Université Lille Nord de France, Lille, France.
PLoS One. 2010 Dec 3;5(12):e14220. doi: 10.1371/journal.pone.0014220.
Pseudomonas aeruginosa is a gram-negative bacterium and an opportunistic pathogen, which causes persisting life-threatening infections in cystic fibrosis (CF) patients. Biofilm mode of growth facilitates its survival in a variety of environments. Most P. aeruginosa isolates, including the non-mucoid laboratory strain PA14, are able to form a thick pellicle, which results in a surface-associated biofilm at the air-liquid (A-L) interface in standing liquid cultures. Exopolysaccharides (EPS) are considered as key components in the formation of this biofilm pellicle. In the non-mucoid P. aeruginosa strain PA14, the "scaffolding" polysaccharides of the biofilm matrix, and the molecules responsible for the structural integrity of rigid A-L biofilm have not been identified. Moreover, the role of LPS in this process is unclear, and the chemical structure of the LPS O-antigen of PA14 has not yet been elucidated.
In the present work we carried out a systematic analysis of cellular and extracellular (EC) carbohydrates of P. aeruginosa PA14. We also elucidated the chemical structure of the LPS O-antigen by chemical methods and 2-D NMR spectroscopy. Our results showed that it is composed of linear trisaccharide repeating units, identical to those described for P. aeruginosa Lanýi type O:2a,c (Lanýi-Bergman O-serogroup 10a, 10c; IATS serotype 19) and having the following structure: -4)-α-L-GalNAcA-(1-3)-α-D-QuiNAc-(1-3)- α-L-Rha-(1-. Furthermore, an EC O-antigen polysaccharide (EC O-PS) and the glycerol-phosphorylated cyclic β-(1,3)-glucans were identified in the culture supernatant of PA14, grown statically in minimal medium. Finally, the extracellular matrix of the thick biofilm formed at the A-L interface contained, in addition to eDNA, important quantities (at least ∼20% of dry weight) of LPS-like material.
We characterized the chemical structure of the LPS O-antigen and showed that the O-antigen polysaccharide is an abundant extracellular carbohydrate of PA14. We present evidence that LPS-like material is found as a component of a biofilm matrix of P. aeruginosa.
铜绿假单胞菌是一种革兰氏阴性细菌和机会性病原体,它会导致囊性纤维化 (CF) 患者持续存在危及生命的感染。生物膜生长模式使其能够在各种环境中存活。包括非粘液性实验室菌株 PA14 在内的大多数铜绿假单胞菌分离株能够形成厚厚的菌膜,从而在静置液体培养物中的气液 (A-L) 界面形成表面相关的生物膜。胞外多糖 (EPS) 被认为是生物膜菌膜形成的关键成分。在非粘液性铜绿假单胞菌菌株 PA14 中,生物膜基质的“支架”多糖以及刚性 A-L 生物膜结构完整性的负责分子尚未被确定。此外,LPS 在这一过程中的作用尚不清楚,PA14 的 LPS O-抗原的化学结构也尚未阐明。
在本工作中,我们对铜绿假单胞菌 PA14 的细胞内和细胞外 (EC) 碳水化合物进行了系统分析。我们还通过化学方法和 2-D NMR 光谱阐明了 LPS O-抗原的化学结构。我们的结果表明,它由线性三糖重复单元组成,与描述的铜绿假单胞菌 Lanýi 型 O:2a,c(Lanýi-Bergman O-血清组 10a、10c;IATS 血清型 19)相同,具有以下结构:-4)-α-L-GalNAcA-(1-3)-α-D-QuiNAc-(1-3)-α-L-Rha-(1-。此外,在 PA14 静态培养于最小培养基时,在培养上清液中鉴定出 EC O-抗原多糖(EC O-PS)和甘油磷酸化环 β-(1,3)-葡聚糖。最后,在气液界面形成的厚生物膜的细胞外基质中,除了 eDNA 外,还含有大量(至少约 20%的干重)类似 LPS 的物质。
我们对 LPS O-抗原的化学结构进行了表征,并表明 O-抗原多糖是 PA14 的一种丰富的细胞外碳水化合物。我们提供的证据表明,LPS 样物质作为铜绿假单胞菌生物膜基质的成分存在。