Literature DB >> 8361360

Lactococcus lactis: high-level expression of tetanus toxin fragment C and protection against lethal challenge.

J M Wells1, P W Wilson, P M Norton, M J Gasson, R W Le Page.   

Abstract

To determine if the food-grade bacterium Lactococcus lactis holds promise as a vaccine antigen delivery vector we have investigated whether this bacterium can be made to produce high levels of a heterologous protein antigen. A regulated expression system has been developed which may be generally suitable for the expression of foreign antigens (and other proteins) in L. lactis. The system utilizes the fast-acting T7 RNA polymerase to transcribe target genes, and provides the first example of the successful use of this polymerase in a Gram-positive bacterium. When the performance of the expression system was characterized using tetanus toxin fragment C (TTFC) up to 22% of soluble cell protein was routinely obtained as TTFC. Mice immunized subcutaneously with L. lactis expressing TTFC were protected from lethal challenge with tetanus toxin. These results show for the first time that L. lactis is able to express substantial quantities of a heterologous protein antigen and that this organism can present this antigen to the immune system in an immunogenic form.

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Year:  1993        PMID: 8361360     DOI: 10.1111/j.1365-2958.1993.tb01660.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  57 in total

1.  Surface expression of the conserved C repeat region of streptococcal M6 protein within the Pip bacteriophage receptor of Lactococcus lactis.

Authors:  B L Geller; N Wade; T D Gilberts; D E Hruby; R Johanson; L Topisirovic
Journal:  Appl Environ Microbiol       Date:  2001-12       Impact factor: 4.792

2.  Expression of the Staphylococcus hyicus lipase in Lactococcus lactis.

Authors:  S Drouault; G Corthier; S D Ehrlich; P Renault
Journal:  Appl Environ Microbiol       Date:  2000-02       Impact factor: 4.792

3.  Induction of mucosal immune response after intranasal or oral inoculation of mice with Lactococcus lactis producing bovine beta-lactoglobulin.

Authors:  J M Chatel; P Langella; K Adel-Patient; J Commissaire; J M Wal; G Corthier
Journal:  Clin Diagn Lab Immunol       Date:  2001-05

4.  Rapid and Efficient Purification Method for Small, Hydrophobic, Cationic Bacteriocins: Purification of Lactococcin B and Pediocin PA-1.

Authors:  K Venema; M L Chikindas; J Seegers; A J Haandrikman; K J Leenhouts; G Venema; J Kok
Journal:  Appl Environ Microbiol       Date:  1997-01       Impact factor: 4.792

5.  Cell surface-exposed tetanus toxin fragment C produced by recombinant Bacillus anthracis protects against tetanus toxin.

Authors:  S Mesnage; M Weber-Levy; M Haustant; M Mock; A Fouet
Journal:  Infect Immun       Date:  1999-09       Impact factor: 3.441

6.  Protective antigen-mediated antibody response against a heterologous protein produced in vivo by Bacillus anthracis.

Authors:  F Brossier; M Weber-Levy; M Mock; J C Sirard
Journal:  Infect Immun       Date:  2000-10       Impact factor: 3.441

7.  Molecular characterization of a phage-inducible middle promoter and its transcriptional activator from the lactococcal bacteriophage phi31.

Authors:  S A Walker; T R Klaenhammer
Journal:  J Bacteriol       Date:  1998-02       Impact factor: 3.490

Review 8.  Progress in the development of Lactococcus lactis as a recombinant mucosal vaccine delivery system.

Authors:  P M Norton; R W Le Page; J M Wells
Journal:  Folia Microbiol (Praha)       Date:  1995       Impact factor: 2.099

9.  TetR is a positive regulator of the tetanus toxin gene in Clostridium tetani and is homologous to botR.

Authors:  J C Marvaud; U Eisel; T Binz; H Niemann; M R Popoff
Journal:  Infect Immun       Date:  1998-12       Impact factor: 3.441

10.  Ability of Lactococcus lactis to export viral capsid antigens: a crucial step for development of live vaccines.

Authors:  Yakhya Dieye; Arjan J W Hoekman; Florence Clier; Vincent Juillard; Hein J Boot; Jean-Christophe Piard
Journal:  Appl Environ Microbiol       Date:  2003-12       Impact factor: 4.792

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