Department of Infectious Diseases, College of Veterinary Medicine, University of Georgiagrid.213876.9, Athens, Georgia, USA.
Department of Molecular Biology and Laboratory for Molecular Infection Medicine Sweden, Umeå Centre for Microbial Research, Umeå University, Umeå, Sweden.
mBio. 2021 Dec 21;12(6):e0309921. doi: 10.1128/mBio.03099-21. Epub 2021 Nov 30.
Gram-negative bacteria resist external stresses due to cell envelope rigidity, which is provided by two membranes and a peptidoglycan layer. The outer membrane (OM) surface contains lipopolysaccharide (LPS; contains O-antigen) or lipooligosaccharide (LOS). LPS/LOS are essential in most Gram-negative bacteria and may contribute to cellular rigidity. Acinetobacter baumannii is a useful tool for testing these hypotheses as it can survive without LOS. Previously, our group found that strains with naturally high levels of penicillin binding protein 1A (PBP1A) could not become LOS deficient unless the gene encoding it was deleted, highlighting the relevance of peptidoglycan biosynthesis and suggesting that high PBP1A levels were toxic during LOS deficiency. Transposon sequencing and follow-up analysis found that axial peptidoglycan synthesis by the elongasome and a peptidoglycan recycling enzyme, ElsL, were vital in LOS-deficient cells. The toxicity of high PBP1A levels during LOS deficiency was clarified to be due to a negative impact on elongasome function. Our data suggest that during LOS deficiency, the strength of the peptidoglycan specifically imparted by elongasome synthesis becomes essential, supporting that the OM and peptidoglycan contribute to cell rigidity. Gram-negative bacteria have a multilayered cell envelope with a layer of cross-linked polymers (peptidoglycan) sandwiched between two membranes. Peptidoglycan was long thought to exclusively provide rigidity to the cell providing mechanical strength. Recently, the most outer membrane of the cell was also proposed to contribute to rigidity due to properties of a unique molecule called lipopolysaccharide (LPS). LPS is located on the cell surface in the outer membrane and is typically required for growth. By using Acinetobacter baumannii, a Gram-negative bacterium that can grow without LPS, we found that key features of the peptidoglycan structure also become essential. This finding supports that both the outer membrane and peptidoglycan contribute to cell rigidity.
革兰氏阴性菌由于细胞包膜的刚性而抵抗外部压力,这种刚性由两层膜和一层肽聚糖层提供。外膜 (OM) 表面含有脂多糖 (LPS;含有 O-抗原) 或脂寡糖 (LOS)。LPS/LOS 在大多数革兰氏阴性菌中是必不可少的,可能有助于细胞刚性。鲍曼不动杆菌是测试这些假设的有用工具,因为它可以在没有 LOS 的情况下存活。以前,我们的小组发现,自然高水平青霉素结合蛋白 1A (PBP1A) 的菌株除非删除其编码基因,否则不能成为 LOS 缺陷型,这突出了肽聚糖生物合成的相关性,并表明在 LOS 缺陷型时高水平的 PBP1A 是有毒的。转座子测序和后续分析发现,伸长体的轴向肽聚糖合成和肽聚糖再循环酶 ElsL 对 LOS 缺陷型细胞至关重要。在 LOS 缺陷型时高水平的 PBP1A 的毒性被阐明是由于对伸长体功能的负面影响。我们的数据表明,在 LOS 缺陷型时,伸长体合成赋予的肽聚糖的强度变得至关重要,支持 OM 和肽聚糖有助于细胞刚性。革兰氏阴性菌的细胞包膜具有多层结构,一层交联聚合物(肽聚糖)夹在两层膜之间。长期以来,人们一直认为肽聚糖仅为细胞提供刚性,提供机械强度。最近,由于一种称为脂多糖 (LPS) 的独特分子的特性,细胞的最外层膜也被认为有助于刚性。LPS 位于外膜的细胞表面,通常是生长所必需的。通过使用革兰氏阴性菌鲍曼不动杆菌,一种可以在没有 LPS 的情况下生长的细菌,我们发现肽聚糖结构的关键特征也变得必不可少。这一发现支持了外膜和肽聚糖都有助于细胞刚性。