate fluid for the microbiologic diagnosis of PJI. PCR sequences generating mixed chromatograms were decatenated using RipSeq Mixed. We studied sonicate fluids from 135 and 231 subjects with PJI and aseptic failure, respectively. Synovial fluid, tissue, and sonicate fluid culture and sonicate fluid PCR had similar sensitivities (64.7, 70.4, 72.6, and 70.4%, respectively; P > 0.05) and specificities (96.9, 98.7, 98.3, and 97.8%, respectively; P > 0.05). Combining sonicate fluid culture and PCR, the sensitivity was higher (78.5%, P < 0.05) than those of individual tests, with similar specificity (97.0%). Thirteen subjects had positive sonicate fluid culture but negative PCR, and 11 had negative sonicate fluid culture but positive PCR (among which 7 had prior use of antimicrobials). Broad-range PCR and culture of sonicate fluid have equivalent performance for PJI diagnosis.
先前已有研究探讨了假体周围组织和/或滑液聚合酶链反应(PCR)在假体关节感染(PJI)诊断中的应用;然而,鲜有研究评估了通过涡旋和超声(即超声液 PCR)从取出的关节假体表面脱落的生物膜进行 PCR 的效用。我们比较了超声液 16S rRNA 基因实时 PCR 和测序与关节滑液、组织和超声液培养在 PJI 微生物学诊断中的应用。对于产生混合色谱的 PCR 序列,我们使用 RipSeq Mixed 进行解链。我们研究了分别患有 PJI 和无菌性失败的 135 名和 231 名受试者的超声液。关节滑液、组织和超声液培养以及超声液 PCR 的敏感性(分别为 64.7%、70.4%、72.6%和 70.4%;P > 0.05)和特异性(分别为 96.9%、98.7%、98.3%和 97.8%;P > 0.05)相似。联合使用超声液培养和 PCR 可提高敏感性(78.5%,P < 0.05),而特异性(97.0%)相似。13 名受试者的超声液培养阳性但 PCR 阴性,11 名受试者的超声液培养阴性但 PCR 阳性(其中 7 名曾使用过抗菌药物)。广谱 PCR 和超声液培养在 PJI 诊断中具有等效性能。