Department of Biological Sciences, Binghamton University, Binghamton, New York, USA.
Binghamton Biofilm Research Center, Binghamton University, Binghamton, New York, USA.
Sci Rep. 2018 Jun 29;8(1):9873. doi: 10.1038/s41598-018-28042-4.
Delivery of cargo to target cells is fundamental to bacterial competitiveness. One important but poorly understood system, ubiquitous among Gram-negative organisms, involves packaging cargo into outer membrane vesicles (OMVs). These biological nanoparticles are involved in processes ranging from toxin delivery to cell-cell communication. Despite this, we know comparatively little about how OMVs are formed. Building upon the discovery that the Pseudomonas Quinolone Signal (PQS) stimulates OMV biogenesis in Pseudomonas aeruginosa, we proposed a model where PQS interacts with the outer membrane to induce curvature and ultimately OMV formation. Though this model is well supported in P. aeruginosa, it remained unclear whether other organisms produce similar compounds. Here we describe the development of a tightly controlled experimental system to test the interaction of bacterially-produced factors with target cells. Using this system, we show that multiple species respond to PQS by increasing OMV formation, that PQS accumulates in the induced vesicles, and that other bacteria secrete OMV-promoting factors. Analysis of induced vesicles indicates that recipient-mediated mechanisms exist to control vesicle size and that relatedness to the producer organism can dictate susceptibility to OMV-inducing compounds. This work provides evidence that small molecule induced OMV biogenesis is a widely conserved process and that cross-talk between systems may influence OMV production in neighboring bacteria.
货物递送到靶细胞是细菌竞争力的基础。有一个重要但尚未被充分理解的系统,在革兰氏阴性生物中普遍存在,涉及将货物包装到外膜囊泡(OMV)中。这些生物纳米颗粒参与了从毒素输送到细胞间通讯的各种过程。尽管如此,我们对 OMV 的形成方式知之甚少。在发现假单胞菌喹诺酮信号(PQS)刺激铜绿假单胞菌中 OMV 的生物发生的基础上,我们提出了一个模型,其中 PQS 与外膜相互作用诱导曲率,最终形成 OMV。虽然这个模型在铜绿假单胞菌中得到了很好的支持,但仍不清楚其他生物体是否产生类似的化合物。在这里,我们描述了一个严格控制的实验系统的开发,以测试细菌产生的因素与靶细胞的相互作用。使用这个系统,我们表明,多种物种通过增加 OMV 的形成来响应 PQS,PQS 在诱导的囊泡中积累,并且其他细菌分泌促进 OMV 的因子。对诱导的囊泡的分析表明,存在受体会介导的机制来控制囊泡的大小,并且与生产者生物体的亲缘关系可以决定对 OMV 诱导化合物的敏感性。这项工作提供了证据表明,小分子诱导的 OMV 生物发生是一个广泛保守的过程,并且系统之间的串扰可能会影响邻近细菌中 OMV 的产生。