经口递送实现肠道细菌原位重编程。
In situ reprogramming of gut bacteria by oral delivery.
机构信息
Department of Biological Sciences, Virginia Tech, Blacksburg, VA, 24061, USA.
Department of Systems Biology, Harvard Medical School, Boston, MA, 02115, USA.
出版信息
Nat Commun. 2020 Oct 6;11(1):5030. doi: 10.1038/s41467-020-18614-2.
Abundant links between the gut microbiota and human health indicate that modification of bacterial function could be a powerful therapeutic strategy. The inaccessibility of the gut and inter-connections between gut bacteria and the host make it difficult to precisely target bacterial functions without disrupting the microbiota and/or host physiology. Herein we describe a multidisciplinary approach to modulate the expression of a specific bacterial gene within the gut by oral administration. We demonstrate that an engineered temperate phage λ expressing a programmable dCas9 represses a targeted E. coli gene in the mammalian gut. To facilitate phage administration while minimizing disruption to host processes, we develop an aqueous-based encapsulation formulation with a microbiota-based release mechanism and show that it facilitates oral delivery of phage in vivo. Finally we combine these technologies and show that bacterial gene expression in the mammalian gut can be precisely modified in situ with a single oral dose.
肠道微生物群与人类健康之间存在着丰富的联系,这表明改变细菌功能可能是一种强大的治疗策略。由于肠道的不可及性以及肠道细菌与宿主之间的相互联系,在不破坏微生物群和/或宿主生理机能的情况下,精确靶向细菌功能是具有挑战性的。在这里,我们描述了一种通过口服给药来调节肠道内特定细菌基因表达的多学科方法。我们证明,表达可编程 dCas9 的工程化温和噬菌体 λ 在哺乳动物肠道中抑制靶向大肠杆菌基因的表达。为了便于噬菌体给药,同时最大限度地减少对宿主过程的干扰,我们开发了一种基于水的包封制剂,具有基于微生物群的释放机制,并证明它有利于噬菌体在体内的口服递送。最后,我们将这些技术结合起来,证明可以通过单次口服剂量在体内精确修饰哺乳动物肠道中的细菌基因表达。