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用于将靶向肽核酸反义剂细胞内递送至耐头孢噻肟大肠杆菌以恢复抗生素敏感性的四面体DNA纳米颗粒载体

Tetrahedral DNA Nanoparticle Vector for Intracellular Delivery of Targeted Peptide Nucleic Acid Antisense Agents to Restore Antibiotic Sensitivity in Cefotaxime-Resistant Escherichia coli.

作者信息

Readman John Benedict, Dickson George, Coldham Nick G

机构信息

1 Bacteriology Department, Animal and Plant Health Agency , Addlestone, Surrey, United Kingdom .

2 Centre for Biomedical Sciences, School of Biological Sciences, Royal Holloway-University of London , Surrey, United Kingdom .

出版信息

Nucleic Acid Ther. 2017 Jun;27(3):176-181. doi: 10.1089/nat.2016.0644. Epub 2017 Jan 12.

DOI:10.1089/nat.2016.0644
PMID:28080251
Abstract

The bacterial cell wall presents a barrier to the uptake of unmodified synthetic antisense oligonucleotides, such as peptide nucleic acids, and so is one of the greatest obstacles to the development of their use as therapeutic anti-bacterial agents. Cell-penetrating peptides have been covalently attached to antisense agents, to facilitate penetration of the bacterial cell wall and deliver their cargo into the cytoplasm. Although they are an effective vector for antisense oligonucleotides, they are not specific for bacterial cells and can exhibit growth inhibitory properties at higher doses. Using a bacterial cell growth assay in the presence of cefotaxime (CTX 16 mg/L), we have developed and evaluated a self-assembling non-toxic DNA tetrahedron nanoparticle vector incorporating a targeted anti-bla antisense peptide nucleic acid (PNA4) in its structure for penetration of the bacterial cell wall. A dose-dependent CTX potentiating effect was observed when PNA4 (0-40 μM) was incorporated into the structure of a DNA tetrahedron vector. The minimum inhibitory concentration (to CTX) of an Escherichia coli field isolate harboring a plasmid carrying bla was reduced from 35 to 16 mg/L in the presence of PNA4 carried by the DNA tetrahedron vector (40 μM), contrasting with no reduction in MIC in the presence of PNA4 alone. No growth inhibitory effects of the DNA tetrahedron vector alone were observed.

摘要

细菌细胞壁对未修饰的合成反义寡核苷酸(如肽核酸)的摄取构成了障碍,因此是将其用作治疗性抗菌剂开发的最大障碍之一。细胞穿透肽已与反义剂共价连接,以促进细菌细胞壁的穿透并将其货物递送至细胞质中。尽管它们是反义寡核苷酸的有效载体,但它们对细菌细胞不具有特异性,并且在较高剂量下可能表现出生长抑制特性。使用在头孢噻肟(CTX 16 mg/L)存在下的细菌细胞生长测定法,我们开发并评估了一种自组装无毒DNA四面体纳米颗粒载体,其结构中包含靶向抗bla反义肽核酸(PNA4)以穿透细菌细胞壁。当PNA4(0-40 μM)掺入DNA四面体载体的结构中时,观察到剂量依赖性的CTX增强作用。携带bla的质粒的大肠杆菌现场分离株对CTX的最低抑菌浓度在DNA四面体载体(40 μM)携带的PNA4存在下从35降低至16 mg/L,而单独存在PNA4时MIC没有降低。未观察到单独的DNA四面体载体的生长抑制作用。

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