Ali Zienab, Abdelkader Karim, Abdel-Fattah Maha M, Azmy Ahmed Farag, El-Gendy Ahmed O, Dishisha Tarek
Department of Pharmaceutical Microbiology and Immunology, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, 62511, Egypt.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, 62511, Egypt.
BMC Microbiol. 2025 Feb 20;25(1):80. doi: 10.1186/s12866-025-03785-z.
In nosocomial settings, vancomycin-resistant Enterococcus faecalis is a major health threat leading to increased morbidities, mortalities, and treatment costs. Nowadays, several approaches are under investigation to enhance the activity of or replace the traditional antibiotics. Bacteriophage therapy was sought as a potential approach for combating E. faecalis infections. The present study focuses on isolating and characterizing bacteriophage against clinical multi-drug resistant (MDR) E. faecalis strain Lb-1492. The phage stability, lytic activity, host-range, latent period, burst size, the ability to detach the pre-formed biofilm and destroy entrapped cells were investigated. The phage genome was purified, sequenced, and subjected to bioinformatics analysis for identifying and characterizing its features, as well as, the suitability for clinical application. Finally, the ability of the phage to rescue mice from deadly, experimentally induced E. faecalis bacteremia was evaluated.
A virulent phage was isolated from sewage water against a clinical MDR E. faecalis isolate. Morphological and genomic studies indicated that the phage belongs to the Efquatrovirus genus, with a long tail, icosahedral head and a linear double-stranded DNA genome of approximately 42.9 kbp. The phage was named vB_Efa_ZAT1 (shortly ZAT1). It demonstrated a shorter latent period and larger burst size than regular-tailed phages, and a characteristic stability over a wide range of pH and temperatures, with the optimum activity at pH 7.4 and 37 °C, respectively. Phage ZAT1 showed a narrow spectrum of activity and a characteristic biofilm disruption ability. The phage managed successfully to control E. faecalis-induced bacteremia in mice models, which was lethal within 48 h in the control group. An intraperitoneal injection of 3 × 10 PFU of the phage solution given 1 h after the bacterial challenge was sufficient to save all the animals, completely reversing the trend of 100% mortality caused by this bacterium.
Phage therapy can be a promising alternative to traditional antibiotics in the post-antibiotic era with a significant antimicrobial and antibiofilm activities against MDR E. faecalis.
在医院环境中,耐万古霉素粪肠球菌是一种主要的健康威胁,会导致发病率、死亡率增加以及治疗成本上升。如今,有几种方法正在研究中,以增强传统抗生素的活性或替代传统抗生素。噬菌体疗法被视为对抗粪肠球菌感染的一种潜在方法。本研究重点在于分离和鉴定针对临床多药耐药(MDR)粪肠球菌菌株Lb - 1492的噬菌体。对噬菌体的稳定性、裂解活性、宿主范围、潜伏期、爆发量、去除预先形成的生物膜的能力以及破坏包埋细胞的能力进行了研究。对噬菌体基因组进行了纯化、测序,并进行了生物信息学分析,以鉴定和表征其特征以及临床应用的适用性。最后,评估了噬菌体拯救小鼠免受致命的、实验性诱导的粪肠球菌菌血症的能力。
从污水中分离出一种针对临床耐多药粪肠球菌分离株的烈性噬菌体。形态学和基因组学研究表明,该噬菌体属于Efquatrovirus属,具有长尾巴、二十面体头部和大约42.9 kbp的线性双链DNA基因组。该噬菌体被命名为vB_Efa_ZAT1(简称ZAT1)。与常规尾噬菌体相比,它表现出更短的潜伏期和更大的爆发量,并且在广泛的pH值和温度范围内具有特征性稳定性,分别在pH 7.4和37°C时活性最佳。噬菌体ZAT1显示出较窄的活性谱和特征性的生物膜破坏能力。在小鼠模型中,噬菌体成功地控制了粪肠球菌诱导的菌血症,在对照组中,这种菌血症在48小时内是致命的。在细菌攻击后1小时腹腔注射3×10 PFU的噬菌体溶液足以拯救所有动物,完全扭转了由这种细菌导致的100%死亡率的趋势。
在抗生素后时代,噬菌体疗法对于耐多药粪肠球菌具有显著的抗菌和抗生物膜活性,有望成为传统抗生素的替代方法。