Center for Orthopedic and Trauma Research, Adelaide Medical School, Faculty of Health and Medical Sciences, University of Adelaide, Adelaide, Australia.
Department of Orthopedics and Trauma, Royal Adelaide Hospital, Adelaide, Australia.
Antimicrob Agents Chemother. 2024 Oct 8;68(10):e0080824. doi: 10.1128/aac.00808-24. Epub 2024 Aug 28.
Osteomyelitis caused by can involve the persistent infection of osteocytes. We sought to determine if current clinically utilized antibiotics were capable of clearing an intracellular osteocyte infection. Rifampicin, vancomycin, levofloxacin, ofloxacin, amoxicillin, oxacillin, doxycycline, linezolid, gentamicin, and tigecycline were assessed for their minimum inhibitory concentration (MIC) and minimum bactericidal concentrations against 12 strains, at pH 5.0 and 7.2 to mimic lysosomal and cytoplasmic environments, respectively. Those antibiotics whose bone estimated achievable concentration was commonly above their respective MIC for the strains tested were further assayed in a human osteocyte infection model under acute and chronic conditions. Osteocyte-like cells were treated at 1×, 4×, and 10× the MIC for 1 and 7 days following infection (acute model), or at 15 and 21 days of infection (chronic model). The intracellular effectivity of each antibiotic was measured in terms of CFU reduction, small colony variant formation, and bacterial mRNA expression change. Only rifampicin, levofloxacin, and linezolid reduced intracellular CFU numbers significantly in the acute model. Consistent with the transition to a non-culturable state, few if any CFU could be recovered from the chronic model. However, no treatment in either model reduced the quantity of bacterial mRNA or prevented non-culturable bacteria from returning to a culturable state. These findings indicate that adapts phenotypically during intracellular infection of osteocytes, adopting a reversible quiescent state that is protected against antibiotics, even at 10× their MIC. Thus, new therapeutic approaches are necessary to cure intracellular infections in osteomyelitis.
由 引起的骨髓炎可能涉及破骨细胞的持续感染。我们试图确定当前临床使用的抗生素是否能够清除细胞内破骨细胞的 感染。利福平、万古霉素、左氧氟沙星、氧氟沙星、阿莫西林、苯唑西林、多西环素、利奈唑胺、庆大霉素和替加环素的最低抑菌浓度(MIC)和最低杀菌浓度在 pH 值为 5.0 和 7.2 时分别针对 12 株进行了评估,以分别模拟溶酶体和细胞质环境。那些骨估计可达浓度通常高于各自 MIC 的抗生素进一步在急性和慢性人破骨细胞感染模型中进行了检测。在感染后 1 天和 7 天(急性模型)或感染后 15 天和 21 天(慢性模型),用 1×、4×和 10×MIC 处理破骨细胞样细胞。用 CFU 减少、小菌落变异形成和细菌 mRNA 表达变化来衡量每种抗生素的细胞内效力。只有利福平、左氧氟沙星和利奈唑胺在急性模型中显著减少了细胞内 CFU 数量。与向不可培养状态的转变一致,从慢性模型中几乎无法回收任何 CFU。然而,在任一模型中,没有一种治疗方法能减少细菌 mRNA 的数量,也不能阻止不可培养的细菌恢复到可培养状态。这些发现表明,在破骨细胞的细胞内感染过程中, 会发生表型适应,形成一种可逆的静止状态,从而对抗生素产生耐药性,即使在其 MIC 的 10 倍时也是如此。因此,需要新的治疗方法来治愈骨髓炎中的细胞内感染。