C. difficile toxin A (TcdA)

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The large clostridial cytotoxins (LCT) are a family of structurally and functionally related exotoxins from Clostridium difficile (toxins A and B [also termed TcdA and TcdB, respectively), C. sordellii (lethal and hemorrhagic toxin) and C. novyi (alpha-toxin). The LCTs are major virulence factors, which in addition to their in vivo effects, are cytotoxic to cultured cell lines, causing reorganization of the cytoskeleton accompanied by morphological changes[1]. The LCTs are single-chain protein toxins, comprising three domains: receptor-binding, translocation and catalysis, which mediate cell entry via receptor-mediated endocytosis, translocation into the cytoplasm, and enzymatic cytotoxic activity, respectively. Enzymatic activity involves transfer of a glucosyl moiety from UDP-glucose (or the N-acetyl-glucosaminyl moiety from UDP-GlcNAc in the case of alpha toxin) to a conserved threonine within the effector regions of the intracellular Rho and Ras GTPases[1]. The C-terminal receptor-binding domain comprises up to one third of the LCT molecule, and contains repetitive peptide elements called combined repetitive oligopetides (CROPs). The repeating units binding regions of certain streptococcal glycosyltransferases[1].

TcdA is the better characterized of the two LCTs produced by C. difficile. Collectively, TcdA and TcdB are directly responsible for the increasingly common and serious human gastrointestinal disease caused when antibiotic treatment enables C. difficile to out-compete commensal gut microflora. Recently, the crystal structure of a C-terminal fragment of TcdA has been solved, revealing a solenoid-like structure, which consists of 32 short repeats with 15–21 residues and seven long repeats with 30 residues[2]. Solenoid structures are often found in bacterial surface proteins, and their extended surface allows protein–protein or protein–carbohydrate interactions. TcdA is known to bind to Galα1-3Galβ1-4GlcNAc- glycans, although this structure is not present in humans. However, it is also known to recognize a variety of other structures with a Galβ[1→4]GlcNAcβ- backbone, including the fucosylated blood group antigens Lewisx and Lewisy, both of which are present in human intestinal epithelium[3]. Clearly, a better understanding of the identity/structure of the human receptor(s) for these toxins will facilitate design of novel therapeutics capable of blocking toxin binding. Glycan array analysis conducted by the CFG showed that TcdA bound most strongly to glycans terminating in Galβ1-3[Fucα1-4]GlcNAcβ1-3Galβ1-4-GlcNAc-, which mimics the blood group antigen Lewisa; other bound structures included Galα1-3[Fucα1-4]GlcNAcβ1-3Galβ1-4GlcNAcβ-, NeuAcα2-3Galβ1-3GlcNAcβ1-3Galβ1-4GlcNAcβ-, and Fucαa1-2[GalNAcαa1-3]Galβ1-4GlcNAcβ1-3Galβb1-4GlcNAcβ-.


CFG Participating Investigators contributing to the understanding of this paradigm

Progress toward understanding this GBP paradigm

Carbohydrate ligands

Cellular expression


Biological roles of GBP-ligand interaction

CFG resources used in investigations

The best examples of CFG contributions to this paradigm are described below, with links to specific data sets. For a complete list of CFG data and resources relating to this paradigm, see the [XXX CFG database search results for XXX].

Glycan profiling

Glycogene microarray

Knockout mouse lines

Glycan array

Related GBPs



The CFG is grateful to the following PIs for their contributions to this wiki page:

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