Department of Pharmacology, School of Pharmacy, Fourth Military Medical University, No. 169, Changle West Road, Xi'an 710032, China.
Department of Neurosurgery, Xijing Hospital, Fourth Military Medical University, No. 169, Changle West Road, Xi'an, Shaanxi Province, China.
Curr Drug Deliv. 2019;16(8):728-736. doi: 10.2174/1567201816666190627141931.
Carbapenem-resistant Acinetobacter baumannii (A. baumannii) was on the top of the list of the most threatening bacteria published by the WHO in 2017. Antisense oligonucleotides (ASOs) based therapy is a promising strategy for combating Multi-Drug Resistant (MDR) bacteria because of its high specificity, easy design and lower induction of resistance, but poor cellular uptake by bacteria has restricted the further utilization of this therapy.
Here, we used CADY, a secondary amphipathic peptide of 20 residues that could successfully carry siRNA into mammalian cells, to prepare CADY/ASOs nanoparticles (CADY-NPs) targeting acpP (encoding acyl carrier protein), and evaluated the uptake features, the inhibitory effects of CADY-NPs on gene expression and the growth of MDR-A. baumannii.
We found that CADY-NPs could be quickly internalized by drug-sensitive and MDR-A. baumannii in an energy independent manner, which could be restrained by chlorpromazine (an inhibitor of clathrin mediated endocytosis) significantly. In addition, CADY-NPs targeting acpP concentrationdependently retarded the growth of MDR-A. baumannii, which was associated with the decreased expression of targeted genes in A. baumannii.
In conclusion, our research is the first to demonstrate that CADY can deliver ASOs into bacteria and provide a novel strategy for the treatment of MDR-A. baumannii.
耐碳青霉烯鲍曼不动杆菌(A.baumannii)在 2017 年世界卫生组织(WHO)发布的最具威胁细菌名单中位居榜首。基于反义寡核苷酸(ASO)的治疗策略是对抗多药耐药(MDR)细菌的一种有前途的策略,因为它具有高度特异性、易于设计和较低的耐药性诱导,但细菌对其的摄取能力差限制了该疗法的进一步利用。
在这里,我们使用 CADY,一种 20 个残基的二级两亲肽,可以成功地将 siRNA 导入哺乳动物细胞,来制备针对 acpP(编码酰基载体蛋白)的 CADY/ASO 纳米颗粒(CADY-NPs),并评估了其摄取特征、CADY-NPs 对基因表达的抑制作用和 MDR-A.baumannii 的生长情况。
我们发现 CADY-NPs 可以快速以能量非依赖的方式被药敏和 MDR-A.baumannii 内吞,氯丙嗪(一种网格蛋白介导的内吞抑制剂)可以显著抑制这一过程。此外,CADY-NPs 靶向 acpP 浓度依赖性地减缓了 MDR-A.baumannii 的生长,这与 A.baumannii 中靶向基因的表达降低有关。
总之,我们的研究首次证明 CADY 可以将 ASO 递送到细菌中,并为治疗 MDR-A.baumannii 提供了一种新策略。