IBB-Institute for Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, Lisbon, Portugal.
Instituto Gulbenkian de Ciência, Oeiras, Portugal.
J Bacteriol. 2018 Aug 10;200(17). doi: 10.1128/JB.00216-18. Print 2018 Sep 1.
Bacteria from the complex grow in different natural and man-made environments and are feared opportunistic pathogens that cause chronic respiratory infections in cystic fibrosis patients. Previous studies showed that mucoid clinical isolates grown under stress conditions give rise to nonmucoid variants devoid of the exopolysaccharide cepacian. Here, we determined that a major cause of the nonmucoid morphotype involves nonsynonymous mutations and small indels in the gene encoding a response regulator of a two-component regulatory system. In complementation of nonmucoid variants (NMVs) with the native gene restored exopolysaccharide production. The loss of functional OmpR had positive effects on growth, adhesion to lung epithelial cells, and biofilm formation in high-osmolarity medium, as well as an increase in swimming and swarming motilities. In contrast, phenotypes such as antibiotic resistance, biofilm formation at low osmolarity, and virulence in were compromised by the absence of functional OmpR. Transcriptomic studies indicated that loss of the gene affects the expression of 701 genes, many associated with outer membrane composition, motility, stress response, iron acquisition, and the uptake of nutrients, consistent with starvation tolerance. Since the stresses here imposed on may strongly resemble the ones found in the cystic fibrosis (CF) airways and mutations in the gene from longitudinally collected CF isolates have been found, this regulator might be important for the production of NMVs in the CF environment. Within the cystic fibrosis (CF) lung, bacteria experience high-osmolarity conditions due to an ion unbalance resulting from defects in CF transmembrane conductance regulator (CFTR) protein activity in epithelial cells. Understanding how bacterial CF pathogens thrive in this environment might help the development of new therapeutic interventions to prevent chronic respiratory infections. Here, we show that the OmpR response regulator of one of the species found in CF respiratory infections, , is involved in the emergence of nonmucoid colony variants and is important for osmoadaptation by regulating several cell envelope components. Specifically, genetic, phenotypic, genomic, and transcriptomic approaches uncover OmpR as a regulator of cell wall remodeling under stress conditions, with implications in several phenotypes such as exopolysaccharide production, motility, antibiotic resistance, adhesion, and virulence.
来自 复合体的细菌在不同的自然和人为环境中生长,被认为是机会性病原体,可导致囊性纤维化患者的慢性呼吸道感染。先前的研究表明,在应激条件下生长的粘液临床分离株会产生缺乏胞外多糖 Cepacian 的非粘液变体。在这里,我们确定非粘液形态的主要原因涉及编码双组分调节系统反应调节剂的基因中的非同义突变和小插入缺失。在非粘液变体(NMVs)与天然基因的互补中,恢复了胞外多糖的产生。功能性 OmpR 的丧失对高渗透压培养基中的生长、对肺上皮细胞的粘附和生物膜形成以及泳动和群集运动性的增加具有积极影响。相比之下,缺失功能性 OmpR 会损害抗生素耐药性、低渗透压下的生物膜形成和 在 中的毒力等表型。转录组学研究表明, 基因的缺失影响了 701 个基因的表达,其中许多与外膜组成、运动性、应激反应、铁摄取和营养物质摄取有关,与饥饿耐受性一致。由于这里对 施加的压力可能与囊性纤维化(CF)气道中发现的压力非常相似,并且已经在从纵向收集的 CF 分离株中发现了 基因的突变,因此该调节剂可能对 CF 环境中 NMV 的产生很重要。在囊性纤维化(CF)肺部中,由于上皮细胞中 CF 跨膜电导调节剂(CFTR)蛋白活性缺陷导致的离子失衡,细菌会经历高渗透压条件。了解细菌 CF 病原体如何在这种环境中茁壮成长可能有助于开发新的治疗干预措施以预防慢性呼吸道感染。在这里,我们表明,在 CF 呼吸道感染中发现的一种物种 中的 OmpR 反应调节剂参与了非粘液菌落变体的出现,并且通过调节几个细胞包膜成分对渗透压适应很重要。具体来说,遗传、表型、基因组和转录组学方法揭示了 OmpR 是应激条件下细胞壁重塑的调节剂,对几种表型(如胞外多糖产生、运动性、抗生素耐药性、粘附和毒力)具有重要意义。