Berberov Kaloyan, Atanasova Nikolina, Krumov Nikolay, Yakimova Boryana, Lazarkevich Irina, Engibarov Stephan, Damyanova Tsvetozara, Boyadzhieva Ivanka, Kabaivanova Lyudmila
Department of General Microbiology, The Stephan Angeloff Institute of Microbiology, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.
Laboratory of Chemistry and Biophysics of Proteins and Enzymes, Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.
Mar Drugs. 2025 Jul 23;23(8):295. doi: 10.3390/md23080295.
Antibiotic resistance is one of the most significant public health issues today. As a consequence, there is an urgent need for novel classes of antibiotics. This necessitates the development of highly efficient screening methods for the rapid identification of antibiotic-producing bacteria. Here, we describe a new method for high-throughput screening of antimicrobial compounds (AMC) producing halophilic bacteria. Our methodology used a newly designed 3D-printed Petri plate replicator used for drop deposition and colony replication. We employed this device in combination with a modified agar overlay assay to screen more than 7400 bacterial colonies. A total of 54 potential AMC producers were discovered at a success rate of 0.7%. Although 40% of them lost their antibacterial activity during the secondary screening, 22 strains retained inhibitory activity and were able to suppress the growth of one or more safe relatives of the ESKAPE group pathogens. The ethyl acetate extract from the most potent strain, POTR191, demonstrated moderate antibacterial activity against , , and with minimal inhibitory concentrations of 128 μg/mL, 128 μg/mL, and 512 μg/mL, respectively. We propose that our replica plate assay could be used for target-based antimicrobial screening of various extremophilic bacteria.
抗生素耐药性是当今最重大的公共卫生问题之一。因此,迫切需要新型抗生素类别。这就需要开发高效的筛选方法,以便快速鉴定产生抗生素的细菌。在此,我们描述了一种用于高通量筛选产生抗菌化合物(AMC)的嗜盐细菌的新方法。我们的方法使用了一种新设计的3D打印培养皿复制器,用于液滴沉积和菌落复制。我们将该设备与改良的琼脂覆盖试验相结合,筛选了7400多个细菌菌落。共发现54个潜在的AMC产生菌,成功率为0.7%。尽管其中40%在二次筛选过程中失去了抗菌活性,但仍有22株保留了抑制活性,能够抑制ESKAPE组病原体的一种或多种安全亲缘菌的生长。最具活性的菌株POTR191的乙酸乙酯提取物对、和表现出中等抗菌活性,最小抑菌浓度分别为128μg/mL、128μg/mL和512μg/mL。我们认为,我们的复制平板试验可用于对各种极端嗜热细菌进行基于靶点的抗菌筛选。