一种靶向多重耐药大肠杆菌的噬菌体的特性和抗菌效果。

IF 3.8 2区 医学 Q2 CHEMISTRY, MEDICINAL
Tianshi Xiao, Chan Wang, Longbo Wang, Lingxian Xiang, Lin Li, Shaoqi Qu
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引用次数: 0

摘要

耐多药大肠杆菌(MDR)的出现对全球公共卫生构成重大威胁,需要采取替代治疗策略。本研究从家禽养殖场污水中分离并鉴定了一种新型噬菌体vB_EcoM_51,并对其抗耐多药大肠杆菌的潜力进行了评价。透射电镜显示,该噬菌体具有典型的肌病毒科形态特征,包括多面体头部(~ 66.62 nm)和可收缩的尾部(~ 97.32 nm)。基因组分析显示该病毒为双链DNA,全长167,016 bp, GC含量为35.54%,属于Tequatrovirus属。该噬菌体对8株大肠杆菌和1株肠道沙门氏菌具有较强的裂解活性。稳定性评估显示广泛的耐热性(-20至50°C)和广泛的pH稳定性(pH 2-11)。一步生长动力学分析表明复制速度快,潜伏期为5分钟,每个感染细胞的爆发大小约为212个斑块形成单位(PFU)。在大肠杆菌感染的小鼠模型中,1 × 109 PFU的噬菌体治疗显著提高了存活率,减少了器官中的细菌负荷,并减轻了炎症反应。总的来说,这些发现表明噬菌体vB_EcoM_51代表了一个有希望的噬菌体治疗耐多药感染的候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization and Antimicrobial Efficacy of a Bacteriophage Targeting Multidrug-Resistant Escherichia coli.

The emergence of multidrug-resistant (MDR) Escherichia coli poses a significant threat to global public health, necessitating alternative therapeutic strategies. In this study, we isolated and characterized a novel lytic bacteriophage (phage), vB_EcoM_51, from poultry farm sewage and evaluated its potential against MDR E. coli. Transmission electron microscopy revealed that the phage exhibits morphological features typical of the Myoviridae family, including a polyhedral head (∼66.62 nm) and a contractile tail (∼97.32 nm). Genome analysis indicated a double-stranded DNA virus of 167,016 bp with a GC content of 35.54%, classifying it within the Tequatrovirus genus. The phage showed potent lytic activity against eight E. coli strains and one Salmonella enterica strain. Stability assessments revealed broad thermal tolerance (-20 to 50 °C) and broad pH stability (pH 2-11). One-step growth kinetics analysis indicated rapid replication, with a latent period of 5 min and a burst size of approximately 212 plaque-forming units (PFU) per infected cell. In a mouse model infected with E. coli, phage treatment at 1 × 109 PFU significantly improved survival rates, reduced bacterial loads in organs, and attenuated inflammatory responses. Collectively, these findings demonstrate that phage vB_EcoM_51 represents a promising candidate for phage therapy against MDR infections.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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