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Sequencing and analysis of the gene encoding the α-toxin of Clostridium novyi proves its homology to toxins A and B of Clostridium difficile

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Abstract

A library of total Clostridium novyi DNA was established and screened for the α-toxin gene (tcnα) by hybridization with oligonucleotides derived from a partial N-terminal sequence and by using specific antisera. Overlapping subgenic tcnα fragments were isolated and subsequently the total sequence of tcnα was determined. The 6534 nucleotide open reading frame encodes a polypeptide of Mr 250 166 and pI 5.9. The N-terminal α-toxin (Tcnα) sequence MLITREQLMKIASIP determined by Edman degradation confirmed the identity of the reading frame and the assignment of the translation start point. The toxin is not modified posttranslationally at its N-terminus nor does it consist of different subunits. Overall the amino acid sequence shows 48% homology between the Tcnα and both toxins A (TcdA) and B (TcdB) of Clostridium difficile. The C-terminal 382 residues of Tcnα constitute a repetitive domain similar to those reported for TcdA and TcdB of C. difficile. The individual repeat motifs of these three toxins consist of oligopeptides some 19–52 amino acids in length, arranged in four to five different groups. Genetic, biochemical and pharmacological data thus confirm that the three toxins belong to one subgroup, designated large clostridial cytotoxins (LCT). Further definition of their structure and detailed molecular action should allow the LCTs to be used tools for the analysis of microfilament assembly and function.

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References

  • Aktories K, Bärmann M, Ohishi I, Tsuyama S, Jakobs KH, Habermann E (1986) Botulinum C2 toxin ADP-ribosylates actin. Nature 322:390–392

    Google Scholar 

  • Ball DW, van Tassell RL, Roberts MD, Hahn PE, Lyerly DM, Wilkins TD (1993) Purification and characterization of alpha-toxin produced by Clostridium novyi type A. Infect Immun 61:2913–2918

    Google Scholar 

  • Banas JA, Russell RR, Ferretti JJ (1990) Sequence analysis of the gene for the glucan-binding protein of Streptococcus mutans Ingbritt. Infect Immun 58:667–673

    Google Scholar 

  • Bette P, Frevert J, Mauler F, Suttorp N, Habermann E (1989) Pharmacological and biochemical studies of cytotoxicity of Clostridium novyi type A alpha-toxin. Infect Immun 57:2507–2513

    Google Scholar 

  • Bette P, Oksche A, Mauler F, von Eichel-Streiber C, Popoff MR, Habermann E (1991) A comparative biochemical, pharmacological and immunological study of Clostridium novyi alpha-toxin, C. difficile toxin B and C. sordellii lethal toxin. Toxicon 29:877–887

    Google Scholar 

  • Binz T, Kurazono H, Wille M, Frevert J, Wernars K, Niemann H (1990) The complete sequence of botulinum neurotoxin A and comparison with other clostridial neurotoxins. J Biol Chem 265:9153–9158

    Google Scholar 

  • Chardin P, Boquet P, Madaule P, Popoff MR, Rubin EJ, Gill DM (1989) The mammalian G protein rhoC is ADP-ribosylated by Clostridium botulinum exoenzyme C3 and affects actin microfilaments in Vero cells. EMBO J 8:1087–1092

    Google Scholar 

  • von Eichel-Streiber C (1993) Molecular biology of the Clostridium difficile toxins In: Sebald M (ed) Genetics and molecular biology of the anaerobic bacteria. Springer-Verlag, New York, pp 264–289

    Google Scholar 

  • von Eichel-Streiber C, Sauerborn M (1990) Clostridium difficile toxin A carries a C-terminal repetitive structure homologous to the carbohydrate binding region of streptococcal glycosyltransferases. Gene 96:107–113

    Google Scholar 

  • von Eichel-Streiber C, Harperath U, Bosse D, Hadding U (1987) Purification of two high molecular weight toxins of Clostridium difficile which are antigenically related. Microbiol Pathogen 2:307–318

    Google Scholar 

  • von Eichel-Streiber C, Suckau D, Wachter M, Hadding U (1989) Cloning and characterization of overlapping DNA fragments of the toxin A gene of Clostridium difficile. J Gen Microbiol 135:55–64

    Google Scholar 

  • von Eichel-Streiber C, Laufenberg Feldmann R, Sartingen S, Schulze J, Sauerborn M (1992a) Comparative sequence analysis of the Clostridium difficile toxins A and B. Mol Gen Genet 233:260–268

    Google Scholar 

  • von Eichel-Streiber C, Sauerborn M, Kuramitsu HK (1992b) Evidence for a modular structure of the homologous repetitive C-terminal carbohydrate-binding sites of Clostridium difficile toxins and Streptococcus mutans glucosyltransferases. J Bacteriol 174:6707–6710

    Google Scholar 

  • Eichel-Streiber C, Meyer zu Heringdorf D, Habermann E, Sartingen S (1994) Closing in on the toxic domain through analysis of a mutant Clostridium difficile cytotoxin. B. Mol Microbiol, in press

  • Eklund MW (1993) The role of bacteriophages and plasmids in the production of toxins and other biologically active substances by Clostridium botulinum and Clostridium novyi. In: Sebald M (ed) Genetics and molecular biology of the anaerobic bacteria. Springer-Verlag, New York, pp 179–194

