Institut Pasteur, Genetics of Biofilms Laboratory, Paris, France.
Institut Pasteur, Genetics of Biofilms Laboratory, Paris, France
mBio. 2018 Aug 21;9(4):e01415-18. doi: 10.1128/mBio.01415-18.
Biofilms are often described as protective shelters that preserve bacteria from hostile surroundings. However, biofilm bacteria are also exposed to various stresses and need to adjust to the heterogeneous physicochemical conditions prevailing within biofilms. In Gram-negative bacteria, such adaptations can result in modifications of the lipopolysaccharide, a major component of the outer membrane characterized by a highly dynamic structure responding to environmental changes. We previously showed that Gram-negative biofilm bacteria undergo an increase in lipid A palmitoylation mediated by the PagP enzyme, contributing to increased resistance to host defenses. Here we describe a regulatory pathway leading to transcriptional induction of in response to specific conditions created in the biofilm environment. We show that expression is induced via the Rcs envelope stress system independently of the Rcs phosphorelay cascade and that it requires the GadE auxiliary regulator. Moreover, we identify an increase in osmolarity (i.e., ionic stress) as a signal able to induce expression in an RcsB-dependent manner. Consistently, we show that the biofilm is a hyperosmolar environment and that RcsB-dependent induction can be dampened in the presence of an osmoprotectant. These results provide new insights into the adaptive mechanisms of bacterial differentiation in biofilm. The development of the dense bacterial communities called biofilms creates a highly heterogeneous environment in which bacteria are subjected to a variety of physicochemical stresses. We investigated the mechanisms of a widespread and biofilm-associated chemical modification of the lipopolysaccharide (LPS), a major component of all Gram-negative bacterial outer membranes. This modification corresponds to the incorporation, mediated by the enzyme PagP, of a palmitate chain into lipid A (palmitoylation) that reduces bacterial recognition by host immune responses. Using biochemical and genetic approaches, we demonstrate that a significant part of biofilm-associated lipid A palmitoylation is triggered upon induction of transcription by the hyperosmolar biofilm environment. induction is regulated by RcsB, the response regulator of the Rcs stress response pathway, and is not observed under planktonic conditions. Our report provides new insights into how physiological adaptations to local biofilm microenvironments can contribute to decreases in susceptibility to antimicrobial agents and host immune defenses.
生物膜通常被描述为保护细菌免受恶劣环境影响的庇护所。然而,生物膜中的细菌也会面临各种压力,并需要适应生物膜内存在的异质物理化学条件。在革兰氏阴性菌中,这种适应性可以导致脂多糖( outer membrane 的主要成分)发生修饰,其结构高度动态,能响应环境变化。我们之前曾表明,革兰氏阴性生物膜细菌中 PagP 酶介导的脂酰化修饰会增加,从而增加对宿主防御的抵抗力。在这里,我们描述了一种调节途径,该途径可导致在生物膜环境中产生特定条件时, 基因的转录诱导。我们发现, 基因的表达是通过 Rcs 包膜应激系统诱导的,而与 Rcs 磷酸传递级联反应无关,并且它需要辅助调节因子 GadE。此外,我们发现渗透压(即离子应激)的增加可以作为一种信号,以 RcsB 依赖的方式诱导 基因的表达。一致地,我们表明生物膜是一种高渗环境,并且在存在渗透压保护剂的情况下,RcsB 依赖的 诱导可以被抑制。这些结果为细菌在生物膜中分化的适应机制提供了新的见解。被称为生物膜的密集细菌群落的发展创造了一个高度异质的环境,其中细菌会受到各种物理化学压力的影响。我们研究了 LPS(所有革兰氏阴性菌外膜的主要成分)的一种广泛存在且与生物膜相关的化学修饰的机制。这种修饰对应于由 PagP 酶介导的将棕榈酸链掺入脂质 A(棕榈酰化),从而减少细菌被宿主免疫反应识别。使用生化和遗传方法,我们证明了由高渗透压生物膜环境诱导的转录诱导会触发生物膜相关的脂酰化的很大一部分。 基因的转录是由 RcsB 调节的,RcsB 是 Rcs 应激反应途径的反应调节因子,并且在浮游状态下观察不到。我们的报告提供了新的见解,即对局部生物膜微环境的生理适应如何有助于降低对抗菌剂和宿主免疫防御的敏感性。