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Characterizing the type 6 secretion system (T6SS) of E. cloacae SBP-8 and its role in pathogenesis and bacterial competition.解析阴沟肠杆菌 SBP-8 的 6 型分泌系统(T6SS)及其在发病机制和细菌竞争中的作用。
Microb Pathog. 2023 Oct;183:106268. doi: 10.1016/j.micpath.2023.106268. Epub 2023 Aug 1.
3
Tyrosine residues initiated photopolymerization in living organisms.酪氨酸残基引发活生物体中的光聚合反应。
Nat Commun. 2023 Jun 16;14(1):3598. doi: 10.1038/s41467-023-39286-8.
4
Intracellular hydrogelation of macrophage conjugated probiotics for hitchhiking delivery and combined treatment of colitis.巨噬细胞共轭益生菌的细胞内水凝胶化用于搭便车递送和联合治疗结肠炎。
Mater Today Bio. 2023 May 19;20:100679. doi: 10.1016/j.mtbio.2023.100679. eCollection 2023 Jun.
5
Biofilm-forming strains of P. aeruginosa and S. aureus isolated from cystic fibrosis patients differently affect inflammatory phenotype of macrophages.从囊性纤维化患者中分离出的生物膜形成型铜绿假单胞菌和金黄色葡萄球菌菌株对巨噬细胞炎症表型的影响不同。
Inflamm Res. 2023 Jun;72(6):1275-1289. doi: 10.1007/s00011-023-01743-x. Epub 2023 May 31.
6
Transcriptome Dynamics of Pseudomonas aeruginosa during Transition from Overlapping To Non-Overlapping Cell Cycles.铜绿假单胞菌在重叠细胞周期到非重叠细胞周期转变过程中的转录组动态。
mSystems. 2023 Apr 27;8(2):e0113022. doi: 10.1128/msystems.01130-22. Epub 2023 Feb 14.
7
Engineering Cyborg Bacteria Through Intracellular Hydrogelation.通过细胞内水凝胶化工程改造细菌。
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8
Pseudomonas aeruginosa: pathogenesis, virulence factors, antibiotic resistance, interaction with host, technology advances and emerging therapeutics.铜绿假单胞菌:发病机制、毒力因子、抗生素耐药性、与宿主的相互作用、技术进展和新兴治疗方法。
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通过细胞内水凝胶化工程化合成半机械细菌病原体。

Engineering Cyborg Pathogens through Intracellular Hydrogelation.

机构信息

Department of Biomedical Engineering, University of California, Davis, Davis, California 95616, United States.

出版信息

ACS Synth Biol. 2024 Nov 15;13(11):3609-3620. doi: 10.1021/acssynbio.4c00420. Epub 2024 Oct 16.

DOI:10.1021/acssynbio.4c00420
PMID:39413025
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11748816/
Abstract

Synthetic biology primarily focuses on two kinds of cell chassis: living cells and nonliving systems. Living cells are autoreplicating systems that have active metabolism. Nonliving systems, including artificial cells and nanoparticles, are nonreplicating systems typically lacking active metabolism. In recent work, Cyborg bacteria that are nonreplicating-but-metabolically active have been engineered through intracellular hydrogelation. Intracellular hydrogelation is conducted by infusing gel monomers and photoactivators into cells, followed by the activation of polymerization of the gel monomers inside the cells. However, the previous work investigated only cells. Extending the Cyborg-Cell method to pathogenic bacteria could enable the exploitation of their pathogenic properties in biomedical applications. Here, we focus on different strains of , , and . To synthesize the Cyborg pathogens, we first reveal the impact of different hydrogel concentrations on the metabolism, replication, and intracellular gelation of Cyborg pathogens. Next, we demonstrate that the Cyborg pathogens are taken up by macrophages in a similar magnitude as wild-type pathogens through confocal microscopy and real-time PCR. Finally, we show that the macrophage that takes up the Cyborg pathogen exhibits a similar phenotypic response to the wild-type pathogen. Our work generalizes the intracellular hydrogelation approach from lab strains of to bacterial pathogens. The new Cyborg pathogens could be applied in biomedical applications ranging from drug delivery to immunotherapy.

摘要

合成生物学主要关注两种细胞底盘

活细胞和无生命系统。活细胞是具有主动代谢的自我复制系统。无生命系统,包括人工细胞和纳米颗粒,是非复制系统,通常缺乏主动代谢。在最近的工作中,通过细胞内水凝胶化工程,制造出了非复制但代谢活跃的半机械细菌。细胞内水凝胶化是通过将凝胶单体和光引发剂注入细胞内,然后在细胞内激活凝胶单体的聚合来进行的。然而,以前的工作只研究了 细胞。将 Cyborg-Cell 方法扩展到致病菌上,可以使我们能够在生物医学应用中利用它们的致病特性。在这里,我们专注于不同的 、 和 菌株。为了合成 Cyborg 病原体,我们首先揭示了不同水凝胶浓度对 Cyborg 病原体代谢、复制和细胞内凝胶化的影响。接下来,我们通过共聚焦显微镜和实时 PCR 证明,Cyborg 病原体被巨噬细胞摄取的程度与野生型病原体相似。最后,我们表明,摄取 Cyborg 病原体的巨噬细胞对野生型病原体表现出相似的表型反应。我们的工作将细胞内水凝胶化方法从实验室的 菌株推广到了细菌病原体。新的 Cyborg 病原体可以应用于从药物输送到免疫治疗的各种生物医学应用中。