Laboratory of Emerging Infectious Diseases (LEID), School of Medicine, Pontifícia Universidade Católica do Paraná, Curitiba, PR, Brazil.
Xenobiotics Research Unit, School of Life Sciences, Pontifícia Universidade Católica do Paraná, Curitiba, PR, Brazil.
Eur J Orthop Surg Traumatol. 2021 Aug;31(6):1113-1120. doi: 10.1007/s00590-020-02856-3. Epub 2021 Jan 4.
The gold standard for microbial detection in prosthetic joint infections is the multiple culture of the peri-prosthetic tissue. The fluid cultures after sonication can improve the recovery of the microorganisms.
The aim of this study was to evaluate the sonication technique with a plastic bag and the effect of refrigeration on microorganism detection with conventional culturing, MALDI-TOF MS and qPCR assay on an orthopedic screw model.
We produced biofilms of Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans on orthopedic screws, which were stored under different conditions and temperatures before sonication. After sonication, the mass spectrometry by MALDI-TOF, qPCR and culture protocols was performed using the sonicated fluid, for detecting the microorganisms involved in the biofilm.
The bacterial bioburden decreased by approximately one log after the refrigeration period, in the screws containing P. aeruginosa and S. aureus biofilms. All the microorganisms involved in the screw biofilms were detected with MALDI-TOF and qPCR. Significant reductions in CFU counts occurred only in groups stored in the plastic bag, indicating that changes in temperature and humidity may favor cell death. However, this variation is not important for this model as it did not affect the detection owing to the high counts obtained.
Microbial identification by MALDI-TOF in sonicated fluid is feasible. With qPCR, there were no differences between the detection in the screws processed immediately or after refrigeration. It is necessary to consider whether or not the refrigeration period would affect microbial recovery in an explanted prosthesis.
关节假体感染的微生物检测金标准是对假体周围组织进行多次培养。超声处理后的液体培养可以提高微生物的回收率。
本研究旨在评估在骨科螺钉模型上,使用塑料袋进行超声处理技术以及冷藏对常规培养、基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)和 qPCR 检测的影响。
我们在骨科螺钉上产生了金黄色葡萄球菌、铜绿假单胞菌和白色念珠菌的生物膜,然后在不同的条件和温度下储存,再进行超声处理。超声处理后,使用超声处理液进行质谱分析 MALDI-TOF、qPCR 和培养方案,以检测生物膜中涉及的微生物。
在含有铜绿假单胞菌和金黄色葡萄球菌生物膜的螺钉中,冷藏期后细菌生物负荷减少了约一个对数级。所有涉及螺钉生物膜的微生物都可以通过 MALDI-TOF 和 qPCR 检测到。只有储存在塑料袋中的组的 CFU 计数显著减少,表明温度和湿度的变化可能有利于细胞死亡。然而,由于获得的高计数,这种变化对于该模型并不重要,因为它不会影响检测。
通过 MALDI-TOF 在超声处理液中进行微生物鉴定是可行的。通过 qPCR,立即处理或冷藏后处理螺钉的检测结果没有差异。有必要考虑冷藏期是否会影响从假体中取出的微生物的恢复。