Molecular Biology Department, Pasteur Institute of Iran, Tehran, Iran.
Immunotherapy and Leishmania Vaccine Research Department, Pasteur Institute of Iran, Tehran, Iran.
PLoS One. 2020 Jul 14;15(7):e0235892. doi: 10.1371/journal.pone.0235892. eCollection 2020.
Today the development of antibiotic resistance, especially in the treatment of bacterial infections associated with biofilms, has led to increasing the importance of antimicrobial peptides (AMPs). In this work, antimicrobial and synergistic activity of three truncated HNP-1 analogs (2Abz14S29, 2Abz23S29, and HNP1ΔC18A) with β-lactam (amoxicillin and cefixime) and fluoroquinolones (ciprofloxacin and norfloxacin) antibiotics against multidrug-resistant (MDR) uropathogenic E. coli clinical isolates were evaluated. The anti-biofilm potential of peptides at different stages was also investigated. All peptides exhibited additive activity just with β-lactam antibiotics in a checkerboard synergy assay. Inhibition and eradication of MDR uropathogenic E. coli biofilm were shown by all test peptides at different concentrations. Thus, truncated HNP-1 analogs (2Abz14S29, 2Abz23S29, and HNP1ΔC18A) may have the potential for the treatment of urinary tract infections (UTIs) caused by biofilm-forming MDR uropathogenic E. coli.
如今,抗生素耐药性的发展,尤其是在治疗与生物膜相关的细菌感染方面,使得抗菌肽(AMPs)的重要性日益增加。在这项工作中,评估了三种截短的 HNP-1 类似物(2Abz14S29、2Abz23S29 和 HNP1ΔC18A)与β-内酰胺(阿莫西林和头孢克肟)和氟喹诺酮类(环丙沙星和诺氟沙星)抗生素对多药耐药(MDR)尿路致病性大肠杆菌临床分离株的抗菌和协同活性。还研究了肽在不同阶段的抗生物膜潜力。在棋盘协同试验中,所有肽与β-内酰胺抗生素均表现出相加活性。所有测试肽在不同浓度下均显示出对 MDR 尿路致病性大肠杆菌生物膜的抑制和清除作用。因此,截短的 HNP-1 类似物(2Abz14S29、2Abz23S29 和 HNP1ΔC18A)可能具有治疗由形成生物膜的 MDR 尿路致病性大肠杆菌引起的尿路感染(UTI)的潜力。