Ivagnes Vittorio, Menchinelli Giulia, Liotti Flora Marzia, De Carolis Elena, Torelli Riccardo, De Lorenzis Desy, Recine Cinzia, Sanguinetti Maurizio, D'Inzeo Tiziana, Posteraro Brunella
Dipartimento di Scienze Biotecnologiche di Base, Cliniche Intensivologiche e Perioperatorie, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Dipartimento di Scienze di Laboratorio e Infettivologiche, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy.
Microorganisms. 2023 Dec 31;12(1):81. doi: 10.3390/microorganisms12010081.
The diagnosis of bloodstream infection (BSI) may rely on a PCR-based analysis of a positive blood culture (PBC) obtained from the patient at the time of BSI. In this study, a yeast DNA extraction protocol for use on PBCs was developed and evaluated with the molecular mouse (MM) yeast blood (YBL) chip-based PCR assay, which allowed us to detect nine medically relevant species. We studied 125 simulated or clinical PBCs for species. A positive correlation between the DNA concentration and colony-forming unit count was found for simulated (Spearman's ρ = 0.58; < 0.0001) and clinical (Spearman's ρ = 0.23, = 0.09) PBCs. The extracted DNA yielded positive results with the MM YBL chip assay that agreed with the species-level identification results for 63 (100%) of 63 isolates from simulated PBCs and 66 (99.5%) of 67 isolates from clinical PBCs. The false-negative result was for one isolate that grew together with in PBC. None of the 30 ()-negative clinical BCs included as negative controls yielded a positive result with the MM YBL chip assay. Our DNA extraction protocol for the species couples efficiency and simplicity together. Nevertheless, further studies are needed before it can be adopted for use with the MM YBL chip assay.
血流感染(BSI)的诊断可能依赖于对患者在发生BSI时采集的阳性血培养物(PBC)进行基于聚合酶链反应(PCR)的分析。在本研究中,我们开发了一种用于PBC的酵母DNA提取方案,并通过基于分子小鼠(MM)酵母血(YBL)芯片的PCR检测进行评估,该检测使我们能够检测9种与医学相关的菌种。我们研究了125份模拟或临床PBC中的菌种。对于模拟PBC(斯皮尔曼相关系数ρ = 0.58;P < 0.0001)和临床PBC(斯皮尔曼相关系数ρ = 0.23,P = 0.09),发现DNA浓度与菌落形成单位计数之间存在正相关。提取的DNA在MM YBL芯片检测中产生了阳性结果,与来自模拟PBC的63株分离株中的63株(100%)以及来自临床PBC的67株分离株中的66株(99.5%)的菌种水平鉴定结果一致。假阴性结果是针对一株在PBC中与其他菌种共同生长的分离株。作为阴性对照纳入的30份()阴性临床血培养物,在MM YBL芯片检测中均未产生阳性结果。我们针对该菌种的DNA提取方案兼具高效性和简便性。然而,在可将其用于MM YBL芯片检测之前,还需要进一步研究。