Department of Animal Biology, School of Life Sciences, University of Hyderabad, Hyderabad, Telangana, India.
Department of Plant Sciences, School of Life Sciences, University of Hyderabad, Hyderabad, Telangana, India.
Microbiol Spectr. 2024 Sep 3;12(9):e0081724. doi: 10.1128/spectrum.00817-24. Epub 2024 Aug 5.
The discovery of Replication Competent Circular DNA molecules in mammalian cells and tissues is being linked to debilitating diseases, such as multiple sclerosis (MS), bovine spongiform encephalopathy (BSE), and colorectal cancer (CRC). These circular DNA molecules, otherwise known as bovine meat and milk factors (BMMFs) and Slow Progressive Hidden INfections of variable (X) latency (SPHINX), bear significant (80%) sequence similarity with the plasmids of strains. Nanostructures, such as bacterial outer membrane vesicles (OMVs) serve as vehicles for transporting biomolecular cargo and have the potential to facilitate interkingdom lateral mobility of DNA. Strengthening the proposed hypothesis, this study demonstrates that OMVs derived from DS002 carrying four plasmids and genome (pTS236) of phage, AbDs1, successfully reached different parts of the body, including the central nervous system, following the injection of fluorescein isothiocyanate (FITC)-labeled OMVs into experimental mice. Out of the four OMV-associated plasmids, three (pTS4586, pTS9900, and pTS134338) were identified within the lumen, and the fourth one (pTS11291) was found on the surface of OMVs. In addition to the indigenous plasmids, the phage-encoded protein, Orf96, anchored on the surface of the OMVs by establishing a strong interaction with the OMV-associated porin, OmpA. Intriguingly, a subset of labeled OMVs, when incubated with Neuro2A cells, translocated across the membrane and reached to the cytoplasmic space of the cells. Collectively, the experimental evidence presented herein underscores the promising potential of OMVs as vehicles for delivering molecular cargo containing plasmids and phage genomes to diverse mammalian tissues and cells.
Several independent studies have demonstrated the existence of replication competent circular DNA molecules of bacterial and viral origin in mammalian cells and tissues. However, studies about their origin and lateral mobility to mammalian cells are scarce. Our work describes the existence of circular DNA, similar to that of DNA molecules identified in mammalian cells, OMVs derived from soil isolate of DS002. Furthermore, the work also provides visual evidence that demonstrates the passage of labeled OMVs to different organs of experimental mice within hours after intravenously administering OMVs into experimental mice. Some of the labeled OMVs have even crossed the membrane of Neuro2A, suggesting the existence of interkingdom horizontal mobility between bacteria and mammals.
在哺乳动物细胞和组织中发现具有复制能力的环形 DNA 分子与多种衰弱性疾病相关联,如多发性硬化症(MS)、牛海绵状脑病(BSE)和结直肠癌(CRC)。这些环形 DNA 分子,也称为牛肉和牛奶因子(BMMFs)和缓慢进展性隐匿感染的可变(X)潜伏期(SPHINX),与 株的质粒具有显著的(80%)序列相似性。纳米结构,如细菌外膜囊泡(OMVs),可作为运输生物分子货物的载体,并有可能促进 DNA 在不同生物界之间的横向移动。本研究证实了这一假设,表明源自携带四个质粒和噬菌体 AbDs1 的基因组(pTS236)的 DS002 的 OMVs,在将荧光素异硫氰酸酯(FITC)标记的 OMVs注入实验小鼠后,成功到达身体的不同部位,包括中枢神经系统。在与 OMV 相关的四个质粒中,有三个(pTS4586、pTS9900 和 pTS134338)在腔中被识别,而第四个(pTS11291)则在 OMV 表面被发现。除了本土质粒外,噬菌体编码的蛋白 Orf96 通过与 OMV 相关的孔蛋白 OmpA 建立强相互作用,锚定在 OMV 表面。有趣的是,一组标记的 OMVs,当与 Neuro2A 细胞孵育时,穿过膜并到达细胞的细胞质空间。总的来说,本文提供的实验证据强调了 OMV 作为载体的有前途的潜力,可以将含有质粒和噬菌体基因组的分子货物递送到不同的哺乳动物组织和细胞中。
几项独立的研究已经证明了具有细菌和病毒起源的复制能力的环形 DNA 分子在哺乳动物细胞和组织中的存在。然而,关于它们的起源和向哺乳动物细胞的横向移动的研究很少。我们的工作描述了在土壤分离株 DS002 衍生的 OMVs 中存在类似于在哺乳动物细胞中鉴定的 DNA 分子的环形 DNA。此外,该工作还提供了视觉证据,表明在将 OMVs 静脉内给予实验小鼠后数小时内,标记的 OMVs 可以到达实验小鼠的不同器官。一些标记的 OMVs 甚至穿过了 Neuro2A 的膜,这表明细菌和哺乳动物之间存在跨生物界的水平移动。