Institute for Bioscience and Biotechnology Research (IBBR), University of Maryland, College Park, Maryland.
Fischell Department of Bioengineering, University of Maryland, College Park, Maryland.
Biotechnol Bioeng. 2018 Feb;115(2):278-289. doi: 10.1002/bit.26397. Epub 2017 Oct 16.
Antibacterial resistance is an issue of increasing severity as current antibiotics are losing their effectiveness and fewer antibiotics are being developed. New methods for combating bacterial virulence are required. Modulating molecular communication among bacteria can alter phenotype, including attachment to epithelia, biofilm formation, and even toxin production. Intercepting and modulating communication networks provide a means to attenuate virulence without directly interacting with the bacteria of interest. In this work, we target communication mediated by the quorum sensing (QS) bacterial autoinducer-2, AI-2. We have assembled a capsule of biological polymers alginate and chitosan, attached an AI-2 processing kinase, LsrK, and provided substrate, ATP, for enzymatic alteration of AI-2 in culture fluids. Correspondingly, AI-2 mediated QS activity is diminished. All components of this system are "biofabricated"-they are biologically derived and their assembly is accomplished using biological means. Initially, component quantities and kinetics were tested as assembled in microtiter plates. Subsequently, the identical components and assembly means were used to create the "artificial cell" capsules. The functionalized capsules, when introduced into populations of bacteria, alter the dynamics of the AI-2 bacterial communication, attenuating QS activated phenotypes. We envision the assembly of these and other capsules or similar materials, as means to alter QS activity in a biologically compatible manner and in many environments, including in humans.
随着现有抗生素的疗效逐渐减弱,而开发的抗生素却越来越少,细菌的抗药性问题日益严重。我们需要新的方法来对抗细菌的毒性。调节细菌之间的分子通讯可以改变表型,包括与上皮细胞的附着、生物膜的形成,甚至毒素的产生。拦截和调节通讯网络提供了一种在不直接与感兴趣的细菌相互作用的情况下减弱毒性的方法。在这项工作中,我们针对由群体感应(QS)细菌自体诱导物-2(AI-2)介导的通讯进行了研究。我们组装了一个由生物聚合物海藻酸盐和壳聚糖组成的胶囊,附着了一个 AI-2 处理激酶 LsrK,并提供了用于在培养物中酶法改变 AI-2 的底物 ATP。相应地,AI-2 介导的 QS 活性减弱。该系统的所有组件都是“生物制造”的-它们是生物衍生的,其组装是使用生物手段完成的。最初,在微量滴定板中测试了组装好的组件数量和动力学。随后,使用相同的组件和组装方法创建了“人工细胞”胶囊。功能化的胶囊在引入细菌群体时,改变了 AI-2 细菌通讯的动力学,减弱了 QS 激活的表型。我们设想组装这些和其他胶囊或类似材料,作为以生物相容的方式改变 QS 活性的手段,并在许多环境中使用,包括在人类中。