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噬菌体与头孢他啶/他唑巴坦在气管内导管生物膜中的协同作用。

The synergistic effect between phages and Ceftolozane/Tazobactam in endotracheal tube biofilm.

机构信息

Department of Dental Materials and Prostheses, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.

Human Exposome and Infectious Diseases Network - HEID, School of Nursing of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.

出版信息

Emerg Microbes Infect. 2024 Dec;13(1):2420737. doi: 10.1080/22221751.2024.2420737. Epub 2024 Nov 17.

Abstract

Although an increased effectiveness has been suggested when phages and antibiotics are combined, this approach has not been tested against a mature biofilm on an endotracheal tube (ETT) surface. This study evaluated the effect of short- and long-term combined phage-antibiotic therapy in a control of a mature biofilm on an ETT surface. strains, including susceptible and resistant clinical samples, were used to develop the ETT biofilm. Biofilm was treated with 10PFU/mL of phage_2, phage_18 or 5 μg/mL of ceftolozane/tazobactam, alone or in combination with phages. The sequential combination of the two different phages and ceftolozane/tazobactam was also tested. Biofilm viability was assessed after short (2, 4, 24 h) and long-(48, 72 h) term treatment exposure using colony forming unit measurement. For long-term exposition, a new treatment shot was added every 24 h. In the sequential combination, the phage type was switched at 24 h of treatment. Regarding the susceptible strains, the treatments had limited antibiofilm effect after 2, 4 and 24 h. After 48 and 72 h, administering phages alone had no effect on biofilm viability, indicating the emergence of phage-resistant phenotypes. Nonetheless, the combined phage-antibiotic treatment reduced the biofilm viability in about 5-log, whilst antibiotic alone reduced in about 3-log. The sequential combination of phages and antibiotic reduced the biofilm viability in about 6-log. With respect to the resistant strains, no antibiofilm activity was observed regarding the treatment arms. The combination of phages and ceftolozane/tazobactam showed a synergism strain-dependent, being more apparent in susceptible strains.

摘要

尽管已经有人提出,噬菌体和抗生素联合使用时效果会增强,但这种方法尚未在成熟的气管内管(ETT)表面生物膜上进行测试。本研究评估了短期和长期联合噬菌体-抗生素治疗对 ETT 表面成熟生物膜的控制效果。 使用包括敏感和耐药临床样本在内的 株来开发 ETT 生物膜。单独或联合噬菌体使用 10PFU/mL 的噬菌体_2、噬菌体_18 或 5μg/mL 的头孢他啶/他唑巴坦处理生物膜。还测试了两种不同噬菌体和头孢他啶/他唑巴坦的序贯联合。使用集落形成单位测量法评估短期(2、4、24 小时)和长期(48、72 小时)暴露于治疗后生物膜的存活能力。对于长期暴露,每 24 小时添加一次新的治疗剂量。在序贯联合中,在治疗 24 小时后切换噬菌体类型。对于敏感菌株,在 2、4 和 24 小时后,治疗对生物膜的抑制效果有限。在 48 和 72 小时后,单独使用噬菌体对生物膜的存活能力没有影响,表明出现了噬菌体耐药表型。尽管如此,联合噬菌体-抗生素治疗使生物膜的存活能力降低了约 5 个对数,而单独使用抗生素降低了约 3 个对数。噬菌体和抗生素的序贯联合使生物膜的存活能力降低了约 6 个对数。对于耐药菌株,治疗组没有观察到任何抗生物膜活性。噬菌体和头孢他啶/他唑巴坦的联合具有依赖于菌株的协同作用,在敏感菌株中更为明显。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2721/11571741/c75f9dd1e3c4/TEMI_A_2420737_UF0001_OC.jpg

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