增强从地衣芽孢杆菌中提取的脂肽作为益生菌对 MDR 鲍曼不动杆菌的抗菌作用

IF 3.3 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mahdi Hosseini Bafghi, Farangis Ghanipour, Razieh Nazari, Seyed Soheil Aghaei, Parvaneh Jafari
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引用次数: 0

摘要

背景:微生物对抗生素的耐药性正在迅速升级。机会性病原体在免疫力低下的人群中引起的感染促使研究人员寻找高效安全的抗菌药物。本研究的目的是通过利用从益生菌中获得的代谢物,探索抑制鲍曼不动杆菌毒力基因表达的方法,特别是抑制鲍曼不动杆菌中负责生物膜形成的 pga 操作子基因的表达:为了评估益生菌的抗菌特性,采用琼脂凝胶扩散技术对五种益生菌的标准菌株与耐多药(MDR)鲍曼不动杆菌的标准菌株进行了测试。在确定了最有效的益生菌菌株(地衣芽孢杆菌)后,使用聚合酶链反应(PCR)测试确认了其 LanA 和 LanM 基因的存在。采用高效液相色谱(HPLC)和傅立叶变换红外光谱(FTIR)技术鉴定了预期代谢物,发现其具有脂肽性质。利用 96 孔微孔稀释法和场发射扫描电子显微镜(FE-SEM)测定了目标代谢物的最低抑菌浓度(MIC)值和抗生物膜活性。利用实时 PCR(qPCR)技术比较了鲍曼不动杆菌在接触衍生脂肽前后 pga 操作子基因(包括 pgaABCD)的表达情况:MIC结果表明,益生菌产品抑制鲍曼不动杆菌生长的浓度低于传统抗生素所需的浓度。此外,还观察到由于这种物质的作用,所需基因的表达量减少:本研究得出结论:地衣芽孢杆菌益生菌产品可以作为一种可行的替代品来对抗鲍曼不动杆菌的耐药性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancing the Antibacterial Impact of Lipopeptide Extracted from Bacillus licheniformis as a Probiotic against MDR Acinetobacter baumannii.

Background: The antibiotic resistance of microorganisms is escalating rapidly. Infections caused by opportunistic pathogens in immunocompromised individuals have prompted researchers to seek for potent and safe antibacterial agents. The purpose of this investigation was to explore the suppression of virulence gene expression, specifically the pga operon genes responsible in biofilm formation in Acinetobacter baumannii, through the utilization of metabolites obtained from probiotic bacteria.

Methods: To assess the antimicrobial properties, standard strains of five probiotic bacteria were tested against a standard strain of multidrug-resistant (MDR) A. baumannii employing the agar gel diffusion technique. Following the identification of the most potent probiotic strain (Bacillus licheniformis), the existence of its LanA and LanM genes was confirmed using the polymerase chain reaction (PCR) test. High-performance liquid chromatography (HPLC) and fourier-transform infrared spectroscopy (FTIR) techniques were employed to identify the intended metabolite, which was found to be a lipopeptide nature. The minimum inhibitory concentration (MIC) values and anti-biofilm activity of the targeted metabolite were determined using a dilution method in 96-well microplates and field emission scanning electron microscopy (FE-SEM). Real-time PCR (qPCR) was utilized for comparing the expression of pga operon genes, including pgaABCD, in A. baumannii pre- and post-exposure to the derived lipopeptide.

Results: The MIC results indicated that the probiotic product inhibited the growth of A. baumannii at concentrations lower than those needed for conventional antibiotics. Furthermore, it was observed that the desired genes' expression decreased due to the effect of this substance.

Conclusions: This research concludes that the B. licheniformis probiotic product could be a viable alternative for combating drug resistance in A. baumannii.

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