    Google Scholar 

  • Florin I (1991) Isolation of a fibroblast mutant resistant to Clostridium difficile toxins A and B. Microbial Pathogen 11:337–346

    Google Scholar 

  • Florin I, Thelestam M (1991) ADP-ribosylation in Clostridium difficile toxin-treated cells is not related to cytopathogenicity of toxin B. Biochim Biophys Acta 1091:51–54

    Google Scholar 

  • Hatheway CL (1990) Toxigenic clostridia. Clin Microbiol Rev 3:66–98

    Google Scholar 

  • Izumi N, Kondo H, Ohishi I, Sakaguchi G (1983) Purification and characterization of alpha-toxin of Clostridium oedematiens type A. Jpn J Med Sci Biol 36:135–146

    Google Scholar 

  • Just I, Fritz G, Aktories K, Giry M, Popoff MR, Boquet P, Hegenbarth S, von Eichel-Streiber C (1994) Clostridium difficile toxin B acts on small GTP-binding protein Rho. J Biol Chem 269:10706–10712

    Google Scholar 

  • Kistner A, Sanders D, Habermann E (1993) Disulfide formation in reduced tetanus toxin by thioredoxin: the pharmacological role of the interchain covalent and noncovalent bonds. Toxicon 31:1423–1434

    Google Scholar 

  • Kyte J, Doolittle RF (1982) A simple method for displaying the hydropathic character of a protein. J Mol Biol 157:105–132

    Google Scholar 

  • Martinez RD, Wilkins TD (1988) Purification and characterization of Clostridium sordellii hemorrhagic toxin and cross-reactivity with Clostridium difficile toxin A (enterotoxin). Infect Immun 56:1215–1221

    Google Scholar 

  • Müller H, von Eichel-Streiber C, Habermann E (1992) Morphological changes of cultured endothelial cells after microinjection of toxins that act on the cytoskeleton. Infect Immun 60:3007–3010

    Google Scholar 

  • Oksche A, Nakov R, Habermann E (1992) Morphological and biochemical study of cytoskeletal changes in cultured cells afterextracellular application of Clostridium novyi alpha-toxin. Infect Immun 60:3002–3006

    Google Scholar 

  • Oswald E, Sugai M, Labigne A, Wu HC, Fiorentim C, Boquet P, O'Brien AD (1994) Cytotoxic necrotizing factor type 2 produced by virulent Escherichia coli modifies the small GTP-binding proteins Rho involved in assembly of actin stress fibers. Proc Natl Acad Sci USA 91:3814–3818

    Google Scholar 

  • Ridley AJ, Hall A (1992) The small GTP-binding protein rho regulates the assembly of focal adhesions and actin stress fibers in response to growth factors. Cell 70:389–399

    Google Scholar 

  • Rolfe RD, Song W (1993) Purification of a functional receptor for Clostridium difficile toxin A from intestinal brush border membranes of infant hamsters. Clin Infect Dis 16 [Suppl 4]:S219–27

    Google Scholar 

  • Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Sauerborn M, Hegenbarth S, Laufenberg-Feldmann R, Leukel P, von Eichel-Streiber C (1994) Monoclonal antibodies discriminating between Clostridium difficile toxins A and B. In: Freer J, Aitken R, Alouf JE, Boulnois GJ, Falmagne P, Fehrenbach FJ, Montecucco C, Piemont Y, Rappuoli R, Wadstöm T and Witholt B (eds) Bacterial protein toxins. Gustav Fischer, Stuttgart Jena New York, Zentralbl Bakteriol Suppl 24:510–511

    Google Scholar 

  • Schiavo G, Benfenati F, Poulain B, Rossetto O, Polverino de Laureto P, DasGupta BR, Montecucco C (1992) Tetanus and botulinum-B neurotoxins block neurotransmitter release by proteolytic cleavage of synaptobrevin. Nature, 359:832–835

    Google Scholar 

  • Selzer J, Just I, Habermann E, Aktories K (1994) A cytosolic factor is involved in the action of Clostridium novyi α-toxin on the GTP-binding protein Rho. Naunyn-Schmied Arch Pharmacol 349 Suppl:R 15

    Google Scholar 

  • Tabor S, Richardson CC (1987) DNA sequence analysis with a modified bacteriophage T7 DNA polymerase. Proc Natl Acad Sci USA 84:4767–4771

    Google Scholar 

  • Thelestam M, Gross R (1990) Toxins acting on the cytoskeleton. In: Shier WT, Mebs D (eds) Handbook of toxinology. Marcel Dekker, New York and Basel, pp 423–492

    Google Scholar 

  • Tucker KD, Wilkins TD (1991) Toxin A of Clostridium difficile binds to the human carbohydrate antigens I, X, and Y. Infect Immun 59:73–78

    Google Scholar 

  • Wren BW (1991) A family of clostridial and streptococcal ligand-binding proteins with conserved C-terminal repeat sequences. Mol Microbiol 5:797–803

    Google Scholar 

  • Yanisch-Perron C, Vieira J, Messing J (1985) Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene 33:103–119

    Google Scholar 

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Communicated by W. Goebel

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Hofmann, F., Herrmann, A., Habermann, E. et al. Sequencing and analysis of the gene encoding the α-toxin of Clostridium novyi proves its homology to toxins A and B of Clostridium difficile . Molec. Gen. Genet. 247, 670–679 (1995). https://doi.org/10.1007/BF00290398

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