Leeds Institute for Biomedical and Clinical Sciences, University of Leeds, Leeds LS1 3EX, UK.
Public Health England, Centre for Infections, London NW9 5EQ, UK.
J Med Microbiol. 2014 Apr;63(Pt 4):489-503. doi: 10.1099/jmm.0.070409-0. Epub 2014 Jan 20.
The soluble proteome of three Clostridium difficile strains of varying pathogenic potential, designated B-1, Tra 5/5 and 027 SM, were compared using differential in-gel electrophoresis in which the proteins of each strain were labelled with CyDyes. This enabled visual inspection of the 2D profiles of strains and identification of differentially expressed proteins using image analysis software. Unlabelled protein reference maps of the predominant proteins were then generated for each strain using 2D gel electrophoresis followed by protein sequencing of each spot using a Reflectron matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometer. Increased coverage of the proteome was achieved using 1D gel electrophoresis in a bottom-up approach using LC-MS/MS of 1 cm gel slices. A total of 888 different proteins were detected by comparative analysis of isolates grown in parallel for 64 h on blood agar plates. Of these, only 38 % were shared between all isolates. One hundred and ten proteins were identified as showing ≥2-fold difference in expression between strains. Differential expression was shown in a number of potential virulence and colonization factors. Toxin B was detected in the more virulent strains B-1 and 027 SM, but not in the lower virulent strain Tra 5/5, despite all strains possessing an intact pathogenicity locus. The S-layer protein (Cwp2) was identified in strains 027 SM and Tra 5/5 but not strain B-1, and differences in the post-translational modification of SlpA were noted for strain B-1. The variant S-layer profile of strain B-1 was confirmed by genomic comparison, which showed a 58 kb insertion in the S-layer operon of strain B-1. Differential post-translation modification events were also noted in flagellar proteins, thought to be due to differential glycosylation. This study highlights genomic and proteomic variation of different Clostridium difficile strains and suggests a number of factors may play a role in mediating the varying virulence of these different strains.
比较了三种不同致病潜能的艰难梭菌(Clostridium difficile)菌株 B-1、Tra 5/5 和 027 SM 的可溶性蛋白质组,使用差异凝胶电泳(differential in-gel electrophoresis)对每种菌株的蛋白质进行 CyDyes 标记。这使得可以通过图像分析软件观察菌株的 2D 图谱并鉴定差异表达的蛋白质。然后使用 2D 凝胶电泳为每种菌株生成主要蛋白质的未标记蛋白质参考图谱,然后使用反射式基质辅助激光解吸/电离飞行时间(matrix-assisted laser desorption/ionization time-of-flight,MALDI-TOF)质谱仪对每个斑点的蛋白质进行测序。通过使用 1D 凝胶电泳进行自上而下的方法,使用 1 cm 凝胶切片的 LC-MS/MS,实现了蛋白质组的更高覆盖率。在血琼脂平板上平行培养 64 小时后,比较分析共检测到 888 种不同的蛋白质。其中,只有 38%在所有分离株中共享。110 种蛋白质被鉴定为在菌株之间的表达差异≥2 倍。在一些潜在的毒力和定植因子中显示出差异表达。毒素 B 在更具毒性的菌株 B-1 和 027 SM 中检测到,但在毒性较低的菌株 Tra 5/5 中未检测到,尽管所有菌株都具有完整的致病基因座。在菌株 027 SM 和 Tra 5/5 中鉴定到 S-层蛋白(Cwp2),但在菌株 B-1 中未鉴定到,并且注意到菌株 B-1 中 SlpA 的翻译后修饰存在差异。通过基因组比较证实了菌株 B-1 的变体 S-层图谱,该图谱显示菌株 B-1 的 S-层操纵子中有 58 kb 的插入。在鞭毛蛋白中也注意到差异的翻译后修饰事件,这被认为是由于差异的糖基化。本研究强调了不同艰难梭菌菌株的基因组和蛋白质组的变异,并提出了一些因素可能在调节这些不同菌株的不同毒力方面发挥作用。