Literature DB >> 24445512

Comparative proteomic analysis of Clostridium difficile isolates of varying virulence.

C H Chilton1, S E Gharbia2, M Fang2, R Misra2, I R Poxton3, S P Borriello4, H N Shah2.   

Abstract

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.

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Year:  2014        PMID: 24445512     DOI: 10.1099/jmm.0.070409-0

Source DB:  PubMed          Journal:  J Med Microbiol        ISSN: 0022-2615            Impact factor:   2.472


  5 in total

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Journal:  Gut Pathog       Date:  2017-08-14       Impact factor: 4.181

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3.  Investigation of metabolic crosstalk between host and pathogenic Clostridioides difficile via multiomics approaches.

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Journal:  Front Bioeng Biotechnol       Date:  2022-09-02

4.  A Metabolic Labeling Strategy for Relative Protein Quantification in Clostridioides difficile.

Authors:  Anke Trautwein-Schult; Sandra Maaß; Kristina Plate; Andreas Otto; Dörte Becher
Journal:  Front Microbiol       Date:  2018-10-16       Impact factor: 5.640

5.  Notch3 promotes 3T3-L1 pre-adipocytes differentiation by up-regulating the expression of LARS to activate the mTOR pathway.

Authors:  Yuxian Guo; Junyu Tan; Wei Xiong; Shuzhao Chen; Liping Fan; Yaochen Li
Journal:  J Cell Mol Med       Date:  2019-11-21       Impact factor: 5.310

  5 in total

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