Tashiro Yosuke, Hasegawa Yusuke, Shintani Masaki, Takaki Kotaro, Ohkuma Moriya, Kimbara Kazuhide, Futamata Hiroyuki
Applied Chemistry and Biochemical Engineering Course, Department of Engineering, Graduate School of Integrated Science and Technology, Shizuoka UniversityHamamatsu, Japan.
Graduate School of Science and Technology, Shizuoka UniversityHamamatsu, Japan.
Front Microbiol. 2017 Apr 7;8:571. doi: 10.3389/fmicb.2017.00571. eCollection 2017.
Membrane vesicles (MVs) are secreted from a wide range of microbial species and transfer their content to other cells. Although MVs play critical roles in bacterial communication, whether MVs selectively interact with bacterial cells in microbial communities is unclear. In this study, we investigated the specificity of the MV-cell interactions and evaluated the potential of MVs to target bacterial cells for delivery. MV association with bacterial cells was examined using a fluorescent membrane dye to label MVs. MVs derived from the enterobacterium specifically interacted with cells of the parent strain but interacted less specifically with those of other genera tested in this study. Electron microscopic analyses showed that MVs were not only attached on cells but also fused to them. The interaction energy, which was characterized by hydrodynamic diameter and zeta potential based on the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory, was significant low between MVs and cells in , compared to those between MVs and cells of other genera. Similar specific interaction was also occurred between MVs and cells of six other species belonging to spp. harboring plasmid pBBR1MCS-1 secreted plasmid-containing MVs (p-MVs), and plasmid DNA in p-MVs was transferred to the same species. Moreover, antibiotic-associated MVs enabled effective killing of target species; the survival rate of was lower than those of and in the presence of gentamicin-associated MVs derived from . Altogether, we provide the evidence that MVs selectively interact with target bacterial cells and offer a new avenue for controlling specific bacterial species using bacterial MVs in microbial communities.
膜泡(MVs)由多种微生物分泌,并将其内含物转移到其他细胞中。尽管MVs在细菌通讯中发挥着关键作用,但MVs在微生物群落中是否与细菌细胞选择性相互作用尚不清楚。在本研究中,我们调查了MV-细胞相互作用的特异性,并评估了MVs靶向细菌细胞进行递送的潜力。使用荧光膜染料标记MVs来检测MVs与细菌细胞的结合。源自肠杆菌的MVs与亲本菌株的细胞特异性相互作用,但与本研究中测试的其他属的细胞相互作用特异性较低。电子显微镜分析表明,MVs不仅附着在细胞上,还与它们融合。基于德亚金-朗道-维韦-奥弗贝克(DLVO)理论,通过流体动力学直径和zeta电位表征的相互作用能,在[具体情况未明确,推测可能是特定条件下]MVs与细胞之间显著低于MVs与其他属细胞之间的相互作用能。属于[具体属名未明确] spp.的其他六个物种的MVs与细胞之间也发生了类似的特异性相互作用。携带质粒pBBR1MCS-1的[具体物种未明确]分泌含质粒的MVs(p-MVs),并且p-MVs中的质粒DNA转移到了同一物种。此外,与抗生素相关的MVs能够有效杀死靶标物种;在源自[具体物种未明确]的庆大霉素相关MVs存在的情况下,[具体物种未明确]的存活率低于[其他两个未明确的物种]。总之,我们提供了证据表明MVs与靶标细菌细胞选择性相互作用,并为在微生物群落中使用细菌MVs控制特定细菌物种提供了一条新途径。