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抗生素亚抑菌浓度通过诱导细菌毒力加剧葡萄球菌感染。

Subinhibitory Concentrations of Antibiotics Exacerbate Staphylococcal Infection by Inducing Bacterial Virulence.

作者信息

Gao Peng, Wei Yuanxin, Wan Rachel Evelyn, Wong Ka Wing, Iu Ho Ting Venice, Tai Sherlock Shing Chiu, Li Yongli, Yam Hin Cheung Bill, Halebeedu Prakash Pradeep, Chen Jonathan Hon Kwan, Ho Pak Leung, Yuen Kwok Yung, Davies Julian, Kao Richard Yi Tsun

机构信息

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Konggrid.194645.b, Pok Fu Lam, Hong Kong.

Department of Microbiology, Queen Mary Hospital, Pok Fu Lam, Hong Kong.

出版信息

Microbiol Spectr. 2022 Aug 31;10(4):e0064022. doi: 10.1128/spectrum.00640-22. Epub 2022 Jun 27.

Abstract

Antibiotics are widely used for the treatment of bacterial infections. However, injudicious use of antibiotics based on an empirical method may lead to the emergence of resistant strains. Despite appropriate administration of antibiotics, their concentrations may remain subinhibitory in the body, due to individual variations in tissue distribution and metabolism rates. This may promote bacterial virulence and complicate the treatment strategies. To investigate whether the administration of certain classes of antibiotics will induce bacterial virulence and worsen the infection under conditions. Different classes of antibiotics were tested for their ability to induce virulence in a methicillin-resistant S. aureus strain Mu3 and clinical isolates. Antibiotic-induced pathogenicity was assessed using mouse peritonitis and bacteremia models. β-lactam antibiotics and tetracyclines induced the expression of multiple surface-associated virulence factors as well as the secretion of toxins. In peritonitis and bacteremia models, mice infected with MRSA and treated with ampicillin, ceftazidime, or tetracycline showed enhanced bacterial pathogenicity. The release of induced virulence factors was confirmed in a histological examination. Subinhibitory concentrations of antibiotics belonging to β-lactam and tetracycline aggravated infection by inducing staphylococcal virulence . Thus, when antibiotics are required, it is preferable to employ combination therapy and to initiate the appropriate treatment plan, following diagnosis. Our findings emphasize the risks associated with antibiotic-based therapy and underline the need for alternative therapeutic options. Antibiotics are widely applied to treat infectious diseases. Empirically treatment with incorrect antibiotics, or even correct antibiotics always falls into subinhibitory concentrations, due to dosing, distribution, or secretion. In this study, we have systematically evaluated virulence induction effect of antibiotics and exacerbated infection. The major highlight of this work is to prove the β-lactam and tetracyclines antibiotics exacerbated disease is due to their induction effect on staphylococcal virulence. This phenomenon is common and suggests that if β-lactam antibiotics remain the first line of defense during empirical therapy, we either need to increase patient reliability or the treatment approach may improve in the future when paired with anti-virulence drugs.

摘要

抗生素被广泛用于治疗细菌感染。然而,基于经验方法的不当使用抗生素可能会导致耐药菌株的出现。尽管抗生素使用得当,但由于个体在组织分布和代谢率方面存在差异,其在体内的浓度可能仍低于抑制水平。这可能会促进细菌的毒力并使治疗策略复杂化。为了研究在某些情况下给予特定类别的抗生素是否会诱导细菌毒力并使感染恶化。对不同类别的抗生素在耐甲氧西林金黄色葡萄球菌菌株Mu3和临床分离株中诱导毒力的能力进行了测试。使用小鼠腹膜炎和菌血症模型评估抗生素诱导的致病性。β-内酰胺类抗生素和四环素诱导多种表面相关毒力因子的表达以及毒素的分泌。在腹膜炎和菌血症模型中,感染耐甲氧西林金黄色葡萄球菌并用氨苄西林、头孢他啶或四环素治疗的小鼠表现出增强的细菌致病性。在组织学检查中证实了诱导的毒力因子的释放。属于β-内酰胺类和四环素类的抗生素的亚抑制浓度通过诱导葡萄球菌毒力而加重感染。因此,当需要使用抗生素时,最好采用联合治疗并在诊断后启动适当的治疗方案。我们的研究结果强调了基于抗生素治疗的风险,并强调了需要替代治疗选择。抗生素被广泛应用于治疗传染病。由于给药、分布或分泌问题,使用不正确的抗生素进行经验性治疗,甚至正确的抗生素也总是处于亚抑制浓度。在这项研究中,我们系统地评估了抗生素的毒力诱导作用和加重感染的情况。这项工作的主要亮点是证明β-内酰胺类和四环素类抗生素加重疾病是由于它们对葡萄球菌毒力的诱导作用。这种现象很常见,这表明如果β-内酰胺类抗生素在经验性治疗期间仍然是一线防御药物,我们要么需要提高患者的依从性,要么在未来与抗毒力药物联合使用时治疗方法可能会有所改进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8868/9431598/daaec7290d3c/spectrum.00640-22-f001.jpg

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