Arthritis and Arthroplasty Design Group, Department of Orthopaedic Surgery, University of Pittsburgh, Pittsburgh, PA, USA.
Department of Orthopaedic Surgery, Ageo Medical Clinic, 3133 Haraichi, Ageo-Shi, Saitama, Japan.
Sci Rep. 2023 Mar 21;13(1):4593. doi: 10.1038/s41598-023-30951-y.
Antibiotic stewardship is viewed as having great public health benefit with limited direct benefit to the patient at the time of administration. The objective of our study was to determine if inappropriate administration of antibiotics could create conditions that would increase the rates of surgical infection. We hypothesized that sub-MIC levels of vancomycin would increase Staphylococcus aureus growth, biofilm formation, and rates of infection. S. aureus MRSA and MSSA strains were used for all experiments. Bacteria were grown planktonically and monitored using spectrophotometry. Quantitative agar culture was used to measure planktonic and biofilm bacterial burden. A mouse abscess model was used to confirm phenotypes in vivo. In the planktonic growth assay, increases in bacterial burden at ¼ MIC vancomycin were observed in USA300 JE2 by 72 h. Similar findings were observed with ½ MIC in Newman and SH1000. For biofilm formation, USA300 JE2 at ¼ and ½ MIC vancomycin increased biofilm formation by approximately 1.3- and 2.3-fold respectively at 72 h as compared to untreated controls. Similar findings were observed with Newman and SH1000 with a 2.4-fold increase in biofilm formation at ½ MIC vancomycin. In a mouse abscess model, there was a 1.2-fold increase with sub-MIC vancomycin at 3 days post infection. Our study showed that Sub-optimal vancomycin dosing promoted S. aureus planktonic growth and biofilm formation, phenotypic measures of bacterial virulence. This phenotype induced by sub-MIC levels of vancomycin was also observed to increase rates of infection and pathogenesis in our mouse model. Risks of exposure to sub-MIC concentrations with vancomycin in surgical procedures are greater as there is decreased bioavailability in tissue in comparison to other antibiotics. This highlights the importance of proper antibiotic selection, stewardship, and dosing for both surgical prophylaxis and treatment of infection.
抗生素管理被认为具有巨大的公共卫生效益,而在给药时对患者的直接益处有限。我们的研究目的是确定抗生素的不当使用是否会导致手术感染率增加。我们假设低于最低抑菌浓度(MIC)的万古霉素水平会增加金黄色葡萄球菌的生长、生物膜形成和感染率。所有实验均使用金黄色葡萄球菌 MRSA 和 MSSA 菌株。细菌在浮游状态下生长,并通过分光光度法进行监测。定量琼脂培养用于测量浮游和生物膜细菌负荷。使用小鼠脓肿模型在体内确认表型。在浮游生长测定中,在 USA300 JE2 中观察到 1/4 MIC 万古霉素在 72 小时时细菌负荷增加。在 Newman 和 SH1000 中也观察到类似的发现,在 1/2 MIC 时细菌负荷增加。对于生物膜形成,在 1/4 和 1/2 MIC 万古霉素时,USA300 JE2 在 72 小时时生物膜形成分别增加了约 1.3-和 2.3 倍,与未处理的对照组相比。在 Newman 和 SH1000 中也观察到类似的发现,在 1/2 MIC 万古霉素时生物膜形成增加了 2.4 倍。在小鼠脓肿模型中,在感染后 3 天,亚 MIC 万古霉素增加了 1.2 倍。我们的研究表明,低于最佳剂量的万古霉素促进了金黄色葡萄球菌浮游生长和生物膜形成,这是细菌毒力的表型衡量标准。在我们的小鼠模型中,还观察到这种由亚 MIC 水平万古霉素引起的表型会增加感染和发病的速度。在手术过程中接触亚 MIC 浓度万古霉素的风险更高,因为与其他抗生素相比,组织中的生物利用度降低。这突显了正确选择抗生素、管理和剂量对于手术预防和治疗感染的重要性。