Preliminary insights into the potential role of Acanthamoeba-Pseudomonas interactions in the development of antibiotic resistance.

Access microbiology Pub Date : 2025-06-30 eCollection Date: 2025-01-01 DOI:10.1099/acmi.0.000999.v3
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Abstract

Interactions between environmental protists and bacteria play a crucial role in shaping bacterial survival strategies and pathogenic potential. Certain bacteria have evolved mechanisms to resist predation by protists such as Acanthamoeba, allowing them to persist intracellularly and, in some cases, enhance their virulence. We hypothesize that Acanthamoeba species may also play a role in promoting antimicrobial resistance (AMR) in amoeba-resistant bacteria. This study investigated whether Acanthamoeba castellanii enhanced AMR development in Pseudomonas putida under lethal ciprofloxacin concentrations. P. putida was co-incubated with A. castellanii and maintained in ciprofloxacin concentrations starting at 2 µg ml-1, four times the planktonic MIC, which was incrementally increased as resistance emerged. The survival of the co-incubated P. putida and the development of resistance were monitored, and antimicrobial susceptibility tests were conducted using multiple antibiotics. P. putida co-incubated with A. castellanii in the presence of ciprofloxacin became increasingly resistant in a dose-dependent manner, with the MIC increasing from 0.5 to 20 µg ml-1 after 17 days. Contrastingly, the naïve strain did not survive sustained exposure at 2 µg ml-1. Co-incubated bacteria maintained under ciprofloxacin pressure developed resistance to ciprofloxacin, chloramphenicol, azithromycin and enrofloxacin while retaining susceptibility to streptomycin and tetracycline. Co-incubation in the absence of ciprofloxacin did not promote resistance in P. putida, suggesting that the combination of extracellular drug pressure and intracellular survival is important in driving resistance. These findings indicate that intracellular survival within Acanthamoeba can significantly accelerate AMR development in P. putida under fluoroquinolone pressure. Further research into the molecular mechanisms involved is warranted to inform strategies for mitigating AMR emergence in clinical and environmental contexts.

棘阿米巴-假单胞菌相互作用在抗生素耐药性发展中的潜在作用的初步见解。
环境原生生物和细菌之间的相互作用在形成细菌生存策略和致病潜力方面起着至关重要的作用。某些细菌已经进化出抵抗棘阿米巴原虫等原生生物捕食的机制,使它们能够在细胞内持续存在,在某些情况下,增强了它们的毒力。我们假设棘阿米巴也可能在促进阿米巴耐药细菌的抗微生物药物耐药性(AMR)中发挥作用。本研究探讨了环丙沙星致死浓度下,卡斯特棘阿米巴是否会促进恶臭假单胞菌AMR的发展。恶臭p.p . putida与A. castellanii共孵育,维持环丙沙星浓度为2µg ml-1,是浮游MIC的4倍,随着耐药性的出现逐渐增加。监测共孵育的恶臭假单胞菌的存活和耐药性的发生,并采用多种抗生素进行药敏试验。在环丙沙星存在下,恶臭假单胞菌与castellani共孵育的耐药呈剂量依赖性增加,17天后MIC从0.5 μ g ml-1增加到20µg ml-1。相比之下,naïve菌株在2µg ml-1的浓度下无法存活。在环丙沙星压力下共同培养的细菌对环丙沙星、氯霉素、阿奇霉素和恩诺沙星产生耐药性,而对链霉素和四环素保持敏感性。在没有环丙沙星的情况下共孵育不促进恶臭假单胞菌的耐药,提示细胞外药物压力和细胞内生存的结合在驱动耐药方面很重要。这些发现表明,棘阿米巴细胞内存活可显著加速氟喹诺酮压力下恶臭假单胞菌AMR的发展。进一步研究所涉及的分子机制是有必要的,以便为减轻临床和环境背景下AMR出现的策略提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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