Department of Microbiology, General Division of Basic Medical Sciences, Egyptian Drug Authority (EDA), Formerly National Organization for Drug Control and Research (NODCAR), 12611, Giza, Egypt.
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Helwan University, 11795, Helwan, Cairo, Egypt; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Modern University for Technology and Information, Egypt.
Anaerobe. 2021 Jun;69:102328. doi: 10.1016/j.anaerobe.2021.102328. Epub 2021 Jan 30.
Human infections caused by the anaerobic bacterium Eggerthia catenaformis are rare. However, a growing number of case reports have presented the bacterium as the causative agent in many serious complications. This study provides data on the isolation and antibiotic susceptibility profiles of E. catenaformis from dental abscess. Identification of isolates was performed using matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS). We also investigated the antibacterial activity of 5-acetyl-4-methyl-2-(3-pyridyl) thiazole (AMPT) on E. catenaformis isolates. Minimum inhibitory concentrations (MICs) were determined by an agar dilution method and bactericidal activity was evaluated by a time-kill assay. Moreover, the mechanism of action of AMPT was also explored by cell membrane disruption assay and scanning electron microscopy (SEM). MALDI-TOF MS results revealed unambiguous identification of all isolates with score values between 2.120 and 2.501. Isolates NY4 and NY9 (20% of isolates) were found resistant to multiple antibiotics judged by MIC values. As multidrug-resistant strains of E. catenaformis were not reported to date, we then confirmed the identity of NY4 and NY9 based on 16S rRNA gene sequence. Favorably, all isolates were susceptible to AMPT with an MIC range of 0.25-1 mg/L. Time-kill kinetics of AMPT indicated that it exhibited potent bactericidal activity against the multidrug-resistant isolates NY4 and NY9. Furthermore, this study also hypothesizes that AMPT exerts its antibacterial effect through damaging the cell membrane and thereby induce the release of intracellular components. AMPT could therefore be considered as a therapeutic option for infections caused by multidrug-resistant bacteria.
人类感染厌氧细菌卡特尼亚菌的情况较为罕见。然而,越来越多的病例报告表明,这种细菌是许多严重并发症的病原体。本研究提供了从牙脓肿中分离出的卡特尼亚菌的分离和抗生素药敏谱数据。使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)对分离物进行鉴定。我们还研究了 5-乙酰基-4-甲基-2-(3-吡啶基)噻唑(AMPT)对卡特尼亚菌分离物的抗菌活性。采用琼脂稀释法测定最小抑菌浓度(MIC),通过时间杀伤试验评估杀菌活性。此外,还通过细胞膜破坏试验和扫描电子显微镜(SEM)探讨了 AMPT 的作用机制。MALDI-TOF MS 结果显示,所有分离物的得分值在 2.120 到 2.501 之间,均得到了明确的鉴定。分离物 NY4 和 NY9(占分离物的 20%)对多种抗生素的 MIC 值显示耐药。由于迄今为止尚未报道卡特尼亚菌的多药耐药株,因此我们根据 16S rRNA 基因序列进一步确认了 NY4 和 NY9 的身份。令人欣慰的是,所有分离物对 AMPT 均敏感,MIC 范围为 0.25-1mg/L。AMPT 的时间杀伤动力学表明,它对多药耐药分离物 NY4 和 NY9 具有很强的杀菌活性。此外,本研究还假设 AMPT 通过破坏细胞膜发挥其抗菌作用,从而诱导细胞内成分的释放。因此,AMPT 可以被认为是治疗多药耐药菌感染的一种选择。