UTI89尿路致病性大肠杆菌BIoVector®(UPEC)E.coli strain BioVector NTCC典型培养物保藏中心
- 价 格:¥99850
- 货 号:BIoVector®-UTI89
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
- 联系人:Dr.Xu, Biovector NTCC Inc.
电话:400-800-2947 工作QQ:1843439339 (微信同号)
邮件:Biovector@163.com
手机:18901268599
地址:北京
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BIoVector® UTI89 strain is a well-characterized, clinically isolated uropathogenic Escherichia coli (UPEC) used as a model organism in urinary tract infection (UTI) research. It was originally isolated from a patient with uncomplicated cystitis and has since been instrumental in studying the molecular mechanisms of UPEC virulence.
Pathogenic origin: UTI89 is a clinical isolate from a human patient with acute bladder inflammation (cystitis). It belongs to phylogroup B2, a lineage of E. coli frequently associated with extraintestinal infections.
Virulence factors: UTI89 is equipped with several genetic features that enhance its ability to cause infection, including:
Pathogenicity Islands (PAIs): It possesses four major PAIs, which are distinct from those in non-pathogenic E. coli strains and contain genes that contribute to its disease-causing potential.
Virulence plasmid (pUTI89): This large extrachromosomal plasmid contains virulence genes and plays a critical role during the initial stages of infection by promoting bladder colonization and invasion.
Adhesins: UTI89 has multiple pilus operons, including type 1 pili, which help it adhere to the urinary tract's epithelial cells. The FimH adhesin on the tip of type 1 pili is particularly important for this process.
Toxins: The strain produces several toxins, including hemolysin and cytotoxic necrotizing factor (CNF), that can damage host cells and aid infection.
Infection cycle: In mouse models, UTI89 replicates within the bladder's urothelial cells, forming intracellular bacterial communities (IBCs). This provides a niche where the bacteria are protected from the host's immune response and antibiotics.
UPEC fitness: Identifying the essential genes required for its survival and growth in different environments, including laboratory media, human urine, and the mouse bladder.
Host-pathogen interactions: Understanding how the bacterium adapts to the host's immune response and manipulates host cell processes.
Biofilm formation: Investigating the complex biofilm structures it creates at the air-liquid interface and how they protect the bacteria.
Therapeutic development: Testing novel strategies to combat antibiotic-resistant UPEC, such as phage therapy.


BioVector NTCC质粒载体菌种细胞蛋白抗体基因保藏中心
BioVector NTCC Inc.
TEL: 400-800-2947, 189-0126-8599
E-mail: biovector@163.com
http://www.biovector.net
致病性来源: UTI89是从一名患有急性膀胱炎的患者身上分离出的临床菌株。它属于系统发育B2群,该谱系的大肠杆菌常与肠道外感染相关。
毒力因子: UTI89拥有多种增强其致病能力的遗传特征,其中包括:
致病岛(PAIs): 它拥有四个主要的致病岛,这些致病岛与非致病性大肠杆菌菌株不同,并包含有助于其致病潜力的基因。
毒力质粒(pUTI89): 这个大型染色体外质粒包含毒力基因,在感染的早期阶段通过促进膀胱定殖和侵袭而发挥关键作用。
黏附素: UTI89拥有多个菌毛操纵子,包括1型菌毛,这有助于它黏附到尿路的表皮细胞上。1型菌毛顶端的FimH黏附素对此过程尤为重要。
毒素: 该菌株产生多种毒素,包括溶血素和细胞毒性坏死因子(CNF),这些毒素可以破坏宿主细胞并帮助感染。
感染周期: 在小鼠模型中,UTI89在膀胱的尿路上皮细胞内复制,形成细胞内细菌群落(IBCs)。这为细菌提供了一个可以躲避宿主免疫反应和抗生素的“庇护所”。
UPEC适应性: 识别其在不同环境(包括实验室培养基、人体尿液和小鼠膀胱)中生存和生长所必需的关键基因。
宿主-病原体相互作用: 理解细菌如何适应宿主的免疫反应并操控宿主细胞过程。
生物膜形成: 研究其在气液界面形成的复杂生物膜结构,以及这些结构如何保护细菌。
治疗方法开发: 测试对抗耐药性UPEC的新策略,例如噬菌体疗法。
BioVector NTCC质粒载体菌种细胞蛋白抗体基因保藏中心
BioVector NTCC Inc.
TEL: 400-800-2947, 189-0126-8599
E-mail: biovector@163.com
http://www.biovector.net
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