Carvacrol对大肠杆菌异源耐药鲍曼不动杆菌临床分离株生物膜形成的抑制作用。

Iraj Pakzad, Fatemeh Yarkarami, Behrooz Sadeghi Kalani, Mahnaz Shafieian, Ali Hematian
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引用次数: 0

摘要

背景:细菌形成生物膜的能力是产生稳定感染的重要策略。这一问题在鲍曼尼不动杆菌作为医院病原体中更为关键。如今,生物膜形成的控制和预防或去除生物膜的解决方案正在开发中。Carvacrol被认为是重要细菌中的一种抗生物膜化合物。本研究研究了Carvacrol对鲍曼不动杆菌临床粘菌素异耐药分离株生物膜形成的抗生物膜作用。方法:2019年从伊朗德黑兰Motahari医院采集了约22株鲍曼不动杆菌临床菌株。生化和基因型方法证实了这些分离株。用标准PAP法测定了粘菌素的异源耐药性。根据标准方案测定Carvacrol的抗菌和抗生物膜活性。结果:大约12个分离株被认为是强大的生物膜生产者,并用于分析。6株菌株对粘菌素具有异源抗性。512g/ml浓度的Carvacrol对所有分离株显示出最佳的抗菌活性。Carvacrol的亚MIC(256g/ml)降低了生物膜的形成能力,这具有统计学意义(P结论:本研究结果表明,Carvacol的亚MIC在临床鲍氏粘菌素异耐药分离株中具有抗生物膜作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitory Effects of Carvacrol on Biofilm Formation in Colistin Heteroresistant Acinetobacter baumannii Clinical Isolates.

Background: The ability of bacteria to form biofilm is an essential strategy for creating stable infections. This issue is more critical in Acinetobacter bauamannii as a hospital pathogen. Today, the control of biofilm formation and solutions to prevent or remove biofilm is being developed. Carvacrol has been considered an anti-biofilm compound in significant bacteria. This study investigated the anti-biofilm effect of Carvacrol on biofilm formation in clinical colistin heteroresistant isolates of A. baumannii.

Methods: 22 clinical strains of A. baumannii were collected from Motahari Hospital in Tehran, Iran, in 2019. Biochemical and genotypic methods confirmed these isolates. Colistin heteroresistance was determined by the Standard PAP method. Carvacrol's antibacterial and anti-biofilm activity was determined according to the standard protocol.

Results: About 12 isolates were considered strong biofilm producers and were used for analysis. Six isolates had hetero-resistance to colistin. Carvacrol at a 512 g/ml concentration showed the best antibacterial activity against all isolates. The sub-MIC of Carvacrol (256 g/ml) reduced the biofilm formation capacity, which was statistically significant (p < 0.05).

Conclusion: The results of this study showed that sub-MIC of Carvacrol has anti-biofilm effects in clinical A.baumannii colistin hetero-resistance isolates.

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