首页> 外文期刊>Biomaterials >Antisense inhibition of gene expression and growth in gram-negative bacteria by cell-penetrating peptide conjugates of peptide nucleic acids targeted to rpoD gene.
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Antisense inhibition of gene expression and growth in gram-negative bacteria by cell-penetrating peptide conjugates of peptide nucleic acids targeted to rpoD gene.

机译:通过靶向rpoD基因的肽核酸的细胞穿透肽结合物对革兰氏阴性细菌中基因表达和生长的反义抑制。

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Gram-negative bacteria (GNB) cause common and severe hospital- and community-acquired infections with a high incidence of multidrug resistance (MDR) and mortality. The emergence and spread of MDR-GNB strains limit therapeutic options and highlight the need to develop new therapeutic strategies. In this study, the peptide (RXR)(4)XB- and (KFF)(3)K-conjugated peptide nucleic acids (PPNAs) were developed to target rpoD, which encodes an RNA polymerase primary sigma(70) that is thought to be essential for bacterial growth. Their antimicrobial activities were tested against different clinical isolates of MDR-GNB in vitro and in infection models. The (RXR)(4)XB- and (KFF)(3)K- conjugated PNAs were bactericidal against different strains of MDR-GNB in concentration-dependent and sequence-selective manner, whereas a PPNA with a scrambled base sequence had no effect on growth. Among tested PPNAs, (RXR)(4)XB conjugate PPNA06 showed more potent and broad spectrum inhibition in multidrug-resistant Escherichia coli, Salmonella enterica, Klebsiella pneumoniae, and Shigella flexneri in vitro and in vivo. The results were associated with suppression of rpoD mRNA and sigma(70) expression, as well as sigma(70) downstream regulated genes including ftsZ, mazF, prfB, rpoS, seqA, turfB and ygjD. The treatment of PPNA06 on mono- or multiple MDR-GBN infected human gastric mucosal epithelial cells demonstrated the complete inhibition on bacterial growth and no influence on morphology and growth of human cells. Also, PPNA06 did not show the induction of antibiotic resistance as compared with classical antibiotics in GNB. These findings firstly demonstrate that rpoD is potential target for developing antisense antibiotics, and indicate that peptide conjugates of anti-rpoD PNA are active against GNBs in vitro and in vivo. Our results offer a feasible strategy for treating MDR-GNB infections.
机译:革兰氏阴性细菌(GNB)导致常见和严重的医院和社区感染,多药耐药性(MDR)和死亡率很高。 MDR-GNB菌株的出现和传播限制了治疗选择,并突出了开发新治疗策略的必要性。在这项研究中,肽(RXR)(4)XB-和(KFF)(3)K缀合的肽核酸(PPNA)被开发为靶向rpoD,后者编码被认为是RNA聚合酶的一级sigma(70)。对细菌生长至关重要。在体外和感染模型中,对它们的抗MDR-GNB临床分离株的抗菌活性进行了测试。 (RXR)(4)XB-和(KFF)(3)K-缀合的PNA以浓度依赖性和序列选择性的方式针对不同菌株的MDR-GNB杀菌,而具有混乱碱基序列的PPNA则没有作用增长。在测试的PPNA中,(RXR)(4)XB共轭PPNA06在体外和体内对多药耐药的大肠杆菌,肠炎沙门氏菌,肺炎克雷伯菌和弗氏志贺氏菌显示出更有效和广谱的抑制作用。结果与抑制rpoD mRNA和sigma(70)表达以及sigma(70)下游调控的基因有关,包括ftsZ,mazF,prfB,rpoS,seqA,turfB和ygjD。对单个或多个感染了MDR-GBN的人胃粘膜上皮细胞进行PPNA06的处理显示出对细菌生长的完全抑制,并且对人细胞的形态和生长没有影响。而且,与GNB中的经典抗生素相比,PPNA06没有显示出对抗生素的抗性诱导。这些发现首先证明rpoD是开发反义抗生素的潜在靶标,并且表明抗rpoD PNA的肽缀合物在体外和体内对GNB具有活性。我们的结果为治疗MDR-GNB感染提供了可行的策略。

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